Caroline A. Sewry
Great Ormond Street Hospital(GB)Salford Royal NHS Foundation Trust(GB)Robert Jones and Agnes Hunt Orthopaedic Hospital(GB)Salford Royal Hospital(GB)University College London(GB)
Publications by Year
Research Areas
Muscle Physiology and Disorders, Cardiomyopathy and Myosin Studies, Neurogenetic and Muscular Disorders Research, Genetic Neurodegenerative Diseases, Nuclear Structure and Function
Most-Cited Works
- → Muscle Biopsy: A Practical Approach(2020)1,343 cited
- → Exon skipping and dystrophin restoration in patients with Duchenne muscular dystrophy after systemic phosphorodiamidate morpholino oligomer treatment: an open-label, phase 2, dose-escalation study(2011)855 cited
- → Mutations in the Fukutin-Related Protein Gene (FKRP) Cause a Form of Congenital Muscular Dystrophy with Secondary Laminin α2 Deficiency and Abnormal Glycosylation of α-Dystroglycan(2001)596 cited
- → Mutations in the skeletal muscle α-actin gene in patients with actin myopathy and nemaline myopathy(1999)399 cited
- → Loss-of-function mutations in MICU1 cause a brain and muscle disorder linked to primary alterations in mitochondrial calcium signaling(2013)367 cited
- → Mutation in BAG3 causes severe dominant childhood muscular dystrophy(2008)361 cited