Crompton, Douglas E
Royal Children's Hospital · The University of Melbourne · University of South Australia · University of California, San Francisco · Northern Health · University of Washington · Florey Institute of Neuroscience and Mental Health · Murdoch Children's Research Institute · Austin Health
3 papers on CoChatORCID 0000-0002-0776-1203
Most cited papers
- Verified
Mutations in DEPDC5 cause familial focal epilepsy with variable foci
Dibbens, L. M., de Vries, B., Donatello, S., Heron, S. E., Hodgson, B. L., Chintawar, S., Crompton, D. E., Hughes, J. N., Bellows, S. T., Klein, K. M., et al. (2013) · Nature Genetics
Epilepsy research and treatmentTuberous Sclerosis Complex Research
Cited by 373
- Verified
Clinical features and natural history of neuroferritinopathy caused by the FTL1 460InsA mutation
Chinnery, P. F., Crompton, D. E., Birchall, D., Jackson, M. J., Coulthard, A., Lombes, A., Quinn, N., Wills, A., Fletcher, N., Mottershead, J. P., et al. (2006) · Brain
Neurological diseases and metabolismParkinson's Disease Mechanisms and Treatments
Cited by 205
- Verified
Epileptic spasms are a feature of DEPDC5 mTORopathy
Carvill, G. L., Crompton, D. E., Regan, B. M., McMahon, J. M., Saykally, J., Zemel, M., Schneider, A. L., Dibbens, L., Howell, K. B., Mandelstam, S., et al. (2015) · Neurology Genetics
Epilepsy research and treatmentTuberous Sclerosis Complex Research
Cited by 76
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