Adnan Y. Manzur

<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 · 266 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

Long-term benefits and adverse effects of intermittent versus daily glucocorticoids in boys with Duchenne muscular dystrophy

Valeria Ricotti, Deborah Ridout, E. Scott et al. · Journal of Neurology Neurosurgery & Psychiatry · 2012 · 260 citations

Medicine, Endocrinology, Musculoskeletal Rehabilitation +13

Mutations in RYR1 are a common cause of exertional myalgia and rhabdomyolysis

Nomazulu Dlamini, Nicol C. Voermans, S. Lillis et al. · Neuromuscular Disorders · 2013 · 199 citations

Medicine, Genetics, Molecular Genetics +5

Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2

A. Reghan Foley, Manoj P. Menezes, Amelie Pandraud et al. · Brain · 2013 · 182 citations · Full text

Life Sciences, Genetics, Neurology +15

Clinical and genetic findings in a large cohort of patients with ryanodine receptor 1 gene-associated myopathies

Andrea Klein, Suzanne Lillis, Iulia Munteanu et al. · Human Mutation · 2012 · 168 citations

Life Sciences, Molecular Biology, Molecular Genetics +16