biotin has been researched along with Developmental Disabilities in 6 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (16.67) | 18.2507 |
| 2000's | 3 (50.00) | 29.6817 |
| 2010's | 2 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Chen, J; Chen, SZ; Fan, CH; Li, R; Liu, XM; Sang, Y | 1 |
| Kluijtmans, LAJ; Koene, S; Mock, D; Morava, E; Pasch, M; Wevers, R | 1 |
| El-Hajj, TI; Karam, PE; Mikati, MA | 1 |
| Buyukkayhan, D; Sancaktar, M; Tanzer, F | 1 |
| Ogundele, MO | 1 |
| Baumgartner, ER; Lehnert, W; Niederhoff, H; Suormala, T | 1 |
2 review(s) available for biotin and Developmental Disabilities
| Article | Year |
|---|---|
Biotin-responsive basal ganglia disease: case report and review of the literature.
Topics: Basal Ganglia Diseases; Biotin; Child, Preschool; Developmental Disabilities; Diagnosis, Differential; Dominance, Cerebral; Dose-Response Relationship, Drug; Electroencephalography; Female; Globus Pallidus; Humans; Magnetic Resonance Imaging; Neurologic Examination | 2008 |
Question 2. What is the incidence of biotin deficiency in preschool children with global developmental delay?
Topics: Biotin; Biotinidase Deficiency; Child, Preschool; Developmental Disabilities; Evidence-Based Medicine; Female; Humans; Incidence; Vitamin B Deficiency | 2011 |
4 other study(ies) available for biotin and Developmental Disabilities
| Article | Year |
|---|---|
Screening of Inherited Metabolic Disorders in Infants with Infantile Spasms.
Topics: Amino Acid Metabolism, Inborn Errors; Anticonvulsants; Biotin; Brain; Brain Diseases, Metabolic; Chromatography, Gas; Developmental Disabilities; Epilepsy; Female; Glutaryl-CoA Dehydrogenase; Humans; Infant; Liver; Liver Function Tests; Magnetic Resonance Imaging; Male; Mass Screening; Mass Spectrometry; Metabolic Diseases; Phenylketonurias; Spasms, Infantile; Succinate-Semialdehyde Dehydrogenase; Tomography, X-Ray Computed | 2015 |
Biotin-sensitive 3-methylcrotonylglycinuria in a patient with severe growth delay, ectodermal abnormalities, neonatal progeroid appearance, and developmental delay.
Topics: Abnormalities, Multiple; Aging, Premature; Biotin; Child, Preschool; Developmental Disabilities; Ectoderm; Female; Glycine; Growth Disorders; Humans; Metabolism, Inborn Errors | 2008 |
Neonatal screening for biotidinidase deficiency: results of a 1-year pilot study in four cities in central Anatolia.
Topics: Administration, Oral; Biotin; Biotinidase Deficiency; Colorimetry; Developmental Disabilities; Female; Humans; Incidence; Infant, Newborn; Male; Neonatal Screening; Pilot Projects; Turkey; Urban Population; Vitamin B Complex | 2009 |
Isolated biotin-resistant 3-methylcrotonyl-CoA carboxylase deficiency: long-term outcome in a case with neonatal onset.
Topics: Age of Onset; Biotin; Carbon-Carbon Ligases; Developmental Disabilities; Diet, Protein-Restricted; Epilepsy, Generalized; Humans; Infant, Newborn; Ligases; Male; Metabolism, Inborn Errors; Patient Compliance; Valerates | 1996 |