Generalized Epilepsy and Myoclonic Seizures in 22q11.2 Deletion Syndrome-Reference-Cited by-同舟云学术

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Generalized Epilepsy and Myoclonic Seizures in 22q11.2 Deletion Syndrome

Published:2016 Issue:4 Volume:7 Page:239-246
ISSN:1661-8769
Container-title:Molecular Syndromology
language:en
Short-container-title:Mol Syndromol

Author:

Strehlow Vincent,Swinkels Marielle E.M.,Thomas Rhys H.,Rapps Nora,Syrbe Steffen,Dorn Thomas,Lemke Johannes R.

Publisher

S. Karger AG

Subject

Genetics (clinical),Genetics

Cited by 19 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Recurrent Seizures in a Patient with Primary Hypoparathyroidism;Journal of the Korean Neurological Association;2024-08-01

2. Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals;Nature Communications;2023-07-20

3. The CLDN5 gene at the blood-brain barrier in health and disease;Fluids and Barriers of the CNS;2023-03-28

4. Df(h22q11)/+ mouse model exhibits reduced binding levels of GABAA receptors and structural and functional dysregulation in the inhibitory and excitatory networks of hippocampus;Molecular and Cellular Neuroscience;2022-09

5. Overlap Between Epilepsy and Neurodevelopmental Disorders: Insights from Clinical and Genetic Studies;Epilepsy;2022-04-04

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