Padraic J. Grattan‐Smith

Infection-Triggered Familial or Recurrent Cases of Acute Necrotizing Encephalopathy Caused by Mutations in a Component of the Nuclear Pore, RANBP2

Derek Neilson, Mark D. Adams, Caitlin M.D. Orr et al. · The American Journal of Human Genetics · 2009 · 349 citations · Full text

Genetic Disorder, Pathogenesis, Nuclear Pore +8

Tyrosine hydroxylase deficiency: a treatable disorder of brain catecholamine biosynthesis

Michèl A.A.P. Willemsen, Marcel M. Verbeek, Erik‐Jan Kamsteeg et al. · Brain · 2010 · 228 citations · Full text

Infantile spinal muscular atrophy with respiratory distress type 1 (SMARD1)

Katja Grohmann, Raymonda Varon, Piroschka Stolz et al. · Annals of Neurology · 2003 · 171 citations

Clinical and neurophysiological features of tick paralysis

Padraic J. Grattan‐Smith · Brain · 1997 · 166 citations · Full text

Generalized Tick Paralysis, Neurorehabilitation, Allergy +14

Clinical features of conversion disorder.

Padraic J. Grattan‐Smith, Michael Fairley, Peter Procopis · Archives of Disease in Childhood · 1988 · 134 citations · Full text

Psychological Co-morbidities, Psychopathology, Psychiatric Disorders +16