1. Clinical and genetic features in pyridoxine‐dependent epilepsy: a Chinese cohort study
    Xianru Jiao et al, 2020, Developmental Medicine & Child Neurology CrossRef
  2. Consensus guidelines for the diagnosis and management of pyridoxine‐dependent epilepsy due to α‐aminoadipic semialdehyde dehydrogenase deficiency
    Curtis R. Coughlin et al, 2021, Journal of Inherited Metabolic Disease CrossRef
  3. Epilepsy Phenotypes of Vitamin B6-Dependent Diseases: An Updated Systematic Review
    Mario Mastrangelo et al, 2023, Children CrossRef
  4. Brain malformations associated to Aldh7a1 gene mutations: Report of a novel homozygous mutation and literature review
    Irene Toldo et al, 2018, European Journal of Paediatric Neurology CrossRef
  5. Update on the treatment of vitamin B6 dependent epilepsies
    Mario Mastrangelo et al, 2019, Expert Review of Neurotherapeutics CrossRef
  6. PYRIDOXINE-dependent epilepsy (PDE): An observational study of neonatal cases on the role of pyridoxine in patients treated with standard anti-seizure medications
    Raffaele Falsaperla et al, 2024, Seizure: European Journal of Epilepsy CrossRef