biotin and Dystonia
biotin has been researched along with Dystonia in 4 studies
Research
Studies (4)
| 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 | 2 (50.00) | 24.3611 |
| 2020's | 2 (50.00) | 2.80 |
Authors
| Authors | Studies |
|---|---|
| Alfadhel, M; Alnozha, A; Alsini, H; Asmat, Z; Hundallah, K; Tabarki, B | 1 |
| Abdelaty, O; Aburezq, M; Al-Tawari, A; Alahmad, A; Albash, B; Alsafi, R; Alsharhan, H; Ayed, M; Bastaki, L; Dashti, F; Elshafie, R; Hayat, A; Makhseed, N; Marafi, D; Ramadan, D; Shafik, M | 1 |
| Cestari, DM; Eichler, FS; Hunt, AL; Rapalino, O; Swoboda, KJ | 1 |
| Bellanger, A; Brice, A; Debs, R; Degos, B; Depienne, C; Galanaud, D; Keren, B; Lyon-Caen, O; Rastetter, A; Sedel, F | 1 |
Other Studies
4 other study(ies) available for biotin and Dystonia
| Article | Year |
|---|---|
Beyond the caudate nucleus: Early atypical neuroimaging findings in biotin-thiamine- responsive basal ganglia disease.
Topics: Basal Ganglia Diseases; Biotin; Caudate Nucleus; Dystonia; Humans; Magnetic Resonance Imaging; Male; Membrane Transport Proteins; Neuroimaging; Thiamine | 2022 |
Biotin-thiamine responsive basal ganglia disease: a retrospective review of the clinical, radiological and molecular findings of cases in Kuwait with novel variants.
Topics: Adult; Basal Ganglia Diseases; Biotin; Brain Diseases; Child, Preschool; Dysarthria; Dystonia; Humans; Infant, Newborn; Kuwait; Membrane Transport Proteins; Retrospective Studies; Seizures | 2023 |
Case 38-2017. A 20-Year-Old Woman with Seizures and Progressive Dystonia.
Topics: Basal Ganglia Diseases; Biotin; Brain; Carbidopa; Diagnosis, Differential; Drug Combinations; Dystonia; Female; Humans; Levodopa; Macula Lutea; Magnetic Resonance Imaging; Membrane Transport Proteins; Metabolism, Inborn Errors; Mutation; Optic Nerve; Seizures; Thiamine; Young Adult | 2017 |
Biotin-responsive basal ganglia disease in ethnic Europeans with novel SLC19A3 mutations.
Topics: Adult; Basal Ganglia; Basal Ganglia Diseases; Biotin; Brain Diseases, Metabolic; DNA Mutational Analysis; Dystonia; Epilepsy; Europe; Female; Genetic Markers; Genetic Predisposition to Disease; Genotype; Humans; Magnetic Resonance Imaging; Male; Membrane Transport Proteins; Mutation; Portugal; Thiamine; Treatment Outcome; Vitamin B Complex; White People | 2010 |