Dravet Syndrome and Mitochondrial Dysfunction
Author:
Affiliation:
1. Servicio de Neuropediatría, Hospital Clínico Universitario, Facultad de Medicina, Universidad de Santiago de Compostela Santiago de Compostela, Spain
Publisher
SAGE Publications
Subject
Clinical Neurology,Pediatrics, Perinatology, and Child Health
Link
http://journals.sagepub.com/doi/pdf/10.1177/0883073811420718
Reference9 articles.
1. Leber’s Hereditary Optic Neuropathy Mutations Associated With Infantile-Onset Myoclonic Epilepsy
2. Severe myoclonic epilepsy associated with mitochondrial cytopathy
3. Severe myoclonic epilepsy and mitochondrial cytopathy
4. Clinical heterogeneity associated with mitochondrial DNA depletion in muscle
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1. Mitochondrial respiratory chain defects in skin fibroblasts from patients with Dravet syndrome;Neurological Sciences;2015-07-14
2. Síndrome de Dravet y enfermedad mitocondrial, ¿patologías comórbidas?;Revista de Neurología;2015
3. Síndrome de Dravet y enfermedad mitocondrial, ¿patologías comórbidas?;Revista de Neurología;2014
4. Mitochondrial Dysfunction and Myoclonic Epilepsy;Journal of Child Neurology;2011-10
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