Douglas E. Crompton
Northern Health(AU)Austin Health(AU)
Publications by Year
Research Areas
Epilepsy research and treatment, Acute Ischemic Stroke Management, Genetics and Neurodevelopmental Disorders, Genomics and Rare Diseases, Neuroscience and Neuropharmacology Research
Most-Cited Works
- → Mutations in DEPDC5 cause familial focal epilepsy with variable foci(2013)359 cited
- → Mortality in Dravet syndrome(2016)304 cited
- → Exome‐based analysis of cardiac arrhythmia, respiratory control, and epilepsy genes in sudden unexpected death in epilepsy(2015)276 cited
- → Mutations in mammalian target of rapamycin regulator DEPDC5 cause focal epilepsy with brain malformations(2014)219 cited
- → Clinical features and natural history of neuroferritinopathy caused by the FTL1 460InsA mutation(2006)201 cited
- → Intronic ATTTC repeat expansions in STARD7 in familial adult myoclonic epilepsy linked to chromosome 2(2019)164 cited
- → Early onset absence epilepsy: 1 in 10 cases is caused by GLUT1 deficiency(2012)115 cited
- → The borderland of epilepsy: clinical and molecular features of phenomena that mimic epileptic seizures(2009)102 cited
- → Deconstruction of Interhospital Transfer Workflow in Large Vessel Occlusion(2017)91 cited
- → Familial mesial temporal lobe epilepsy: a benign epilepsy syndrome showing complex inheritance(2010)89 cited