Page last updated: 2024-09-05

biotin and Orphan Diseases

biotin has been researched along with Orphan Diseases in 2 studies

Research

Studies (2)

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	0 (0.00)	24.3611
2020's	2 (100.00)	2.80

Authors

Authors	Studies
Jiang, YL; Li, KY; Tang, JP; Wei, Z; Wen, R; Yue, SZ; Zhou, B; Zhou, ZT	1
Bennaoui, F; El Idrissi Slitine, N; El Moussaoui, S; Houcar, O; Maoulainine, FMR	1

Other Studies

2 other study(ies) available for biotin and Orphan Diseases

Article	Year
[Holocarboxylase synthetase deficiency induced by Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics, 2023, Apr-15, Volume: 25, Issue:4 Topics: Biotin; Holocarboxylase Synthetase Deficiency; Homozygote; Humans; Infant; Male; Mutation; Rare Diseases	2023
Biotinidase deficiency in a newborn. Journal of neonatal-perinatal medicine, 2020, Volume: 13, Issue:1 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

Article

Year

[Holocarboxylase synthetase deficiency induced by

Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics, 2023, Apr-15, Volume: 25, Issue:4

Topics: Biotin; Holocarboxylase Synthetase Deficiency; Homozygote; Humans; Infant; Male; Mutation; Rare Diseases

2023

Biotinidase deficiency in a newborn.

Journal of neonatal-perinatal medicine, 2020, Volume: 13, Issue:1

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