Chromosomal microarray in unexplained severe early onset epilepsy – A single centre cohort-Reference-Cited by-同舟云学术

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Chromosomal microarray in unexplained severe early onset epilepsy – A single centre cohort

Published:2015-07 Issue:4 Volume:19 Page:390-394
ISSN:1090-3798
Container-title:European Journal of Paediatric Neurology
language:en
Short-container-title:European Journal of Paediatric Neurology

Author:

Allen Nicholas M.,Conroy Judith,Shahwan Amre,Ennis Sean,Lynch Bryan,Lynch Sally A.,King Mary D.

Publisher

Elsevier BV

Subject

Clinical Neurology,General Medicine,Pediatrics, Perinatology, and Child Health

Reference17 articles.

1. Revised terminology and concepts for organization of seizures and epilepsies: report of the ILAE commission on classification and terminology, 2005–2009;Berg;Epilepsia,2010

2. A population-based study of newly diagnosed epilepsy in infants;Eltze;Epilepsia,2013

3. Deletions involving both KCNQ2 and CHRNA4 present with benign familial neonatal seizures;Kurahashi;Neurology,2009

4. The variable phenotypes of KCNQ-related epilepsy;Allen;Epilepsia,2014

5. Identification of single gene deletions at 15q13.3: further evidence that CHRNA7 causes the 15q13.3 microdeletion syndrome phenotype;Hoppman-Chaney;Clin Genet,2013

Cited by 14 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. Copy Number Variation and Epilepsy: State of the Art in the Era of High-Throughput Sequencing—A Multicenter Cohort Study;Pediatric Neurology;2024-10

2. Exome sequencing as first-tier genetic testing in infantile-onset pharmacoresistant epilepsy: diagnostic yield and treatment impact;European Journal of Human Genetics;2022-10-05

3. Chromosomal microarray and exome sequencing in unexplained early infantile epileptic encephalopathies in a highly consanguineous population;International Journal of Neuroscience;2021-08-23

4. Diagnostic Considerations in the Epilepsies—Testing Strategies, Test Type Advantages, and Limitations;Neurotherapeutics;2021-07

5. Genetic Factors Underlying Sudden Infant Death Syndrome;The Application of Clinical Genetics;2021-02

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