Hemiconvulsion-Hemiplegia-Epilepsy Syndrome Associated With CACNA1A S218L Mutation-Reference-Cited by-同舟云学术

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Hemiconvulsion-Hemiplegia-Epilepsy Syndrome Associated With CACNA1A S218L Mutation

Published:2011-09 Issue:3 Volume:45 Page:193-196
ISSN:0887-8994
Container-title:Pediatric Neurology
language:en
Short-container-title:Pediatric Neurology

Author:

Yamazaki Sawako,Ikeno Kanju,Abe Tokinari,Tohyama Jun,Adachi Yoshiki

Publisher

Elsevier BV

Subject

Neurology (clinical),Developmental Neuroscience,Neurology,Pediatrics, Perinatology and Child Health

Reference14 articles.

1. Hemiconvulsion-hemiplegia-epilepsy syndrome: Characteristic early magnetic resonance imaging findings;Freeman;J Child Neurol,2002

2. Long-term cognitive outcome of hemiconvulsion-hemiplegia-epilepsy syndrome affecting the left cerebral hemisphere;Mirsattari;Epilepsy Behav,2008

3. The international classification of headache disorders, 2nd edition;Cephalalgia,2004

4. Familial hemiplegic migraine;Pietrobon;Neurotherapeutics,2007

5. Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4;Ophoff;Cell,1996

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1. Familial hemiplegic migraine;Handbook of Clinical Neurology;2024

2. The genotype–phenotype correlations of the CACNA1A-related neurodevelopmental disorders: a small case series and literature reviews;Frontiers in Molecular Neuroscience;2023-07-24

3. A neurodevelopmental disorder caused by a dysfunctional CACNA1A allele;eNeurologicalSci;2023-06

4. Genetic and environmental risk factors of acute infection-triggered encephalopathy;Frontiers in Neuroscience;2023-01-24

5. CACNA1A-Related Channelopathies: Clinical Manifestations and Treatment Options;Voltage-gated Ca2+ Channels: Pharmacology, Modulation and their Role in Human Disease;2023

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