s-adenosylmethionine has been researched along with Intellectual Disability in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (25.00) | 29.6817 |
| 2010's | 2 (50.00) | 24.3611 |
| 2020's | 1 (25.00) | 2.80 |
| Authors | Studies |
|---|---|
| Hall, K; Hasadsri, L; Kimonis, V; Rose, L; Tang, S | 1 |
| Arias, A; Artuch, R; Campistol, J; Desviat, LR; Farré, G; García-Cazorla, A; García-Villoria, J; Merinero, B; Ribes, A; Rodríguez-Pombo, P; Sempere, A; Vilaseca, MA | 1 |
| Andresen, BS; Berry, SA; He, M; Lussky, RC; Madsen, PP; Matern, D; Rinaldo, P; van Calcar, SC; Vockley, J; Whitley, CB; Wolff, JA | 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 |
2 review(s) available for s-adenosylmethionine and Intellectual Disability
| Article | Year |
|---|---|
Prospective diagnosis of 2-methylbutyryl-CoA dehydrogenase deficiency in the Hmong population by newborn screening using tandem mass spectrometry.
Topics: Amino Acid Metabolism, Inborn Errors; Carnitine; Diagnosis, Differential; Diet, Protein-Restricted; DNA Mutational Analysis; Ethnicity; Exons; Female; Genetic Testing; Humans; Infant, Newborn; Intellectual Disability; Isoleucine; Male; Mass Spectrometry; Neonatal Screening; Oxidoreductases Acting on CH-CH Group Donors; Sequence Deletion; Treatment Outcome | 2003 |
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 |
2 other study(ies) available for s-adenosylmethionine and Intellectual Disability
| Article | Year |
|---|---|
Homozygous B4GALNT1 mutation and biochemical glutaric acidemia type II: A case report.
Topics: Adult; Carnitine; Epilepsy, Temporal Lobe; Female; Frameshift Mutation; Homozygote; Humans; Intellectual Disability; Multiple Acyl Coenzyme A Dehydrogenase Deficiency; N-Acetylgalactosaminyltransferases; Spastic Paraplegia, Hereditary | 2020 |
Study of inborn errors of metabolism in urine from patients with unexplained mental retardation.
Topics: Adenylosuccinate Lyase; Adolescent; Adult; Aged; Carnitine; Child; Child, Preschool; Chromium; Cohort Studies; Creatine; Female; Humans; Intellectual Disability; Male; Metabolism, Inborn Errors; Middle Aged; Phenylketonurias; Purines; Pyrimidines | 2010 |