biotin has been researched along with Ataxias, Hereditary in 1 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Kien, CL; Tsao, CY | 1 |
1 other study(ies) available for biotin and Ataxias, Hereditary
Article | Year |
---|---|
Complete biotinidase deficiency presenting as reversible progressive ataxia and sensorineural deafness.
Topics: Amidohydrolases; Biotin; Biotinidase; Brain; Deafness; Disease Progression; Female; Follow-Up Studies; Genetic Carrier Screening; Humans; Infant; Neurologic Examination; Spinocerebellar Degenerations; Tomography, X-Ray Computed | 2002 |