Cognitive abilities in children with congenital muscular dystrophy: correlation with brain MRI and merosin status

Author:

Mercuri Eugenio,Gruter-Andrew Jackie,Philpot Jo,Sewry Caroline,Counsell Serena,Henderson Sheila,Jensen Alan,Naom Isam,Bydder Graeme,Dubowitz Victor,Muntoni Francesco

Publisher

Elsevier BV

Subject

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

Reference22 articles.

1. Workshop report on 22nd ENMC-sponsored meeting on congenital muscular dystrophy held in Baarn, The Netherlands, May 14–16;Dubowitz;Neuromusc Disord,1993

2. Workshop report on 27th ENMC-sponsored meeting on congenital muscular dystrophy held in Baarn, The Netherlands, April 22–24;Dubowitz;Neuromusc Disord,1994

3. Clinical phenotype in congenital muscular dystrophy: correlation with expression of merosin in skeletal muscle;Philpot;Neuromusc Disord,1995

4. Van der Knaap MS, Valk J, Congenital muscular dystrophy. In Magnetic resonance of myelin, myelination and myelin disorders.2.nd edition Springer, New York, 1995: pp 267-276.

5. Deficiency of merosin (laminin M or 2) in congenital muscular dystrophy associated with cerebral white matter alterations;Vainzof;Neuropediatrics,1995

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