Page last updated: 2024-09-05
biotin and Xeroderma
biotin has been researched along with Xeroderma in 3 studies
Research
Studies (3)
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 2 (66.67) | 2.80 |
Authors
| Authors | Studies |
|---|---|
| Bennaoui, F; El Idrissi Slitine, N; El Moussaoui, S; Houcar, O; Maoulainine, FMR | 1 |
| Cadieux-Dion, M; Gannon, J; Heese, B; Jenkins, J; Newell, B; Nopper, AJ; Saunders, C | 1 |
| Anand, A; Chatterjee, A; Hiremagalore, R; Mani, RS; Pandey, N; Rajashekhar, B; Tharakan, A; Xavier, DF | 1 |
Other Studies
3 other study(ies) available for biotin and Xeroderma
| 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 |
Delayed diagnosis of holocarboxylase synthetase deficiency in three patients with prominent skin findings.
Topics: Biotin; Delayed Diagnosis; Holocarboxylase Synthetase Deficiency; Humans; Ichthyosis; Seizures | 2021 |
Functional Analysis of a Novel Connexin30 Mutation in a Large Family with Hearing Loss, Pesplanus, Ichthyosis, Cutaneous Nodules, and Keratoderma.
Topics: Biotin; Connexin 30; Connexins; DNA Mutational Analysis; Female; Genetic Linkage; Hearing Loss, Sensorineural; Humans; Ichthyosis; Keratoderma, Palmoplantar, Diffuse; Male; Pedigree; Phenotype; Skin Diseases, Genetic | 2016 |