Susan Treves

<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

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

Nomazulu Dlamini, Nicol C. Voermans, S. Lillis et al. · Neuromuscular Disorders · 2013 · 195 citations

Neuromusculoskeletal Disorder, Mendelian Disorder, Genetics +6

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

Chlorocresol: an activator of ryanodine receptor-mediated Ca2+ release.

Francesco Zorzato, Erica Scutari, Vincenzo Tegazzin et al. · PubMed · 1993 · 139 citations

Neurotransmitter, Intracellular Ca2+ Homeostasis, Neurotransmission +18

<i><scp>RYR</scp>1</i>‐related myopathies: a wide spectrum of phenotypes throughout life

Marc Snoeck, Baziel G.M. van Engelen, Benno Küsters et al. · European Journal of Neurology · 2015 · 138 citations