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Douglas Crompton
Douglas Crompton
Northern Health, University of Melbourne
Verified email at unimelb.edu.au
Title
Cited by
Cited by
Year
Mutations in DEPDC5 cause familial focal epilepsy with variable foci
LM Dibbens, B De Vries, S Donatello, SE Heron, BL Hodgson, ...
Nature genetics 45 (5), 546-551, 2013
3792013
Mortality in Dravet syndrome
MS Cooper, A Mcintosh, DE Crompton, JM McMahon, A Schneider, ...
Epilepsy research 128, 43-47, 2016
2652016
Mutations in mammalian target of rapamycin regulator DEPDC5 cause focal epilepsy with brain malformations
IE Scheffer, SE Heron, BM Regan, S Mandelstam, DE Crompton, ...
Annals of neurology 75 (5), 782-787, 2014
2602014
Mutations in mammalian target of rapamycin regulator DEPDC5 cause focal epilepsy with brain malformations
IE Scheffer, SE Heron, BM Regan, S Mandelstam, DE Crompton, ...
Annals of neurology 75 (5), 782-787, 2014
2602014
Exome‐based analysis of cardiac arrhythmia, respiratory control, and epilepsy genes in sudden unexpected death in epilepsy
RD Bagnall, DE Crompton, S Petrovski, L Lam, C Cutmore, SI Garry, ...
Annals of neurology 79 (4), 522-534, 2016
2412016
Clinical features and natural history of neuroferritinopathy caused by the FTL1 460InsA mutation
PF Chinnery, DE Crompton, D Birchall, MJ Jackson, A Coulthard, ...
Brain 130 (1), 110-119, 2007
2222007
Mutations in the mammalian target of rapamycin pathway regulators NPRL2 and NPRL3 cause focal epilepsy
MG Ricos, BL Hodgson, T Pippucci, A Saidin, YS Ong, SE Heron, ...
Annals of neurology 79 (1), 120-131, 2016
2082016
Intronic ATTTC repeat expansions in STARD7 in familial adult myoclonic epilepsy linked to chromosome 2
MA Corbett, T Kroes, L Veneziano, MF Bennett, R Florian, AL Schneider, ...
Nature communications 10 (1), 4920, 2019
1212019
Early onset absence epilepsy: 1 in 10 cases is caused by GLUT1 deficiency
T Arsov, SA Mullen, JA Damiano, KM Lawrence, LL Huh, M Nolan, ...
Epilepsia 53 (12), e204-e207, 2012
1182012
The borderland of epilepsy: clinical and molecular features of phenomena that mimic epileptic seizures
DE Crompton, SF Berkovic
The Lancet Neurology 8 (4), 370-381, 2009
1142009
Familial mesial temporal lobe epilepsy: a benign epilepsy syndrome showing complex inheritance
DE Crompton, IE Scheffer, I Taylor, MJ Cook, PA McKelvie, DF Vears, ...
Brain 133 (11), 3221-3231, 2010
1032010
Neuroferritinopathy: a window on the role of iron in neurodegeneration
DE Crompton, PF Chinnery, C Fey, ARJ Curtis, CM Morris, J Kierstan, ...
Blood Cells, Molecules, and Diseases 29 (3), 522-531, 2002
982002
Deconstruction of interhospital transfer workflow in large vessel occlusion: real-world data in the thrombectomy era
FC Ng, E Low, E Andrew, K Smith, BCV Campbell, PJ Hand, ...
Stroke 48 (7), 1976-1979, 2017
962017
Genetic basis of sudden unexpected death in epilepsy
RD Bagnall, DE Crompton, C Semsarian
Frontiers in neurology 8, 260615, 2017
822017
Melbourne mobile stroke unit and reperfusion therapy: greater clinical impact of thrombectomy than thrombolysis
H Zhao, S Coote, D Easton, F Langenberg, M Stephenson, K Smith, ...
Stroke 51 (3), 922-930, 2020
742020
Epileptic spasms are a feature of DEPDC5 mTORopathy
GL Carvill, DE Crompton, BM Regan, JM McMahon, J Saykally, M Zemel, ...
Neurology: Genetics 1 (2), e17, 2015
712015
Essential and neural transcripts from the Drosophila shaking-B locus are differentially expressed in the embryonic mesoderm and pupal nervous system
D Crompton, M Todman, M Wilkin, S Ji, J Davies
Developmental biology 170 (1), 142-158, 1995
661995
Neuroferritinopathy in a French family with late onset dominant dystonia
PF Chinnery, ARJ Curtis, C Fey, A Coulthard, D Crompton, A Curtis, ...
Journal of medical genetics 40 (5), e69-e69, 2003
632003
Spectrum of movement disorders in neuroferritinopathy
DE Crompton, PF Chinnery, D Bates, TJ Walls, MJ Jackson, AJ Curtis, ...
Movement Disorders: Official Journal of the Movement Disorder Society 20 (1 …, 2005
532005
Risk‐adjusted hospital mortality rates for stroke: evidence from the Australian Stroke Clinical Registry (AuSCR)
DA Cadilhac, MF Kilkenny, CR Levi, NA Lannin, AG Thrift, J Kim, ...
Medical Journal of Australia 206 (8), 345-350, 2017
472017
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