biotin has been researched along with Beriberi, Cerebral 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 | 0 (0.00) | 29.6817 |
| 2010's | 4 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Artuch, R; Dupuits, C; Gargallo, E; Muchart, J; Pérez-Dueñas, B; Rebollo, M; Serrano, M | 1 |
| Al Balwi, M; Al Rifai, MT; Al Rumayan, A; Al Shalaan, H; Al-Twaijri, W; Alfadhel, M; Almuntashri, M; Bashiri, FA; Eyaid, W; Jadah, RH | 1 |
| Carr, LJ; Chong, WK; DeVile, CJ; Fassone, E; Rahman, S; Wedatilake, Y | 1 |
| Hara, K; Ishihara, N; Kumagai, T; Kuwano, R; Miura, K; Nakanishi, K; Suzuki, M; Tsuji, S; Wakamatsu, N; Yamada, K; Yamada, Y | 1 |
1 review(s) available for biotin and Beriberi, Cerebral
| Article | Year |
|---|---|
Biotin-responsive basal ganglia disease should be renamed biotin-thiamine-responsive basal ganglia disease: a retrospective review of the clinical, radiological and molecular findings of 18 new cases.
Topics: Adolescent; Adult; Basal Ganglia; Basal Ganglia Diseases; Biotin; Child; Child, Preschool; Female; Humans; Infant; Magnetic Resonance Imaging; Male; Membrane Transport Proteins; Mutation; Radiography; Thiamine; Wernicke Encephalopathy; Young Adult | 2013 |
3 other study(ies) available for biotin and Beriberi, Cerebral
| Article | Year |
|---|---|
Reversible lactic acidosis in a newborn with thiamine transporter-2 deficiency.
Topics: Acidosis, Lactic; Biotin; Blood Chemical Analysis; Carnitine; Diagnosis, Differential; Drug Therapy, Combination; Follow-Up Studies; Gene Expression Regulation; Humans; Infant, Newborn; Magnetic Resonance Imaging; Male; Membrane Transport Proteins; Mutation; Risk Assessment; Thiamine; Thiamine Deficiency; Treatment Outcome; Wernicke Encephalopathy | 2013 |
Treatable Leigh-like encephalopathy presenting in adolescence.
Topics: Adolescent; Biopsy; Biotin; Diagnosis, Differential; Diagnostic Imaging; Female; Humans; Thiamine; Wernicke Encephalopathy | 2013 |
A wide spectrum of clinical and brain MRI findings in patients with SLC19A3 mutations.
Topics: Adolescent; Adult; Asian People; Basal Ganglia Diseases; Biotin; Brain; Child; Female; Genome-Wide Association Study; Humans; Magnetic Resonance Imaging; Male; Membrane Transport Proteins; Mutation; Thiamine; Wernicke Encephalopathy | 2010 |