Hepatic coma culminating in severe brain damage in a child with a SCN1A mutation-Reference-Cited by-同舟云学术

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Hepatic coma culminating in severe brain damage in a child with a SCN1A mutation

Published:2010-09 Issue:5 Volume:14 Page:456-459
ISSN:1090-3798
Container-title:European Journal of Paediatric Neurology
language:en
Short-container-title:European Journal of Paediatric Neurology

Author:

Nishri Daniella,Blumkin Lubov,Lev Dorit,Leshinsky-Silver Esther,Abu-Rashid Mohammad,Birch Rachael,Zuberi Sameer M.,Lerman-Sagie Tally

Publisher

Elsevier BV

Subject

Neurology (clinical),General Medicine,Pediatrics, Perinatology and Child Health

Reference13 articles.

1. Severe myoclonic epilepsy in infancy (Dravet syndrome);Dravet,2002

2. Catalog of SCN1A variants;Lossin;Brain Dev,2009

3. The spectrum of SCN1A-related infantile epileptic encephalopathies;Harkin;Brain,2007

4. POLG mutations associated with Alpers’ syndrome and mitochondrial DNA depletion;Naviaux;Ann Neurol,2004

5. Spectrum of SCN1A gene mutations associated with Dravet syndrome: analysis of 333 patients;Depienne;J Med Genet,2009

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1. Epilepsy-Related Voltage-Gated Sodium Channelopathies: A Review;Frontiers in Pharmacology;2020-08-18

2. Mining for mitochondrial mechanisms: Linking known syndromes to mitochondrial function;Clinical Genetics;2017-12-11

3. Fatal Cerebral Edema With Status Epilepticus in Children With Dravet Syndrome: Report of 5 Cases;Pediatrics;2017-04-01

4. Síndrome de Dravet y enfermedad mitocondrial, ¿patologías comórbidas?;Revista de Neurología;2014

5. Dravet syndrome: New potential genetic modifiers, imaging abnormalities, and ictal findings;Epilepsia;2013-06-28

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