Michael Harbord

The spectrum of SCN1A-related infantile epileptic encephalopathies

Louise A. Harkin, Jacinta M. McMahon, Xenia Iona et al. · Brain · 2007 · 530 citations · Full text

Medicine, Genetics, Neurology +17

Disruption of the Serine/Threonine Kinase 9 Gene Causes Severe X-Linked Infantile Spasms and Mental Retardation

Vera M. Kalscheuer, Jiong Tao, Andrew J. Donnelly et al. · The American Journal of Human Genetics · 2003 · 297 citations · Full text

Life Sciences, Genetics, Molecular Genetics +9

In-depth analysis of delays to patient discharge: a metropolitan teaching hospital experience

Peter Hendy, JH Patel, T Kordbacheh et al. · Clinical Medicine · 2012 · 102 citations · Full text

Health Professions, Health Care Management, Health Services Administration +13

14q12 and severe Rett-like phenotypes: new clinical insights and physical mapping of FOXG1-regulatory elements

Lila Allou, Laëtitia Lambert, Daniel Amsallem et al. · European Journal of Human Genetics · 2012 · 87 citations · Full text

Life Sciences, Genetics, Molecular Genetics +8

Anti-tumour necrosis factor-α therapy for severe enteropathy in patients with common variable immunodeficiency (CVID)

Ignatius Chua, Richard Standish, Sara Lear et al. · Clinical & Experimental Immunology · 2007 · 85 citations · Full text

Veterinary Medicine, Immunology, Pharmacotherapy +15