s-adenosylmethionine has been researched along with Mental Retardation, X-Linked in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 5 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Akiba, K; Aoyama, Y; Fukao, T; Goto, M; Hasegawa, Y; Hashimoto, T; Hori, T; Kuwayama, N; Morita, M; Moriyama, Y; Murayama, K; Ohtake, A; Shigematsu, Y; Usuda, N; Venkatesan, R; Wierenga, R | 1 |
| Aydin, HI | 1 |
| Collet, JP; Dunbar, M; Edgar, V; Elango, R; Jaggumantri, S; Mignone, C; Newlove, T; Sargent, M; Stockler-Ipsiroglu, S; van Karnebeek, CD | 1 |
| Cheillan, D; Dessein, AF; Dobbelaere, D; Fontaine, M; Joncquel-Chevalier Curt, M; Mention-Mulliez, K; Porchet, N; Soto-Ares, G; Vamecq, J; Voicu, PM | 1 |
| McCloskey, DE; Pegg, AE; Schwartz, CE; Wang, X | 1 |
1 review(s) available for s-adenosylmethionine and Mental Retardation, X-Linked
| Article | Year |
|---|---|
Creatine biosynthesis and transport in health and disease.
Topics: Amidinotransferases; Amino Acid Metabolism, Inborn Errors; Amino Acid Transport Systems, Basic; AMP-Activated Protein Kinases; Animals; Biological Transport, Active; Brain Diseases, Metabolic, Inborn; Creatine; Developmental Disabilities; Energy Metabolism; Guanidinoacetate N-Methyltransferase; Gyrate Atrophy; Humans; Hyperammonemia; Intellectual Disability; Language Development Disorders; Mental Retardation, X-Linked; Methylation; Mitochondrial Membrane Transport Proteins; Movement Disorders; Mutation; Nerve Tissue Proteins; Ornithine; Plasma Membrane Neurotransmitter Transport Proteins; Prenatal Diagnosis; S-Adenosylmethionine; Speech Disorders; Urea Cycle Disorders, Inborn | 2015 |
4 other study(ies) available for s-adenosylmethionine and Mental Retardation, X-Linked
| Article | Year |
|---|---|
The first case in Asia of 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency (HSD10 disease) with atypical presentation.
Topics: 3-Hydroxyacyl CoA Dehydrogenases; Acetyl-CoA C-Acetyltransferase; Base Sequence; Carnitine; Child; Diagnosis, Differential; DNA Mutational Analysis; Dyskinesias; Fibroblasts; Glycine; Humans; Hydroxybutyrates; Immunoblotting; Lipid Metabolism, Inborn Errors; Male; Mental Retardation, X-Linked; Mitochondria; Models, Molecular; Point Mutation; Protein Structure, Tertiary | 2014 |
Creatine Transporter Deficiency in Two Brothers with Autism Spectrum Disorder.
Topics: Adolescent; Arginine; Autism Spectrum Disorder; Brain Diseases, Metabolic, Inborn; Child; Creatine; Glycine; Humans; Male; Mental Retardation, X-Linked; Nerve Tissue Proteins; Plasma Membrane Neurotransmitter Transport Proteins; S-Adenosylmethionine; Siblings | 2018 |
Treatment of Creatine Transporter (SLC6A8) Deficiency With Oral S-Adenosyl Methionine as Adjunct to L-arginine, Glycine, and Creatine Supplements.
Topics: Administration, Oral; Arginine; Basal Ganglia; Brain Diseases, Metabolic, Inborn; Central Nervous System Agents; Child; Creatine; Drug Therapy, Combination; Follow-Up Studies; Glycine; Humans; Magnetic Resonance Spectroscopy; Male; Medication Adherence; Mental Retardation, X-Linked; Plasma Membrane Neurotransmitter Transport Proteins; S-Adenosylmethionine; Treatment Outcome | 2015 |
Spermine synthase activity affects the content of decarboxylated S-adenosylmethionine.
Topics: Animals; Biogenic Amines; Cells, Cultured; Decarboxylation; Humans; Mental Retardation, X-Linked; Mice; Mice, Knockout; S-Adenosylmethionine; Spermine Synthase | 2011 |