Towards the identification of a genetic basis for Landau-Kleffner syndrome-Reference-Cited by-同舟云学术

Towards the identification of a genetic basis for Landau-Kleffner syndrome

Published:2014-05-14 Issue:6 Volume:55 Page:858-865
ISSN:0013-9580
Container-title:Epilepsia
language:en
Short-container-title:Epilepsia

Author:

Conroy Judith¹²,McGettigan Paul A.²³,McCreary Dara⁴,Shah Naisha⁵,Collins Kevin⁶,Parry-Fielder Bronwyn⁶,Moran Margaret⁴⁶,Hanrahan Donncha⁷,Deonna Thierry W.⁸,Korff Christian M.⁹,Webb David¹⁰,Ennis Sean²¹¹,Lynch Sally A.¹²¹¹,King Mary D.²⁴

Affiliation:

1. Department of Genetics; Children's University Hospital; Dublin Ireland

2. Academic Centre on Rare Diseases; School of Medicine and Medical Science; University College Dublin; Dublin Ireland

3. School of Agriculture and Food Science; University College Dublin; Dublin Ireland

4. Department of Neurology; Children's University Hospital; Dublin Ireland

5. School of Medicine and Medical Science; University College Dublin; Dublin Ireland

6. Royal Children's Hospital; Melbourne VIC Australia

7. Royal Belfast Hospital for Sick Children; Belfast United Kingdom

8. University Hospital of Lausanne; Lausanne Switzerland

9. University Hospitals; Geneva Switzerland

10. Department of Neurology; Our Lady's Children's Hospital Crumlin; Dublin Ireland

11. The National Centre for Medical Genetics; Our Lady's Children's Hospital Crumlin; Dublin Ireland

Funder

Childrens Fund for Health, Childrens University Hospital, Temple Street

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/epi.12645/fullpdf

Reference40 articles.

1. Acquired auditory agnosia in childhood and normal sleep electroencephalography subsequently diagnosed as Landau-Kleffner Syndrome: a report of three cases;Bogaert;Dev Med Child Neurol,2013

2. Deletions in 16p13 including GRIN2A in patients with intellectual disability, various dysmorphic features, and seizure disorders of the rolandic region;Reutlinger;Epilepsia,2010

3. 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

4. A subset of genomic alterations in rolandic epilepsies containing candidate or known epilepsy genes including GRIN2A and PRRT2;Dimassi;Epilepsia,2014

5. GRIN2A mutations cause epilepsy-aphasia spectrum disorders;Carvill;Nat Genet,2013

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