Clinical Diagnosis, Treatment, and ALDH7A1 Mutations in Pyridoxine-Dependent Epilepsy in Three Chinese Infants
Author:
Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
Reference33 articles.
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1. A rare case of pyridoxine-dependent epilepsy with novel ALDH7A1 mutation;Asian Journal of Surgery;2024-09
2. PYRIDOXINE-dependent epilepsy (PDE): An observational study of neonatal cases on the role of pyridoxine in patients treated with standard anti-seizure medications;Seizure: European Journal of Epilepsy;2024-05
3. Genotype and phenotype features and prognostic factors of neonatal-onset pyridoxine-dependent epilepsy: A systematic review;Epilepsy Research;2024-05
4. Molecular analysis and prenatal diagnosis of seven Chinese families with genetic epilepsy;Frontiers in Neuroscience;2023-05-12
5. A case of pyridoxine-dependent epilepsy with novel ALDH7A1 mutation;2023-04-12
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