Compounds > methionine
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methionine and Brain Diseases, Metabolic, Familial

methionine has been researched along with Brain Diseases, Metabolic, Familial in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's4 (80.00)29.6817
2010's1 (20.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Abdenur, JE; Boyer, M; Di Meo, I; Eftekharian, S; Sowa, M; Steenari, MR; Tiranti, V1
Barshop, BA; Haas, RH; McGowan, KA; Naviaux, RK; Nyhan, WL; Townsend, JJ; Yu, A1
Baris, H; Eichler, FS; Grant, PE; Hanley, CA; Hoda, S; Krishnamoorthy, KS; Lee, MS; Shih, VE; Tan, WH1
De Vivo, DC; Fujii, T; Ho, YY; Ito, M; Kudo, T; Miyajima, T; Shirasaka, Y; Tsang, PT; Wang, D; Wong, HY1
Giraudier, S; Michot, JM; Papo, T; Sedel, F; Smiejan, JM1

Reviews

1 review(s) available for methionine and Brain Diseases, Metabolic, Familial

ArticleYear
Isolated sulfite oxidase deficiency: a case report with a novel mutation and review of the literature.
    Pediatrics, 2005, Volume: 116, Issue:3

    Topics: Amino Acid Metabolism, Inborn Errors; Base Pairing; Brain Diseases, Metabolic, Inborn; Cysteine; Humans; Infant; Infant, Newborn; Male; Methionine; Mutation; Sequence Deletion; Sulfite Oxidase

2005

Other Studies

4 other study(ies) available for methionine and Brain Diseases, Metabolic, Familial

ArticleYear
Response to medical and a novel dietary treatment in newborn screen identified patients with ethylmalonic encephalopathy.
    Molecular genetics and metabolism, 2018, Volume: 124, Issue:1

    Topics: Acetylcysteine; Amino Acids; Biomarkers; Brain Diseases, Metabolic, Inborn; Cysteine; Diet; Female; Humans; Infant; Infant, Newborn; Lactic Acid; Male; Malonates; Methionine; Metronidazole; Mitochondrial Proteins; Mutation; Neonatal Screening; Nucleocytoplasmic Transport Proteins; Purpura; Sulfur

2018
The role of methionine in ethylmalonic encephalopathy with petechiae.
    Archives of neurology, 2004, Volume: 61, Issue:4

    Topics: Amino Acids; Brain; Brain Diseases, Metabolic, Inborn; Caudate Nucleus; Fatal Outcome; Female; Follow-Up Studies; Humans; Infant; Isoleucine; Male; Malonates; Methionine; Pedigree; Purpura; Substantia Nigra; Syndrome

2004
Three Japanese patients with glucose transporter type 1 deficiency syndrome.
    Brain & development, 2007, Volume: 29, Issue:2

    Topics: 3-Hydroxybutyric Acid; Adult; Arginine; Brain Diseases, Metabolic, Inborn; Brain Mapping; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Female; Glucose Transporter Type 1; Humans; Japan; Male; Methionine; Mutation, Missense; Positron-Emission Tomography; Threonine; Tryptophan

2007
Psychosis, paraplegia and coma revealing methylenetetrahydrofolate reductase deficiency in a 56-year-old woman.
    Journal of neurology, neurosurgery, and psychiatry, 2008, Volume: 79, Issue:8

    Topics: Brain; Brain Diseases, Metabolic, Inborn; Catatonia; Chromosome Aberrations; Chromosomes, Human, Pair 1; Coma; Dementia; Exons; Folic Acid; Genes, Recessive; Homocysteine; Humans; Magnetic Resonance Imaging; Methionine; Methylenetetrahydrofolate Reductase (NADPH2); Mutation, Missense; Neurologic Examination; Paraplegia; Polymorphism, Genetic; Psychotic Disorders

2008