Rosaline C. M. Quinlivan

Consensus on Exercise Reporting Template (CERT): Modified Delphi Study

Susan C. Slade, Clermont E. Dionne, Martin Underwood et al. · Physical Therapy · 2016 · 447 citations · Full text

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

Ataluren treatment of patients with nonsense mutation dystrophinopathy

K. Bushby, Richard S. Finkel, Brenda Wong et al. · Muscle & Nerve · 2014 · 416 citations · Full text

Changes in Spirometry Over Time as a Prognostic Marker in Patients with Duchenne Muscular Dystrophy

Margaret Phillips, Rosaline C. M. Quinlivan, R. H. T. Edwards et al. · American Journal of Respiratory and Critical Care Medicine · 2001 · 280 citations

<i>RYR1</i> mutations are a common cause of congenital myopathies with central nuclei

Jo M. Wilmshurst, Suzanne Lillis, Haiyan Zhou et al. · Annals of Neurology · 2010 · 261 citations · Full text