Neurodevelopmental, emotional, and behavioural problems in Duchenne muscular dystrophy in relation to underlying dystrophin gene mutations-Reference-Cited by-同舟云学术

Neurodevelopmental, emotional, and behavioural problems in Duchenne muscular dystrophy in relation to underlying dystrophin gene mutations

Published:2015-09-14 Issue:1 Volume:58 Page:77-84
ISSN:0012-1622
Container-title:Developmental Medicine & Child Neurology
language:en
Short-container-title:Dev Med Child Neurol

Author:

Ricotti Valeria¹,Mandy William P L²,Scoto Mariacristina¹,Pane Marika³,Deconinck Nicolas⁴⁵,Messina Sonia⁶,Mercuri Eugenio¹³,Skuse David H²,Muntoni Francesco¹

Affiliation:

1. Dubowitz Neuromuscular Centre; UCL Institute of Child Health; London UK

2. Behavioural and Brain Sciences Unit; UCL Institute of Child Health; London UK

3. Department of Paediatric Neurology; Catholic University; Rome Italy

4. Department of Paediatric Neurology; NMRC; Universitair Ziekenhuis Gent; Gent Belgium

5. Paediatric Neurology Department; Hôpital Universitaire des Enfants Reine Fabiola; Universite Libre de Bruxelles; Brussels Belgium

6. Department of Neurosciences and Nemo Sud Clinical Centre; University of Messina; Messina Italy

Funder

Great Ormond Street Hospital for Children

GOSH Biomedical Research centre

Muscular Dystrophy Campaign Centre Grant

Association Française contre les Myopathies

AVI

Parametric Technology Corporation

Italian Telethon

SMA Europe

Publisher

Wiley

Subject

Clinical Neurology,Developmental Neuroscience,Pediatrics, Perinatology, and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/dmcn.12922/fullpdf

Reference38 articles.

1. Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management;Bushby;Lancet Neurol,2010

2. Early neurodevelopmental assessment in Duchenne muscular dystrophy;Pane;Neuromuscul Disord,2013

3. Dystrophin and mutations: one gene, several proteins, multiple phenotypes;Muntoni;Lancet Neurol,2003

4. Loss of Dp140 dystrophin isoform and intellectual impairment in Duchenne dystrophy;Felisari;Neurology,2000

5. Analysis of Dp71 contribution in the severity of mental retardation through comparison of Duchenne and Becker patients differing by mutation consequences on Dp71 expression;Daoud;Hum Mol Genet,2009

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