C. Sewry

Refining genotype phenotype correlations in muscular dystrophies with defective glycosylation of dystroglycan

C. Godfrey, Emma Clement, R. Mein et al. · Brain · 2007 · 433 citations · Full text

Molecular mechanisms and phenotypic variation in RYR1-related congenital myopathies

Haiyan Zhou, Heinz Jungbluth, C. Sewry et al. · Brain · 2007 · 173 citations · Full text

Mendelian Disorder, Ryr1-related Congenital Myopathies, Skeletal Muscle +11

Collagen VI involvement in Ullrich syndrome

Eugenio Mercuri, Yeliz Yuva, S. Brown et al. · Neurology · 2002 · 102 citations

Muscle magnetic resonance imaging in patients with congenital muscular dystrophy and Ullrich phenotype

Eugenio Mercuri, C. Cini, Anna Pichiecchio et al. · Neuromuscular Disorders · 2003 · 86 citations

Imaging Anatomy, Health Sciences, Medical Imaging +6

Myopathy with unique ultrastructural feature in marchinesco‐sjögren syndrome

C. Sewry, T. Voit, Victor Dubowitz · Annals of Neurology · 1988 · 72 citations

Pathology, Unique Ultrastructural Feature, Anatomy +16