Richard Webster

Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1

Gemma L. Carvill, Sinéad B. Heavin, Simone C. Yendle et al. · Nature Genetics · 2013 · 683 citations · Full text

Genetics, Novo Mutations, Neurotransmission +5

Long-term effects of glucocorticoids on function, quality of life, and survival in patients with Duchenne muscular dystrophy: a prospective cohort study

Craig M. McDonald, Erik Henricson, Richard T. Abresch et al. · The Lancet · 2017 · 446 citations

Long-term Effects, Duchenne Muscular Dystrophy, Degenerative Disease +4

GRIN2A mutations cause epilepsy-aphasia spectrum disorders

Gemma L. Carvill, Brigid M. Regan, Simone C. Yendle et al. · Nature Genetics · 2013 · 372 citations · Full text

Genetic Disorder, Grin2a Mutations, Neurology +4

N‐methyl‐<scp>D</scp>‐aspartate receptor antibodies in pediatric dyskinetic encephalitis lethargica

Russell C. Dale, Sarosh R. Irani, Fabienne Brilot et al. · Annals of Neurology · 2009 · 219 citations

Pediatric Hydrocephalus, Neurological Disorder, Corticobasal Degeneration +17

Prednisone/prednisolone and deflazacort regimens in the CINRG Duchenne Natural History Study

Luca Bello, Heather Gordish‐Dressman, Lauren P. Morgenroth et al. · Neurology · 2015 · 197 citations · Full text