Peter Uldall

De novo mutations in ATP1A3 cause alternating hemiplegia of childhood

Erin L. Heinzen, Kathryn J. Swoboda, Yuki Hitomi et al. · Nature Genetics · 2012 · 423 citations · Full text

Life Sciences, Genetics, Neurology +9

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 · 355 citations · Full text

Life Sciences, Genetics, Molecular Genetics +8

The landscape of epilepsy-related GATOR1 variants

Sara Baldassari, Fabienne Picard, Nienke E. Verbeek et al. · Genetics in Medicine · 2018 · 239 citations · Full text

Medicine, Genetics, Molecular Genetics +17

The misdiagnosis of epilepsy in children admitted to a tertiary epilepsy centre with paroxysmal events

Peter Uldall · Archives of Disease in Childhood · 2006 · 235 citations · Full text

Medicine, Maternal Health, Obstetrics +16

Lamotrigine plasma levels reduced by oral contraceptives

Anne Sabers, Jette Buchholt, Peter Uldall et al. · Epilepsy Research · 2001 · 223 citations

Medicine, Pharmacokinetics, Pharmacotherapy +14