Mena Abdelsayed

Exome Sequencing and the Management of Neurometabolic Disorders

Maja Tarailo‐Graovac, Casper Shyr, Colin J.D. Ross et al. · New England Journal of Medicine · 2016 · 274 citations · Full text

Loss-of-function mutations in<i>SCN4A</i>cause severe foetal hypokinesia or ‘classical’ congenital myopathy

Irina Zaharieva, Michael G. Thor, Emily C. Oates et al. · Brain · 2015 · 120 citations · Full text

Congenital Myopathy, Muscle Function, Genetics +29

SCN5A mutations in 442 neonates and children: genotype–phenotype correlation and identification of higher-risk subgroups

Alban‐Elouen Baruteau, Florence Kyndt, Elijah R. Behr et al. · European Heart Journal · 2018 · 48 citations · Full text

Differential thermosensitivity in mixed syndrome cardiac sodium channel mutants

Mena Abdelsayed, Colin H. Peters, Peter C. Ruben · The Journal of Physiology · 2015 · 38 citations · Full text

Cardiac Muscle, Nav 1.5, Genetics +18

Effects of Amiodarone and N-desethylamiodarone on Cardiac Voltage-Gated Sodium Channels

Mohammad‐Reza Ghovanloo, Mena Abdelsayed, Peter C. Ruben · Frontiers in Pharmacology · 2016 · 33 citations · Full text