Emma Matthews

To tell or not to tell: barriers and facilitators in family communication about genetic risk

Karen Forrest, SA Simpson, Wilson Bj et al. · Clinical Genetics · 2003 · 370 citations

Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysis

Emma Matthews, Robyn Labrum, Mary G. Sweeney et al. · Neurology · 2008 · 195 citations · Full text

Prevalence study of genetically defined skeletal muscle channelopathies in England

Alejandro Horga, D.L. Raja Rayan, Emma Matthews et al. · Neurology · 2013 · 135 citations · Full text

Dihydropyridine receptor (DHPR, CACNA1S) congenital myopathy

Vanessa Schartner, Norma B. Romero, Sandra Donkervoort et al. · Acta Neuropathologica · 2016 · 132 citations · Full text

Congenital Myopathy, Mendelian Disorder, Degenerative Disease +1

Effect of Mexiletine on Muscle Stiffness in Patients With Nondystrophic Myotonia Evaluated Using Aggregated N-of-1 Trials

Bas C. Stunnenberg, Joost Raaphorst, Hans Groenewoud et al. · JAMA · 2018 · 129 citations · Full text