biotin has been researched along with Hypermyotonia in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (33.33) | 18.2507 |
| 2000's | 2 (66.67) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Rathi, M; Rathi, N | 1 |
| Ficicioglu, C; Hoffman, TL; Simon, EM | 1 |
| Berry, SA; Nyhan, WL; Thuy, LP; Tuchman, M | 1 |
3 other study(ies) available for biotin and Hypermyotonia
| Article | Year |
|---|---|
Biotinidase deficiency with hypertonia as unusual feature.
Topics: Biotin; Biotinidase Deficiency; Humans; Infant; Male; Muscle Hypertonia; Vitamin B Complex | 2009 |
Biotinidase deficiency: the importance of adequate follow-up for an inconclusive newborn screening result.
Topics: Acidosis, Lactic; Ataxia; Biotin; Biotinidase Deficiency; Brain; Continuity of Patient Care; Hearing Loss, Bilateral; Hearing Loss, Sensorineural; Humans; Infant; Infant, Newborn; Magnetic Resonance Imaging; Male; Muscle Hypertonia; Neonatal Screening; Pakistan; Pennsylvania; Respiratory Sounds; Speech Disorders | 2005 |
Partial methylcrotonyl-coenzyme A carboxylase deficiency in an infant with failure to thrive, gastrointestinal dysfunction, and hypertonia.
Topics: Biotin; Carbon-Carbon Ligases; Failure to Thrive; Gastrointestinal Diseases; Glycine; Humans; Infant; Ligases; Male; Metabolism, Inborn Errors; Muscle Hypertonia; Valerates | 1993 |