Page last updated: 2024-09-05

biotin and Dystonia

biotin has been researched along with Dystonia in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's2 (50.00)24.3611
2020's2 (50.00)2.80

Authors

AuthorsStudies
Alfadhel, M; Alnozha, A; Alsini, H; Asmat, Z; Hundallah, K; Tabarki, B1
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, M1
Cestari, DM; Eichler, FS; Hunt, AL; Rapalino, O; Swoboda, KJ1
Bellanger, A; Brice, A; Debs, R; Degos, B; Depienne, C; Galanaud, D; Keren, B; Lyon-Caen, O; Rastetter, A; Sedel, F1

Other Studies

4 other study(ies) available for biotin and Dystonia

ArticleYear
Beyond the caudate nucleus: Early atypical neuroimaging findings in biotin-thiamine- responsive basal ganglia disease.
    Brain & development, 2022, Volume: 44, Issue:9

    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.
    Orphanet journal of rare diseases, 2023, 09-05, Volume: 18, Issue:1

    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.
    The New England journal of medicine, 2017, Dec-14, Volume: 377, Issue:24

    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.
    Archives of neurology, 2010, Volume: 67, Issue:1

    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