Two definite cases of sudden unexpected death in epilepsy in a family with aDEPDC5mutation-Reference-Cited by-同舟云学术

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Two definite cases of sudden unexpected death in epilepsy in a family with aDEPDC5mutation

Published:2015-10-15 Issue:4 Volume:1 Page:e28
ISSN:2376-7839
Container-title:Neurology Genetics
language:en
Short-container-title:Neurol Genet

Author:

Nascimento Fábio A.,Borlot Felippe,Cossette Patrick,Minassian Berge A.,Andrade Danielle M.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Genetics (clinical),Neurology (clinical)

Reference8 articles.

1. Mutations in DEPDC5 cause familial focal epilepsy with variable foci

2. Mutations in mammalian target of rapamycin regulatorDEPDC5cause focal epilepsy with brain malformations

3. Familial focal epilepsy with focal cortical dysplasia due toDEPDC5mutations

4. Epileptic spasms are a feature ofDEPDC5mTORopathy

5. Long-Term Prognosis of Seizures with Onset in Childhood

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1. Ictal and Postictal Central Apnea in DEPDC5 -Related Epilepsy;Neurology Genetics;2024-10

2. DEPDC5 plays a vital role in epilepsy: Genotypic and phenotypic features in cohort and literature;Epileptic Disorders;2024-05-16

3. Cardiac arrhythmia and epilepsy genetic variants in sudden unexpected death in epilepsy;Frontiers in Neurology;2024-05-02

4. The Genetics of Tuberous Sclerosis Complex and Related mTORopathies: Current Understanding and Future Directions;Genes;2024-03-04

5. GATOR1 Mutations Impair PI3 Kinase-Dependent Growth Factor Signaling Regulation of mTORC1;International Journal of Molecular Sciences;2024-02-08

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