glycine has been researched along with Syndrome in 113 studies
Syndrome: A characteristic symptom complex.
| Excerpt | Relevance | Reference |
|---|---|---|
| "An increase in serum glycine was associated with TUR syndrome; there were large variations in the amounts of glycine absorbed, reaching levels many times the upper limit of normal." | 9.11 | A comparison of the effect of 1.5% glycine and 5% glucose irrigants on plasma serum physiology and the incidence of transurethral resection syndrome during prostate resection. ( Bradbrook, RA; Collins, JW; Keeley, FX; Macdermott, S; Timoney, AG, 2005) |
| "We present the case of a 34-year-old female with relapsed acute myeloid leukemia post-allogeneic transplant who developed ivosidenib-induced differentiation syndrome complicated by myopericarditis and cardiogenic shock." | 9.05 | Ivosidenib induction therapy complicated by myopericarditis and cardiogenic shock: A case report and literature review. ( Chen, A; Hernandez Burgos, P; Patel, J, 2020) |
| "Cerebral creatine deficiency syndromes (CCDSs) are a group of inborn errors of creatine metabolism comprising two autosomal recessive disorders that affect the biosynthesis of creatine--i." | 8.84 | Cerebral creatine deficiency syndromes: clinical aspects, treatment and pathophysiology. ( Salomons, GS; Schutz, PW; Stockler, S, 2007) |
| "Cerebral creatine deficiency syndromes are caused by the dysfunctional creatine biosynthesis or transport and comprise three hereditary neurodevelopmental defects including arginine-glycine amidinotransferase (AGAT), guanidinoacetate methyltransferase (GAMT), and creatine transporter deficiencies." | 8.12 | Laboratory Diagnosis of Cerebral Creatine Deficiency Syndromes by Determining Creatine and Guanidinoacetate in Plasma and Urine. ( Liu, N; Sun, Q, 2022) |
| "We report a case of differentiation syndrome in a patient receiving the IDH1 inhibitor ivosidenib, with skin biopsy showing isocitrate dehydrogenase (IDH) R132H-mutated leukemia cutis." | 7.96 | Differentiation syndrome during ivosidenib treatment with immunohistochemistry showing isocitrate dehydrogenase R132H mutation. ( Chase, M; Fernandez-Pol, S; Kwong, BY; Novoa, RA; Tabata, MM, 2020) |
| "To further facilitate the diagnosis of creatine deficiency syndromes (CDS) a modified method was developed for the quantification of urinary creatine and guanidinoacetoacetate using gas chromatography/mass spectrometry (GC/MS) and having the additional advantage of using the same derivatizing agents, column and equipment usually used for the diagnosis of the organic acidurias in the clinical biochemistry laboratories." | 7.76 | GC/MS determination of guanidinoacetate and creatine in urine: A routine method for creatine deficiency syndrome diagnosis. ( Briand, G; Feki, M; Kaabachi, N; Nasrallah, F, 2010) |
| " Creatine deficiency syndrome (CDS) is one form of inborn error of metabolism where affected individuals have similar clinical features to individuals with ASD." | 7.76 | Is there a role for routinely screening children with autism spectrum disorder for creatine deficiency syndrome? ( Angley, MT; Gerber, JP; McKinnon, RA; Sorich, MJ; Wang, L; Young, RL, 2010) |
| "To test whether the presence of indolyl-3-acryloylglycine (IAG) is associated with autism, we analyzed urine from population-based, blinded cohorts." | 7.73 | Is the presence of urinary indolyl-3-acryloylglycine associated with autism spectrum disorder? ( Brzozowski, AM; Calvert, E; Farnworth, H; Goodall, DM; Holbrook, I; Imrie, G; Jordan, J; Kelly, A; Miles, J; Smith, R; Town, J; Wright, B, 2005) |
| "In a prospective study it was our intention to evaluate the reliability and the predictive value of expiratory ethanol for the early detection of the occurrence of TURP syndrome and emphasize the role of the serum levels of glycine in clinical manifestation." | 7.71 | The TURP syndrome: importance of expiratory ethanol measurement and high serum levels of glycine. ( Bartoloni, A; Capotosto, C; Ficarra, V; Finco, G; Gottin, L; Malossini, G; Tallarigo, C, 2001) |
| "Post-prostatectomy syndrome (PPS) is characterized by hyponatremia after absorption of glycine irrigant." | 7.69 | Glycine-induced hyponatremia in the rat: a model of post-prostatectomy syndrome. ( Baer, JE; Kozlowski, SA; Rogers, SJ; Silver, SM; Sterns, RH, 1995) |
| "We describe a newborn infant with 9p- syndrome and nonketotic hyperglycinemia." | 7.67 | Nonketotic hyperglycinemia in a patient with the 9p- syndrome. ( Bensen, J; Block, SM; Burton, BK; Pettenati, MJ; Roach, ES, 1989) |
| "Hypersarcosinemia with craniostenosis-syndactylism syndrome." | 7.65 | Hypersarcosinemia with craniostenosis-syndactylism syndrome. ( Minami, R; Olek, K; Wardenbach, P, 1975) |
| "Glycine solution was used as the irrigant and ethanol served as a tracer for fluid absorption." | 5.29 | Symptoms of the transurethral resection syndrome using glycine as the irrigant. ( Hahn, RG; Nilsson, A; Olsson, J, 1995) |
| "An increase in serum glycine was associated with TUR syndrome; there were large variations in the amounts of glycine absorbed, reaching levels many times the upper limit of normal." | 5.11 | A comparison of the effect of 1.5% glycine and 5% glucose irrigants on plasma serum physiology and the incidence of transurethral resection syndrome during prostate resection. ( Bradbrook, RA; Collins, JW; Keeley, FX; Macdermott, S; Timoney, AG, 2005) |
| "We present the case of a 34-year-old female with relapsed acute myeloid leukemia post-allogeneic transplant who developed ivosidenib-induced differentiation syndrome complicated by myopericarditis and cardiogenic shock." | 5.05 | Ivosidenib induction therapy complicated by myopericarditis and cardiogenic shock: A case report and literature review. ( Chen, A; Hernandez Burgos, P; Patel, J, 2020) |
| "Cerebral creatine deficiency syndromes (CCDSs) are a group of inborn errors of creatine metabolism comprising two autosomal recessive disorders that affect the biosynthesis of creatine--i." | 4.84 | Cerebral creatine deficiency syndromes: clinical aspects, treatment and pathophysiology. ( Salomons, GS; Schutz, PW; Stockler, S, 2007) |
| "Cerebral creatine deficiency syndromes are caused by the dysfunctional creatine biosynthesis or transport and comprise three hereditary neurodevelopmental defects including arginine-glycine amidinotransferase (AGAT), guanidinoacetate methyltransferase (GAMT), and creatine transporter deficiencies." | 4.12 | Laboratory Diagnosis of Cerebral Creatine Deficiency Syndromes by Determining Creatine and Guanidinoacetate in Plasma and Urine. ( Liu, N; Sun, Q, 2022) |
| "We report a case of differentiation syndrome in a patient receiving the IDH1 inhibitor ivosidenib, with skin biopsy showing isocitrate dehydrogenase (IDH) R132H-mutated leukemia cutis." | 3.96 | Differentiation syndrome during ivosidenib treatment with immunohistochemistry showing isocitrate dehydrogenase R132H mutation. ( Chase, M; Fernandez-Pol, S; Kwong, BY; Novoa, RA; Tabata, MM, 2020) |
| " We report a patient who developed hyponatremia, hemolysis and oliguric acute renal failure as a major complication following TURP using glycine as irrigating fluid." | 3.85 | Acute tubular necrosis following transurethral resection of the Prostate using Glycine as irrigating fluid. ( Beji, S; Ben Fatma, L; Ben Hamida, F; Ben Moussa, F; El Ati, Z; Jebali, H; Kheder, R; Krid, M; Rais, L; Smaoui, W; Zouaghi, MK, 2017) |
| " Creatine deficiency syndrome (CDS) is one form of inborn error of metabolism where affected individuals have similar clinical features to individuals with ASD." | 3.76 | Is there a role for routinely screening children with autism spectrum disorder for creatine deficiency syndrome? ( Angley, MT; Gerber, JP; McKinnon, RA; Sorich, MJ; Wang, L; Young, RL, 2010) |
| "To further facilitate the diagnosis of creatine deficiency syndromes (CDS) a modified method was developed for the quantification of urinary creatine and guanidinoacetoacetate using gas chromatography/mass spectrometry (GC/MS) and having the additional advantage of using the same derivatizing agents, column and equipment usually used for the diagnosis of the organic acidurias in the clinical biochemistry laboratories." | 3.76 | GC/MS determination of guanidinoacetate and creatine in urine: A routine method for creatine deficiency syndrome diagnosis. ( Briand, G; Feki, M; Kaabachi, N; Nasrallah, F, 2010) |
| "To test whether the presence of indolyl-3-acryloylglycine (IAG) is associated with autism, we analyzed urine from population-based, blinded cohorts." | 3.73 | Is the presence of urinary indolyl-3-acryloylglycine associated with autism spectrum disorder? ( Brzozowski, AM; Calvert, E; Farnworth, H; Goodall, DM; Holbrook, I; Imrie, G; Jordan, J; Kelly, A; Miles, J; Smith, R; Town, J; Wright, B, 2005) |
| "In a prospective study it was our intention to evaluate the reliability and the predictive value of expiratory ethanol for the early detection of the occurrence of TURP syndrome and emphasize the role of the serum levels of glycine in clinical manifestation." | 3.71 | The TURP syndrome: importance of expiratory ethanol measurement and high serum levels of glycine. ( Bartoloni, A; Capotosto, C; Ficarra, V; Finco, G; Gottin, L; Malossini, G; Tallarigo, C, 2001) |
| "Post-prostatectomy syndrome (PPS) is characterized by hyponatremia after absorption of glycine irrigant." | 3.69 | Glycine-induced hyponatremia in the rat: a model of post-prostatectomy syndrome. ( Baer, JE; Kozlowski, SA; Rogers, SJ; Silver, SM; Sterns, RH, 1995) |
| " Considering postoperative hyponatremia and hypoosmality, we discuss the possible role of glycine-induced visual disturbances as described in the TURP reaction syndrome, to our knowledge an entity almost unknown in the neurologic literature." | 3.69 | Visual disturbances and transurethral resection of the prostate: the TURP syndrome. ( Bogousslavsky, J; Borruat, FX; Radziwill, AJ; Vuadens, P, 1997) |
| "5% glycine solution causes a well known clinical and metabolic syndrome called TURP-syndrome." | 3.68 | [The intravascular transfer of glycine during percutaneous kidney surgery]. ( Antonini, A; Bellezza, M; Cathala, B; Fellahi, JL; Richard, JP; Thouvenot, JP, 1992) |
| "To study the potential contribution of glycine toxicity in the transurethral resection syndrome, we evaluated hemodynamic and visual evoked potential responses to glycine infusion (1 g/kg) in 22 dogs anesthetized with halothane (1." | 3.67 | Effects of glycine on hemodynamic responses and visual evoked potentials in the dog. ( Clark, WM; Creel, DJ; Shahangian, S; Wang, JM; Wong, KC, 1985) |
| "We describe a newborn infant with 9p- syndrome and nonketotic hyperglycinemia." | 3.67 | Nonketotic hyperglycinemia in a patient with the 9p- syndrome. ( Bensen, J; Block, SM; Burton, BK; Pettenati, MJ; Roach, ES, 1989) |
| "Complications of transurethral resection of the prostate (TURP syndrome) when glycine is used as the irrigating fluid include cardiovascular and central nervous system abnormalities that occasionally include transient blindness." | 3.67 | Transurethral resection of the prostate, serum glycine levels, and ocular evoked potentials. ( Creel, DJ; Wang, JM; Wong, KC, 1989) |
| "Thirteen patients undergoing resection of benign prostatic hyperplasia were given furosemide 40 mg at the end of the procedure." | 3.66 | Changes in oncotic pressure, osmolality and electrolytes following transurethral resection of the prostate using glycine as irrigating solution. ( Breivik, H; Sellevold, O; Tveter, K, 1983) |
| "Hypersarcosinemia with craniostenosis-syndactylism syndrome." | 3.65 | Hypersarcosinemia with craniostenosis-syndactylism syndrome. ( Minami, R; Olek, K; Wardenbach, P, 1975) |
| "Multiple endocrine neoplasia type 2A (MEN2A) is an autosomal dominant hereditary disorder, associated with a cluster of germline gain-of-function mutations of the RET proto-oncogene (RET), mainly in exons 10-15." | 2.44 | Multiple endocrine neoplasia type 2A in two families with the familial medullary thyroid carcinoma associated G533C mutation of the RET proto-oncogene. ( Boutati, E; Economopoulos, T; Hadjidakis, D; Kamakari, S; Panayiotides, IG; Peppa, M; Peros, G; Pikounis, V; Raptis, SA, 2008) |
| "The PTX-induced thermal hyperalgesia peaked between day 2 and 4, but no cold allodynia is observed; i." | 2.42 | Implications of intrathecal pertussis toxin animal model on the cellular mechanisms of neuropathic pain syndrome. ( Chang, YC; Wen, ZH; Wong, CS, 2003) |
| "The TUR syndrome is a clinical disorder consisting of circulatory, gastrointestinal, and neurologic signs that are infrequently seen in some patients undergoing endoscopic surgery of the prostate gland with the use of nonconductive irrigating fluids." | 2.39 | Temporary blindness in the TUR syndrome. ( Barletta, JP; Fanous, MM; Hamed, LM, 1994) |
| "A 78-year-old man with prostatic hypertrophy was scheduled for transurethral resection of the prostate under spinal anesthesia." | 1.39 | Transurethral resection of prostate syndrome: report of a case. ( Boukatta, B; El Bouazzaoui, A; Kanjaa, N; Lafrayiji, Z; Messaoudi, F; Sbai, H, 2013) |
| "The MELAS has been related to mutation A3243G in most cases, but some other mitochondrial DNA mutations were described in the background of this syndrome as well." | 1.37 | A8344G mutation of the mitochondrial DNA with typical mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome. ( Gál, A; Lukács, T; Molnár, MJ; Reményi, V; Semjén, J; Valikovics, A; Vastagh, I, 2011) |
| "Several of these syndromes are associated with an encephalopathy that characteristically shows episodes of rapid neurological deterioration and the development of acute cerebral lesions." | 1.36 | Localized cerebral energy failure in DNA polymerase gamma-associated encephalopathy syndromes. ( Bindoff, LA; Engelsen, BE; Ersland, L; Moen, G; Mørk, SJ; Neckelmann, G; Tzoulis, C; Viscomi, C; Zeviani, M, 2010) |
| "The Timothy syndrome is a multisystem disorder associated with the mutation of a Gly residue (G402 or G406) in the Ca(v)1." | 1.35 | Introduction into Ca(v)2.1 of the homologous mutation of Ca(v)1.2 causing the Timothy syndrome questions the role of V421 in the phenotypic definition of P-type Ca(2+) channel. ( Cens, T; Charnet, P; Leyris, JP, 2008) |
| "Creatine plays an important role in the storage and transmission of phosphate-bound energy." | 1.35 | Simultaneous determination of guanidinoacetate, creatine and creatinine in urine and plasma by un-derivatized liquid chromatography-tandem mass spectrometry. ( Calvin, J; Carling, RS; Hogg, SL; Wood, TC, 2008) |
| "Dropped head syndrome is characterized by severe weakness of neck extensor muscles with sparing of the flexors." | 1.33 | Two patients with 'Dropped head syndrome' due to mutations in LMNA or SEPN1 genes. ( Benedetti, S; Bertini, E; Bonne, G; D'Amico, A; Ferreiro, A; Guicheney, P; Haliloglu, G; Maugenre, S; Menditto, I; Richard, P; Talim, B; Topaloglu, H, 2005) |
| "The observed constellation of microcephaly, deafness, cryptorchidism, developmental delay, hypertension, and bilateral pheochromocytoma in association with a VHL mutation A451G in a patient with negative family history has not previously been described in the literature." | 1.32 | Bilateral pheochromocytomas and congenital anomalies associated with a de novo germline mutation in the von Hippel-Lindau gene. ( Assadi, F; Brackbill, EL, 2003) |
| "Stickler syndrome is a dominantly inherited disorder characterized by arthropathy, midline clefting, hearing loss, midfacial hypoplasia, myopia, and retinal detachment." | 1.31 | Variation in the vitreous phenotype of Stickler syndrome can be caused by different amino acid substitutions in the X position of the type II collagen Gly-X-Y triple helix. ( Baguley, DM; Harper, PS; Lane, C; Nicol, M; Richards, AJ; Scott, JD; Snead, MP; Yates, JR, 2000) |
| "The TUR syndrome is well described after transurethral resection of the prostate." | 1.30 | TUR syndrome and endoscopic transanal resection: no evidence for a clinically important association in 38 procedures. ( Boyle, JR; Kelly, MJ; Lopez, B; Thompson, MM; Twist, MH, 1997) |
| "Early infantile epileptic encephalopathy (EIEE) with suppression burst activity in EEG (Ohtahara syndrome) is a rare type of epileptic encephalopathy in infancy and represents the earliest type of age-related symptomatic generalized epilepsy." | 1.30 | [Early infantile epileptic encephalopathy and glycine encephalopathy]. ( Carratalà, F; González de Dios, J; Izura, V; Moya, M; Pastore, C, 1997) |
| "This leukoencephalopathy has an autosomal-recessive mode of inheritance." | 1.30 | Increased cerebrospinal fluid glycine: a biochemical marker for a leukoencephalopathy with vanishing white matter. ( Gabreëls, FJ; Jaeken, J; Kure, S; van der Knaap, MS; van Raaij-Selten, B; Verhoeven, NM; Wevers, RA, 1999) |
| "Glycine solution was used as the irrigant and ethanol served as a tracer for fluid absorption." | 1.29 | Symptoms of the transurethral resection syndrome using glycine as the irrigant. ( Hahn, RG; Nilsson, A; Olsson, J, 1995) |
| " The high absorption rate suggests that continued resection would have promoted a severe transurethral resection syndrome." | 1.29 | Ethanol monitoring of the transurethral resection syndrome. ( Hahn, RG; Olsson, J, 1996) |
| "This post-resection syndrome is caused by resorption of a large amount of the hypotonic solution used during the surgical procedure and containing 1." | 1.28 | [Resorption of the lavage fluid during transurethral resection of the prostate. Apropos of 13 cases]. ( Clément, P; Paulet, C, 1990) |
| "Glycine 2." | 1.27 | Hallucination and visual disturbances in transurethral prostatic resection. ( Hahn, RG, 1988) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 34 (30.09) | 18.7374 |
| 1990's | 27 (23.89) | 18.2507 |
| 2000's | 35 (30.97) | 29.6817 |
| 2010's | 10 (8.85) | 24.3611 |
| 2020's | 7 (6.19) | 2.80 |
| Authors | Studies |
|---|---|
| Liu, N | 1 |
| Sun, Q | 1 |
| Nakakura, S | 1 |
| Terao, E | 1 |
| Fujisawa, Y | 1 |
| Tabuchi, H | 1 |
| Kiuchi, Y | 1 |
| Tabata, MM | 1 |
| Chase, M | 1 |
| Kwong, BY | 1 |
| Novoa, RA | 1 |
| Fernandez-Pol, S | 1 |
| Boiten, HJ | 1 |
| Buijze, M | 1 |
| Zweegman, S | 1 |
| Levin, MD | 1 |
| Martelli, MP | 1 |
| Martino, G | 1 |
| Cardinali, V | 1 |
| Falini, B | 1 |
| Martinelli, G | 1 |
| Cerchione, C | 1 |
| Sterrett, MC | 1 |
| Enyenihi, L | 1 |
| Leung, SW | 1 |
| Hess, L | 1 |
| Strassler, SE | 1 |
| Farchi, D | 1 |
| Lee, RS | 1 |
| Withers, ES | 1 |
| Kremsky, I | 1 |
| Baker, RE | 1 |
| Basrai, MA | 1 |
| van Hoof, A | 1 |
| Fasken, MB | 1 |
| Corbett, AH | 1 |
| Rais, L | 1 |
| El Ati, Z | 1 |
| Ben Fatma, L | 1 |
| Kheder, R | 1 |
| Jebali, H | 1 |
| Smaoui, W | 1 |
| Krid, M | 1 |
| Ben Hamida, F | 1 |
| Ben Moussa, F | 1 |
| Beji, S | 1 |
| Zouaghi, MK | 1 |
| Fox, WC | 1 |
| Moon, RE | 1 |
| Takeuchi, I | 1 |
| Yanagawa, Y | 1 |
| Nagasawa, H | 1 |
| Jitsuiki, K | 1 |
| Madokoro, S | 1 |
| Takahashi, N | 1 |
| Ohsaka, H | 1 |
| Ishikawa, K | 1 |
| Omori, K | 1 |
| Hernandez Burgos, P | 1 |
| Patel, J | 1 |
| Chen, A | 1 |
| Boukatta, B | 1 |
| Sbai, H | 1 |
| Messaoudi, F | 1 |
| Lafrayiji, Z | 1 |
| El Bouazzaoui, A | 1 |
| Kanjaa, N | 1 |
| Hahn, RG | 9 |
| Gebäck, T | 1 |
| Cens, T | 1 |
| Leyris, JP | 1 |
| Charnet, P | 1 |
| Stockler, S | 1 |
| Schutz, PW | 1 |
| Salomons, GS | 2 |
| Carling, RS | 1 |
| Hogg, SL | 1 |
| Wood, TC | 1 |
| Calvin, J | 1 |
| Peppa, M | 1 |
| Boutati, E | 1 |
| Kamakari, S | 1 |
| Pikounis, V | 1 |
| Peros, G | 1 |
| Panayiotides, IG | 1 |
| Economopoulos, T | 1 |
| Raptis, SA | 1 |
| Hadjidakis, D | 1 |
| Braissant, O | 1 |
| Béard, E | 1 |
| Torrent, C | 1 |
| Henry, H | 1 |
| Tzoulis, C | 1 |
| Neckelmann, G | 1 |
| Mørk, SJ | 1 |
| Engelsen, BE | 1 |
| Viscomi, C | 1 |
| Moen, G | 1 |
| Ersland, L | 1 |
| Zeviani, M | 1 |
| Bindoff, LA | 1 |
| Wang, L | 1 |
| Angley, MT | 1 |
| Sorich, MJ | 1 |
| Young, RL | 1 |
| McKinnon, RA | 1 |
| Gerber, JP | 1 |
| Nasrallah, F | 1 |
| Feki, M | 1 |
| Briand, G | 1 |
| Kaabachi, N | 1 |
| Vastagh, I | 1 |
| Gál, A | 1 |
| Reményi, V | 1 |
| Semjén, J | 1 |
| Lukács, T | 1 |
| Valikovics, A | 1 |
| Molnár, MJ | 1 |
| Breitinger, HG | 1 |
| Becker, CM | 1 |
| Assadi, F | 1 |
| Brackbill, EL | 1 |
| Van der Knaap, MS | 3 |
| Bishop, P | 1 |
| Kim, Y | 1 |
| Park, JY | 1 |
| Lee, TJ | 1 |
| Yoo, HW | 1 |
| PALMIERI, A | 1 |
| GIACCA, S | 1 |
| KAESER, H | 2 |
| COTTIER, P | 1 |
| ANTENER, I | 1 |
| Wen, ZH | 1 |
| Chang, YC | 1 |
| Wong, CS | 1 |
| Marszał, E | 1 |
| Jamroz, E | 1 |
| Paprocka, J | 1 |
| Kluczewska, E | 1 |
| Sokół, M | 1 |
| Schmidt, MR | 1 |
| Birkebaek, N | 1 |
| Gonzalez, I | 1 |
| Sunde, L | 1 |
| Almeida, LS | 1 |
| Verhoeven, NM | 3 |
| Roos, B | 1 |
| Valongo, C | 1 |
| Cardoso, ML | 1 |
| Vilarinho, L | 1 |
| Jakobs, C | 2 |
| Item, CB | 1 |
| Turhani, D | 1 |
| Thurnher, D | 1 |
| Yerit, K | 1 |
| Sinko, K | 1 |
| Wittwer, G | 1 |
| Adeyemo, WL | 1 |
| Frei, K | 1 |
| Erginel-Unaltuna, N | 1 |
| Watzinger, F | 1 |
| Ewers, R | 1 |
| Wright, B | 1 |
| Brzozowski, AM | 1 |
| Calvert, E | 1 |
| Farnworth, H | 1 |
| Goodall, DM | 1 |
| Holbrook, I | 1 |
| Imrie, G | 1 |
| Jordan, J | 1 |
| Kelly, A | 1 |
| Miles, J | 1 |
| Smith, R | 1 |
| Town, J | 1 |
| Sijens, PE | 2 |
| Verbruggen, KT | 2 |
| Meiners, LC | 1 |
| Soorani-Lunsing, RJ | 2 |
| Rake, JP | 1 |
| Oudkerk, M | 2 |
| Splawski, I | 1 |
| Timothy, KW | 1 |
| Decher, N | 1 |
| Kumar, P | 1 |
| Sachse, FB | 1 |
| Beggs, AH | 1 |
| Sanguinetti, MC | 1 |
| Keating, MT | 1 |
| D'Amico, A | 1 |
| Haliloglu, G | 1 |
| Richard, P | 1 |
| Talim, B | 1 |
| Maugenre, S | 1 |
| Ferreiro, A | 1 |
| Guicheney, P | 1 |
| Menditto, I | 1 |
| Benedetti, S | 1 |
| Bertini, E | 1 |
| Bonne, G | 1 |
| Topaloglu, H | 1 |
| Collins, JW | 1 |
| Macdermott, S | 1 |
| Bradbrook, RA | 1 |
| Keeley, FX | 1 |
| Timoney, AG | 1 |
| van Spronsen, FJ | 1 |
| Klepper, J | 1 |
| Salas-Burgos, A | 1 |
| Gertsen, E | 1 |
| Fischbarg, J | 1 |
| Jacob, G | 1 |
| Garland, EM | 1 |
| Costa, F | 1 |
| Stein, CM | 1 |
| Xie, HG | 1 |
| Robertson, RM | 1 |
| Biaggioni, I | 1 |
| Robertson, D | 1 |
| Kimura, M | 1 |
| Taketani, T | 1 |
| Horie, A | 1 |
| Isumi, H | 1 |
| Sejima, H | 1 |
| Yamaguchi, S | 1 |
| Weiss, G | 1 |
| Madsen, HO | 1 |
| Garred, P | 1 |
| Schmahl, K | 1 |
| Atamna, N | 1 |
| Schönijahn, T | 1 |
| Lülsdorf, P | 1 |
| Göller, T | 1 |
| Jacob, R | 1 |
| Bhakta, P | 1 |
| Goel, A | 1 |
| Acharjee, P | 1 |
| Biswas, BK | 1 |
| Young, S | 1 |
| Struys, E | 1 |
| Wood, T | 1 |
| Bowser-Riley, F | 1 |
| Sellevold, O | 1 |
| Breivik, H | 1 |
| Tveter, K | 1 |
| Phanichphant, S | 1 |
| Bunyaratavej, S | 1 |
| Kurathong, S | 1 |
| Soranastaporn, S | 1 |
| Tazawa, Y | 1 |
| Yamada, M | 1 |
| Nakagawa, M | 1 |
| Konno, T | 1 |
| Tada, K | 1 |
| Aicardi, J | 1 |
| Hoekstra, PT | 1 |
| Kahnoski, R | 1 |
| McCamish, MA | 1 |
| Bergen, W | 1 |
| Heetderks, DR | 1 |
| Desroches, J | 1 |
| Spahr, L | 1 |
| Leduc, F | 1 |
| Pomier-Layrargues, G | 1 |
| Picard, M | 1 |
| Picard, D | 1 |
| Chartrand, R | 1 |
| Morais, J | 1 |
| Silver, SM | 1 |
| Kozlowski, SA | 1 |
| Baer, JE | 1 |
| Rogers, SJ | 1 |
| Sterns, RH | 1 |
| Olsson, J | 3 |
| Nilsson, A | 1 |
| Barletta, JP | 1 |
| Fanous, MM | 1 |
| Hamed, LM | 1 |
| Körkkö, J | 1 |
| Ritvaniemi, P | 1 |
| Haataja, L | 1 |
| Kääriäinen, H | 1 |
| Kivirikko, KI | 1 |
| Prockop, DJ | 2 |
| Ala-Kokko, L | 2 |
| Nakao, R | 1 |
| Yanase, T | 1 |
| Sakai, Y | 1 |
| Haji, M | 1 |
| Nawata, H | 1 |
| Siddiqui, MA | 1 |
| Berns, JS | 1 |
| Baime, MJ | 1 |
| Berglund, L | 1 |
| Boyle, JR | 1 |
| Thompson, MM | 1 |
| Lopez, B | 1 |
| Twist, MH | 1 |
| Kelly, MJ | 1 |
| Delcenserie, R | 1 |
| Yzet, T | 1 |
| Duchmann, JC | 1 |
| Delamarre, J | 1 |
| Dupas, JL | 1 |
| Capron, JP | 1 |
| Radziwill, AJ | 1 |
| Vuadens, P | 1 |
| Borruat, FX | 1 |
| Bogousslavsky, J | 1 |
| Spritz, RA | 1 |
| Beighton, P | 1 |
| Antman, EM | 1 |
| González de Dios, J | 1 |
| Moya, M | 1 |
| Pastore, C | 1 |
| Izura, V | 1 |
| Carratalà, F | 1 |
| Pihlajamaa, T | 1 |
| Faber, J | 1 |
| Winterpacht, A | 1 |
| Zabel, B | 1 |
| Giedion, A | 1 |
| Wiesbauer, P | 1 |
| Spranger, J | 1 |
| Wevers, RA | 1 |
| Kure, S | 1 |
| Gabreëls, FJ | 1 |
| van Raaij-Selten, B | 1 |
| Jaeken, J | 1 |
| Richards, AJ | 1 |
| Baguley, DM | 1 |
| Yates, JR | 1 |
| Lane, C | 1 |
| Nicol, M | 1 |
| Harper, PS | 1 |
| Scott, JD | 1 |
| Snead, MP | 1 |
| Guérand, WS | 1 |
| Struys, EA | 1 |
| Bouman, AA | 1 |
| Lankes, W | 1 |
| Fleischer, K | 1 |
| Gulba, DC | 1 |
| Bartoloni, A | 1 |
| Gottin, L | 1 |
| Ficarra, V | 1 |
| Capotosto, C | 1 |
| Malossini, G | 1 |
| Tallarigo, C | 1 |
| Finco, G | 1 |
| Byard, RW | 1 |
| Harrison, R | 1 |
| Wells, R | 1 |
| Gilbert, JD | 1 |
| Schofield, PR | 1 |
| Minami, R | 1 |
| Olek, K | 1 |
| Wardenbach, P | 1 |
| Fischer, MH | 1 |
| Fortune, JS | 1 |
| Foster, SH | 1 |
| Gilbert, EF | 1 |
| Bank, WJ | 1 |
| Pizer, L | 1 |
| Pfendner, W | 1 |
| Lasley, L | 1 |
| Scriver, CR | 1 |
| Shuman, RM | 1 |
| Leech, RW | 1 |
| Scott, CR | 1 |
| von Wendt, L | 1 |
| Similä, S | 1 |
| Hirvasniemi, A | 1 |
| Suvanto, E | 1 |
| Kolvraa, S | 1 |
| Rasmussen, K | 1 |
| Brandt, NJ | 1 |
| Schmidt, RT | 1 |
| Stahl, SM | 1 |
| Spehlmann, R | 1 |
| Hahn, R | 1 |
| Essén, P | 1 |
| Wernerman, J | 1 |
| Fellahi, JL | 1 |
| Richard, JP | 1 |
| Bellezza, M | 1 |
| Antonini, A | 1 |
| Thouvenot, JP | 1 |
| Cathala, B | 1 |
| Tauzin-Fin, P | 1 |
| Sanz, L | 1 |
| Hirose, M | 1 |
| Tanaka, Y | 1 |
| Agius, AM | 1 |
| Cutajar, CL | 1 |
| Ellis, RE | 1 |
| Carmichael, JK | 1 |
| Clément, P | 1 |
| Paulet, C | 1 |
| Ghanem, AN | 1 |
| Ward, JP | 2 |
| Sasaki, H | 1 |
| Matsuda, M | 1 |
| Terasawa, T | 1 |
| Ito, T | 1 |
| Fukushima, Y | 1 |
| Kuroki, Y | 1 |
| Matsuyama, S | 1 |
| Burton, BK | 1 |
| Pettenati, MJ | 1 |
| Block, SM | 1 |
| Bensen, J | 1 |
| Roach, ES | 1 |
| Wang, JM | 2 |
| Creel, DJ | 2 |
| Wong, KC | 2 |
| Bernstein, GT | 1 |
| Loughlin, KR | 1 |
| Gittes, RF | 1 |
| Shepard, RL | 1 |
| Kraus, SE | 1 |
| Babayan, RK | 1 |
| Siroky, MB | 1 |
| Rhymer, JC | 1 |
| Bell, TJ | 1 |
| Perry, KC | 1 |
| Clark, WM | 1 |
| Shahangian, S | 1 |
| Dotchev, D | 1 |
| Hungerland, H | 1 |
| Liappis, N | 1 |
| Oyanagi, K | 1 |
| Holmgren, G | 1 |
| Kryzhanovskiĭ, GN | 1 |
| Grafova, VN | 1 |
| Danilova, EI | 1 |
| Igon'kina, SI | 1 |
| Keating, JP | 1 |
| Feigin, RD | 1 |
| Tenenbaum, SM | 1 |
| Hillman, RE | 1 |
| Hofmann, AF | 2 |
| Tacker, MM | 1 |
| Fromm, H | 1 |
| Thomas, PJ | 1 |
| Smith, LH | 2 |
| Ionasescu, V | 1 |
| Stegink, L | 1 |
| Mueller, S | 1 |
| Weinstein, M | 1 |
| Bartsocas, CS | 1 |
| Erbe, RW | 1 |
| Balci, S | 1 |
| Say, B | 1 |
| Firat, T | 1 |
10 reviews available for glycine and Syndrome
| Article | Year |
|---|---|
Enasidenib and ivosidenib in AML.
Topics: Aminopyridines; Antineoplastic Agents; Cell Differentiation; Clinical Trials as Topic; Glutarates; G | 2020 |
Ivosidenib induction therapy complicated by myopericarditis and cardiogenic shock: A case report and literature review.
Topics: Adult; Female; Glycine; Humans; Leukemia, Myeloid, Acute; Mutation; Myocarditis; Pyridines; Recurren | 2020 |
Cerebral creatine deficiency syndromes: clinical aspects, treatment and pathophysiology.
Topics: Adult; Amidinotransferases; Animals; Brain Diseases, Metabolic, Inborn; Cerebellar Diseases; Child; | 2007 |
Multiple endocrine neoplasia type 2A in two families with the familial medullary thyroid carcinoma associated G533C mutation of the RET proto-oncogene.
Topics: Adult; Aged; Aged, 80 and over; Amino Acid Substitution; Carcinoma, Medullary; Cysteine; Female; Gly | 2008 |
Implications of intrathecal pertussis toxin animal model on the cellular mechanisms of neuropathic pain syndrome.
Topics: Animals; Disease Models, Animal; Excitatory Amino Acids; Glycine; Hyperalgesia; Injections, Spinal; | 2003 |
[Myoclonias as a manifestation of degenerative disorders of the central nervous system in childhood].
Topics: Adolescent; Age Factors; Brain Diseases; Cerebellar Diseases; Ceroid; Child; Child, Preschool; Diagn | 1982 |
Temporary blindness in the TUR syndrome.
Topics: Ammonia; Blindness; Glycine; Humans; Hyponatremia; Male; Middle Aged; Postoperative Complications; P | 1994 |
[Direct thrombin antagonists].
Topics: Acute Disease; Angina, Unstable; Angioplasty, Balloon, Coronary; Animals; Anticoagulants; Antithromb | 2001 |
The role of glycine and glycine receptors in myoclonus and startle syndromes.
Topics: Amino Acid Sequence; Animals; Glycine; Humans; Molecular Sequence Data; Mutation; Myoclonus; Nervous | 2002 |
[Prostate transurethral resection syndrome].
Topics: Glycine; Humans; Hyponatremia; Male; Prostatectomy; Syndrome; Therapeutic Irrigation; Water-Electrol | 1992 |
1 trial available for glycine and Syndrome
| Article | Year |
|---|---|
A comparison of the effect of 1.5% glycine and 5% glucose irrigants on plasma serum physiology and the incidence of transurethral resection syndrome during prostate resection.
Topics: Absorption; Aged; Aged, 80 and over; Blood Loss, Surgical; Glucose; Glycine; Humans; Hypernatremia; | 2005 |
102 other studies available for glycine and Syndrome
| Article | Year |
|---|---|
Laboratory Diagnosis of Cerebral Creatine Deficiency Syndromes by Determining Creatine and Guanidinoacetate in Plasma and Urine.
Topics: Creatine; Glycine; Guanidinoacetate N-Methyltransferase; Humans; Infant, Newborn; Neonatal Screening | 2022 |
Changes in Prostaglandin-associated Periorbital Syndrome After Switch from Conventional Prostaglandin F2α Treatment to Omidenepag Isopropyl in 11 Consecutive Patients.
Topics: Aged; Antihypertensive Agents; Bimatoprost; Drug Substitution; Eyelid Diseases; Female; Glycine; Hum | 2020 |
Differentiation syndrome during ivosidenib treatment with immunohistochemistry showing isocitrate dehydrogenase R132H mutation.
Topics: Aged; Antineoplastic Agents; Diagnosis, Differential; Glycine; Humans; Immunohistochemistry; Isocitr | 2020 |
Ixazomib Treatment of IgA Multiple Myeloma With Hyperviscosity Syndrome.
Topics: Aged; Blood Viscosity; Boron Compounds; Female; Glycine; Humans; Multiple Myeloma; Syndrome; Treatme | 2020 |
A budding yeast model for human disease mutations in the
Topics: Amino Acid Sequence; Amino Acid Substitution; Aspartic Acid; Dwarfism; Exoribonucleases; Exosome Mul | 2021 |
Acute tubular necrosis following transurethral resection of the Prostate using Glycine as irrigating fluid.
Topics: Acute Kidney Injury; Glycine; Humans; Hyponatremia; Kidney Tubular Necrosis, Acute; Male; Middle Age | 2017 |
Blue Vision (Cyanopsia) Associated With TURP Syndrome: A Case Report.
Topics: Aged; Glycine; Humans; Hyponatremia; Male; Postoperative Complications; Prostatic Hyperplasia; Syndr | 2018 |
Decrease in Butyrylcholinesterase Accompanied by Intermediate-like Syndrome after Massive Ingestion of a Glyphosate-surfactant.
Topics: Aged, 80 and over; Biomarkers; Butyrylcholinesterase; Coma; Eating; Female; Glycine; Glyphosate; Hum | 2019 |
Transurethral resection of prostate syndrome: report of a case.
Topics: Absorption; Aged; Anesthesia, Spinal; Bradycardia; Coma; Combined Modality Therapy; Glycine; Humans; | 2013 |
Fluid volume kinetics of dilutional hyponatremia; a shock syndrome revisited.
Topics: Animals; Cardiac Output; Diuretics, Osmotic; Electrolytes; Glycine; Glycine Agents; Hemodynamics; Hy | 2014 |
Introduction into Ca(v)2.1 of the homologous mutation of Ca(v)1.2 causing the Timothy syndrome questions the role of V421 in the phenotypic definition of P-type Ca(2+) channel.
Topics: Alanine; Animals; Arginine; Arrhythmias, Cardiac; Calcium; Calcium Channels, L-Type; Calcium Channel | 2008 |
What happens if you infuse 1 l of glycine 1.5%?
Topics: Anesthesiology; Animals; Blood Pressure; Dose-Response Relationship, Drug; Ethics, Research; Glycine | 2008 |
Simultaneous determination of guanidinoacetate, creatine and creatinine in urine and plasma by un-derivatized liquid chromatography-tandem mass spectrometry.
Topics: Adult; Blood Chemical Analysis; Brain Diseases, Metabolic, Inborn; Child; Child, Preschool; Chromato | 2008 |
Dissociation of AGAT, GAMT and SLC6A8 in CNS: relevance to creatine deficiency syndromes.
Topics: Amidinotransferases; Animals; Brain Diseases, Metabolic, Inborn; Brain Mapping; Cell Count; Cells, C | 2010 |
Localized cerebral energy failure in DNA polymerase gamma-associated encephalopathy syndromes.
Topics: Arginine; Brain; Brain Diseases; Cerebellum; Cysteine; Diffuse Cerebral Sclerosis of Schilder; Diffu | 2010 |
Is there a role for routinely screening children with autism spectrum disorder for creatine deficiency syndrome?
Topics: Biomarkers; Brain Diseases, Metabolic, Inborn; Child; Child Development Disorders, Pervasive; Chroma | 2010 |
GC/MS determination of guanidinoacetate and creatine in urine: A routine method for creatine deficiency syndrome diagnosis.
Topics: Adolescent; Adult; Brain Diseases, Metabolic, Inborn; Calibration; Child; Child, Preschool; Chromato | 2010 |
A8344G mutation of the mitochondrial DNA with typical mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome.
Topics: Acidosis, Lactic; Adult; Alanine; Brain Ischemia; DNA, Mitochondrial; Glycine; Humans; Male; MELAS S | 2011 |
Statistical coassembly of glycine receptor alpha1 wildtype and the hyperekplexia mutant alpha1(P250T) in HEK 293 cells: impaired channel function is not dominant in the recombinant system.
Topics: Cell Line, Transformed; Electrophysiology; Glycine; Humans; Kinetics; Models, Chemical; Mutation; Ne | 2002 |
Bilateral pheochromocytomas and congenital anomalies associated with a de novo germline mutation in the von Hippel-Lindau gene.
Topics: Adrenal Gland Neoplasms; Amino Acid Substitution; Child; Cryptorchidism; Developmental Disabilities; | 2003 |
Forget About "van der Knaap syndrome," forget about glycine.
Topics: Brain; Brain Diseases; Diagnosis, Differential; Glycine; Humans; Magnetic Resonance Spectroscopy; Sy | 2003 |
Bipolar transurethral resection of the prostate--a new approach.
Topics: Aged; Aged, 80 and over; Electrosurgery; Glycine; Humans; Hyponatremia; Male; Middle Aged; Periopera | 2003 |
Identification of two novel mutations of IRF6 in Korean families affected with Van der Woude syndrome.
Topics: Alanine; Amino Acid Sequence; Cleft Lip; Cleft Palate; Codon; DNA-Binding Proteins; Frameshift Mutat | 2003 |
[New trends in therapy of hemochromatosis syndromes; report of dioxyethylglycine therapy of a case].
Topics: Fabaceae; Glycine; Hemochromatosis; Humans; Syndrome | 1955 |
[Gluco-glycinuria, a new familial syndrome].
Topics: Body Fluids; Cystic Fibrosis; Glycine; Glycosuria; Humans; Kidney Diseases; Medical Records; Syndrom | 1961 |
[Glyco-glycinuric diabetes, a new familial syndrome].
Topics: Body Fluids; Diabetes Mellitus; Glycine; Glycosuria; Humans; Syndrome | 1962 |
Leukoencephalopathy with macrocephaly and mild clinical course.
Topics: Abnormalities, Multiple; Aspartic Acid; Brain; Child; Child, Preschool; Choline; Creatinine; Dementi | 2004 |
Barth syndrome without 3-methylglutaconic aciduria.
Topics: Arginine; Cardiomyopathies; Chromosomes, Human, X; Fatal Outcome; Glutarates; Glycine; Humans; Infan | 2004 |
Creatine and guanidinoacetate: diagnostic markers for inborn errors in creatine biosynthesis and transport.
Topics: Adolescent; Adult; Age Factors; Aged; Amino Acid Metabolism, Inborn Errors; Child; Child, Preschool; | 2004 |
Van Der Woude syndrome: variable penetrance of a novel mutation (p.Arg 84Gly) of the IRF6 gene in a Turkish family.
Topics: 5' Untranslated Regions; Abnormalities, Multiple; Anodontia; Arginine; Base Sequence; Cleft Lip; Cle | 2005 |
Is the presence of urinary indolyl-3-acryloylglycine associated with autism spectrum disorder?
Topics: Adolescent; Autistic Disorder; Child; Child, Preschool; Cohort Studies; Diagnosis, Differential; Edu | 2005 |
1H chemical shift imaging of the brain in guanidino methyltransferase deficiency, a creatine deficiency syndrome; guanidinoacetate accumulation in the gray matter.
Topics: Aspartic Acid; Brain Chemistry; Child, Preschool; Choline; Creatine; Glutamic Acid; Glycine; Guanidi | 2005 |
Severe arrhythmia disorder caused by cardiac L-type calcium channel mutations.
Topics: Action Potentials; Amino Acid Sequence; Animals; Arrhythmias, Cardiac; Brain; Calcium Channels, L-Ty | 2005 |
Two patients with 'Dropped head syndrome' due to mutations in LMNA or SEPN1 genes.
Topics: Arginine; Child; DNA Mutational Analysis; Female; Glycine; Humans; Infant; Lamin Type A; Lamins; Mal | 2005 |
1H MR spectroscopy of the brain in Cr transporter defect.
Topics: Brain; Creatine; Glycine; Humans; Magnetic Resonance Spectroscopy; Male; Membrane Transport Proteins | 2005 |
Bench meets bedside: a 10-year-old girl and amino acid residue glycine 75 of the facilitative glucose transporter GLUT1.
Topics: 3-O-Methylglucose; Amino Acid Sequence; Child; Epilepsy; Female; Glycine; Humans; Models, Molecular; | 2005 |
Beta2-adrenoceptor genotype and function affect hemodynamic profile heterogeneity in postural tachycardia syndrome.
Topics: Adrenergic beta-Agonists; Adult; Arteries; Catecholamines; Codon; Dose-Response Relationship, Drug; | 2006 |
Two Japanese families with hyperekplexia who have a Arg271Gln mutation in the glycine receptor alpha 1 subunit gene.
Topics: Child, Preschool; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Glycine; Hip D | 2006 |
A novel mannose-binding lectin-associated serine protease 1/3 gene variant.
Topics: Amino Acid Substitution; Genetic Variation; Glutamic Acid; Glycine; Humans; Inflammation; Lupus Eryt | 2007 |
Ethics of infusing irrigating fluid.
Topics: Anesthesiology; Biomarkers; Dose-Response Relationship, Drug; Ethanol; Ethics, Research; Glycine; Hu | 2008 |
[Uncommon case of paraganglioma syndrome in combination with malignant paraganglioma].
Topics: Aged; Amino Acid Substitution; Asparagine; Carotid Body Tumor; Chromosomes, Human, Pair 11; Diagnosi | 2008 |
Propofol for the management of glycine-mediated excitatory symptoms of TURP syndrome.
Topics: Aged; Akathisia, Drug-Induced; Glycine; Glycine Agents; Humans; Hyperammonemia; Hypnotics and Sedati | 2008 |
Quantification of creatine and guanidinoacetate using GC-MS and LC-MS/MS for the detection of cerebral creatine deficiency syndromes.
Topics: Chromatography, High Pressure Liquid; Creatine; Gas Chromatography-Mass Spectrometry; Glycine; Human | 2007 |
Mechanistic studies on the high pressure neurological syndrome.
Topics: Animals; Atmospheric Pressure; Biogenic Amines; Biomechanical Phenomena; Central Nervous System Dise | 1984 |
Changes in oncotic pressure, osmolality and electrolytes following transurethral resection of the prostate using glycine as irrigating solution.
Topics: Aged; Body Weight; Furosemide; Glycine; Humans; Male; Osmolar Concentration; Osmotic Pressure; Posto | 1983 |
Adult hypophosphatemic osteomalacia: a case report.
Topics: Adult; Glycine; Humans; Male; Osteomalacia; Phosphates; Syndrome | 1984 |
Serum bile acid patterns determined by an enzymatic method and high-performance liquid chromatography in young infants with cholestasis.
Topics: 3-alpha-Hydroxysteroid Dehydrogenase (B-Specific); 3-Hydroxysteroid Dehydrogenases; Bile Acids and S | 1984 |
Transurethral prostatic resection syndrome--a new perspective: encephalopathy with associated hyperammonemia.
Topics: Aged; Ammonia; Coma; Glycine; Humans; Male; Methods; Postoperative Complications; Prostate; Syndrome | 1983 |
Life-threatening transurethral resection syndrome despite monitoring of fluid absorption with ethanol.
Topics: Absorption; Aged; Edema; Ethanol; Fluid Therapy; Glycine; Humans; Hypotension; Indicators and Reagen | 1995 |
Noninvasive diagnosis of Caroli syndrome associated with congenital hepatic fibrosis using hepatobiliary scintigraphy.
Topics: Adult; Aniline Compounds; Bile Ducts; Caroli Disease; Glycine; Humans; Imino Acids; Liver; Liver Cir | 1995 |
Glycine-induced hyponatremia in the rat: a model of post-prostatectomy syndrome.
Topics: Animals; Central Nervous System Diseases; Disease Models, Animal; Glycine; Hyponatremia; Infusions, | 1995 |
Symptoms of the transurethral resection syndrome using glycine as the irrigant.
Topics: Absorption; Aged; Aged, 80 and over; Bradycardia; Chest Pain; Confusion; Ethanol; Extravasation of D | 1995 |
Transurethral resection syndrome after transurethral resection of bladder tumours.
Topics: Abdominal Pain; Absorption; Aged; Aged, 80 and over; Ethanol; Extravasation of Diagnostic and Therap | 1995 |
Mutation in type II procollagen (COL2A1) that substitutes aspartate for glycine alpha 1-67 and that causes cataracts and retinal detachment: evidence for molecular heterogeneity in the Wagner syndrome and the Stickler syndrome (arthro-ophthalmopathy)
Topics: Adolescent; Adult; Amino Acid Sequence; Aspartic Acid; Base Sequence; Cataract; Child; Child, Presch | 1993 |
A single amino acid substitution (gly743 --> val) in the steroid-binding domain of the human androgen receptor leads to Reifenstein syndrome.
Topics: Adult; Androgens; Base Sequence; Binding Sites; Blotting, Western; Cells, Cultured; Disorders of Sex | 1993 |
Glycine irrigant absorption syndrome following cystoscopy.
Topics: Absorption; Aged; Cystoscopy; Female; Glycine; Humans; Hyponatremia; Mental Disorders; Seizures; Syn | 1996 |
Early detection of 'endometrial resection syndrome'.
Topics: Absorption; Breath Tests; Endometrium; Ethanol; Female; Glycine; Humans; Hyponatremia; Middle Aged; | 1996 |
Ethanol monitoring of the transurethral resection syndrome.
Topics: Absorption; Aged; Blood Loss, Surgical; Breath Tests; Equipment Failure; Ethanol; Fluid Therapy; Gly | 1996 |
TUR syndrome and endoscopic transanal resection: no evidence for a clinically important association in 38 procedures.
Topics: Adenoma; Aged; Aged, 80 and over; Endoscopy; Female; Glycine; Humans; Male; Middle Aged; Prospective | 1997 |
[Late pseudo-appendicular syndrome after Roundup poisoning].
Topics: Adult; Appendicitis; Diagnosis, Differential; Glycine; Glyphosate; Herbicides; Humans; Male; Syndrom | 1997 |
Visual disturbances and transurethral resection of the prostate: the TURP syndrome.
Topics: Aged; Glycine; Humans; Male; Prostatectomy; Remission, Spontaneous; Syndrome; Therapeutic Irrigation | 1997 |
Piebaldism with deafness: molecular evidence for an expanded syndrome.
Topics: Amino Acid Substitution; Arginine; Child; Female; Glycine; Hearing Disorders; Humans; Piebaldism; Po | 1998 |
Another chapter of the antithrombin story has been written...
Topics: Acute Disease; Antithrombins; Coronary Disease; Glycine; Heparin; Hirudin Therapy; Humans; Piperidin | 1997 |
[Early infantile epileptic encephalopathy and glycine encephalopathy].
Topics: Brain Diseases; Electroencephalography; Epilepsy, Generalized; Fatal Outcome; Female; Glycine; Human | 1997 |
Heterozygous glycine substitution in the COL11A2 gene in the original patient with the Weissenbacher-Zweymüller syndrome demonstrates its identity with heterozygous OSMED (nonocular Stickler syndrome).
Topics: Abnormalities, Multiple; Amino Acid Sequence; Base Sequence; Collagen; DNA Primers; Glycine; Heteroz | 1998 |
Increased cerebrospinal fluid glycine: a biochemical marker for a leukoencephalopathy with vanishing white matter.
Topics: Adolescent; Adult; Biomarkers; Brain; Brain Diseases; Child; Child, Preschool; Excitatory Amino Acid | 1999 |
Variation in the vitreous phenotype of Stickler syndrome can be caused by different amino acid substitutions in the X position of the type II collagen Gly-X-Y triple helix.
Topics: Abnormalities, Multiple; Amino Acid Sequence; Amino Acid Substitution; Base Sequence; Biopolymers; C | 2000 |
Plasma creatinine assessment in creatine deficiency: A diagnostic pitfall.
Topics: Creatinine; Diagnostic Errors; Glycine; Guanidinoacetate N-Methyltransferase; Humans; Methyltransfer | 2000 |
The TURP syndrome: importance of expiratory ethanol measurement and high serum levels of glycine.
Topics: Aged; Aged, 80 and over; Breath Tests; Cardiovascular Diseases; Ethanol; Glycine; Humans; Male; Midd | 2001 |
Glycine toxicity and unexpected intra-operative death.
Topics: Aged; Autopsy; Cause of Death; Fatal Outcome; Forensic Medicine; Glycine; Heart Arrest; Humans; Hypo | 2001 |
Hypersarcosinemia with craniostenosis-syndactylism syndrome.
Topics: Amino Acid Metabolism, Inborn Errors; Craniosynostoses; Female; Glycine; Humans; Male; Sarcosine; Sy | 1975 |
Chemical analysis of an angiofibroma from a patient with tuberous sclerosis.
Topics: Adult; Alanine; Collagen; Dermatan Sulfate; Facial Neoplasms; Galactosidases; Glucuronidase; Glycine | 1977 |
Glycine metabolism and spinal cord disorders.
Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Animals; Ataxia; Cats; Cells, Cultured; Chi | 1978 |
Ontogeny of amino acid reabsorption in human kidney. Evidence from the homozygous infant with familial renal iminoglycinuria for multiple proline and glycine systems.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Glycine; Humans; Imino Acids; Infant, Newborn; Ki | 1979 |
The neuropathology of the nonketotic and ketotic hyperglycinemias: three cases.
Topics: Amino Acid Metabolism, Inborn Errors; Child, Preschool; Corpus Callosum; Demyelinating Diseases; Fem | 1978 |
Nonketotic hyperglycinemia: a clinical analysis of 19 Finnish patients.
Topics: Amino Acid Metabolism, Inborn Errors; Female; Finland; Glycine; Humans; Infant; Infant, Newborn; Int | 1978 |
D-glyceric acidemia: biohcemical studies of a new syndrome.
Topics: Alcohol Oxidoreductases; Amino Acid Metabolism, Inborn Errors; Child, Preschool; Chromatography, Gas | 1976 |
A pharmacologic study of the stiff-man syndrome. Correlation of clinical symptoms with urinary 3-methoxy-4-hydroxy-phenyl glycol excretion.
Topics: Diazepam; Glycine; Glycols; Homovanillic Acid; Humans; Levodopa; Male; Metanephrine; Methoxyhydroxyp | 1975 |
Amino acid concentrations in plasma and skeletal muscle after transurethral resection syndrome.
Topics: Acid-Base Equilibrium; Aged; Amino Acids; Blood Pressure; Glycine; Humans; Male; Middle Aged; Muscle | 1992 |
[The intravascular transfer of glycine during percutaneous kidney surgery].
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Female; Glycine; Hemodilution; Humans; Male; Middle Aged | 1992 |
Serum potassium change during the TURP syndrome by cell volume regulation.
Topics: Absorption; Cells; Extracellular Space; Glycine; Humans; Male; Potassium; Prostatectomy; Syndrome | 1992 |
Hyponatraemia after transurethral resection of the prostate.
Topics: Aged; Bradycardia; Confusion; Glycine; Humans; Hyponatremia; Hypotension; Intraoperative Complicatio | 1991 |
Hyponatremia and volume overload as a complication of transurethral resection of the prostate.
Topics: Absorption; Aged; Glycine; Humans; Hyponatremia; Male; Plasma Volume; Postoperative Complications; P | 1991 |
[Resorption of the lavage fluid during transurethral resection of the prostate. Apropos of 13 cases].
Topics: Absorption; Diplopia; Glycine; Humans; Hypotonic Solutions; Male; Nausea; Osmolar Concentration; Pro | 1990 |
Osmotic and metabolic sequelae of volumetric overload in relation to the TUR syndrome.
Topics: Aged; Blood Volume; Glycine; Heart Rate; Humans; Infusions, Intravenous; Intraoperative Complication | 1990 |
[Analysis of the relative rates of synthesis of G gamma and A gamma globin chains in the erythropoietic bursts in patients with trisomy 13 syndrome].
Topics: Alanine; Chromosomes, Human, Pair 13; Erythroid Precursor Cells; Female; Fetal Hemoglobin; Globins; | 1989 |
Nonketotic hyperglycinemia in a patient with the 9p- syndrome.
Topics: Abnormalities, Multiple; Chromosome Deletion; Chromosomes, Human, Pair 9; Genes, Recessive; Genetic | 1989 |
Transurethral resection of the prostate, serum glycine levels, and ocular evoked potentials.
Topics: Aged; Evoked Potentials, Visual; Glycine; Humans; Male; Middle Aged; Prostatectomy; Syndrome; Vision | 1989 |
The physiologic basis of the TUR syndrome.
Topics: Ammonia; Animals; Cardiovascular Diseases; Central Nervous System Diseases; Female; Glycine; Hyponat | 1989 |
Hallucination and visual disturbances in transurethral prostatic resection.
Topics: Absorption; Aged; Blood Volume; Glycine; Hallucinations; Humans; Male; Prostatectomy; Syndrome; Ther | 1988 |
The role of ammonia toxicity in the post transurethral prostatectomy syndrome.
Topics: Aged; Ammonia; Glycine; Humans; Male; Postoperative Period; Prostatectomy; Sodium; Syndrome; Therape | 1987 |
Hyponatraemia following transurethral resection of the prostate.
Topics: Aged; Glycine; Humans; Hyponatremia; Hypotension; Male; Middle Aged; Organ Size; Postoperative Compl | 1985 |
Effects of glycine on hemodynamic responses and visual evoked potentials in the dog.
Topics: Ammonia; Animals; Arginine; Blood Pressure; Cardiac Output; Dogs; Evoked Potentials, Visual; Glycine | 1985 |
[Hyperiminoaciduria and disaminoaciduria in endemic (Balkan-)nephropathy (author's transl)].
Topics: Adult; Aged; Alanine; Amino Acids; Chromatography, Thin Layer; Chronic Disease; Creatinine; Female; | 1974 |
Urinary metabolic screening of mentally retarded patients from institutions in the northern part of Sweden.
Topics: Abnormalities, Multiple; Adolescent; Adult; Amino Acids; Child; Eye Diseases; Female; Glycine; Glyco | 1973 |
[Study of the pain syndrome of spinal origin (the concept of a generative mechanism for the pain syndrome)].
Topics: Animals; Denervation; Femoral Nerve; Glycine; Injections, Spinal; Lumbosacral Plexus; Neural Inhibit | 1974 |
Hyperglycinemia with ketosis due to a defect in isoleucine metabolism: a preliminary report.
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Amino Acids; Ammonia; Diet Therapy; Dietary Proteins | 1972 |
Acquired hyperoxaluria and intestinal disease. Evidence that bile acid glycine is not a precursor of oxalate.
Topics: Adult; Aged; Bacteria; Bacterial Infections; Bile Acids and Salts; Carbon Isotopes; Crohn Disease; F | 1973 |
Amino acid abnormality in Sjögren-Larsson syndrome.
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Dental Enamel Hypoplasia; Epilepsy; Ethylamines; G | 1973 |
Lowe's syndrome. Absence of amino acid transport defect in cultured fibroblasts.
Topics: Ammonia; Biological Transport; Carbon Radioisotopes; Culture Techniques; Eye Diseases; Fibroblasts; | 1973 |
Acquired hyperoxaluria, urolithiasis, and intestinal disease: a new digestive disorder?
Topics: Bile Acids and Salts; Carbon Dioxide; Carbon Radioisotopes; Cholestyramine Resin; Female; Glycine; H | 1974 |
Corneal opacity, microphthalmia, mental retardation, microcephaly and generalized muscular spasticity associated with hyperglycinemia.
Topics: Alkaline Phosphatase; Calcium; Cerebral Palsy; Chromosomes; Consanguinity; Corneal Opacity; Female; | 1974 |