biotin has been researched along with Myoclonic Jerk in 3 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 2 (66.67) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 1 (33.33) | 2.80 |
Authors | Studies |
---|---|
Bennaoui, F; El Idrissi Slitine, N; El Moussaoui, S; Houcar, O; Maoulainine, FMR | 1 |
Bartlett, K; Low, LC; Seakins, JW; Shaikh, SA; Stephenson, JB | 1 |
Bressman, S; Brin, M; Eisenberg, M; Fahn, S; Maltese, W | 1 |
3 other study(ies) available for biotin and Myoclonic Jerk
Article | Year |
---|---|
Biotinidase deficiency in a newborn.
Topics: Age of Onset; Alopecia; Biotin; Biotinidase Deficiency; Consanguinity; Dermatitis, Exfoliative; Eyebrows; Fatal Outcome; Health Services Accessibility; Humans; Ichthyosis; Infant, Newborn; Intensive Care Units, Neonatal; Male; Morocco; Muscle Hypotonia; Myoclonus; Rare Diseases; Vitamin B Complex | 2020 |
Biotin-reversible neurodegenerative disease in infancy.
Topics: Acidosis; Biotin; Carbon-Carbon Ligases; Carboxy-Lyases; Failure to Thrive; Female; Humans; Infant; Ligases; Methylmalonyl-CoA Decarboxylase; Muscular Diseases; Myoclonus; Pyruvate Carboxylase Deficiency Disease | 1986 |
Biotin-responsive encephalopathy with myoclonus, ataxia, and seizures.
Topics: Adult; Amidohydrolases; Ataxia; Biotin; Biotinidase; Brain Diseases, Metabolic; Electroencephalography; Electromyography; Female; Hearing Loss; Humans; Myoclonus; Pyruvate Carboxylase; Seizures | 1986 |