Epilepsy in 22q11.2 Deletion Syndrome: A Case Series and Literature Review-Reference-Cited by-同舟云学术

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Epilepsy in 22q11.2 Deletion Syndrome: A Case Series and Literature Review

Published:2017-11 Issue: Volume:76 Page:86-90
ISSN:0887-8994
Container-title:Pediatric Neurology
language:en
Short-container-title:Pediatric Neurology

Author:

Mudigoudar Basanagoud,Nune Sunitha,Fulton Stephen,Dayyat Ehab,Wheless James W.

Funder

Neuroscience Institute, Le Bonheur Children's Hospital

Publisher

Elsevier BV

Subject

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

Reference24 articles.

1. A population study of chromosome 22q11 deletions in infancy;Goodship;Arch Dis Child,1998

2. Velocardiofacial syndrome, DiGeorge syndrome: the chromosome 22q11.2 deletion syndromes;Kobrynski;Lancet,2007

3. Molecular definition of 22q11 deletions in 151 velo-cardio-facial syndrome patients;Carlson;Am J Hum Genet,1997

4. Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis;Shaikh;Hum Mol Genet,2000

5. Polymicrogyria and deletion 22q11.2 syndrome: window to the etiology of a common cortical malformation;Robin;Am J Med Genet A,2006

Cited by 12 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. Successful Hemispherotomy in a Patient With 22q11.2 Deletion Syndrome Who Had Developmental and Epileptic Encephalopathy With Spike-and-Wave Activation During Sleep;Cureus;2024-04-16

2. Short Report: Clinical Features and Epilepsy Monitoring in an Adult With 22q11.2 Deletion Syndrome;The Neurohospitalist;2024-01-17

3. Severe Hypocalcemia in the Adolescent as the Only Manifestation of <i>22q11</i> Microdeletion Syndrome: Clinical Case;Current Pediatrics;2023-07-08

4. Chromosome 22q11.2 Deletion Syndrome: A Comprehensive Review of Molecular Genetics in the Context of Multidisciplinary Clinical Approach;International Journal of Molecular Sciences;2023-05-05

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

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