sulfur has been researched along with Brain Diseases, Metabolic, Familial in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (66.67) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Abdenur, JE; Boyer, M; Di Meo, I; Eftekharian, S; Sowa, M; Steenari, MR; Tiranti, V | 1 |
| Dawson, PA; Eyles, DW; Kesby, JP; Lee, S; Markovich, D; Muslim, MD; Steane, SE | 1 |
| Akisu, M; Arslanoglu, S; Ciriş, M; Coker, M; Darcan, S; Demirtaş, E; Gökşen, D; Kultursay, N; Tütüncüoglu, S; Yalaz, M | 1 |
3 other study(ies) available for sulfur and Brain Diseases, Metabolic, Familial
| Article | Year |
|---|---|
Response to medical and a novel dietary treatment in newborn screen identified patients with ethylmalonic encephalopathy.
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 |
Hyperserotonaemia and reduced brain serotonin levels in NaS1 sulphate transporter null mice.
Topics: Animals; Brain; Brain Chemistry; Brain Diseases, Metabolic, Inborn; Cation Transport Proteins; Down-Regulation; Hydroxyindoleacetic Acid; Male; Mice; Mice, Knockout; Receptors, Serotonin; RNA, Messenger; Serotonin; Sodium Sulfate Cotransporter; Sulfur Compounds; Symporters; Up-Regulation | 2007 |
Molybdenum cofactor deficiency associated with Dandy-Walker complex.
Topics: Brain; Brain Diseases, Metabolic, Inborn; Coenzymes; Dandy-Walker Syndrome; Humans; Infant, Newborn; Magnetic Resonance Imaging; Male; Metalloproteins; Molybdenum Cofactors; Oxidoreductases Acting on Sulfur Group Donors; Pteridines; Sulfur Compounds; Uric Acid; Xanthine Dehydrogenase; Xanthines | 2001 |