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Practical Neurology|September 5, 2015
Glut1 deficiency syndrome: Absence epilepsy and La Soupe du JourAnaïs Thouin, Douglas E Crompton
The Lancet. Neurology|March 20, 2009
The borderland of epilepsy: clinical and molecular features of phenomena that mimic epileptic seizuresDouglas E Crompton, Samuel F Berkovic
Epileptic Disorders : International Epilepsy Journal with Videotape|December 10, 2021
ILAE Genetic Literacy Series: familial focal epilepsy syndromesSamuel Gooley, Douglas E Crompton, Samuel F Berkovic
Frontiers in Neurology|August 5, 2017
Genetic Basis of Sudden Unexpected Death in EpilepsyRichard D Bagnall, Douglas E Crompton, Christopher Semsarian
Clinical & Experimental Ophthalmology|September 27, 2007
Optic perineuritis as a rare initial presentation of sarcoidosisPatrick Yu-Wai-Man, Douglas E Crompton, James Y Graham, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 25, 2004
Spectrum of movement disorders in neuroferritinopathyDouglas E Crompton, Patrick F Chinnery, David Bates, et al.
Neurology|August 3, 2014
Genetic analysis of PHOX2B in sudden unexpected death in epilepsy casesRichard D Bagnall, Douglas E Crompton, Carina Cutmore, et al.
Archives of Neurology|April 12, 2012
Familial adult myoclonic epilepsy: recognition of mild phenotypes and refinement of the 2q locusDouglas E Crompton, Lynette G Sadleir, Catherine J Bromhead, et al.
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