Compounds > s-adenosylmethionine
Page last updated: 2024-08-23

s-adenosylmethionine and Acidosis

s-adenosylmethionine has been researched along with Acidosis in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (40.00)29.6817
2010's2 (40.00)24.3611
2020's1 (20.00)2.80

Authors

AuthorsStudies
Cai, R; Chang, R; Chen, D; Huang, L; Jiang, Y; Ning, H; Pan, L; Tan, J; Wei, B; Wei, J; Yang, J; Yin, B; Yuan, D; Zeng, T; Zheng, M1
Liu, H; Miao, JK; Wan, KX; Wang, DJ; Yang, J; Yu, CW; Yuan, ZJ; Zeng, Y; Zhang, J; Zou, L1
Burgard, P; Haege, G; Hoffmann, GF; Hörster, F; Kölker, S; Riderer, A; Zwickler, T1
Bain, MD; Baric, I; Chalmers, RA; Feyh, P; Hoffmann, GF; Jakobs, C; Jeffrey, I; Kölker, S; Okun, JG; Pourfarzam, M; Schor, DS; Wagner, L; Zschocke, J1
al-Essa, MA; Bakheet, SM; Ozand, PT; Patay, ZJ; Rashed, MS1

Other Studies

5 other study(ies) available for s-adenosylmethionine and Acidosis

ArticleYear
[Analysis of IVD gene variants in four children with isovalerate acidemia].
    Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics, 2022, Dec-10, Volume: 39, Issue:12

    Topics: Acidosis; Carnitine; Child; Erythrocytes; High-Throughput Nucleotide Sequencing; Humans; Infant, Newborn

2022
Severe clinical manifestation of mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency associated with two novel mutations: a case report.
    BMC pediatrics, 2019, 10-09, Volume: 19, Issue:1

    Topics: Acidosis; Acyl Coenzyme A; Adipates; Carnitine; Diarrhea; Dicarboxylic Acids; Exome Sequencing; Fatal Outcome; Frameshift Mutation; Glutarates; Humans; Hydroxymethylglutaryl-CoA Synthase; Infant; Male; Mitochondria; Multiple Organ Failure; Mutation; Respiratory Tract Infections

2019
Metabolic decompensation in methylmalonic aciduria: which biochemical parameters are discriminative?
    Journal of inherited metabolic disease, 2012, Volume: 35, Issue:5

    Topics: Acid-Base Equilibrium; Acidosis; Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Ammonia; Bicarbonates; Carnitine; Child; Child, Preschool; Female; Follow-Up Studies; Humans; Infant; Infant, Newborn; Male; Young Adult

2012
Glutaryl-CoA dehydrogenase deficiency: region-specific analysis of organic acids and acylcarnitines in post mortem brain predicts vulnerability of the putamen.
    Neuropediatrics, 2003, Volume: 34, Issue:5

    Topics: Acidosis; Acute Disease; Adolescent; Anticonvulsants; Atrophy; Brain; Carnitine; DNA Mutational Analysis; Fatal Outcome; Gas Chromatography-Mass Spectrometry; Gene Expression; Glutarates; Glutaryl-CoA Dehydrogenase; Humans; Male; Muscle Hypotonia; N-Methylaspartate; Oxidoreductases Acting on CH-CH Group Donors; Point Mutation; Putamen; Spasm; Vigabatrin

2003
Glutaric aciduria type II: observations in seven patients with neonatal- and late-onset disease.
    Journal of perinatology : official journal of the California Perinatal Association, 2000, Volume: 20, Issue:2

    Topics: Acidosis; Age of Onset; Brain; Carnitine; Child; Consanguinity; Female; Glutarates; Humans; Infant; Infant, Newborn; Magnetic Resonance Imaging; Male; Mass Spectrometry; Metabolism, Inborn Errors; Tomography, Emission-Computed

2000