Prospective longitudinal overnight video-EEG evaluation in Phelan–McDermid Syndrome-Reference-Cited by-同舟云学术

Prospective longitudinal overnight video-EEG evaluation in Phelan–McDermid Syndrome

Published:2018-03 Issue: Volume:80 Page:312-320
ISSN:1525-5050
Container-title:Epilepsy & Behavior
language:en
Short-container-title:Epilepsy & Behavior

Author:

Khan Omar I.,Zhou Xiangping,Leon Jill,Kessler Riley,Gaughan Thomas,D'Souza Precilla,Gropman Andrea,Cohen Ninette,Rennert Owen,Buckley Ashura,Inati Sara,Thurm Audrey

Funder

National Institute of Mental Health

NCATS

National Institute of Neurological Disorders and Stroke

Publisher

Elsevier BV

Subject

Behavioral Neuroscience,Neurology (clinical),Neurology

Reference45 articles.

1. The 22q13.3 deletion syndrome (Phelan-McDermid syndrome);Phelan;Mol Syndromol,2012

2. Seizures and EEG pattern in the 22q13.3 deletion syndrome: clinical report of six Italian cases;Figura;Seizure,2014

3. SHANK3 overexpression causes manic-like behaviour with unique pharmacogenetic properties;Han;Nature,2013

4. Epileptic encephalopathies of the Landau-Kleffner and continuous spike and waves during slow-wave sleep types: genomic dissection makes the link with autism;Lesca;Epilepsia,2012

5. 22q13 deletion syndrome;Phelan;Am J Med Genet,2001

Cited by 13 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. A roadmap for SHANK3-related Epilepsy Research: recommendations from the 2023 strategic planning workshop;Therapeutic Advances in Rare Disease;2024-01

2. Late onset and regional heterogeneity of synaptic deficits in cortical PV interneurons ofShank3B^−/−mice;2023-11-23

3. Neurophysiological markers that links genes and behavior in humans: examples from rare genetic syndromes associated with autism spectrum disorders;Genes & Cells;2023-10-19

4. Updated consensus guidelines on the management of Phelan–McDermid syndrome;American Journal of Medical Genetics Part A;2023-07

5. Consensus recommendations on Epilepsy in Phelan-McDermid syndrome;European Journal of Medical Genetics;2023-06