Biotinidase deficiency: Initial clinical features and rapid diagnosis
Author:
Publisher
Wiley
Subject
Clinical Neurology,Neurology
Reference17 articles.
1. BIOTIN-RESPONSIVE ALOPECIA AND DEVELOPMENTAL REGRESSION
2. MULTIPLE BIOTIN-DEPENDENT CARBOXYLASE DEFICIENCIES ASSOCIATED WITH DEFECTS IN T-CELL AND B-CELL IMMUNITY
3. DEFICIENT LIVER BIOTINIDASE ACTIVITY IN MULTIPLE CARBOXYLASE DEFICIENCY
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1. Evaluation of clinical, laboratory, and molecular genetic features of patients with biotinidase deficiency;European Journal of Pediatrics;2023-12-23
2. Inborn Errors of Metabolism with Ataxia: Current and Future Treatment Options;Cells;2023-09-19
3. Tetraparesis as an initial manifestation of biotinidase deficiency: case report;Annals of Medicine & Surgery;2023-04-12
4. Neuroimaging Features of Biotinidase Deficiency;American Journal of Neuroradiology;2023-02-09
5. Overview on Pathophysiology, Diagnosis, and Management of Biotinidase Deficiency in Pediatrics;Archives of Pharmacy Practice;2023
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