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Brain : a Journal of Neurology|December 5, 2006
Clinical features and natural history of neuroferritinopathy caused by the FTL1 460InsA mutationPatrick F Chinnery, Douglas E Crompton, Daniel Birchall, et al.
Brain : a Journal of Neurology|September 25, 2010
Familial mesial temporal lobe epilepsy: a benign epilepsy syndrome showing complex inheritanceDouglas E Crompton, Ingrid E Scheffer, Isabella Taylor, et al.
Annals of Neurology|July 7, 2017
Familial mesial temporal lobe epilepsy and the borderland of déjà vuPiero Perucca, Douglas E Crompton, Susannah T Bellows, et al.
Blood Cells, Molecules & Diseases|January 28, 2003
Neuroferritinopathy: a window on the role of iron in neurodegenerationDouglas E Crompton, Patrick F Chinnery, Constanze Fey, et al.
Epilepsia|October 31, 2012
Early onset absence epilepsy: 1 in 10 cases is caused by GLUT1 deficiencyTodor Arsov, Saul A Mullen, John A Damiano, et al.
Epilepsy Research|November 5, 2016
Mortality in Dravet syndromeMonica S Cooper, Anne Mcintosh, Douglas E Crompton, et al.
Annals of Neurology|December 26, 2015
Exome-based analysis of cardiac arrhythmia, respiratory control, and epilepsy genes in sudden unexpected death in epilepsyRichard D Bagnall, Douglas E Crompton, Slavé Petrovski, et al.
Stroke|July 28, 2021
Greater Adherence to Secondary Prevention Medications Improves Survival After Stroke or Transient Ischemic Attack: A Linked Registry StudyLachlan L Dalli, Joosup Kim, Dominique A Cadilhac, et al.
Annals of Neurology|March 4, 2014
Mutations in mammalian target of rapamycin regulator DEPDC5 cause focal epilepsy with brain malformationsIngrid E Scheffer, Sarah E Heron, Brigid M Regan, et al.
European Journal of Human Genetics : EJHG|March 24, 2020
Familial adult myoclonic epilepsy type 1 SAMD12 TTTCA repeat expansion arose 17,000 years ago and is present in Sri Lankan and Indian familiesMark F Bennett, Karen L Oliver, Brigid M Regan, et al.
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