Biotinidase deficiency in differential diagnosis of neuromyelitis optica spectrum disorder
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Neurology,General Medicine
Reference23 articles.
1. Neuromyelitis optica spectrum disorders;Akaishi;Neuroimaging Clin. N. Am.,2017
2. Incidence of biotinidase deficiency in Turkish newborns;Baykal;Acta Paediatr.,1998
3. Diagnosis and Treatment of NMO Spectrum Disorder and MOG-Encephalomyelitis;Borisow;Frontiers in Neurology,2018
4. Biotinidase deficiency mimicking neuromyelitis optica: Initially exhibiting symptoms in adulthood;Bottin;Mult. Scler. J.,2015
5. Biotinidase deficiency mimicking neuromyelitis optica: Initially exhibiting symptoms in adulthood;Bottin;Mult. Sclerosis J.,2017
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1. Atypical presentation of biotinidase deficiency: masquerading neuromyelitis optica spectrum disorder;BMJ Case Reports;2024-07
2. Biotin Homeostasis and Human Disorders: Recent Findings and Perspectives;International Journal of Molecular Sciences;2024-06-14
3. Démarche diagnostique devant une leucodystrophie métabolique de l’adulte;Pratique Neurologique - FMC;2024-03
4. Ophthalmic manifestations of biotinidase deficiency: report of a case and review of literature;Ophthalmic Genetics;2024-01-17
5. Biotinidase deficiency: What have we learned in forty years?;Molecular Genetics and Metabolism;2023-04
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