Page last updated: 2024-10-16

betaine and Amino Acid Metabolism Disorders, Inborn

betaine has been researched along with Amino Acid Metabolism Disorders, Inborn in 16 studies

glycine betaine : The amino acid betaine derived from glycine.

Research Excerpts

ExcerptRelevanceReference
"Patients with combined methylmalonic acidemia and homocystinuria respond to a combined treatment consisting of supplementation of hydroxycobalamin, betaine, folic acid, vitamin B6 and L-carnitine with clinical and biochemical improvement."7.79[Outcomes of patients with combined methylmalonic acidemia and homocystinuria after treatment]. ( Gao, XL; Gu, XF; Han, LS; Huang, Z; Ji, WJ; Li, XY; Qiu, WJ; Wang, Y; Ye, J; Zhang, HW, 2013)
"The use of hydroxocobalamin (OH-B12), betaine, carnitine, and folinic acid were studied in two children with the cobalamin C form of methylmalonic acidemia and homocystinuria."7.67Therapeutic approaches to cobalamin-C methylmalonic acidemia and homocystinuria. ( Allen, RH; Bartholomew, DW; Batshaw, ML; Francomano, CA; Roe, CR; Rosenblatt, D; Valle, DL, 1988)
"Elevation of homocysteine is implicated in multiple medical conditions, including classical homocystinuria, a variety of remethylation disorders, and most recently in coronary artery disease."4.83The use of betaine in the treatment of elevated homocysteine. ( Lawson-Yuen, A; Levy, HL, 2006)
"Patients with combined methylmalonic acidemia and homocystinuria respond to a combined treatment consisting of supplementation of hydroxycobalamin, betaine, folic acid, vitamin B6 and L-carnitine with clinical and biochemical improvement."3.79[Outcomes of patients with combined methylmalonic acidemia and homocystinuria after treatment]. ( Gao, XL; Gu, XF; Han, LS; Huang, Z; Ji, WJ; Li, XY; Qiu, WJ; Wang, Y; Ye, J; Zhang, HW, 2013)
"The use of hydroxocobalamin (OH-B12), betaine, carnitine, and folinic acid were studied in two children with the cobalamin C form of methylmalonic acidemia and homocystinuria."3.67Therapeutic approaches to cobalamin-C methylmalonic acidemia and homocystinuria. ( Allen, RH; Bartholomew, DW; Batshaw, ML; Francomano, CA; Roe, CR; Rosenblatt, D; Valle, DL, 1988)
"Among 13 patients who exhibited spastic paraplegia as the main manifestation, 11 patients carried c."1.72Late-onset cblC deficiency around puberty: a retrospective study of the clinical characteristics, diagnosis, and treatment. ( Chen, Z; Dong, H; He, R; Jin, Y; Kang, L; Li, D; Li, M; Liu, X; Liu, Y; Qi, J; Song, J; Wang, F; Xiao, H; Yan, H; Yang, Y; Zhang, Y; Zheng, H, 2022)
"Malignant hypertension was diagnosed."1.40Adult-onset eculizumab-resistant hemolytic uremic syndrome associated with cobalamin C deficiency. ( Benoist, JF; Cornec-Le Gall, E; De Parscau, L; Delmas, Y; Doucet, L; Fremeaux-Bacchi, V; Le Meur, Y; Ogier, H, 2014)

Research

Studies (16)

TimeframeStudies, this research(%)All Research%
pre-19905 (31.25)18.7374
1990's2 (12.50)18.2507
2000's3 (18.75)29.6817
2010's4 (25.00)24.3611
2020's2 (12.50)2.80

Authors

AuthorsStudies
Chen, Z1
Dong, H1
Liu, Y2
He, R1
Song, J1
Jin, Y1
Li, M1
Liu, X1
Yan, H1
Qi, J1
Wang, F1
Xiao, H1
Zheng, H1
Kang, L1
Li, D1
Zhang, Y1
Yang, Y1
Tanaka, Y1
Kawano, M1
Nakashima, S1
Yamaguchi, C1
Asahina, M1
Sakamoto, M1
Shirouchi, B1
Tashiro, K1
Imaizumi, K1
Sato, M1
Huang, Z1
Han, LS1
Ye, J1
Qiu, WJ1
Zhang, HW1
Gao, XL1
Wang, Y1
Ji, WJ1
Li, XY1
Gu, XF1
Liu, YP1
Yang, YL1
Cornec-Le Gall, E1
Delmas, Y1
De Parscau, L1
Doucet, L1
Ogier, H1
Benoist, JF1
Fremeaux-Bacchi, V1
Le Meur, Y1
Minkler, PE1
Stoll, MS1
Ingalls, ST1
Kerner, J1
Hoppel, CL1
HOSEIN, EA1
SMART, M1
HAWKINS, K1
Tsina, EK1
Marsden, DL1
Hansen, RM1
Fulton, AB1
Lawson-Yuen, A1
Levy, HL1
Wikoff, WR1
Gangoiti, JA1
Barshop, BA1
Siuzdak, G1
Komrower, GM1
Lundberg, P1
Dudman, NP1
Kuchel, PW1
Wilcken, DE1
Engelbrecht, V1
Rassek, M1
Huismann, J1
Wendel, U1
Bartholomew, DW1
Batshaw, ML1
Allen, RH1
Roe, CR1
Rosenblatt, D1
Valle, DL1
Francomano, CA1
Iles, RA1
Chalmers, RA1
Hind, AJ1
Mudd, SH1
Levy, H1
Morrow, G1

Reviews

2 reviews available for betaine and Amino Acid Metabolism Disorders, Inborn

ArticleYear
[Advances in the clinical and laboratory studies on methylmalonic aciduria combined with homocysteinemia type cblC].
    Zhonghua er ke za zhi = Chinese journal of pediatrics, 2013, Volume: 51, Issue:4

    Topics: Adult; Age of Onset; Amino Acid Metabolism, Inborn Errors; Betaine; Carrier Proteins; Child; China;

2013
The use of betaine in the treatment of elevated homocysteine.
    Molecular genetics and metabolism, 2006, Volume: 88, Issue:3

    Topics: Amino Acid Metabolism, Inborn Errors; Betaine; Homocysteine; Homocystinuria; Humans; Hyperhomocystei

2006

Other Studies

14 other studies available for betaine and Amino Acid Metabolism Disorders, Inborn

ArticleYear
Late-onset cblC deficiency around puberty: a retrospective study of the clinical characteristics, diagnosis, and treatment.
    Orphanet journal of rare diseases, 2022, 09-02, Volume: 17, Issue:1

    Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Betaine; Carnitine; Child; Female; Homocyst

2022
Mutation in Smek2 regulating hepatic glucose metabolism causes hypersarcosinemia and hyperhomocysteinemia in rats.
    Scientific reports, 2023, 02-21, Volume: 13, Issue:1

    Topics: Amino Acid Metabolism, Inborn Errors; Animals; Betaine; Glucose; Homocysteine; Hypercholesterolemia;

2023
[Outcomes of patients with combined methylmalonic acidemia and homocystinuria after treatment].
    Zhonghua er ke za zhi = Chinese journal of pediatrics, 2013, Volume: 51, Issue:3

    Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Betaine; Carnitine; Child; Child, Preschool

2013
Adult-onset eculizumab-resistant hemolytic uremic syndrome associated with cobalamin C deficiency.
    American journal of kidney diseases : the official journal of the National Kidney Foundation, 2014, Volume: 63, Issue:1

    Topics: Adult; Amino Acid Metabolism, Inborn Errors; Antibodies, Monoclonal, Humanized; Betaine; Biopsy; Car

2014
Quantitative acylcarnitine determination by UHPLC-MS/MS--Going beyond tandem MS acylcarnitine "profiles".
    Molecular genetics and metabolism, 2015, Volume: 116, Issue:4

    Topics: Acetyl-CoA C-Acyltransferase; Acyl-CoA Dehydrogenase; Amino Acid Metabolism, Inborn Errors; Betaine;

2015
Aminoaciduria in rats after treatment with the ethyl ester of gamma-butyrobetaine.
    Canadian journal of biochemistry and physiology, 1960, Volume: 38

    Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Animals; Betaine; Carnitine; Choline; Rats

1960
Maculopathy and retinal degeneration in cobalamin C methylmalonic aciduria and homocystinuria.
    Archives of ophthalmology (Chicago, Ill. : 1960), 2005, Volume: 123, Issue:8

    Topics: Amino Acid Metabolism, Inborn Errors; Betaine; Cobamides; Female; Homocysteine; Homocystinuria; Huma

2005
Metabolomics identifies perturbations in human disorders of propionate metabolism.
    Clinical chemistry, 2007, Volume: 53, Issue:12

    Topics: Acetylcarnitine; Adult; Amino Acid Metabolism, Inborn Errors; Betaine; Biomarkers; Carnitine; Child;

2007
Dietary treatment of homocystinuria.
    American journal of diseases of children (1960), 1967, Volume: 113, Issue:1

    Topics: Amino Acid Metabolism, Inborn Errors; Betaine; Child, Preschool; Diet Therapy; Female; Folic Acid; G

1967
1H NMR determination of urinary betaine in patients with premature vascular disease and mild homocysteinemia.
    Clinical chemistry, 1995, Volume: 41, Issue:2

    Topics: Adult; Amino Acid Metabolism, Inborn Errors; Betaine; Creatinine; Glycine; Homocysteine; Humans; Hyd

1995
MR and proton MR spectroscopy of the brain in hyperhomocysteinemia caused by methylenetetrahydrofolate reductase deficiency.
    AJNR. American journal of neuroradiology, 1997, Volume: 18, Issue:3

    Topics: Amino Acid Metabolism, Inborn Errors; Betaine; Brain; Brain Diseases, Metabolic; Energy Metabolism;

1997
Therapeutic approaches to cobalamin-C methylmalonic acidemia and homocystinuria.
    The Journal of pediatrics, 1988, Volume: 112, Issue:1

    Topics: Administration, Oral; Amino Acid Metabolism, Inborn Errors; Betaine; Carnitine; Child, Preschool; Fe

1988
Methylmalonic aciduria and propionic acidaemia studied by proton nuclear magnetic resonance spectroscopy.
    Clinica chimica acta; international journal of clinical chemistry, 1986, Dec-15, Volume: 161, Issue:2

    Topics: Amino Acid Metabolism, Inborn Errors; Betaine; Creatine; Female; Gas Chromatography-Mass Spectrometr

1986
Deranged B 12 metabolism: effects on sulfur amino acid metabolism.
    Biochemical medicine, 1970, Volume: 4, Issue:3

    Topics: Adenosine Triphosphate; Adult; Amino Acid Metabolism, Inborn Errors; Amino Acids; Betaine; Brain Che

1970