David Webb

Epidemiology of Tuberous Sclerosis

J. OSBORNE, Alan Fryer, David Webb · Annals of the New York Academy of Sciences · 1991 · 731 citations

Neurological Disorder, Clinical Epidemiology, Histopathology +4

De novo mutations in ATP1A3 cause alternating hemiplegia of childhood

Erin L. Heinzen, Kathryn J. Swoboda, Yuki Hitomi et al. · Nature Genetics · 2012 · 417 citations · Full text

Rare Diseases, Mendelian Disorder, Genetic Disorder +8

Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorder

Willemijn G. Leen, Jörg Klepper, Marcel M. Verbeek et al. · Brain · 2010 · 406 citations · Full text

The phenotypic spectrum of rapid-onset dystonia-parkinsonism (RDP) and mutations in the ATP1A3 gene

Alison Brashear, William B. Dobyns, Patrícia de Carvalho Aguiar et al. · Brain · 2007 · 274 citations

Two loci for Tuberous Sclerosis: one on 9q34 and one on 16p13

Sue Povey, Mari‐Wyn Burley, Frances Benham et al. · Annals of Human Genetics · 1994 · 266 citations