Levetiracetam-induced a new seizure type in a girl with a novel SV2A gene mutation-Reference-Cited by-同舟云学术

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Levetiracetam-induced a new seizure type in a girl with a novel SV2A gene mutation

Published:2019-06 Issue: Volume:181 Page:64-66
ISSN:0303-8467
Container-title:Clinical Neurology and Neurosurgery
language:en
Short-container-title:Clinical Neurology and Neurosurgery

Author:

Wang Di,Zhou Qilin,Ren Liankun,Lin Yicong,Gao Lehong,Du Jialin,Wang Yuping

Funder

National Natural Science Foundation of China

Beijing Municipal Education Commission

Publisher

Elsevier BV

Subject

Clinical Neurology,General Medicine,Surgery

Reference5 articles.

1. The synaptic vesicle protein SV2A is the binding site for the antiepileptic drug levetiracetam;Lynch;Proc. Natl. Acad. Sci. U. S. A.,2004

2. Homozygous mutation in synaptic vesicle glycoprotein 2A gene results in intractable epilepsy, involuntary movements, microcephaly, and developmental and growth retardation;Serajee;Pediatr. Neurol.,2015

3. SV2 modulates the size of the readily releasable pool of secretory vesicles;Xu;Nat. Cell Biol.,2001

4. Abnormal neurotransmission in mice lacking synaptic vesicle protein 2A (SV2A);Crowder;Proc. Natl. Acad. Sci. U. S. A.,1999

5. Proepileptic phenotype of SV2A-deficient mice is associated with reduced anticonvulsant efficacy of levetiracetam;Kaminski;Epilepsia,2009

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1. Structures of synaptic vesicle protein 2A and 2B bound to anticonvulsants;Nature Structural & Molecular Biology;2024-06-19

2. Structural basis for antiepileptic drugs and botulinum neurotoxin recognition of SV2A;Nature Communications;2024-04-18

3. Crystal structure of 1-(E)- [(5‑bromo-2-hydroxybenzylidene amino) pyrrolidin-2-one]: Design, synthesis and computational evaluation of a novel racetam congener for epilepsy;Journal of Molecular Structure;2024-03

4. Biallelic variants in the synaptic vesicle glycoprotein 2 A are associated with epileptic encephalopathy;European Journal of Human Genetics;2023-11-20

5. Genetic Factors of Reflex Epilepsies;Russian Journal of Genetics;2023-10

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