191st ENMC International Workshop: Recent advances in oculopharyngeal muscular dystrophy research: From bench to bedside 8-10 June 2012, Naarden, The Netherlands-Reference-Cited by-同舟云学术

191st ENMC International Workshop: Recent advances in oculopharyngeal muscular dystrophy research: From bench to bedside 8-10 June 2012, Naarden, The Netherlands

Published:2013-06 Issue:6 Volume:23 Page:516-523
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Raz Vered,Butler-Browne Gillian,van Engelen Baziel,Brais Bernard

Funder

Muskelsvindfonden (Denmark)

Association Française contre les Myopathies (France)

Deutsche Gesellschaft für Muskelkranke (Germany)

Telethon Foundation (Italy)

Schweizerische Stiftung für die Erforschung der Muskelkrankheiten (Switzerland)

Prinses Beatrix Spierfonds (The Netherlands)

Spierziekten Nederland (The Netherlands)

Muscular Dystrophy Campaign (UK)

Finnish Neuromuscular Association (Finland)

Dutch ZonMw

Publisher

Elsevier BV

Subject

Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health

Reference32 articles.

1. The other trinucleotide repeat: polyalanine expansion disorders;Albrecht;Curr Opin Genet Dev,2005

2. Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy;Brais;Nat Genet,1998

3. Cognitive impairment and reduced life span of oculopharyngeal muscular dystrophy homozygotes;Blumen;Neurology,2009

4. Executive functions are impaired in heterozygote patients with oculopharyngeal muscular dystrophy;Dubbioso;J Neurol,2012

5. Oculopharyngeal muscular dystrophy associated with dementia;Mizoi;Int Med,2011

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