Mike Pike

Genotypic and phenotypic spectrum of pyridoxine-dependent epilepsy (ALDH7A1 deficiency)

Philippa B. Mills, Emma Footitt, Kevin Mills et al. · Brain · 2010 · 266 citations · Full text

Medicine, Neurology, Biochemical Genetics +16

Vigabatrin with hormonal treatment versus hormonal treatment alone (ICISS) for infantile spasms: 18-month outcomes of an open-label, randomised controlled trial

Finbar O’Callaghan, Stuart W. Edwards, Fabienne Dietrich Alber et al. · The Lancet Child & Adolescent Health · 2018 · 165 citations · Full text

Medicine, Neurology, Pharmacotherapy +7

Extreme Variability of Phenotype in Patients With an Identical Missense Mutation in the Lamin A/C Gene

Eugenio Mercuri, Maja Poppe, Rosaline C. M. Quinlivan et al. · Archives of Neurology · 2004 · 125 citations

Medicine, Genetics, Molecular Genetics +15

NMDA receptor antibodies associated with distinct white matter syndromes

Yael Hacohen, Michael Absoud, Cheryl Hemingway et al. · Neurology Neuroimmunology & Neuroinflammation · 2014 · 99 citations · Full text

Medicine, Neurology, Pediatrics +17

Cerebral infarct and meningitis secondary to Lemierre's syndrome

Jamie Bentham, Andrew J. Pollard, Christopher Milford et al. · Pediatric Neurology · 2004 · 71 citations

Medicine, Neurology, Neuroscience +9