Skeletal muscle mitochondrial dysfunction in alternating hemiplegia of childhood
Author:
Publisher
Wiley
Subject
Clinical Neurology,Neurology
Reference25 articles.
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1. Molecular genetic and mitochondrial metabolic analyses confirm the suspected mitochondrial etiology in a pediatric patient with an atypical form of alternating hemiplegia of childhood;Molecular Genetics and Metabolism Reports;2020-09
2. The Expanding Spectrum of Neurological Phenotypes in Children With ATP1A3 Mutations, Alternating Hemiplegia of Childhood, Rapid-onset Dystonia-Parkinsonism, CAPOS and Beyond;Pediatric Neurology;2015-01
3. Alternating hemiplegia of childhood;Pediatric Neurology Part II;2013
4. Hemiplejía alternante de la infancia. Primer caso clínico descrito en El Salvador;Revista de Neurología;2013
5. Alternating hemiplegia of childhood: Metabolic studies in the largest European series of patients;European Journal of Paediatric Neurology;2012-01
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