Page last updated: 2024-10-17

creatine and Disease Exacerbation

creatine has been researched along with Disease Exacerbation in 132 studies

Research Excerpts

ExcerptRelevanceReference
"To investigate whether creatine administration could slow progressive functional decline in adults with early symptoms of Huntington disease."9.24The CREST-E study of creatine for Huntington disease: A randomized controlled trial. ( Bredlau, AL; Hersch, SM; Meyers, CM; Nahin, R; Oakes, D; Rosas, HD; Schifitto, G, 2017)
"To determine whether creatine monohydrate was more effective than placebo in slowing long-term clinical decline in participants with Parkinson disease."9.20Effect of creatine monohydrate on clinical progression in patients with Parkinson disease: a randomized clinical trial. ( Aminoff, MJ; Augustine, AH; Augustine, EU; Babcock, D; Bodis-Wollner, IG; Boyd, J; Cambi, F; Chou, K; Christine, CW; Cines, M; Dahodwala, N; Derwent, L; Dewey, RB; Elm, JJ; Hauser, R; Hawthorne, K; Houghton, DJ; Kamp, C; Kieburtz, K; Leehey, M; Lew, MF; Liang, GS; Luo, ST; Mari, Z; Morgan, JC; Parashos, S; Pérez, A; Petrovitch, H; Rajan, S; Reichwein, S; Ross, GW; Roth, JT; Schneider, JS; Shannon, KM; Simon, DK; Simuni, T; Singer, C; Sudarsky, L; Tanner, CM; Tilley, BC; Umeh, CC; Williams, K; Wills, AM, 2015)
"We performed serial (1)H-MRSI examinations to assess intratumoral metabolite intensities in 16 patients receiving high-dose oral tamoxifen monotherapy for recurrent malignant glioma (WHO grade III or IV) as part of a phase II clinical trial."9.13Prospective serial proton MR spectroscopic assessment of response to tamoxifen for recurrent malignant glioma. ( Arnold, DL; Assina, R; Caramanos, Z; Langleben, A; Leblanc, R; Preul, MC; Sankar, T; Villemure, JG, 2008)
"Creatine, a naturally-occurring nitrogenous organic acid involved in adenosine triphosphate (ATP) production, has been shown to increase survival in mouse models of amyotrophic lateral sclerosis (ALS), also known as motor neuron disease (MND)."8.88Creatine for amyotrophic lateral sclerosis/motor neuron disease. ( Bedlack, RS; Moore, DH; Pastula, DM, 2012)
"Creatine, a naturally-occurring nitrogenous organic acid involved in adenosine triphosphate (ATP) production, has been shown to increase survival in mouse models of amyotrophic lateral sclerosis (ALS)."8.86Creatine for amyotrophic lateral sclerosis/motor neuron disease. ( Bedlack, RS; Moore, DH; Pastula, DM, 2010)
"Creatine has a neuroprotective effect in mutant superoxide dismutase (G93A) transgenic mice, an animal model of motor neuron disease (MND)."7.70Oral administration of creatine monohydrate retards progression of motor neuron disease in the wobbler mouse. ( Ikeda, K; Iwasaki, Y; Kinoshita, M, 2000)
"To investigate whether creatine administration could slow progressive functional decline in adults with early symptoms of Huntington disease."5.24The CREST-E study of creatine for Huntington disease: A randomized controlled trial. ( Bredlau, AL; Hersch, SM; Meyers, CM; Nahin, R; Oakes, D; Rosas, HD; Schifitto, G, 2017)
"To determine whether creatine monohydrate was more effective than placebo in slowing long-term clinical decline in participants with Parkinson disease."5.20Effect of creatine monohydrate on clinical progression in patients with Parkinson disease: a randomized clinical trial. ( Aminoff, MJ; Augustine, AH; Augustine, EU; Babcock, D; Bodis-Wollner, IG; Boyd, J; Cambi, F; Chou, K; Christine, CW; Cines, M; Dahodwala, N; Derwent, L; Dewey, RB; Elm, JJ; Hauser, R; Hawthorne, K; Houghton, DJ; Kamp, C; Kieburtz, K; Leehey, M; Lew, MF; Liang, GS; Luo, ST; Mari, Z; Morgan, JC; Parashos, S; Pérez, A; Petrovitch, H; Rajan, S; Reichwein, S; Ross, GW; Roth, JT; Schneider, JS; Shannon, KM; Simon, DK; Simuni, T; Singer, C; Sudarsky, L; Tanner, CM; Tilley, BC; Umeh, CC; Williams, K; Wills, AM, 2015)
"We performed serial (1)H-MRSI examinations to assess intratumoral metabolite intensities in 16 patients receiving high-dose oral tamoxifen monotherapy for recurrent malignant glioma (WHO grade III or IV) as part of a phase II clinical trial."5.13Prospective serial proton MR spectroscopic assessment of response to tamoxifen for recurrent malignant glioma. ( Arnold, DL; Assina, R; Caramanos, Z; Langleben, A; Leblanc, R; Preul, MC; Sankar, T; Villemure, JG, 2008)
"Our objective was to determine the effect of creatine monohydrate on disease progression in patients with amyotrophic lateral sclerosis (ALS)."5.13Creatine monohydrate in ALS: effects on strength, fatigue, respiratory status and ALSFRS. ( Barohn, RJ; Bedlack, RS; Chapin, J; Dick, A; Gelinas, DF; Jackson, CE; King, RM; Lou, JS; Phillips, LH; Rosenfeld, J, 2008)
"We sought to measure the temporal evolution and spatial distribution of lesion macromolecules and small molecules (lactate, N-acetyl compounds, creatine, and choline) in stroke patients by using short echo time in vivo proton MR spectroscopy."5.09Spectroscopic assessment of alterations in macromolecule and small-molecule metabolites in human brain after stroke. ( Graham, GD; Hwang, JH; Prichard, JW; Rothman, DL, 2001)
"Creatine, a naturally-occurring nitrogenous organic acid involved in adenosine triphosphate (ATP) production, has been shown to increase survival in mouse models of amyotrophic lateral sclerosis (ALS), also known as motor neuron disease (MND)."4.88Creatine for amyotrophic lateral sclerosis/motor neuron disease. ( Bedlack, RS; Moore, DH; Pastula, DM, 2012)
"Creatine, a naturally-occurring nitrogenous organic acid involved in adenosine triphosphate (ATP) production, has been shown to increase survival in mouse models of amyotrophic lateral sclerosis (ALS)."4.86Creatine for amyotrophic lateral sclerosis/motor neuron disease. ( Bedlack, RS; Moore, DH; Pastula, DM, 2010)
"To evaluate the prognostic value of the cortical N-acetyl aspartate to creatine ratio (NAA/Cr) in early relapsing-remitting multiple sclerosis (RRMS)."3.80Cortical N-acetyl aspartate is a predictor of long-term clinical disability in multiple sclerosis. ( Blinkenberg, M; Hanson, LG; Mathiesen, HK; Paulson, OB; Skimminge, A; Sorensen, PS; Wu, X, 2014)
" Primary central nervous system lymphoma (PCNSL) is a highly aggressive tumor responsive to high-dose methotrexate based regimens."3.73Proton magnetic resonance spectroscopy in immunocompetent patients with primary central nervous system lymphoma. ( Abrey, LE; DeAngelis, LM; Koutcher, JA; Lis, E; Panageas, KS; Raizer, JJ; Xu, S; Zakian, KL, 2005)
"Creatine has a neuroprotective effect in mutant superoxide dismutase (G93A) transgenic mice, an animal model of motor neuron disease (MND)."3.70Oral administration of creatine monohydrate retards progression of motor neuron disease in the wobbler mouse. ( Ikeda, K; Iwasaki, Y; Kinoshita, M, 2000)
"Weight loss is a common symptom of Parkinson's disease and is associated with impaired quality of life."2.84Predictors of weight loss in early treated Parkinson's disease from the NET-PD LS-1 cohort. ( Boyd, J; Li, R; Pérez, A; Ren, X; Wills, AM, 2017)
"Late infantile metachromatic leukodystrophy (MLD) is an autosomal recessive lysosomal storage disorder that causes severe demyelination of the nervous system."2.75Brain N-acetylaspartate levels correlate with motor function in metachromatic leukodystrophy. ( Barton, NW; Fogh, J; Hanson, LG; i Dali, C; Lund, AM; Nair, N, 2010)
"Diabetic nephropathy is the leading cause of end-stage renal disease."2.70Effects of losartan on renal and cardiovascular outcomes in patients with type 2 diabetes and nephropathy. ( Brenner, BM; Cooper, ME; de Zeeuw, D; Keane, WF; Mitch, WE; Parving, HH; Remuzzi, G; Shahinfar, S; Snapinn, SM; Zhang, Z, 2001)
"However, an objective measure of disease progression and therapeutic response is sorely needed."2.40Biological markers in the diagnosis and treatment of ALS. ( Arnold, DL; Cashman, NR; Kalra, S, 1999)
"With respect to the severity of autosomal recessive polycystic kidney disease, there is a wide spectrum of phenotypic manifestations, ranging from stillbirths to mildly affected of phenotypic manifestations, ranging from stillbirths to mildly affected adults, while intrafamilial variability of the clinical picture is generally small with multiple allelism as the most likely genetic explanation."2.39Course of autosomal recessive polycystic kidney disease (ARPKD) in siblings: a clinical comparison of 20 sibships. ( Deget, F; Rudnik-Schöneborn, S; Zerres, K, 1995)
"To investigate disease progression and aging, we utilized young (1 month old) and old (21-25 months old) mdx and wild-type tongue muscles."1.91Biomarkers for Duchenne muscular dystrophy progression: impact of age in the mdx tongue spared muscle. ( Chamberlain, JS; Ferretti, R; Lorena, MDSV; Matsumura, CY; Nagana Gowda, GA; Odom, GL; Santos, EKD, 2023)
"Disease progression was investigated at 4 time points, from 9 to 18 months of age, and in 4 regions: cortex, hippocampus, striatum, and thalamus."1.72Spatio-temporal metabolic rewiring in the brain of TgF344-AD rat model of Alzheimer's disease. ( López-Gil, X; Muñoz-Moreno, E; Simões, RV; Soria, G; Tudela, R, 2022)
"From a total of 1,174 IgAN patients in a multicenter retrospective cohort analysis in Japan, 195 patients were treated by tonsillectomy combined with corticosteroid."1.62Impact of the number of steroid pulses in tonsillectomy combined with steroid pulse therapy: a nationwide retrospective study in Japan. ( Hirano, K; Kataoka, H; Kawamura, T; Koike, K; Maruyama, S; Matsuo, S; Matsuzaki, K; Moriyama, T; Nitta, K; Suzuki, Y; Yasuda, T; Yasuda, Y; Yokoo, T, 2021)
"Serum TP levels at delivery in the preeclampsia group (53 ± 7 g/L) were lower than in the control group (61 ± 4 g/L, P < 0."1.56Hypoproteinemia as a parameter of poor perinatal/neonatal outcomes in women with preeclampsia diagnosed as hypertension plus proteinuria. ( Akabane-Nakagawa, K; Chiba, K; Cho, K; Kawaguchi, S; Mayama, M; Morikawa, M; Saito, Y; Umazume, T; Watari, H, 2020)
"Bioenergetic failure is a feature of Alzheimer's disease (AD)."1.40Reduced levels of mitochondrial complex I subunit NDUFB8 and linked complex I + III oxidoreductase activity in the TgCRND8 mouse model of Alzheimer's disease. ( Bazinet, RP; Francis, BM; Gupta, S; Maj, M; Mount, HT; Robinson, B; Song, BJ; Yang, J, 2014)
"Lumbrokinase treatment attenuated diabetic nephropathy in rats, possibly through increasing the activity of MMPs and the subsequent degradation of extracellular matrix."1.39Lumbrokinase attenuates diabetic nephropathy through regulating extracellular matrix degradation in Streptozotocin-induced diabetic rats. ( Cheng, X; Ge, N; Li, S; Li, Y; Shao, M; Shen, J; Sun, H, 2013)
"Recently, the clinical spectrum of dominant optic atrophy has been extended to frequent syndromic forms, exhibiting various degrees of neurological and muscle impairments frequently found in mitochondrial diseases."1.38The human OPA1delTTAG mutation induces premature age-related systemic neurodegeneration in mouse. ( Angebault, C; Bielicki, G; Boddaert, N; Brabet, P; Cazevieille, C; Chaix, B; Delettre, C; Gueguen, N; Hamel, CP; Lenaers, G; Mausset-Bonnefont, AL; Puel, JL; Renou, JP; Reynier, P; Rigau, V; Sarzi, E; Seveno, M; Wang, J, 2012)
"Fourteen patients with juvenile absence epilepsy with typical absence seizures and 10 healthy volunteer controls were included in this study."1.36A proton magnetic resonance spectroscopic study in juvenile absence epilepsy in early stages. ( Erdinc, O; Gumustas, OG; Kabay, SC; Karaman, HO; Ozden, H, 2010)
"Large variation in diabetic nephropathy prevalence remains and is associated with diabetes registry size, screening and treatment practices, suggesting that understanding this variation may help detect and better manage diabetic nephropathy."1.36Identifying additional patients with diabetic nephropathy using the UK primary care initiative. ( Cardwell, CR; Fogarty, DG; Hunter, SJ; Kee, F; Magee, GM; Murphy, MC; Savage, G, 2010)
"Cerebral fat embolism induced by a triolein emulsion resulted in no significant change in the major metabolites of the brain in the acute stage, except for an elevated lipid/Cr ratio, which suggests the absence of any significant hypoxic-ischemic changes in the lesions embolized using a fat emulsion."1.35Proton magnetic resonance spectroscopic findings of cerebral fat embolism induced by triolein emulsion in cats. ( Baik, SK; Chang, KH; Cho, BM; Choi, SH; Kim, DH; Kim, HJ; Kim, YW; Lee, JW; Lee, SH, 2008)
"Prion diseases are fatal chronic neurodegenerative diseases."1.34MRI and MRS alterations in the preclinical phase of murine prion disease: association with neuropathological and behavioural changes. ( Anthony, DC; Blamire, AM; Broom, KA; Griffin, JL; Lowe, JP; Perry, VH; Scott, H; Sibson, NR; Styles, P, 2007)
"However, diabetic patients with ESRD secondary to dNP were significantly younger than those with vNP."1.33Rate of decline of GFR and progression of vascular disease in type 2 diabetic patients with diabetic or vascular nephropathy during the last three years before starting dialysis therapy. ( Biesenbach, G; Janko, O; Pieringer, H; Schmekal, B, 2006)
"Pretreatment with pargyline attenuated the MPTP-induced clinical signs, MRI and MRS changes, and the histopathological and immunoreactivity alterations."1.32Proton magnetic resonance imaging and spectroscopy identify metabolic changes in the striatum in the MPTP feline model of parkinsonism. ( Hadjiconstantinou, M; Neff, NH; Podell, M; Smith, MA, 2003)
"Creatine treatment started at 6, 8, and 10 weeks of age, analogous to early, middle, and late stages of human HD, significantly extended survival at both the 6- and 8-week starting points."1.32Creatine therapy provides neuroprotection after onset of clinical symptoms in Huntington's disease transgenic mice. ( Beal, MF; Dedeoglu, A; Ferrante, KL; Ferrante, RJ; Hersch, SM; Kubilus, JK; Yang, L, 2003)
"Bladder cancer is the fourth most common malignant neoplasm in men and the tenth most common in women."1.32Analytical and clinical evaluation of a new urinary tumor marker: bladder tumor fibronectin in diagnosis and follow-up of bladder cancer. ( Emerk, K; Mutlu, N; Turkeri, L, 2003)
"The fulminating form of subacute sclerosing panencephalitis is an extremely rare condition."1.32Subacute sclerosing panencephalitis with fulminating course: follow-up magnetic resonance spectroscopy (MRS) findings. ( Alkan, A; Aslan, M; Kutlu, R; Sarac, K; Sigirci, A; Yakinci, C, 2004)
"The diagnosis of gliomatosis cerebri with MR imaging is known to be difficult."1.31MR spectroscopy in gliomatosis cerebri. ( Bendszus, M; Burger, R; Klein, R; Schichor, C; Solymosi, L; Tonn, JC; Warmuth-Metz, M, 2000)
"Cystic kidney disease progression was assessed by measuring kidney size and fluid content and determining cyst scores."1.31Creatine supplementation increases renal disease progression in Han:SPRD-cy rats. ( Aukema, HM; DiMarco, NM; Edmunds, JW; Jayapalan, S; Saboorian, MH, 2001)
"The metabolic disturbances indicate disease progression but are less pronounced than in older patients with hemimegalencephaly."1.30Proton magnetic resonance spectroscopy of linear nevus sebaceus syndrome. ( Christen, HJ; Frahm, J; Hanefeld, FA; Kruse, B; Pouwels, PJ, 1998)

Research

Studies (132)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's14 (10.61)18.2507
2000's64 (48.48)29.6817
2010's49 (37.12)24.3611
2020's5 (3.79)2.80

Authors

AuthorsStudies
Muñoz-Moreno, E1
Simões, RV1
Tudela, R1
López-Gil, X1
Soria, G1
Lorena, MDSV1
Santos, EKD1
Ferretti, R1
Nagana Gowda, GA1
Odom, GL1
Chamberlain, JS1
Matsumura, CY1
Han, X1
Xiao, Y1
Tang, Y1
Zheng, X1
Anwar, M1
Qin, W1
Blicher, JU1
Eskildsen, SF1
Stærmose, TG1
Møller, AT1
Figlewski, K1
Near, J1
Morikawa, M1
Mayama, M1
Saito, Y1
Akabane-Nakagawa, K1
Umazume, T1
Chiba, K1
Kawaguchi, S1
Cho, K1
Watari, H1
Moriyama, T1
Kataoka, H1
Nitta, K1
Hirano, K1
Matsuzaki, K1
Yasuda, T1
Yasuda, Y1
Koike, K1
Maruyama, S1
Yokoo, T1
Matsuo, S2
Kawamura, T1
Suzuki, Y1
Shiga, Y1
Nezu, T1
Nakamori, M1
Hosomi, N1
Akiyama, Y1
Tachiyama, K1
Kamimura, T1
Kinoshita, N1
Hayashi, Y1
Matsushima, H1
Imamura, E1
Aoki, S1
Ueno, H1
Ohshita, T1
Wakabayashi, S1
Yamasaki, F1
Awai, K1
Maruyama, H1
Simon, DK2
Wu, C1
Tilley, BC2
Lohmann, K1
Klein, C1
Payami, H1
Wills, AM3
Aminoff, MJ2
Bainbridge, J1
Dewey, R1
Hauser, RA1
Schaake, S1
Schneider, JS2
Sharma, S1
Singer, C2
Tanner, CM2
Truong, D1
Wei, P1
Wong, PS1
Yang, T1
Kirov, II1
Liu, S1
Tal, A1
Wu, WE1
Davitz, MS1
Babb, JS1
Rusinek, H1
Herbert, J1
Gonen, O1
Hersch, SM2
Schifitto, G1
Oakes, D1
Bredlau, AL1
Meyers, CM1
Nahin, R1
Rosas, HD1
Li, R1
Pérez, A2
Ren, X1
Boyd, J2
Fedele, TA1
Galdos-Riveros, AC1
Jose de Farias e Melo, H1
Magalhães, A1
Maria, DA1
Kantarci, K4
Stromillo, ML1
Giorgio, A1
Rossi, F1
Battaglini, M1
Hakiki, B1
Malentacchi, G1
Santangelo, M1
Gasperini, C1
Bartolozzi, ML1
Portaccio, E1
Amato, MP1
De Stefano, N6
Bellenberg, B1
Busch, M1
Trampe, N1
Gold, R1
Chan, A1
Lukas, C1
Targosz-Gajniak, MG1
Siuda, JS1
Wicher, MM1
Banasik, TJ1
Bujak, MA1
Augusciak-Duma, AM1
Opala, G1
Bruggers, CS1
Moore, K1
Francis, BM1
Yang, J1
Song, BJ1
Gupta, S1
Maj, M1
Bazinet, RP1
Robinson, B1
Mount, HT1
Bayer-Karpinska, A1
Schwarz, F1
Wollenweber, FA1
Poppert, H1
Boeckh-Behrens, T1
Becker, A1
Clevert, DA1
Nikolaou, K1
Opherk, C1
Dichgans, M1
Saam, T1
Wu, X1
Hanson, LG2
Skimminge, A1
Sorensen, PS1
Paulson, OB1
Mathiesen, HK1
Blinkenberg, M1
Gerber, LM1
Mann, SJ1
Chase, HS1
Hirsch, JS1
Mohan, S1
Rao, MK1
Radhakrishnan, J1
Kieburtz, K1
Elm, JJ1
Babcock, D1
Hauser, R1
Ross, GW1
Augustine, AH1
Augustine, EU1
Bodis-Wollner, IG1
Cambi, F1
Chou, K1
Christine, CW1
Cines, M1
Dahodwala, N1
Derwent, L1
Dewey, RB1
Hawthorne, K1
Houghton, DJ1
Kamp, C1
Leehey, M1
Lew, MF1
Liang, GS1
Luo, ST1
Mari, Z1
Morgan, JC1
Parashos, S1
Petrovitch, H1
Rajan, S1
Reichwein, S1
Roth, JT1
Shannon, KM1
Simuni, T1
Sudarsky, L1
Umeh, CC1
Williams, K1
Zhou, L1
Fan, Y1
Almuqbel, M1
Melzer, TR1
Myall, DJ1
MacAskill, MR1
Pitcher, TL1
Livingston, L1
Wood, KL1
Keenan, RJ1
Dalrymple-Alford, JC1
Anderson, TJ1
Norouzi, J1
Yadollahpour, A1
Mirbagheri, SA1
Mazdeh, MM1
Hosseini, SA1
Löbel, U1
Hwang, S1
Edwards, A1
Li, Y2
Li, X1
Broniscer, A1
Patay, Z1
Drew, L1
Sankar, T1
Caramanos, Z1
Assina, R1
Villemure, JG1
Leblanc, R1
Langleben, A1
Arnold, DL7
Preul, MC1
Rosenfeld, J1
King, RM1
Jackson, CE1
Bedlack, RS3
Barohn, RJ1
Dick, A1
Phillips, LH1
Chapin, J1
Gelinas, DF1
Lou, JS1
Bonello, L1
De Labriolle, A1
Roy, P1
Steinberg, DH1
Okabe, T1
Pinto Slottow, TL1
Xue, Z1
Torguson, R1
Suddath, WO1
Satler, LF1
Kent, KM1
Pichard, AD1
Lindsay, J1
Waksman, R1
Damman, K1
van Veldhuisen, DJ1
Navis, G1
Voors, AA1
Hillege, HL1
Baik, SK1
Kim, YW1
Kim, HJ1
Lee, JW1
Cho, BM1
Kim, DH1
Choi, SH1
Lee, SH1
Chang, KH1
Pyra, T1
Hui, B1
Hanstock, C1
Concha, L1
Wong, JC1
Beaulieu, C1
Johnston, W1
Kalra, S2
Imamura, A1
Miyajima, H1
Ito, R1
Orii, KO1
Peters, HP1
van den Brand, JA1
Wetzels, JF2
Weigand, SD2
Przybelski, SA1
Shiung, MM1
Whitwell, JL1
Negash, S1
Knopman, DS2
Boeve, BF3
O'Brien, PC3
Petersen, RC3
Jack, CR3
Pilatus, U2
Lais, C1
Rochmont, Adu M1
Kratzsch, T1
Frölich, L1
Maurer, K1
Zanella, FE1
Lanfermann, H2
Pantel, J1
Kabay, SC1
Gumustas, OG1
Karaman, HO1
Ozden, H1
Erdinc, O1
Jickling, G1
Salam, A1
Mohammad, A1
Hussain, MS1
Scozzafava, J1
Nasser, AM1
Jeerakathil, T1
Shuaib, A1
Camicioli, R1
Hattingen, E1
Delic, O1
Franz, K1
Raab, P1
Gerlach, R1
Matsusue, E1
Fink, JR1
Rockhill, JK1
Ogawa, T1
Maravilla, KR1
Qian, J1
Herrera, JJ1
Narayana, PA1
Acosta, ML1
Shin, YS1
Ready, S1
Fletcher, EL1
Christie, DL1
Kalloniatis, M1
Tan, JC1
Pastula, DM2
Moore, DH2
Magee, GM1
Hunter, SJ1
Cardwell, CR1
Savage, G1
Kee, F1
Murphy, MC1
Fogarty, DG1
i Dali, C1
Barton, NW1
Fogh, J1
Nair, N1
Lund, AM1
Kim, JH1
Choi, BS1
Jung, C1
Chang, Y1
Kim, S1
Astor, BC4
Matsushita, K4
Gansevoort, RT4
van der Velde, M4
Woodward, M4
Levey, AS3
Jong, PE1
Coresh, J4
de Jong, PE2
El-Nahas, M2
Eckardt, KU2
Kasiske, BL2
Wright, J1
Appel, L1
Greene, T1
Levin, A1
Djurdjev, O1
Wheeler, DC1
Landray, MJ1
Townend, JN1
Emberson, J1
Clark, LE1
Macleod, A1
Marks, A1
Ali, T1
Fluck, N1
Prescott, G1
Smith, DH1
Weinstein, JR1
Johnson, ES1
Thorp, ML1
Blankestijn, PJ1
van Zuilen, AD1
Menon, V1
Sarnak, M1
Beck, G1
Kronenberg, F1
Kollerits, B1
Froissart, M1
Stengel, B1
Metzger, M1
Remuzzi, G2
Ruggenenti, P1
Perna, A1
Heerspink, HJ1
Brenner, B1
de Zeeuw, D2
Rossing, P1
Parving, HH2
Auguste, P2
Veldhuis, K2
Wang, Y2
Camarata, L2
Thomas, B2
Manley, T2
Levey, A2
de Jong, P1
Ninomiya, T1
Chalmers, J1
Macmahon, S1
Tonelli, M1
Hemmelgarn, B1
Sacks, F1
Curhan, G1
Collins, AJ1
Li, S2
Chen, SC1
Hawaii Cohort, KP1
Lee, BJ1
Ishani, A1
Neaton, J1
Svendsen, K1
Mann, JF1
Yusuf, S1
Teo, KK1
Gao, P1
Nelson, RG1
Knowler, WC1
Bilo, HJ1
Joosten, H1
Kleefstra, N1
Groenier, KH1
Johnson, KR1
Akira, K1
Masu, S1
Imachi, M1
Mitome, H1
Hashimoto, T1
Nicolasjilwan, M1
Lopes, MB1
Larner, J1
Wintermark, M1
Schiff, D1
Yu, MK1
Ye, W1
Cherney, DZ1
Scholey, JW1
Daneman, D1
Dunger, DB1
Dalton, RN1
Moineddin, R1
Mahmud, FH1
Dekker, R1
Elia, Y1
Sochett, E1
Reich, HN1
Wadman, RI1
Bosboom, WM1
van der Pol, WL1
van den Berg, LH2
Wokke, JH2
Iannaccone, ST1
Vrancken, AF1
Lim, TS1
Hong, YH1
Lee, HY1
Choi, JY1
Kim, HS1
Moon, SY1
Lucarelli, G1
Ditonno, P1
Bettocchi, C1
Grandaliano, G1
Gesualdo, L1
Selvaggi, FP1
Battaglia, M1
Ikeda, K2
Murata, K1
Kawase, Y1
Kawabe, K1
Kano, O1
Yoshii, Y1
Takazawa, T1
Hirayama, T1
Iwasaki, Y2
Wang, PS1
Chen, HC1
Wu, HM1
Lirng, JF1
Wu, YT1
Soong, BW1
Sarzi, E1
Angebault, C1
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Gueguen, N1
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Sun, H1
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Cheng, X1
Shen, J1
Sarchielli, P1
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Tarducci, R2
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Liantonio, A1
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Rüegg, UT1
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Blamire, AM2
Palace, J1
Narayanan, S5
Arnold, D1
Styles, P2
Matthews, PM4
Podell, M1
Hadjiconstantinou, M1
Smith, MA1
Neff, NH1
Groeneveld, GJ1
Veldink, JH1
van der Tweel, I1
Kalmijn, S1
Beijer, C1
de Visser, M1
Franssen, H1
Dedeoglu, A1
Kubilus, JK1
Yang, L1
Ferrante, KL1
Beal, MF1
Ferrante, RJ1
Mutlu, N1
Turkeri, L1
Emerk, K1
Sener, RN1
Bassuk, AG1
Joshi, A1
Burton, BK1
Larsen, MB1
Burrowes, DM1
Stack, C1
Nakae, I1
Mitsunami, K1
Omura, T1
Yabe, T1
Tsutamoto, T1
Takahashi, M1
Morikawa, S1
Inubushi, T1
Nakamura, Y1
Kinoshita, M2
Horie, M1
Fuller, RA1
Westmoreland, SV1
Ratai, E1
Greco, JB1
Kim, JP1
Lentz, MR1
He, J1
Sehgal, PK1
Masliah, E1
Halpern, E1
Lackner, AA1
González, RG1
Vidt, DG1
Cressman, MD1
Harris, S1
Pears, JS1
Hutchinson, HG1
Nagae-Poetscher, LM1
Bibat, G1
Philippart, M1
Rosemberg, S1
Fatemi, A1
Lacerda, MT1
Costa, MO1
Kok, F1
Costa Leite, C1
Horská, A1
Barker, PB1
Naidu, S1
Willemsen, MA1
Van Der Graaf, M1
Van Der Knaap, MS1
Heerschap, A1
Van Domburg, PH1
Gabreëls, FJ1
Rotteveel, JJ1
Alkan, A1
Kutlu, R1
Sigirci, A1
Aslan, M1
Sarac, K1
Yakinci, C1
Shefner, JM1
Cudkowicz, ME1
Zhang, H1
Schoenfeld, D1
Jillapalli, D1
Chan, AA1
Lau, A1
Pirzkall, A2
Chang, SM1
Verhey, LJ1
Larson, D1
McDermott, MW1
Dillon, WP2
Nelson, SJ2
Caravati, EM1
Heileson, HL1
Jones, M1
Katz-Brull, R1
Lenkinski, RE1
Du Pasquier, RA1
Koralnik, IJ1
Raizer, JJ1
Koutcher, JA1
Abrey, LE1
Panageas, KS1
DeAngelis, LM1
Lis, E1
Xu, S1
Zakian, KL1
Oz, G1
Tkác, I1
Charnas, LR1
Choi, IY1
Bjoraker, KJ1
Shapiro, EG1
Gruetter, R1
Laprie, A1
Haas-Kogan, DA1
Cha, S1
Banerjee, A1
Le, TP1
Lu, Y1
Nelson, S1
McKnight, TR1
Metastasio, A1
Rinaldi, P1
Mariani, E1
Feliziani, FT1
Cherubini, A1
Senin, U1
Mecocci, P1
Kleefstra, T1
Rosenberg, EH1
Salomons, GS1
Stroink, H1
van Bokhoven, H1
Hamel, BC1
de Vries, BB1
Ito-Ihara, T1
Ono, T1
Nogaki, F1
Suyama, K1
Tanaka, M1
Yonemoto, S1
Fukatsu, A1
Kita, T1
Suzuki, K1
Muso, E1
Kawamura, K1
Okada, S1
Li, B1
Suwa, M1
Yao, J1
Morioka, T1
Gejyo, F1
Oite, T1
Gunter, J1
Reyes, D1
Shiung, M1
Smith, GE2
Ivnik, RJ2
Tangalos, EG2
Appenzeller, S1
Costallat, LT1
Li, LM1
Cendes, F2
Biesenbach, G1
Schmekal, B1
Pieringer, H1
Janko, O1
Ingwall, JS1
Broom, KA1
Anthony, DC1
Lowe, JP1
Griffin, JL1
Scott, H1
Perry, VH1
Sibson, NR1
Pascual, JM1
Solivera, J1
Prieto, R1
Barrios, L1
López-Larrubia, P1
Cerdán, S1
Roda, JM1
Pascual, AM1
Martínez-Bisbal, MC1
Boscá, I1
Valero, C1
Coret, F1
Martínez-Granados, B1
Marti-Bonmati, L1
Mir, A1
Celda, B1
Casanova, B1
Gordeuk, VR1
Sachdev, V1
Taylor, JG1
Gladwin, MT1
Kato, G1
Castro, OL1
Alimenti, A1
Delavelle, J1
Lazeyras, F1
Yilmaz, H1
Dietrich, PY1
de Tribolet, N1
Lövblad, KO1
Azevedo, D1
Tatsch, M1
Hototian, SR1
Bazzarella, MC1
Castro, CC1
Bottino, CM1
Casey, PA1
McKenna, MC1
Fiskum, G1
Saraswati, M1
Robertson, CL1
Patra, S1
Bera, S1
SinhaRoy, S1
Ghoshal, S1
Ray, S1
Basu, A1
Schlattner, U1
Wallimann, T1
Ray, M1
Deget, F1
Rudnik-Schöneborn, S1
Zerres, K1
Andermann, F1
Silver, K1
Owada, A2
Shiigai, T2
Fu, L2
Wolfson, C1
Worsley, KJ1
Collins, DL1
Tedeschi, G1
Lundbom, N1
Raman, R1
Bonavita, S1
Duyn, JH1
Alger, JR1
Di Chiro, G1
Wald, LL1
Day, MR1
Noworolski, SE1
Henry, RG1
Huhn, SL1
Chang, S1
Prados, MD1
Sneed, PK1
Larson, DA1
Wara, WM1
McDermott, M1
Gutin, PH1
Vigneron, DB1
Nakao, M1
Koike, J1
Ujiie, K1
Tomita, K1
Falini, A1
Calabrese, G1
Filippi, M1
Origgi, D1
Lipari, S1
Colombo, B1
Comi, G1
Scotti, G1
Kruse, B1
Pouwels, PJ1
Christen, HJ1
Frahm, J1
Hanefeld, FA1
Stanley, J1
Francis, GS2
Antel, JP2
Terakawa, H1
Abe, K1
Watanabe, Y1
Nakamura, M1
Fujita, N1
Hirabuki, N1
Yanagihara, T1
Stratta, P1
Canavese, C1
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Barolo, S1
Dall'Omo, AM1
Fasano, ME1
Mazzola, G1
Berutti, S1
Fop, F1
Curtoni, ES1
Piccoli, G1
Cashman, NR1
Federico, F1
Simone, IL1
Lucivero, V1
Mezzapesa, DM1
de Mari, M1
Lamberti, P1
Petruzzellis, M1
Ferrari, E1
Bendszus, M1
Warmuth-Metz, M1
Klein, R1
Burger, R1
Schichor, C1
Tonn, JC1
Solymosi, L1
Cucurella, MG1
Rovira, A1
Río, J1
Pedraza, S1
Tintoré, MM1
Montalbán, X1
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Xu, YC1
Campeau, NG1
Kokmen, E1
Mizuno, S1
Takahashi, Y1
Kato, Z1
Goto, H1
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Edmunds, JW1
Jayapalan, S1
DiMarco, NM1
Saboorian, MH1
Aukema, HM1
Arnaoutelis, R1
Tartaglia, MC1
Suzuki, H1
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Snapinn, SM1
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Kobayashi, M1
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Suga, S1
Mihara, B1
Graham, GD1
Hwang, JH1
Rothman, DL1
Prichard, JW1
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Weiner, MW1

Clinical Trials (25)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
Creatine Safety, Tolerability, & Efficacy in Huntington's Disease (CREST-E)[NCT00712426]Phase 3553 participants (Actual)Interventional2009-09-30Terminated (stopped due to Results of an interim analysis showed that it was unlikely that creatine was effective in slowing loss of function in early symptomatic Huntington's Disease.)
A Multicenter, Double-Blind, Parallel Group, Placebo Controlled Study of Creatine in Subjects With Treated Parkinson's Disease (PD) Long Term Study (LS-1)[NCT00449865]Phase 31,741 participants (Actual)Interventional2007-03-31Terminated (stopped due to Futility)
Open Label Study for the Use of Tyrosine Kinase Inhibitors for Treatment of Cognitive Decline Due to Degenerative Dementias[NCT02921477]Phase 1150 participants (Anticipated)Interventional2016-09-30Enrolling by invitation
Focused Ultrasound Delivery of Exosomes for Treatment of Refractory Depression, Anxiety, and Neurodegenerative Dementias[NCT04202770]300 participants (Anticipated)Interventional2019-12-01Suspended (stopped due to Pending COVID-19 pandemic; pending status of product development)
Carotid Plaque Imaging in Acute Stroke[NCT01284933]234 participants (Actual)Observational2011-02-28Completed
Pragmatic Randomized Controlled Trial Comparing Treatment Effectiveness of Guideline Indicated Anti-platelet Therapy for Acute Coronary Syndrome in Patients With Chronic Kidney Disease[NCT03150667]Phase 4220 participants (Anticipated)Interventional2017-04-10Recruiting
MRI Biomarkers of Risk in Sedentary and Exercise Trained Humans[NCT02729428]71 participants (Actual)Observational2016-04-30Completed
Multi-paramEtric Imaging to Assess Treatment REsponse After Stereotactic Radiosurgery of Brain Metastases[NCT04626206]12 participants (Anticipated)Observational2020-12-31Not yet recruiting
A Phase I/II, Open Labeled, Monocentric Study of Direct Intracranial Administration of a Replication Deficient Adeno-associated Virus Gene Transfer Vector Serotype rh.10 Expressing the Human ARSA cDNA to Children With Metachromatic Leukodystrophy.[NCT01801709]Phase 1/Phase 25 participants (Anticipated)Interventional2014-06-30Active, not recruiting
A Phase III Trial to Evaluate the Efficacy and Safety of Biweekly Alirocumab in Patients on a Stable Dialysis Regimen: The Alidial Study[NCT03480568]Phase 320 participants (Anticipated)Interventional2018-05-01Recruiting
Randomised, Double Blind, Placebo Controlled Trial of Angiotensin Converting Enzyme Inhibitors and Statins in the Prevention of Long Term Complications in Young People With Type 1 Diabetes[NCT01581476]Phase 3443 participants (Actual)Interventional2009-01-31Completed
Coenzyme Q10 in Huntington's Disease (HD)[NCT00608881]Phase 3609 participants (Actual)Interventional2008-03-31Terminated (stopped due to Futility analysis failed to showed likelihoo of benefit of CoQ 2400 mg/day.)
Premanifest Huntington's Disease: Creatine Safety & Tolerability Extension Study[NCT01411150]Phase 238 participants (Actual)Interventional2009-05-31Completed
Premanifest Huntington's Disease Extension Study II: Creatine Safety & Tolerability[NCT01411163]Phase 224 participants (Actual)Interventional2010-04-30Completed
Creatine Safety and Tolerability in Premanifest HD: PRECREST[NCT00592995]Phase 264 participants (Actual)Interventional2007-12-31Completed
Creatine Safety & Tolerability in Huntington's Disease (CREST-X): A Single-Center, Open-Label, Long-Term Safety & Tolerability Extension Study of Creatine in Subjects With HD[NCT01412151]Phase 210 participants (Actual)Interventional2005-04-30Completed
Sjogren-Larsson Syndrome: A Longitudinal Study of Natural History, Clinical Variation and Evaluation of Biochemical Markers[NCT01971957]20 participants (Actual)Observational [Patient Registry]2013-04-01Completed
An Open-label, Non-randomized, Phase I/II Study of Autologous Bone Marrow-Derived Mononuclear Stem Cells (BM-MNC) and Liberation Therapy (When Associated With CCSVI) in Patients With RRMS[NCT02587806]Phase 1/Phase 269 participants (Anticipated)Interventional2015-02-28Recruiting
An Open-label, Non-randomized, Phase I/II Study of Allogeneic Human Umbilical Cord Tissue-Derived Mesenchymal Stem Cells (UC-MSC) and Liberation Therapy (When Associated With Chronic Cerebrovascular Venous Insufficiency) in Patients With Relapsing Remitti[NCT02587715]Phase 1/Phase 269 participants (Anticipated)Interventional2015-02-28Recruiting
An Open-label, Non-randomized, Phase I/II Study of Allogeneic Human Umbilical Cord Tissue-Derived Mesenchymal Stem Cells (UC-MSC) and Liberation Therapy (When Associated With Chronic Cerebrovascular Venous Insufficiency) in Patients With Relapsing Remitti[NCT02418325]Phase 1/Phase 269 participants (Anticipated)Interventional2015-02-28Terminated (stopped due to Lack of funding)
Creatine Monohydrate Use for Preventing Altitude Induced Depression[NCT03433651]Phase 40 participants (Actual)Interventional2019-01-01Withdrawn (stopped due to Unable to locate grant funding.)
Open, Randomized, Unicenter Study Comparing Metabolic Surgery With Intensive Medical Therapy to Treat Diabetic Kidney Disease[NCT04626323]Phase 260 participants (Anticipated)Interventional2021-05-25Recruiting
A Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Renal Protective Effects of Losartan in Patients With Non-insulin Dependent Diabetes Mellitus and Nephropathy[NCT00308347]Phase 31,513 participants (Actual)Interventional1996-05-31Completed
SGLT-2 Inhibitors in Prevention of Post-procedural Renal and Cardiovascular Complications aFter PCI Among Patients With Diabetes Mellitus and Coronary Artery Disease: a Prospective, Randomized, Pilot Study (SAFE-PCI)[NCT05037695]Phase 440 participants (Anticipated)Interventional2021-07-21Recruiting
Determinants of Diabetic Nephropathy in American Indians[NCT01878045]141 participants (Actual)Observational2013-11-07Suspended (stopped due to This study is on a temporary Administrative Hold pending further discussion for NIDDK and Tribal Leadership.)
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

The Global Outcome Combined Information on Change From Baseline in Schwab England Activities of Daily Living, 39-Item Parkinson's Disease Questionnaire, Ambulatory Capacity, Symbol Digit Modalities, and Modified Rankin at 5 Years.

All outcomes were coded such that higher scores indicated worse outcomes. Patients were ranked on each outcome and their ranks were summed (summed-ranks). Higher summed ranks (range, 5-4775) indicate worse outcomes. The mean summed ranks were compared by treatment group by a global statistical test (GST). (NCT00449865)
Timeframe: Change from baseline to 5 YEARS

Interventionsummed-ranks (Mean)
Placebo2360
Creatine2414

Change in Behavioral Frequency Score From Baseline to Month 60

The Unified Huntington's Disease Rating Scale (UHDRS) behavioral subscale assesses frequency and severity of psychiatric-related symptoms, including depressed mood, apathy, low self-esteem/guilt, suicidal thoughts, anxiety, irritable behavior, aggressive behavior, obsessional thinking, compulsive behavior, delusions, and hallucinations. A total score was calculated by summing up all the individual behavioral frequency items (range 0-56) with higher scores representing more severe behavioral impairment. (NCT00608881)
Timeframe: Baseline and Month 60

Interventionunits on a scale (Least Squares Mean)
A - Coenzyme Q10 2400 mg/Day1.39
B - Placebo1.43

Change in Behavioral Frequency x Severity Score From Baseline to Month 60

The Unified Huntington's Disease Rating Scale (UHDRS) behavioral subscale assesses frequency and severity of psychiatric-related symptoms, including depressed mood, apathy, low self-esteem/guilt, suicidal thoughts, anxiety, irritable behavior, aggressive behavior, obsessional thinking, compulsive behavior, delusions, and hallucinations. The total score is the sum of the product of the individual behavioral frequency and severity items (range 0-176) with higher scores representing more severe behavioral impairment. (NCT00608881)
Timeframe: Baseline and Month 60

Interventionunits on a scale (Least Squares Mean)
A - Coenzyme Q10 2400 mg/Day4.29
B - Placebo5.06

Change in Functional Checklist Score From Baseline to Month 60

"The functional assessment checklist includes 25 questions about common daily tasks. A score of 1 is given for each yes reply and a score of 0 is given for each no reply (scale range is 0-25). Higher scores indicate better functioning." (NCT00608881)
Timeframe: Baseline and Month 60

Interventionunits on a scale (Mean)
A - Coenzyme Q10 2400 mg/Day-7.93
B - Placebo-8.02

Change in Independence Scale Score From Baseline to Month 60

The independence scale assesses independence on a 0 to 100 scale with higher scores indicating better functioning. (NCT00608881)
Timeframe: Baseline and Month 60

Interventionunits on a scale (Mean)
A - Coenzyme Q10 2400 mg/Day-26.30
B - Placebo-24.86

Change in Stroop Interference Test - Color Naming From Baseline to Month 60

Stroop Interference Test - color naming score is the total number of correct colors identified in 45 seconds and reflects processing speed. (NCT00608881)
Timeframe: Baseline and Month 60

Interventionunits on a scale (Least Squares Mean)
A - Coenzyme Q10 2400 mg/Day-14.21
B - Placebo-14.51

Change in Stroop Interference Test - Interference From Baseline to Month 60

Stroop Interference Test - interference score is the total number of correct items identified in 45 seconds and reflects an executive measure of inhibitory ability. (NCT00608881)
Timeframe: Baseline and Month 60

Interventionunits on a scale (Least Squares Mean)
A - Coenzyme Q10 2400 mg/Day-7.57
B - Placebo-8.61

Change in Stroop Interference Test - Word Reading From Baseline to Month 60

Stroop Interference Test - word reading score is the total number of correct words read in 45 seconds and reflects processing speed. (NCT00608881)
Timeframe: Baseline and Month 60

Interventionunits on a scale (Least Squares Mean)
A - Coenzyme Q10 2400 mg/Day-15.25
B - Placebo-19.13

Change in Symbol Digit Modalities Test (SDMT) From Baseline to Month 60

The SDMT assesses attention, visuoperceptual processing, working memory, and cognitive/psychomotor speed. The score is the number of correctly paired abstract symbols and specific numbers in 90 seconds with higher scores indicating better cognitive functioning. (NCT00608881)
Timeframe: Baseline and Month 60

Interventionunits on a scale (Least Squares Mean)
A - Coenzyme Q10 2400 mg/Day-10.95
B - Placebo-11.36

Change in Total Functional Capacity (TFC) Score From Baseline to Month 60

TFC consists of five ordinally scaled items assessing a person's capacity with: (1) occupation; (2) financial affairs; (3) domestic responsibilities; (4) activities of daily living; and (5) independent living. Total score ranges from zero (worst) to 13 (best). (NCT00608881)
Timeframe: Baseline and Month 60

Interventionunits on a scale (Least Squares Mean)
A - Coenzyme Q10 2400 mg/Day-4.53
B - Placebo-4.76

Change in Total Motor Score From Baseline to Month 60

The motor section of the Unified Huntington's Disease Rating Scale (UHDRS) assesses motor features of Huntington disease with standardized ratings of oculomotor function, dysarthria, chorea, dystonia, gait, and postural stability. The total motor score is the sum of all the individual motor ratings, with higher scores (124) indicating more severe motor impairment than lower scores. The score ranges from 0 to 124. (NCT00608881)
Timeframe: Baseline and Month 60

Interventionunits on a scale (Least Squares Mean)
A - Coenzyme Q10 2400 mg/Day18.06
B - Placebo19.18

Change in Verbal Fluency Test From Baseline to Month 60

The verbal fluency test is typically considered a measure of executive function. The score is the number of correct words produced across three 1-minute trials. (NCT00608881)
Timeframe: Baseline and Month 60

Interventionunits on a scale (Least Squares Mean)
A - Coenzyme Q10 2400 mg/Day-5.07
B - Placebo-4.47

Joint Rank (Combination of Time to Death (for Subjects Who Died) and Change in Total Functional Capacity Score (TFC) From Baseline to Month 60 (for Subjects Who Survived))

The primary outcome variable at the start of the trial was the change in TFC score from baseline to Month 60. The Data and Safety Monitoring Board recommended to the trial leadership that they reconsider how they accommodate missing data from subjects who die in their primary analysis of the change in TFC score. Based on these recommendations, the trial leadership changed the primary analysis to that of a joint rank approach. TFC consists of five ordinally scaled items assessing a person's capacity with: (1) occupation; (2) financial affairs; (3) domestic responsibilities; (4) activities of daily living; and (5) independent living. Total score ranges from zero (worst) to 13 (best). (NCT00608881)
Timeframe: 5 years

Interventionrank (Mean)
A - Coenzyme Q10 2400 mg/Day303.3
B - Placebo306.7

Number Completing Study at Assigned Dosage Level

(NCT00608881)
Timeframe: 5 years

Interventionparticipants completing study on drug (Number)
A - Coenzyme Q10 2400 mg/Day98
B - Placebo108

Time to a Three-Point Decline in TFC Score or Death

TFC consists of five ordinally scaled items assessing a person's capacity with: (1) occupation; (2) financial affairs; (3) domestic responsibilities; (4) activities of daily living; and (5) independent living. Total score ranges from zero (worst) to 13 (best). (NCT00608881)
Timeframe: 5 years

Interventiondays to event (Median)
A - Coenzyme Q10 2400 mg/Day917
B - Placebo911

Time to a Two-Point Decline in TFC Score or Death

TFC consists of five ordinally scaled items assessing a person's capacity with: (1) occupation; (2) financial affairs; (3) domestic responsibilities; (4) activities of daily living; and (5) independent living. Total score ranges from zero (worst) to 13 (best). (NCT00608881)
Timeframe: 5 years

Interventiondays to event (Median)
A - Coenzyme Q10 2400 mg/Day553
B - Placebo549

Tolerability

Proportion of subjects able to complete treatment (NCT01412151)
Timeframe: 306 Weeks

InterventionParticipants (Number)
Creatine Monohydrate5

Reviews

12 reviews available for creatine and Disease Exacerbation

ArticleYear
Proton MRS in mild cognitive impairment.
    Journal of magnetic resonance imaging : JMRI, 2013, Volume: 37, Issue:4

    Topics: Alzheimer Disease; Animals; Aspartic Acid; Biomarkers; Brain; Choline; Cognitive Dysfunction; Creati

2013
Creatine for amyotrophic lateral sclerosis/motor neuron disease.
    The Cochrane database of systematic reviews, 2010, Jun-16, Issue:6

    Topics: Amyotrophic Lateral Sclerosis; Creatine; Disease Progression; Humans; Motor Neuron Disease; Neuropro

2010
Lower estimated glomerular filtration rate and higher albuminuria are associated with mortality and end-stage renal disease. A collaborative meta-analysis of kidney disease population cohorts.
    Kidney international, 2011, Volume: 79, Issue:12

    Topics: Adult; Aged; Albuminuria; Biomarkers; Chi-Square Distribution; Cohort Studies; Creatine; Disease Pro

2011
Lower estimated glomerular filtration rate and higher albuminuria are associated with all-cause and cardiovascular mortality. A collaborative meta-analysis of high-risk population cohorts.
    Kidney international, 2011, Volume: 79, Issue:12

    Topics: Adult; Aged; Albuminuria; Biomarkers; Cardiovascular Diseases; Cause of Death; Chi-Square Distributi

2011
Drug treatment for spinal muscular atrophy types II and III.
    The Cochrane database of systematic reviews, 2012, Apr-18, Issue:4

    Topics: Acetylcarnitine; Adolescent; Amines; Child; Child, Preschool; Creatine; Cyclohexanecarboxylic Acids;

2012
Creatine for amyotrophic lateral sclerosis/motor neuron disease.
    The Cochrane database of systematic reviews, 2012, Dec-12, Volume: 12

    Topics: Amyotrophic Lateral Sclerosis; Creatine; Disease Progression; Humans; Motor Neuron Disease; Neuropro

2012
Rosuvastatin-induced arrest in progression of renal disease.
    Cardiology, 2004, Volume: 102, Issue:1

    Topics: Aged; Atorvastatin; Controlled Clinical Trials as Topic; Creatine; Disease Progression; Drug Adminis

2004
Magnetic resonance spectroscopy in the evaluation of central nervous system manifestations of systemic lupus erythematosus.
    Arthritis and rheumatism, 2006, Oct-15, Volume: 55, Issue:5

    Topics: Aspartic Acid; Brain; Central Nervous System; Creatine; Disease Progression; Humans; Lupus Vasculiti

2006
On the hypothesis that the failing heart is energy starved: lessons learned from the metabolism of ATP and creatine.
    Current hypertension reports, 2006, Volume: 8, Issue:6

    Topics: Adenosine Triphosphate; Animals; Creatine; Disease Progression; Energy Metabolism; Heat-Shock Protei

2006
Course of autosomal recessive polycystic kidney disease (ARPKD) in siblings: a clinical comparison of 20 sibships.
    Clinical genetics, 1995, Volume: 47, Issue:5

    Topics: Adolescent; Adult; Age of Onset; Child; Child, Preschool; Creatine; Disease Progression; Female; Hum

1995
Biological markers in the diagnosis and treatment of ALS.
    Journal of the neurological sciences, 1999, Volume: 165 Suppl 1

    Topics: Amyotrophic Lateral Sclerosis; Aspartic Acid; Biomarkers; Brain; Creatine; Disease Progression; Elec

1999
Proton MR spectroscopy in multiple sclerosis.
    Neuroimaging clinics of North America, 2000, Volume: 10, Issue:4

    Topics: Aspartic Acid; Brain; Choline; Creatine; Disability Evaluation; Disease Progression; Energy Metaboli

2000

Trials

17 trials available for creatine and Disease Exacerbation

ArticleYear
The CREST-E study of creatine for Huntington disease: A randomized controlled trial.
    Neurology, 2017, Aug-08, Volume: 89, Issue:6

    Topics: Australia; Creatine; Disease Progression; Double-Blind Method; Female; Follow-Up Studies; Humans; Hu

2017
Predictors of weight loss in early treated Parkinson's disease from the NET-PD LS-1 cohort.
    Journal of neurology, 2017, Volume: 264, Issue:8

    Topics: Age Factors; Antiparkinson Agents; Creatine; Disease Progression; Dopamine Agents; Double-Blind Meth

2017
1H-magnetic resonance spectroscopy in diffuse and focal cervical cord lesions in multiple sclerosis.
    European radiology, 2013, Volume: 23, Issue:12

    Topics: Adult; Analysis of Variance; Aspartic Acid; Cervical Vertebrae; Creatine; Cross-Sectional Studies; D

2013
Effect of creatine monohydrate on clinical progression in patients with Parkinson disease: a randomized clinical trial.
    JAMA, 2015, Feb-10, Volume: 313, Issue:6

    Topics: Aged; Antiparkinson Agents; Creatine; Disease Progression; Double-Blind Method; Drug Therapy, Combin

2015
Randomized trial of erhuangfang for relapsing multiple sclerosis.
    Neurological research, 2015, Volume: 37, Issue:7

    Topics: Adolescent; Adult; Anti-Inflammatory Agents; Aspartic Acid; Brain; Creatine; Disability Evaluation;

2015
Prospective serial proton MR spectroscopic assessment of response to tamoxifen for recurrent malignant glioma.
    Journal of neuro-oncology, 2008, Volume: 90, Issue:1

    Topics: Adult; Aged; Antineoplastic Agents, Hormonal; Aspartic Acid; Brain Neoplasms; Choline; Creatine; Dis

2008
Creatine monohydrate in ALS: effects on strength, fatigue, respiratory status and ALSFRS.
    Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases, 2008, Volume: 9, Issue:5

    Topics: Aged; Amyotrophic Lateral Sclerosis; Biomarkers; Creatine; Disease Progression; Double-Blind Method;

2008
Brain N-acetylaspartate levels correlate with motor function in metachromatic leukodystrophy.
    Neurology, 2010, Nov-23, Volume: 75, Issue:21

    Topics: Aspartic Acid; Biomarkers; Brain; Child, Preschool; Choline; Cognition; Creatine; Disease Progressio

2010
Urinary markers of renal inflammation in adolescents with Type 1 diabetes mellitus and normoalbuminuria.
    Diabetic medicine : a journal of the British Diabetic Association, 2012, Volume: 29, Issue:10

    Topics: Adolescent; Albuminuria; Biomarkers; Chemokines; Child; Creatine; Cytokines; Diabetes Mellitus, Type

2012
Beta-Interferon treatment does not always slow the progression of axonal injury in multiple sclerosis.
    Journal of neurology, 2003, Volume: 250, Issue:2

    Topics: Adult; Aspartic Acid; Axons; Body Water; Brain Chemistry; Cohort Studies; Creatine; Disease Progress

2003
A randomized sequential trial of creatine in amyotrophic lateral sclerosis.
    Annals of neurology, 2003, Volume: 53, Issue:4

    Topics: Aged; Amyotrophic Lateral Sclerosis; Creatine; Disease Progression; Double-Blind Method; Female; Hum

2003
The use of statistical MUNE in a multicenter clinical trial.
    Muscle & nerve, 2004, Volume: 30, Issue:4

    Topics: Action Potentials; Amyotrophic Lateral Sclerosis; Cell Count; Creatine; Data Interpretation, Statist

2004
Proton spectroscopy in Alzheimer's disease and cognitive impairment no dementia: a community-based study.
    Dementia and geriatric cognitive disorders, 2008, Volume: 25, Issue:6

    Topics: Aged; Aged, 80 and over; Alzheimer Disease; Aspartic Acid; Atrophy; Brain; Choline; Cognition Disord

2008
Effects of oral adsorbent AST-120 on the progression of chronic renal failure: a randomized controlled study.
    Kidney international. Supplement, 1997, Volume: 63

    Topics: Carbon; Creatine; Creatinine; Diet, Protein-Restricted; Disease Progression; Humans; Kidney Failure,

1997
Effects of losartan on renal and cardiovascular outcomes in patients with type 2 diabetes and nephropathy.
    The New England journal of medicine, 2001, Sep-20, Volume: 345, Issue:12

    Topics: Adult; Aged; Angiotensin Receptor Antagonists; Antihypertensive Agents; Cardiovascular Diseases; Cre

2001
Effects of losartan on renal and cardiovascular outcomes in patients with type 2 diabetes and nephropathy.
    The New England journal of medicine, 2001, Sep-20, Volume: 345, Issue:12

    Topics: Adult; Aged; Angiotensin Receptor Antagonists; Antihypertensive Agents; Cardiovascular Diseases; Cre

2001
Effects of losartan on renal and cardiovascular outcomes in patients with type 2 diabetes and nephropathy.
    The New England journal of medicine, 2001, Sep-20, Volume: 345, Issue:12

    Topics: Adult; Aged; Angiotensin Receptor Antagonists; Antihypertensive Agents; Cardiovascular Diseases; Cre

2001
Effects of losartan on renal and cardiovascular outcomes in patients with type 2 diabetes and nephropathy.
    The New England journal of medicine, 2001, Sep-20, Volume: 345, Issue:12

    Topics: Adult; Aged; Angiotensin Receptor Antagonists; Antihypertensive Agents; Cardiovascular Diseases; Cre

2001
Effects of losartan on renal and cardiovascular outcomes in patients with type 2 diabetes and nephropathy.
    The New England journal of medicine, 2001, Sep-20, Volume: 345, Issue:12

    Topics: Adult; Aged; Angiotensin Receptor Antagonists; Antihypertensive Agents; Cardiovascular Diseases; Cre

2001
Effects of losartan on renal and cardiovascular outcomes in patients with type 2 diabetes and nephropathy.
    The New England journal of medicine, 2001, Sep-20, Volume: 345, Issue:12

    Topics: Adult; Aged; Angiotensin Receptor Antagonists; Antihypertensive Agents; Cardiovascular Diseases; Cre

2001
Effects of losartan on renal and cardiovascular outcomes in patients with type 2 diabetes and nephropathy.
    The New England journal of medicine, 2001, Sep-20, Volume: 345, Issue:12

    Topics: Adult; Aged; Angiotensin Receptor Antagonists; Antihypertensive Agents; Cardiovascular Diseases; Cre

2001
Effects of losartan on renal and cardiovascular outcomes in patients with type 2 diabetes and nephropathy.
    The New England journal of medicine, 2001, Sep-20, Volume: 345, Issue:12

    Topics: Adult; Aged; Angiotensin Receptor Antagonists; Antihypertensive Agents; Cardiovascular Diseases; Cre

2001
Effects of losartan on renal and cardiovascular outcomes in patients with type 2 diabetes and nephropathy.
    The New England journal of medicine, 2001, Sep-20, Volume: 345, Issue:12

    Topics: Adult; Aged; Angiotensin Receptor Antagonists; Antihypertensive Agents; Cardiovascular Diseases; Cre

2001
Effects of losartan on renal and cardiovascular outcomes in patients with type 2 diabetes and nephropathy.
    The New England journal of medicine, 2001, Sep-20, Volume: 345, Issue:12

    Topics: Adult; Aged; Angiotensin Receptor Antagonists; Antihypertensive Agents; Cardiovascular Diseases; Cre

2001
Effects of losartan on renal and cardiovascular outcomes in patients with type 2 diabetes and nephropathy.
    The New England journal of medicine, 2001, Sep-20, Volume: 345, Issue:12

    Topics: Adult; Aged; Angiotensin Receptor Antagonists; Antihypertensive Agents; Cardiovascular Diseases; Cre

2001
Effects of losartan on renal and cardiovascular outcomes in patients with type 2 diabetes and nephropathy.
    The New England journal of medicine, 2001, Sep-20, Volume: 345, Issue:12

    Topics: Adult; Aged; Angiotensin Receptor Antagonists; Antihypertensive Agents; Cardiovascular Diseases; Cre

2001
Effects of losartan on renal and cardiovascular outcomes in patients with type 2 diabetes and nephropathy.
    The New England journal of medicine, 2001, Sep-20, Volume: 345, Issue:12

    Topics: Adult; Aged; Angiotensin Receptor Antagonists; Antihypertensive Agents; Cardiovascular Diseases; Cre

2001
Effects of losartan on renal and cardiovascular outcomes in patients with type 2 diabetes and nephropathy.
    The New England journal of medicine, 2001, Sep-20, Volume: 345, Issue:12

    Topics: Adult; Aged; Angiotensin Receptor Antagonists; Antihypertensive Agents; Cardiovascular Diseases; Cre

2001
Effects of losartan on renal and cardiovascular outcomes in patients with type 2 diabetes and nephropathy.
    The New England journal of medicine, 2001, Sep-20, Volume: 345, Issue:12

    Topics: Adult; Aged; Angiotensin Receptor Antagonists; Antihypertensive Agents; Cardiovascular Diseases; Cre

2001
Effects of losartan on renal and cardiovascular outcomes in patients with type 2 diabetes and nephropathy.
    The New England journal of medicine, 2001, Sep-20, Volume: 345, Issue:12

    Topics: Adult; Aged; Angiotensin Receptor Antagonists; Antihypertensive Agents; Cardiovascular Diseases; Cre

2001
Longitudinal changes of metabolites in frontal lobes after hemorrhagic stroke of basal ganglia: a proton magnetic resonance spectroscopy study.
    Stroke, 2001, Volume: 32, Issue:10

    Topics: Aged; Aged, 80 and over; Aspartic Acid; Basal Ganglia Hemorrhage; Creatine; Disease Progression; Fem

2001
Spectroscopic assessment of alterations in macromolecule and small-molecule metabolites in human brain after stroke.
    Stroke, 2001, Dec-01, Volume: 32, Issue:12

    Topics: Adult; Age Factors; Aged; Aged, 80 and over; Brain; Choline; Creatine; Disease Progression; Female;

2001

Other Studies

103 other studies available for creatine and Disease Exacerbation

ArticleYear
Spatio-temporal metabolic rewiring in the brain of TgF344-AD rat model of Alzheimer's disease.
    Scientific reports, 2022, 10-10, Volume: 12, Issue:1

    Topics: Alzheimer Disease; Animals; Brain; Choline; Creatine; Disease Models, Animal; Disease Progression; G

2022
Biomarkers for Duchenne muscular dystrophy progression: impact of age in the mdx tongue spared muscle.
    Skeletal muscle, 2023, 09-13, Volume: 13, Issue:1

    Topics: Acetic Acid; Alanine; Animals; Creatine; Disease Progression; Glycerol; Isoleucine; Methionine; Mice

2023
Clinical and pathological features of immunoglobulin A nephropathy patients with nephrotic syndrome.
    Clinical and experimental medicine, 2019, Volume: 19, Issue:4

    Topics: Adult; China; Creatine; Disease Progression; Female; Glomerular Filtration Rate; Glomerulonephritis,

2019
Short echo-time Magnetic Resonance Spectroscopy in ALS, simultaneous quantification of glutamate and GABA at 3 T.
    Scientific reports, 2019, 11-26, Volume: 9, Issue:1

    Topics: Aged; Amyotrophic Lateral Sclerosis; Aspartic Acid; Atrophy; Choline; Creatine; Disease Progression;

2019
Hypoproteinemia as a parameter of poor perinatal/neonatal outcomes in women with preeclampsia diagnosed as hypertension plus proteinuria.
    Pregnancy hypertension, 2020, Volume: 21

    Topics: Adult; Case-Control Studies; Creatine; Disease Progression; Female; Gestational Age; Humans; Pre-Ecl

2020
Impact of the number of steroid pulses in tonsillectomy combined with steroid pulse therapy: a nationwide retrospective study in Japan.
    Clinical and experimental nephrology, 2021, Volume: 25, Issue:1

    Topics: Adrenal Cortex Hormones; Adult; Combined Modality Therapy; Creatine; Disease Progression; Female; Gl

2021
Utility of Magnetic Resonance Spectroscopy for the Progression of Neurological Symptoms in Lenticulostriate Artery Territory Infarction.
    Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association, 2021, Volume: 30, Issue:6

    Topics: Aged; Aged, 80 and over; Basal Ganglia Cerebrovascular Disease; Biomarkers; Brain Infarction; Cholin

2021
Caffeine, creatine, GRIN2A and Parkinson's disease progression.
    Journal of the neurological sciences, 2017, Apr-15, Volume: 375

    Topics: Aged; Caffeine; Creatine; Disease Progression; Female; Gene-Environment Interaction; Genetic Predisp

2017
Proton MR spectroscopy of lesion evolution in multiple sclerosis: Steady-state metabolism and its relationship to conventional imaging.
    Human brain mapping, 2017, Volume: 38, Issue:8

    Topics: Adult; Aspartic Acid; Brain; Choline; Creatine; Cross-Sectional Studies; Disease Progression; Female

2017
Prognostic relationship of metabolic profile obtained of melanoma B16F10.
    Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie, 2013, Volume: 67, Issue:2

    Topics: Animals; Apoptosis; Biomarkers, Tumor; Caspase 3; Cell Cycle; Cell Line, Tumor; Cell Proliferation;

2013
Brain metabolic changes suggestive of axonal damage in radiologically isolated syndrome.
    Neurology, 2013, Jun-04, Volume: 80, Issue:23

    Topics: Adult; Aspartic Acid; Axons; Brain; Choline; Creatine; Disease Progression; Female; Humans; Magnetic

2013
Magnetic resonance spectroscopy as a predictor of conversion of mild cognitive impairment to dementia.
    Journal of the neurological sciences, 2013, Dec-15, Volume: 335, Issue:1-2

    Topics: Aged; Aged, 80 and over; Aspartic Acid; Brain; Choline; Cognitive Dysfunction; Creatine; Dementia; D

2013
Magnetic resonance spectroscopy as a predictor of conversion of mild cognitive impairment to dementia.
    Journal of the neurological sciences, 2013, Dec-15, Volume: 335, Issue:1-2

    Topics: Aged; Aged, 80 and over; Aspartic Acid; Brain; Choline; Cognitive Dysfunction; Creatine; Dementia; D

2013
Magnetic resonance spectroscopy as a predictor of conversion of mild cognitive impairment to dementia.
    Journal of the neurological sciences, 2013, Dec-15, Volume: 335, Issue:1-2

    Topics: Aged; Aged, 80 and over; Aspartic Acid; Brain; Choline; Cognitive Dysfunction; Creatine; Dementia; D

2013
Magnetic resonance spectroscopy as a predictor of conversion of mild cognitive impairment to dementia.
    Journal of the neurological sciences, 2013, Dec-15, Volume: 335, Issue:1-2

    Topics: Aged; Aged, 80 and over; Aspartic Acid; Brain; Choline; Cognitive Dysfunction; Creatine; Dementia; D

2013
Magnetic resonance imaging spectroscopy in pediatric atypical teratoid rhabdoid tumors of the brain.
    Journal of pediatric hematology/oncology, 2014, Volume: 36, Issue:6

    Topics: Brain; Brain Neoplasms; Child, Preschool; Choline; Chromosomal Proteins, Non-Histone; Creatine; Diag

2014
Reduced levels of mitochondrial complex I subunit NDUFB8 and linked complex I + III oxidoreductase activity in the TgCRND8 mouse model of Alzheimer's disease.
    Journal of Alzheimer's disease : JAD, 2014, Volume: 39, Issue:2

    Topics: Adenosine Triphosphate; Aging; Alzheimer Disease; Amyloid beta-Protein Precursor; Animals; Cardiolip

2014
The carotid plaque imaging in acute stroke (CAPIAS) study: protocol and initial baseline data.
    BMC neurology, 2013, Dec-13, Volume: 13

    Topics: Aged; Carotid Stenosis; Cerebral Cortex; Cognition Disorders; Cohort Studies; Creatine; Disease Prog

2013
Cortical N-acetyl aspartate is a predictor of long-term clinical disability in multiple sclerosis.
    Neurological research, 2014, Volume: 36, Issue:8

    Topics: Adult; Aspartic Acid; Cerebral Cortex; Creatine; Disability Evaluation; Disease Progression; Female;

2014
Development of a model to estimate 24-hour urinary creatinine excretion.
    Journal of clinical hypertension (Greenwich, Conn.), 2014, Volume: 16, Issue:5

    Topics: Biomarkers; Circadian Rhythm; Creatine; Disease Progression; Female; Follow-Up Studies; Humans; Hype

2014
Presence of early CKD-related metabolic complications predict progression of stage 3 CKD: a case-controlled study.
    BMC nephrology, 2014, Nov-27, Volume: 15

    Topics: Acidosis; Aged; Aged, 80 and over; Anemia; Bicarbonates; Calcium; Case-Control Studies; Creatine; Di

2014
Metabolite ratios in the posterior cingulate cortex do not track cognitive decline in Parkinson's disease in a clinical setting.
    Parkinsonism & related disorders, 2016, Volume: 22

    Topics: Aged; Aged, 80 and over; Aspartic Acid; Bayes Theorem; Case-Control Studies; Choline; Cognitive Dysf

2016
Predicting Renal Failure Progression in Chronic Kidney Disease Using Integrated Intelligent Fuzzy Expert System.
    Computational and mathematical methods in medicine, 2016, Volume: 2016

    Topics: Adult; Aged; Artificial Intelligence; Blood Pressure; Calcium; Creatine; Disease Progression; Expert

2016
Discrepant longitudinal volumetric and metabolic evolution of diffuse intrinsic Pontine gliomas during treatment: implications for current response assessment strategies.
    Neuroradiology, 2016, Volume: 58, Issue:10

    Topics: Adolescent; Aging; Aspartic Acid; Biomarkers, Tumor; Brain Stem; Brain Stem Neoplasms; Child; Child,

2016
Two hundred steps.
    Nature, 2016, 10-27, Volume: 538, Issue:7626

    Topics: alpha-Synuclein; Creatine; Deep Brain Stimulation; Disease Progression; Dopamine; Fetal Tissue Trans

2016
Impact of optimal medical therapy and revascularization on outcome of patients with chronic kidney disease and on dialysis who presented with acute coronary syndrome.
    The American journal of cardiology, 2008, Sep-01, Volume: 102, Issue:5

    Topics: Acute Disease; Aged; Confidence Intervals; Coronary Angiography; Coronary Disease; Creatine; Disease

2008
Urinary neutrophil gelatinase associated lipocalin (NGAL), a marker of tubular damage, is increased in patients with chronic heart failure.
    European journal of heart failure, 2008, Volume: 10, Issue:10

    Topics: Acute-Phase Proteins; Albumins; Case-Control Studies; Chronic Disease; Creatine; Disease Progression

2008
Proton magnetic resonance spectroscopic findings of cerebral fat embolism induced by triolein emulsion in cats.
    Acta radiologica (Stockholm, Sweden : 1987), 2008, Volume: 49, Issue:10

    Topics: Animals; Aspartic Acid; Brain; Cats; Choline; Contrast Media; Creatine; Disease Models, Animal; Dise

2008
Combined structural and neurochemical evaluation of the corticospinal tract in amyotrophic lateral sclerosis.
    Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases, 2010, Volume: 11, Issue:1-2

    Topics: Amyotrophic Lateral Sclerosis; Aspartic Acid; Choline; Creatine; Diffusion Tensor Imaging; Disease P

2010
Serial MR imaging and 1H-MR spectroscopy in monozygotic twins with Tay-Sachs disease.
    Neuropediatrics, 2008, Volume: 39, Issue:5

    Topics: Aspartic Acid; Basal Ganglia; Brain; Cerebral Cortex; Child, Preschool; Choline; Corpus Callosum; Cr

2008
Urinary excretion of low-molecular-weight proteins as prognostic markers in IgA nephropathy.
    The Netherlands journal of medicine, 2009, Volume: 67, Issue:2

    Topics: Adolescent; Adult; Aged; Alpha-Globulins; beta 2-Microglobulin; Biomarkers; Creatine; Disease Progre

2009
Risk of dementia in MCI: combined effect of cerebrovascular disease, volumetric MRI, and 1H MRS.
    Neurology, 2009, Apr-28, Volume: 72, Issue:17

    Topics: Aged; Aged, 80 and over; Aspartic Acid; Atrophy; Biomarkers; Brain; Cerebrovascular Disorders; Cogni

2009
Conversion to dementia in mild cognitive impairment is associated with decline of N-actylaspartate and creatine as revealed by magnetic resonance spectroscopy.
    Psychiatry research, 2009, Jul-15, Volume: 173, Issue:1

    Topics: Aged; Alzheimer Disease; Aspartic Acid; Brain; Choline; Cognition; Cognition Disorders; Creatine; De

2009
A proton magnetic resonance spectroscopic study in juvenile absence epilepsy in early stages.
    European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society, 2010, Volume: 14, Issue:3

    Topics: Adolescent; Aspartic Acid; Brain; Child; Choline; Creatine; Disease Progression; Down-Regulation; El

2010
Circulating endothelial progenitor cells and age-related white matter changes.
    Stroke, 2009, Volume: 40, Issue:10

    Topics: Age Distribution; Aged; Aging; Angiotensin-Converting Enzyme Inhibitors; Brain; C-Reactive Protein;

2009
(1)H MRSI and progression-free survival in patients with WHO grades II and III gliomas.
    Neurological research, 2010, Volume: 32, Issue:6

    Topics: Adult; Aged; Brain Neoplasms; Choline; Creatine; Disease Progression; Disease-Free Survival; Female;

2010
Distinction between glioma progression and post-radiation change by combined physiologic MR imaging.
    Neuroradiology, 2010, Volume: 52, Issue:4

    Topics: Adult; Aspartic Acid; Blood Volume; Brain; Brain Neoplasms; Cerebrovascular Circulation; Choline; Cr

2010
Neuronal and axonal degeneration in experimental spinal cord injury: in vivo proton magnetic resonance spectroscopy and histology.
    Journal of neurotrauma, 2010, Volume: 27, Issue:3

    Topics: Animals; Aspartic Acid; Choline; Creatine; Disease Models, Animal; Disease Progression; Gliosis; Imm

2010
Retinal metabolic state of the proline-23-histidine rat model of retinitis pigmentosa.
    American journal of physiology. Cell physiology, 2010, Volume: 298, Issue:3

    Topics: Adenosine Triphosphate; Age Factors; Animals; Apoptosis; Ca(2+) Mg(2+)-ATPase; Coumaric Acids; Creat

2010
Chronic hepatitis C and chronic kidney disease.
    Digestive diseases and sciences, 2010, Volume: 55, Issue:5

    Topics: Creatine; Disease Progression; Global Health; Glomerular Filtration Rate; Hepatitis C, Chronic; Huma

2010
Identifying additional patients with diabetic nephropathy using the UK primary care initiative.
    Diabetic medicine : a journal of the British Diabetic Association, 2010, Volume: 27, Issue:12

    Topics: Creatine; Cross-Sectional Studies; Diabetes Mellitus, Type 2; Diabetic Nephropathies; Disease Progre

2010
Diffusion-weighted imaging and magnetic resonance spectroscopy of sporadic Creutzfeldt-Jakob disease: correlation with clinical course.
    Neuroradiology, 2011, Volume: 53, Issue:12

    Topics: Aged; Aspartic Acid; Biomarkers; Brain; Choline; Creatine; Creutzfeldt-Jakob Syndrome; Diffusion Mag

2011
Strengths and weaknesses of renal markers as risk factors and surrogate markers.
    Kidney international, 2011, Volume: 79, Issue:12

    Topics: Albuminuria; Biomarkers; Cardiovascular Diseases; Creatine; Disease Progression; Evidence-Based Medi

2011
A metabonomic study of biochemical changes characteristic of genetically hypertensive rats based on (1)H NMR spectroscopic urinalysis.
    Hypertension research : official journal of the Japanese Society of Hypertension, 2012, Volume: 35, Issue:4

    Topics: Animals; Citric Acid; Creatine; Disease Progression; Hippurates; Hypertension; Magnetic Resonance Sp

2012
Subependymal seeding of low-grade oligodendroglial neoplasms: a case series.
    Journal of neuro-oncology, 2012, Volume: 108, Issue:1

    Topics: Adult; Aspartic Acid; Creatine; Disease Progression; Ependyma; Fourth Ventricle; Glioma; Humans; Iso

2012
The imaging diagnosis and prognosis assessment of patients with midbrain injury in the acute phase of craniocerebral injury.
    Acta neurochirurgica. Supplement, 2012, Volume: 114

    Topics: Adolescent; Adult; Aspartic Acid; Child; Choline; Craniocerebral Trauma; Creatine; Disease Progressi

2012
Metabolite investigation in both anterior and posterior cingulate gyri in Alzheimer's disease spectrum using 3-tesla MR spectroscopy.
    Dementia and geriatric cognitive disorders, 2012, Volume: 33, Issue:2-3

    Topics: Aged; Aged, 80 and over; Alzheimer Disease; Aspartic Acid; Cognition Disorders; Creatine; Disease Pr

2012
Delayed relief of ureteral obstruction is implicated in the long-term development of renal damage and arterial hypertension in patients with unilateral ureteral injury.
    The Journal of urology, 2013, Volume: 189, Issue:3

    Topics: Adolescent; Adult; Aged; Aged, 80 and over; Biomarkers; Blood Pressure; Chemokine CCL2; Child; Child

2013
Relationship between cervical cord 1H-magnetic resonance spectroscopy and clinoco-electromyographic profile in amyotrophic lateral sclerosis.
    Muscle & nerve, 2013, Volume: 47, Issue:1

    Topics: Amyotrophic Lateral Sclerosis; Cervical Vertebrae; Choline; Creatine; Disease Progression; Electromy

2013
Association between proton magnetic resonance spectroscopy measurements and CAG repeat number in patients with spinocerebellar ataxias 2, 3, or 6.
    PloS one, 2012, Volume: 7, Issue:10

    Topics: Adult; Age of Onset; Aged; Aspartic Acid; Case-Control Studies; Cerebellum; Creatine; Disease Progre

2012
The human OPA1delTTAG mutation induces premature age-related systemic neurodegeneration in mouse.
    Brain : a journal of neurology, 2012, Volume: 135, Issue:Pt 12

    Topics: Acoustic Stimulation; Age Factors; Aging, Premature; Animals; Aspartic Acid; Chi-Square Distribution

2012
Lumbrokinase attenuates diabetic nephropathy through regulating extracellular matrix degradation in Streptozotocin-induced diabetic rats.
    Diabetes research and clinical practice, 2013, Volume: 100, Issue:1

    Topics: Animals; Blotting, Western; Collagen Type IV; Creatine; Diabetes Mellitus, Experimental; Diabetic Ne

2013
Localized (1)H magnetic resonance spectroscopy in mainly cortical gray matter of patients with multiple sclerosis.
    Journal of neurology, 2002, Volume: 249, Issue:7

    Topics: Adult; Aspartic Acid; Atrophy; Creatine; Disease Progression; Female; Humans; Magnetic Resonance Spe

2002
Enhanced dystrophic progression in mdx mice by exercise and beneficial effects of taurine and insulin-like growth factor-1.
    The Journal of pharmacology and experimental therapeutics, 2003, Volume: 304, Issue:1

    Topics: Animals; Creatine; Disease Progression; Electrophysiology; Insulin-Like Growth Factor I; Ion Channel

2003
Proton magnetic resonance imaging and spectroscopy identify metabolic changes in the striatum in the MPTP feline model of parkinsonism.
    Experimental neurology, 2003, Volume: 179, Issue:2

    Topics: 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine; Animals; Aspartic Acid; Brain; Cats; Choline; Corpus S

2003
Creatine therapy provides neuroprotection after onset of clinical symptoms in Huntington's disease transgenic mice.
    Journal of neurochemistry, 2003, Volume: 85, Issue:6

    Topics: Adenosine Triphosphate; Administration, Oral; Animals; Body Weight; Brain; Corpus Striatum; Creatine

2003
Creatine therapy provides neuroprotection after onset of clinical symptoms in Huntington's disease transgenic mice.
    Journal of neurochemistry, 2003, Volume: 85, Issue:6

    Topics: Adenosine Triphosphate; Administration, Oral; Animals; Body Weight; Brain; Corpus Striatum; Creatine

2003
Creatine therapy provides neuroprotection after onset of clinical symptoms in Huntington's disease transgenic mice.
    Journal of neurochemistry, 2003, Volume: 85, Issue:6

    Topics: Adenosine Triphosphate; Administration, Oral; Animals; Body Weight; Brain; Corpus Striatum; Creatine

2003
Creatine therapy provides neuroprotection after onset of clinical symptoms in Huntington's disease transgenic mice.
    Journal of neurochemistry, 2003, Volume: 85, Issue:6

    Topics: Adenosine Triphosphate; Administration, Oral; Animals; Body Weight; Brain; Corpus Striatum; Creatine

2003
Creatine therapy provides neuroprotection after onset of clinical symptoms in Huntington's disease transgenic mice.
    Journal of neurochemistry, 2003, Volume: 85, Issue:6

    Topics: Adenosine Triphosphate; Administration, Oral; Animals; Body Weight; Brain; Corpus Striatum; Creatine

2003
Creatine therapy provides neuroprotection after onset of clinical symptoms in Huntington's disease transgenic mice.
    Journal of neurochemistry, 2003, Volume: 85, Issue:6

    Topics: Adenosine Triphosphate; Administration, Oral; Animals; Body Weight; Brain; Corpus Striatum; Creatine

2003
Creatine therapy provides neuroprotection after onset of clinical symptoms in Huntington's disease transgenic mice.
    Journal of neurochemistry, 2003, Volume: 85, Issue:6

    Topics: Adenosine Triphosphate; Administration, Oral; Animals; Body Weight; Brain; Corpus Striatum; Creatine

2003
Creatine therapy provides neuroprotection after onset of clinical symptoms in Huntington's disease transgenic mice.
    Journal of neurochemistry, 2003, Volume: 85, Issue:6

    Topics: Adenosine Triphosphate; Administration, Oral; Animals; Body Weight; Brain; Corpus Striatum; Creatine

2003
Creatine therapy provides neuroprotection after onset of clinical symptoms in Huntington's disease transgenic mice.
    Journal of neurochemistry, 2003, Volume: 85, Issue:6

    Topics: Adenosine Triphosphate; Administration, Oral; Animals; Body Weight; Brain; Corpus Striatum; Creatine

2003
Creatine therapy provides neuroprotection after onset of clinical symptoms in Huntington's disease transgenic mice.
    Journal of neurochemistry, 2003, Volume: 85, Issue:6

    Topics: Adenosine Triphosphate; Administration, Oral; Animals; Body Weight; Brain; Corpus Striatum; Creatine

2003
Creatine therapy provides neuroprotection after onset of clinical symptoms in Huntington's disease transgenic mice.
    Journal of neurochemistry, 2003, Volume: 85, Issue:6

    Topics: Adenosine Triphosphate; Administration, Oral; Animals; Body Weight; Brain; Corpus Striatum; Creatine

2003
Creatine therapy provides neuroprotection after onset of clinical symptoms in Huntington's disease transgenic mice.
    Journal of neurochemistry, 2003, Volume: 85, Issue:6

    Topics: Adenosine Triphosphate; Administration, Oral; Animals; Body Weight; Brain; Corpus Striatum; Creatine

2003
Creatine therapy provides neuroprotection after onset of clinical symptoms in Huntington's disease transgenic mice.
    Journal of neurochemistry, 2003, Volume: 85, Issue:6

    Topics: Adenosine Triphosphate; Administration, Oral; Animals; Body Weight; Brain; Corpus Striatum; Creatine

2003
Creatine therapy provides neuroprotection after onset of clinical symptoms in Huntington's disease transgenic mice.
    Journal of neurochemistry, 2003, Volume: 85, Issue:6

    Topics: Adenosine Triphosphate; Administration, Oral; Animals; Body Weight; Brain; Corpus Striatum; Creatine

2003
Creatine therapy provides neuroprotection after onset of clinical symptoms in Huntington's disease transgenic mice.
    Journal of neurochemistry, 2003, Volume: 85, Issue:6

    Topics: Adenosine Triphosphate; Administration, Oral; Animals; Body Weight; Brain; Corpus Striatum; Creatine

2003
Creatine therapy provides neuroprotection after onset of clinical symptoms in Huntington's disease transgenic mice.
    Journal of neurochemistry, 2003, Volume: 85, Issue:6

    Topics: Adenosine Triphosphate; Administration, Oral; Animals; Body Weight; Brain; Corpus Striatum; Creatine

2003
Creatine therapy provides neuroprotection after onset of clinical symptoms in Huntington's disease transgenic mice.
    Journal of neurochemistry, 2003, Volume: 85, Issue:6

    Topics: Adenosine Triphosphate; Administration, Oral; Animals; Body Weight; Brain; Corpus Striatum; Creatine

2003
Creatine therapy provides neuroprotection after onset of clinical symptoms in Huntington's disease transgenic mice.
    Journal of neurochemistry, 2003, Volume: 85, Issue:6

    Topics: Adenosine Triphosphate; Administration, Oral; Animals; Body Weight; Brain; Corpus Striatum; Creatine

2003
Creatine therapy provides neuroprotection after onset of clinical symptoms in Huntington's disease transgenic mice.
    Journal of neurochemistry, 2003, Volume: 85, Issue:6

    Topics: Adenosine Triphosphate; Administration, Oral; Animals; Body Weight; Brain; Corpus Striatum; Creatine

2003
Creatine therapy provides neuroprotection after onset of clinical symptoms in Huntington's disease transgenic mice.
    Journal of neurochemistry, 2003, Volume: 85, Issue:6

    Topics: Adenosine Triphosphate; Administration, Oral; Animals; Body Weight; Brain; Corpus Striatum; Creatine

2003
Creatine therapy provides neuroprotection after onset of clinical symptoms in Huntington's disease transgenic mice.
    Journal of neurochemistry, 2003, Volume: 85, Issue:6

    Topics: Adenosine Triphosphate; Administration, Oral; Animals; Body Weight; Brain; Corpus Striatum; Creatine

2003
Creatine therapy provides neuroprotection after onset of clinical symptoms in Huntington's disease transgenic mice.
    Journal of neurochemistry, 2003, Volume: 85, Issue:6

    Topics: Adenosine Triphosphate; Administration, Oral; Animals; Body Weight; Brain; Corpus Striatum; Creatine

2003
Creatine therapy provides neuroprotection after onset of clinical symptoms in Huntington's disease transgenic mice.
    Journal of neurochemistry, 2003, Volume: 85, Issue:6

    Topics: Adenosine Triphosphate; Administration, Oral; Animals; Body Weight; Brain; Corpus Striatum; Creatine

2003
Creatine therapy provides neuroprotection after onset of clinical symptoms in Huntington's disease transgenic mice.
    Journal of neurochemistry, 2003, Volume: 85, Issue:6

    Topics: Adenosine Triphosphate; Administration, Oral; Animals; Body Weight; Brain; Corpus Striatum; Creatine

2003
Creatine therapy provides neuroprotection after onset of clinical symptoms in Huntington's disease transgenic mice.
    Journal of neurochemistry, 2003, Volume: 85, Issue:6

    Topics: Adenosine Triphosphate; Administration, Oral; Animals; Body Weight; Brain; Corpus Striatum; Creatine

2003
Creatine therapy provides neuroprotection after onset of clinical symptoms in Huntington's disease transgenic mice.
    Journal of neurochemistry, 2003, Volume: 85, Issue:6

    Topics: Adenosine Triphosphate; Administration, Oral; Animals; Body Weight; Brain; Corpus Striatum; Creatine

2003
Creatine therapy provides neuroprotection after onset of clinical symptoms in Huntington's disease transgenic mice.
    Journal of neurochemistry, 2003, Volume: 85, Issue:6

    Topics: Adenosine Triphosphate; Administration, Oral; Animals; Body Weight; Brain; Corpus Striatum; Creatine

2003
Creatine therapy provides neuroprotection after onset of clinical symptoms in Huntington's disease transgenic mice.
    Journal of neurochemistry, 2003, Volume: 85, Issue:6

    Topics: Adenosine Triphosphate; Administration, Oral; Animals; Body Weight; Brain; Corpus Striatum; Creatine

2003
Creatine therapy provides neuroprotection after onset of clinical symptoms in Huntington's disease transgenic mice.
    Journal of neurochemistry, 2003, Volume: 85, Issue:6

    Topics: Adenosine Triphosphate; Administration, Oral; Animals; Body Weight; Brain; Corpus Striatum; Creatine

2003
Creatine therapy provides neuroprotection after onset of clinical symptoms in Huntington's disease transgenic mice.
    Journal of neurochemistry, 2003, Volume: 85, Issue:6

    Topics: Adenosine Triphosphate; Administration, Oral; Animals; Body Weight; Brain; Corpus Striatum; Creatine

2003
Creatine therapy provides neuroprotection after onset of clinical symptoms in Huntington's disease transgenic mice.
    Journal of neurochemistry, 2003, Volume: 85, Issue:6

    Topics: Adenosine Triphosphate; Administration, Oral; Animals; Body Weight; Brain; Corpus Striatum; Creatine

2003
Creatine therapy provides neuroprotection after onset of clinical symptoms in Huntington's disease transgenic mice.
    Journal of neurochemistry, 2003, Volume: 85, Issue:6

    Topics: Adenosine Triphosphate; Administration, Oral; Animals; Body Weight; Brain; Corpus Striatum; Creatine

2003
Creatine therapy provides neuroprotection after onset of clinical symptoms in Huntington's disease transgenic mice.
    Journal of neurochemistry, 2003, Volume: 85, Issue:6

    Topics: Adenosine Triphosphate; Administration, Oral; Animals; Body Weight; Brain; Corpus Striatum; Creatine

2003
Creatine therapy provides neuroprotection after onset of clinical symptoms in Huntington's disease transgenic mice.
    Journal of neurochemistry, 2003, Volume: 85, Issue:6

    Topics: Adenosine Triphosphate; Administration, Oral; Animals; Body Weight; Brain; Corpus Striatum; Creatine

2003
Creatine therapy provides neuroprotection after onset of clinical symptoms in Huntington's disease transgenic mice.
    Journal of neurochemistry, 2003, Volume: 85, Issue:6

    Topics: Adenosine Triphosphate; Administration, Oral; Animals; Body Weight; Brain; Corpus Striatum; Creatine

2003
Creatine therapy provides neuroprotection after onset of clinical symptoms in Huntington's disease transgenic mice.
    Journal of neurochemistry, 2003, Volume: 85, Issue:6

    Topics: Adenosine Triphosphate; Administration, Oral; Animals; Body Weight; Brain; Corpus Striatum; Creatine

2003
Analytical and clinical evaluation of a new urinary tumor marker: bladder tumor fibronectin in diagnosis and follow-up of bladder cancer.
    Clinical chemistry and laboratory medicine, 2003, Volume: 41, Issue:8

    Topics: Biomarkers, Tumor; Creatine; Data Interpretation, Statistical; Disease Progression; Female; Fibronec

2003
Pantothenate kinase-associated neurodegeneration: MR imaging, proton MR spectroscopy, and diffusion MR imaging findings.
    AJNR. American journal of neuroradiology, 2003, Volume: 24, Issue:8

    Topics: Adolescent; Aspartic Acid; Brain; Cerebellar Nuclei; Choline; Creatine; Diagnosis, Differential; Dif

2003
Alexander disease with serial MRS and a new mutation in the glial fibrillary acidic protein gene.
    Neurology, 2003, Oct-14, Volume: 61, Issue:7

    Topics: Acidosis, Respiratory; Alexander Disease; Basal Ganglia; Choline; Creatine; Disease Progression; DNA

2003
Proton magnetic resonance spectroscopy can detect creatine depletion associated with the progression of heart failure in cardiomyopathy.
    Journal of the American College of Cardiology, 2003, Nov-05, Volume: 42, Issue:9

    Topics: Adult; Cardiomyopathy, Dilated; Creatine; Disease Progression; Female; Humans; Image Processing, Com

2003
A prospective longitudinal in vivo 1H MR spectroscopy study of the SIV/macaque model of neuroAIDS.
    BMC neuroscience, 2004, Mar-05, Volume: 5

    Topics: Acute Disease; AIDS Dementia Complex; Animals; Aspartic Acid; Brain; Choline; Chronic Disease; Creat

2004
Leukoencephalopathy, cerebral calcifications, and cysts: new observations.
    Neurology, 2004, Apr-13, Volume: 62, Issue:7

    Topics: Adolescent; Aspartic Acid; Brain; Brain Diseases; Calcinosis; Central Nervous System Cysts; Child; C

2004
MR imaging and proton MR spectroscopic studies in Sjögren-Larsson syndrome: characterization of the leukoencephalopathy.
    AJNR. American journal of neuroradiology, 2004, Volume: 25, Issue:4

    Topics: Adolescent; Adult; Aspartic Acid; Brain; Cerebral Ventricles; Child; Child, Preschool; Choline; Crea

2004
Subacute sclerosing panencephalitis with fulminating course: follow-up magnetic resonance spectroscopy (MRS) findings.
    Journal of child neurology, 2004, Volume: 19, Issue:3

    Topics: Aspartic Acid; Brain; Cerebral Cortex; Child, Preschool; Choline; Creatine; Diagnosis, Differential;

2004
Proton magnetic resonance spectroscopy imaging in the evaluation of patients undergoing gamma knife surgery for Grade IV glioma.
    Journal of neurosurgery, 2004, Volume: 101, Issue:3

    Topics: Adult; Aged; Aged, 80 and over; Aspartic Acid; Brain; Brain Mapping; Brain Neoplasms; Choline; Cohor

2004
Treatment of severe pediatric ethylene glycol intoxication without hemodialysis.
    Journal of toxicology. Clinical toxicology, 2004, Volume: 42, Issue:3

    Topics: Acidosis; Adolescent; Antidotes; Bicarbonates; Child; Creatine; Disease Progression; Ethylene Glycol

2004
Elevation of myoinositol is associated with disease containment in progressive multifocal leukoencephalopathy.
    Neurology, 2004, Sep-14, Volume: 63, Issue:5

    Topics: Adult; Aspartic Acid; Cerebellum; Cerebral Cortex; Choline; Creatine; Disease Progression; Female; H

2004
Proton magnetic resonance spectroscopy in immunocompetent patients with primary central nervous system lymphoma.
    Journal of neuro-oncology, 2005, Volume: 71, Issue:2

    Topics: Adult; Aged; Aged, 80 and over; Antimetabolites, Antineoplastic; Aspartic Acid; Central Nervous Syst

2005
Assessment of adrenoleukodystrophy lesions by high field MRS in non-sedated pediatric patients.
    Neurology, 2005, Feb-08, Volume: 64, Issue:3

    Topics: Adolescent; Adrenoleukodystrophy; Aspartic Acid; Brain Chemistry; Child; Child, Preschool; Creatine;

2005
Longitudinal multivoxel MR spectroscopy study of pediatric diffuse brainstem gliomas treated with radiotherapy.
    International journal of radiation oncology, biology, physics, 2005, May-01, Volume: 62, Issue:1

    Topics: Aspartic Acid; Brain Stem Neoplasms; Child; Child, Preschool; Choline; Creatine; Disease Progression

2005
Conversion of MCI to dementia: Role of proton magnetic resonance spectroscopy.
    Neurobiology of aging, 2006, Volume: 27, Issue:7

    Topics: Aged; Amnesia; Aspartic Acid; Cerebral Cortex; Choline; Cognition Disorders; Creatine; Dementia; Dis

2006
Progressive intestinal, neurological and psychiatric problems in two adult males with cerebral creatine deficiency caused by an SLC6A8 mutation.
    Clinical genetics, 2005, Volume: 68, Issue:4

    Topics: Aged; Amino Acid Transport Disorders, Inborn; Brain; Creatine; Depression; Disease Progression; Fema

2005
Clinical efficacy of intravenous immunoglobulin for patients with MPO-ANCA-associated rapidly progressive glomerulonephritis.
    Nephron. Clinical practice, 2006, Volume: 102, Issue:1

    Topics: Aged; Aged, 80 and over; Antibodies, Antineutrophil Cytoplasmic; C-Reactive Protein; Creatine; Cyclo

2006
Turbulence of glomerular hemodynamics involved in progressive glomerulosclerosis.
    Kidney international, 2006, Volume: 69, Issue:10

    Topics: Albumins; Animals; Antibodies, Monoclonal; Blood Proteins; Blood Urea Nitrogen; Cholesterol; Creatin

2006
Longitudinal 1H MRS changes in mild cognitive impairment and Alzheimer's disease.
    Neurobiology of aging, 2007, Volume: 28, Issue:9

    Topics: Aged; Aged, 80 and over; Alzheimer Disease; Analysis of Variance; Aspartic Acid; Choline; Cognition

2007
Rate of decline of GFR and progression of vascular disease in type 2 diabetic patients with diabetic or vascular nephropathy during the last three years before starting dialysis therapy.
    Kidney & blood pressure research, 2006, Volume: 29, Issue:5

    Topics: Aged; Blood Pressure; Cholesterol; Creatine; Diabetes Mellitus, Type 2; Diabetic Angiopathies; Diabe

2006
MRI and MRS alterations in the preclinical phase of murine prion disease: association with neuropathological and behavioural changes.
    Neurobiology of disease, 2007, Volume: 26, Issue:3

    Topics: Animals; Aspartic Acid; Astrocytes; Body Water; Brain; Choline; Creatine; Diffusion; Disease Models,

2007
Time course of early metabolic changes following diffuse traumatic brain injury in rats as detected by (1)H NMR spectroscopy.
    Journal of neurotrauma, 2007, Volume: 24, Issue:6

    Topics: Amino Acids; Animals; Aspartic Acid; Brain; Brain Chemistry; Brain Injuries; Creatine; Diffuse Axona

2007
Axonal loss is progressive and partly dissociated from lesion load in early multiple sclerosis.
    Neurology, 2007, Jul-03, Volume: 69, Issue:1

    Topics: Adult; Aspartic Acid; Axons; Brain; Brain Chemistry; Choline; Creatine; Disease Progression; Female;

2007
Axonal loss is progressive and partly dissociated from lesion load in early multiple sclerosis.
    Neurology, 2007, Jul-03, Volume: 69, Issue:1

    Topics: Adult; Aspartic Acid; Axons; Brain; Brain Chemistry; Choline; Creatine; Disease Progression; Female;

2007
Axonal loss is progressive and partly dissociated from lesion load in early multiple sclerosis.
    Neurology, 2007, Jul-03, Volume: 69, Issue:1

    Topics: Adult; Aspartic Acid; Axons; Brain; Brain Chemistry; Choline; Creatine; Disease Progression; Female;

2007
Axonal loss is progressive and partly dissociated from lesion load in early multiple sclerosis.
    Neurology, 2007, Jul-03, Volume: 69, Issue:1

    Topics: Adult; Aspartic Acid; Axons; Brain; Brain Chemistry; Choline; Creatine; Disease Progression; Female;

2007
Axonal loss is progressive and partly dissociated from lesion load in early multiple sclerosis.
    Neurology, 2007, Jul-03, Volume: 69, Issue:1

    Topics: Adult; Aspartic Acid; Axons; Brain; Brain Chemistry; Choline; Creatine; Disease Progression; Female;

2007
Axonal loss is progressive and partly dissociated from lesion load in early multiple sclerosis.
    Neurology, 2007, Jul-03, Volume: 69, Issue:1

    Topics: Adult; Aspartic Acid; Axons; Brain; Brain Chemistry; Choline; Creatine; Disease Progression; Female;

2007
Axonal loss is progressive and partly dissociated from lesion load in early multiple sclerosis.
    Neurology, 2007, Jul-03, Volume: 69, Issue:1

    Topics: Adult; Aspartic Acid; Axons; Brain; Brain Chemistry; Choline; Creatine; Disease Progression; Female;

2007
Axonal loss is progressive and partly dissociated from lesion load in early multiple sclerosis.
    Neurology, 2007, Jul-03, Volume: 69, Issue:1

    Topics: Adult; Aspartic Acid; Axons; Brain; Brain Chemistry; Choline; Creatine; Disease Progression; Female;

2007
Axonal loss is progressive and partly dissociated from lesion load in early multiple sclerosis.
    Neurology, 2007, Jul-03, Volume: 69, Issue:1

    Topics: Adult; Aspartic Acid; Axons; Brain; Brain Chemistry; Choline; Creatine; Disease Progression; Female;

2007
Relative systemic hypertension in patients with sickle cell disease is associated with risk of pulmonary hypertension and renal insufficiency.
    American journal of hematology, 2008, Volume: 83, Issue:1

    Topics: Adult; Anemia, Sickle Cell; Creatine; Disease Progression; Female; Follow-Up Studies; Humans; Hypert

2008
Monovoxel 1H magnetic resonance spectroscopy in the progression of gliomas.
    European neurology, 2007, Volume: 58, Issue:4

    Topics: Adult; Aged; Aspartic Acid; Brain Neoplasms; Choline; Creatine; Disease Progression; Female; Glioma;

2007
Early and sustained alterations in cerebral metabolism after traumatic brain injury in immature rats.
    Journal of neurotrauma, 2008, Volume: 25, Issue:6

    Topics: Aging; Alanine; Animals; Animals, Newborn; Aspartic Acid; Brain; Brain Injuries; Cell Respiration; C

2008
Progressive decrease of phosphocreatine, creatine and creatine kinase in skeletal muscle upon transformation to sarcoma.
    The FEBS journal, 2008, Volume: 275, Issue:12

    Topics: Adenocarcinoma; Animals; Cell Transformation, Neoplastic; Colorectal Neoplasms; Creatine; Creatine K

2008
Imaging of axonal damage in vivo in Rasmussen's syndrome.
    Brain : a journal of neurology, 1995, Volume: 118 ( Pt 3)

    Topics: Adolescent; Aspartic Acid; Brain Chemistry; Child; Chronic Disease; Creatine; Disease Progression; E

1995
Effects of oral adsorbent AST-120 concurrent with a low-protein diet on the progression of chronic renal failure.
    American journal of nephrology, 1996, Volume: 16, Issue:2

    Topics: Administration, Oral; Adsorption; Carbon; Combined Modality Therapy; Creatine; Creatinine; Diet, Pro

1996
Statistics for investigation of multimodal MR imaging data and an application to multiple sclerosis patients.
    NMR in biomedicine, 1996, Volume: 9, Issue:8

    Topics: Aspartic Acid; Brain; Creatine; Disease Progression; Humans; Image Interpretation, Computer-Assisted

1996
Increased choline signal coinciding with malignant degeneration of cerebral gliomas: a serial proton magnetic resonance spectroscopy imaging study.
    Journal of neurosurgery, 1997, Volume: 87, Issue:4

    Topics: Adult; Aged; Aspartic Acid; Biomarkers, Tumor; Biopsy; Brain Neoplasms; Cell Transformation, Neoplas

1997
Serial proton magnetic resonance spectroscopy imaging of glioblastoma multiforme after brachytherapy.
    Journal of neurosurgery, 1997, Volume: 87, Issue:4

    Topics: Aspartic Acid; Brachytherapy; Brain; Brain Neoplasms; Choline; Contrast Media; Creatine; Disease Pro

1997
Benign versus secondary-progressive multiple sclerosis: the potential role of proton MR spectroscopy in defining the nature of disability.
    AJNR. American journal of neuroradiology, 1998, Volume: 19, Issue:2

    Topics: Adult; Aspartic Acid; Brain; Choline; Creatine; Disease Progression; Female; Follow-Up Studies; Huma

1998
Proton magnetic resonance spectroscopy of linear nevus sebaceus syndrome.
    Pediatric neurology, 1998, Volume: 18, Issue:2

    Topics: Aspartic Acid; Brain Chemistry; Cerebral Cortex; Child, Preschool; Choline; Creatine; Disease Progre

1998
Axonal damage correlates with disability in patients with relapsing-remitting multiple sclerosis. Results of a longitudinal magnetic resonance spectroscopy study.
    Brain : a journal of neurology, 1998, Volume: 121 ( Pt 8)

    Topics: Aspartic Acid; Axons; Brain; Creatine; Disability Evaluation; Disease Progression; Humans; Longitudi

1998
Proton magnetic resonance spectroscopy (1H MRS) in patients with sporadic cerebellar degeneration.
    Journal of neuroimaging : official journal of the American Society of Neuroimaging, 1999, Volume: 9, Issue:2

    Topics: Adult; Aged; Aspartic Acid; Atrophy; Cerebellar Diseases; Cerebellum; Choline; Creatine; Disease Pro

1999
Angiotensin I-converting enzyme genotype significantly affects progression of IgA glomerulonephritis in an italian population.
    American journal of kidney diseases : the official journal of the National Kidney Foundation, 1999, Volume: 33, Issue:6

    Topics: Adult; Creatine; Disease Progression; Female; Genotype; Glomerulonephritis, IGA; Humans; Hypertensio

1999
Usefulness of proton magnetic resonance spectroscopy in differentiating parkinsonian syndromes.
    Italian journal of neurological sciences, 1999, Volume: 20, Issue:4

    Topics: Adult; Aged; Aspartic Acid; Brain; Choline; Creatine; Diagnosis, Differential; Disease Progression;

1999
MR spectroscopy in gliomatosis cerebri.
    AJNR. American journal of neuroradiology, 2000, Volume: 21, Issue:2

    Topics: Adolescent; Adult; Aged; Aspartic Acid; Biopsy; Brain; Brain Neoplasms; Child; Choline; Creatine; Di

2000
Proton magnetic resonance spectroscopy in primary and secondary progressive multiple sclerosis.
    NMR in biomedicine, 2000, Volume: 13, Issue:2

    Topics: Adult; Aged; Aspartic Acid; Brain; Choline; Creatine; Disease Progression; Female; Humans; Magnetic

2000
Regional metabolic patterns in mild cognitive impairment and Alzheimer's disease: A 1H MRS study.
    Neurology, 2000, Jul-25, Volume: 55, Issue:2

    Topics: Aged; Aged, 80 and over; Alzheimer Disease; Aspartic Acid; Brain Mapping; Choline; Cognition Disorde

2000
Magnetic resonance spectroscopy of tubers in patients with tuberous sclerosis.
    Acta neurologica Scandinavica, 2000, Volume: 102, Issue:3

    Topics: Adult; Age Factors; Aspartic Acid; Case-Control Studies; Child; Child, Preschool; Creatine; Disease

2000
Creatine supplementation increases renal disease progression in Han:SPRD-cy rats.
    American journal of kidney diseases : the official journal of the National Kidney Foundation, 2001, Volume: 37, Issue:1

    Topics: Administration, Oral; Animals; Creatine; Dietary Supplements; Disease Progression; Female; Humans; K

2001
Evidence of axonal damage in the early stages of multiple sclerosis and its relevance to disability.
    Archives of neurology, 2001, Volume: 58, Issue:1

    Topics: Adult; Aspartic Acid; Atrophy; Axons; Brain; Chromatography, High Pressure Liquid; Creatine; Disabil

2001
Effects of calcium antagonist, benidipine, on the progression of chronic renal failure in the elderly: a 1-year follow-up.
    Clinical and experimental hypertension (New York, N.Y. : 1993), 2001, Volume: 23, Issue:3

    Topics: Aged; Aged, 80 and over; Angiotensin-Converting Enzyme Inhibitors; Blood Pressure; Calcium Channel B

2001
Proton magnetic resonance spectroscopy of the motor cortex in 70 patients with amyotrophic lateral sclerosis.
    Archives of neurology, 2001, Volume: 58, Issue:5

    Topics: Adult; Amyotrophic Lateral Sclerosis; Aspartic Acid; Choline; Creatine; Disease Progression; Female;

2001
Correlation of cerebral metabolites with clinical outcome among patients with severe congestive heart failure.
    Circulation, 2001, Jun-12, Volume: 103, Issue:23

    Topics: Aspartic Acid; Brain; Choline; Cognition Disorders; Creatine; Disease Progression; Heart Failure; Hu

2001
Severe metabolic abnormalities in the white matter of patients with vacuolating megalencephalic leukoencephalopathy with subcortical cysts. A proton MR spectroscopic imaging study.
    Journal of neurology, 2001, Volume: 248, Issue:5

    Topics: Adolescent; Adult; Aspartic Acid; Creatine; Cysts; Dementia, Vascular; Disease Progression; Female;

2001
Oral administration of creatine monohydrate retards progression of motor neuron disease in the wobbler mouse.
    Amyotrophic lateral sclerosis and other motor neuron disorders : official publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases, 2000, Volume: 1, Issue:3

    Topics: Administration, Oral; Animals; Cell Count; Creatine; Disease Models, Animal; Disease Progression; Fo

2000
Early detection and longitudinal changes in amyotrophic lateral sclerosis by (1)H MRSI.
    Neurology, 2002, Mar-12, Volume: 58, Issue:5

    Topics: Amyotrophic Lateral Sclerosis; Aspartic Acid; Choline; Creatine; Disease Progression; Female; Humans

2002