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Neuropediatrics|April 4, 2002
Selective muscle involvement on magnetic resonance imaging in autosomal dominant Emery-Dreifuss muscular dystrophyE Mercuri, S Counsell, J Allsop, et al.Lancet (London, England)|May 13, 1989
Cyclosporin in juvenile dermatomyositisJ Heckmatt, N Hasson, C Saunders, et al.American Journal of Human Genetics|March 21, 2000
Assignment of a form of congenital muscular dystrophy with secondary merosin deficiency to chromosome 1q42M Brockington, C A Sewry, R Herrmann, et al.Journal of Medical Genetics|September 1, 1995
The myotubular myopathies: differential diagnosis of the X linked recessive, autosomal dominant, and autosomal recessive forms and present state of DNA studiesC Wallgren-Pettersson, A Clarke, F Samson, et al.Lancet (London, England)|March 2, 1996
Diagnosis of merosin (laminin-2) deficient congenital muscular dystrophy by skin biopsyC A Sewry, J Philpot, L M Sorokin, et al.Neuropediatrics|August 1, 1997
Expression of laminin chains in skin in merosin-deficient congenital muscular dystrophyC A Sewry, M D'Alessandro, L A Wilson, et al.Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|December 1, 1995
Readjusting the localization of merosin (laminin alpha 2-chain) deficient congenital muscular dystrophy locus on chromosome 6q2A Helbling-Leclerc, H Topaloglu, F M Tomé, et al.Neuromuscular Disorders : NMD|March 1, 1993
Manifesting carriers of Xp21 muscular dystrophy; lack of correlation between dystrophin expression and clinical weaknessC A Sewry, A Sansome, A Clerk, et al.Developmental Medicine and Child Neurology|December 1, 1991
A new system for cotside display and analysis of the preterm neonatal electroencephalogramD F Wertheim, D G Murdoch Eaton, R C Oozeer, et al.Neuromuscular Disorders : NMD|June 3, 1998
Early presentation of X-linked Emery-Dreifuss muscular dystrophy resembling limb-girdle muscular dystrophyF Muntoni, E J Lichtarowicz-Krynska, C A Sewry, et al.Pageof 24