Karen Rafferty

The TREAT-NMD Duchenne Muscular Dystrophy Registries: Conception, Design, and Utilization by Industry and Academia

Catherine L. Bladen, Karen Rafferty, Volker Straub et al. · Human Mutation · 2013 · 103 citations

Rare Diseases, Dmd Registries, Duchenne Muscular Dystrophy +14

Mapping the differences in care for 5,000 Spinal Muscular Atrophy patients, a survey of 24 national registries in North America, Australasia and Europe

Catherine L. Bladen, Rachel Thompson, J. Jackson et al. · Journal of Neurology · 2013 · 102 citations

Spine Care, Primary Care, Health Policy +9

A general purpose reporter for cations: absorption, fluorescence and electrochemical sensing of zinc(ii)

Andrew C. Benniston, Anthony Harriman, Donald J. Lawrie et al. · Dalton Transactions · 2003 · 51 citations

Engineering, Chemistry, Chemical Engineering +18

Global FKRP Registry: observations in more than 300 patients with Limb Girdle Muscular Dystrophy R9

L. Murphy, Olivia Schreiber‐Katz, Karen Rafferty et al. · Annals of Clinical and Translational Neurology · 2020 · 40 citations · Full text

Design, set-up and utility of the UK facioscapulohumeral muscular dystrophy patient registry

Teresinha Evangelista, Libby Wood, Roberto Fernández‐Torrón et al. · Journal of Neurology · 2016 · 31 citations · Full text

Public Health, Primary Care, Health Informatics +1