An update on Alpers-Huttenlocher syndrome: pathophysiology of disease and rational treatment designs
Author:
Affiliation:
1. Department of Neurology, Division of Pediatric Neurology, University of Washington and Seattle Children’s Hospital, Seattle, WA, USA
2. Neuroscience Institute, Center for Integrative Brain Research, Seattle Children’s Hospital, Seattle, WA, USA
Publisher
Informa UK Limited
Subject
Pharmacology (medical),Health Policy,Pharmacology, Toxicology and Pharmaceutics (miscellaneous)
Link
https://www.tandfonline.com/doi/pdf/10.1080/21678707.2018.1540979
Reference82 articles.
1. Review Article: Progressive Neuronal Degeneration of Childhood With Liver Disease (Alpers-Huttenlocher Syndrome): A Personal Review
2. Alpers-Huttenlocher Syndrome
3. Epilepsy due to mutations in the mitochondrial polymerase gamma (POLG) gene: A clinical and molecular genetic review
4. Status epilepticus in children with Alpers’ disease caused byPOLG1mutations: EEG and MRI features
5. POLG DNA testing as an emerging standard of care before instituting valproic acid therapy for pediatric seizure disorders
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