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Items: 27

1.

Genetic Basis of Sudden Unexpected Death in Epilepsy.

Bagnall RD, Crompton DE, Semsarian C.

Front Neurol. 2017 Jul 20;8:348. doi: 10.3389/fneur.2017.00348. eCollection 2017. Review.

2.

Familial mesial temporal lobe epilepsy and the borderland of déjà vu.

Perucca P, Crompton DE, Bellows ST, McIntosh AM, Kalincik T, Newton MR, Vajda FJE, Scheffer IE, Kwan P, O'Brien TJ, Tan KM, Berkovic SF.

Ann Neurol. 2017 Aug;82(2):166-176. doi: 10.1002/ana.24984. Epub 2017 Jul 19.

PMID:
28681459
3.

Deconstruction of Interhospital Transfer Workflow in Large Vessel Occlusion: Real-World Data in the Thrombectomy Era.

Ng FC, Low E, Andrew E, Smith K, Campbell BCV, Hand PJ, Crompton DE, Wijeratne T, Dewey HM, Choi PM.

Stroke. 2017 Jul;48(7):1976-1979. doi: 10.1161/STROKEAHA.117.017235. Epub 2017 May 16.

PMID:
28512170
4.

Adverse clinical outcomes after dabigatran reversal with idarucizumab to facilitate acute stroke thrombolysis.

Ng FC, Bice J, Rodda A, Lee-Archer M, Crompton DE.

J Neurol. 2017 Mar;264(3):591-594. doi: 10.1007/s00415-017-8410-6. Epub 2017 Feb 6. No abstract available.

PMID:
28168523
5.

Mortality in Dravet syndrome.

Cooper MS, Mcintosh A, Crompton DE, McMahon JM, Schneider A, Farrell K, Ganesan V, Gill D, Kivity S, Lerman-Sagie T, McLellan A, Pelekanos J, Ramesh V, Sadleir L, Wirrell E, Scheffer IE.

Epilepsy Res. 2016 Dec;128:43-47. doi: 10.1016/j.eplepsyres.2016.10.006. Epub 2016 Oct 26.

PMID:
27810515
6.

Identity by descent fine mapping of familial adult myoclonus epilepsy (FAME) to 2p11.2-2q11.2.

Henden L, Freytag S, Afawi Z, Baldassari S, Berkovic SF, Bisulli F, Canafoglia L, Casari G, Crompton DE, Depienne C, Gecz J, Guerrini R, Helbig I, Hirsch E, Keren B, Klein KM, Labauge P, LeGuern E, Licchetta L, Mei D, Nava C, Pippucci T, Rudolf G, Scheffer IE, Striano P, Tinuper P, Zara F, Corbett M, Bahlo M.

Hum Genet. 2016 Oct;135(10):1117-25. doi: 10.1007/s00439-016-1700-8. Epub 2016 Jul 1.

PMID:
27368338
7.

Epileptic spasms are a feature of DEPDC5 mTORopathy.

Carvill GL, Crompton DE, Regan BM, McMahon JM, Saykally J, Zemel M, Schneider AL, Dibbens L, Howell KB, Mandelstam S, Leventer RJ, Harvey AS, Mullen SA, Berkovic SF, Sullivan J, Scheffer IE, Mefford HC.

Neurol Genet. 2015 Jul 23;1(2):e17. doi: 10.1212/NXG.0000000000000016. eCollection 2015 Aug.

8.

Exome-based analysis of cardiac arrhythmia, respiratory control, and epilepsy genes in sudden unexpected death in epilepsy.

Bagnall RD, Crompton DE, Petrovski S, Lam L, Cutmore C, Garry SI, Sadleir LG, Dibbens LM, Cairns A, Kivity S, Afawi Z, Regan BM, Duflou J, Berkovic SF, Scheffer IE, Semsarian C.

Ann Neurol. 2016 Apr;79(4):522-34. doi: 10.1002/ana.24596. Epub 2016 Feb 2.

PMID:
26704558
9.

Glut1 deficiency syndrome: Absence epilepsy and La Soupe du Jour.

Thouin A, Crompton DE.

Pract Neurol. 2016 Feb;16(1):50-2. doi: 10.1136/practneurol-2015-001194. Epub 2015 Sep 3.

PMID:
26336901
10.

Large basilar tip aneurysm causing anterior internuclear ophthalmoplegia.

Khan SA, Brooks M, Crompton DE.

Pract Neurol. 2015 Jun;15(3):230. doi: 10.1136/practneurol-2014-001062. Epub 2015 Feb 10. No abstract available.

PMID:
25670869
11.

Genetic analysis of PHOX2B in sudden unexpected death in epilepsy cases.

Bagnall RD, Crompton DE, Cutmore C, Regan BM, Berkovic SF, Scheffer IE, Semsarian C.

Neurology. 2014 Sep 9;83(11):1018-21. doi: 10.1212/WNL.0000000000000781. Epub 2014 Aug 1.

PMID:
25085640
12.

Mutations in mammalian target of rapamycin regulator DEPDC5 cause focal epilepsy with brain malformations.

Scheffer IE, Heron SE, Regan BM, Mandelstam S, Crompton DE, Hodgson BL, Licchetta L, Provini F, Bisulli F, Vadlamudi L, Gecz J, Connelly A, Tinuper P, Ricos MG, Berkovic SF, Dibbens LM.

Ann Neurol. 2014 May;75(5):782-7. doi: 10.1002/ana.24126. Epub 2014 Apr 14.

PMID:
24585383
13.

Mutations in DEPDC5 cause familial focal epilepsy with variable foci.

Dibbens LM, de Vries B, Donatello S, Heron SE, Hodgson BL, Chintawar S, Crompton DE, Hughes JN, Bellows ST, Klein KM, Callenbach PM, Corbett MA, Gardner AE, Kivity S, Iona X, Regan BM, Weller CM, Crimmins D, O'Brien TJ, Guerrero-López R, Mulley JC, Dubeau F, Licchetta L, Bisulli F, Cossette P, Thomas PQ, Gecz J, Serratosa J, Brouwer OF, Andermann F, Andermann E, van den Maagdenberg AM, Pandolfo M, Berkovic SF, Scheffer IE.

Nat Genet. 2013 May;45(5):546-51. doi: 10.1038/ng.2599. Epub 2013 Mar 31.

PMID:
23542697
14.

Early onset absence epilepsy: 1 in 10 cases is caused by GLUT1 deficiency.

Arsov T, Mullen SA, Damiano JA, Lawrence KM, Huh LL, Nolan M, Young H, Thouin A, Dahl HH, Berkovic SF, Crompton DE, Sadleir LG, Scheffer IE.

Epilepsia. 2012 Dec;53(12):e204-7. doi: 10.1111/epi.12007. Epub 2012 Oct 25.

15.

Familial adult myoclonic epilepsy: recognition of mild phenotypes and refinement of the 2q locus.

Crompton DE, Sadleir LG, Bromhead CJ, Bahlo M, Bellows ST, Arsov T, Harty R, Lawrence KM, Dunne JW, Berkovic SF, Scheffer IE.

Arch Neurol. 2012 Apr;69(4):474-81. doi: 10.1001/archneurol.2011.584.

PMID:
22491192
16.

Familial mesial temporal lobe epilepsy: a benign epilepsy syndrome showing complex inheritance.

Crompton DE, Scheffer IE, Taylor I, Cook MJ, McKelvie PA, Vears DF, Lawrence KM, McMahon JM, Grinton BE, McIntosh AM, Berkovic SF.

Brain. 2010 Nov;133(11):3221-31. doi: 10.1093/brain/awq251. Epub 2010 Sep 23.

PMID:
20864493
17.

The borderland of epilepsy: a clinical and molecular view, 100 years on.

Berkovic SF, Crompton DE.

Epilepsia. 2010 Feb;51 Suppl 1:3-4. doi: 10.1111/j.1528-1167.2009.02432.x. No abstract available.

18.

The borderland of epilepsy: clinical and molecular features of phenomena that mimic epileptic seizures.

Crompton DE, Berkovic SF.

Lancet Neurol. 2009 Apr;8(4):370-81. doi: 10.1016/S1474-4422(09)70059-6. Review.

PMID:
19296920
19.

A neurologist's guide to genome-wide association studies.

Mullen SA, Crompton DE, Carney PW, Helbig I, Berkovic SF.

Neurology. 2009 Feb 10;72(6):558-65. doi: 10.1212/01.wnl.0000341942.29513.bd. Review.

PMID:
19204266
20.

Optic perineuritis as a rare initial presentation of sarcoidosis.

Yu-Wai-Man P, Crompton DE, Graham JY, Black FM, Dayan MR.

Clin Exp Ophthalmol. 2007 Sep-Oct;35(7):682-4.

PMID:
17894695
21.

Pandemic influenza: compliance with public health quarantine laws and policies.

Crompton DE.

Caring. 2007 May;26(5):12-4, 16-8, 20-1.

PMID:
17578214
22.

Clinical features and natural history of neuroferritinopathy caused by the FTL1 460InsA mutation.

Chinnery PF, Crompton DE, Birchall D, Jackson MJ, Coulthard A, Lombès A, Quinn N, Wills A, Fletcher N, Mottershead JP, Cooper P, Kellett M, Bates D, Burn J.

Brain. 2007 Jan;130(Pt 1):110-9. Epub 2006 Dec 2.

PMID:
17142829
23.

Spectrum of movement disorders in neuroferritinopathy.

Crompton DE, Chinnery PF, Bates D, Walls TJ, Jackson MJ, Curtis AJ, Burn J.

Mov Disord. 2005 Jan;20(1):95-9.

PMID:
15390132
24.

Neuroferritinopathy: a window on the role of iron in neurodegeneration.

Crompton DE, Chinnery PF, Fey C, Curtis AR, Morris CM, Kierstan J, Burt A, Young F, Coulthard A, Curtis A, Ince PG, Bates D, Jackson MJ, Burn J.

Blood Cells Mol Dis. 2002 Nov-Dec;29(3):522-31.

PMID:
12547246
25.

Analysis of a cDNA from the neurologically active locus shaking-B (Passover) of Drosophila melanogaster.

Crompton DE, Griffin A, Davies JA, Miklos GL.

Gene. 1992 Dec 15;122(2):385-6.

PMID:
1487155
26.

Ice and snow--and lawsuits.

Crompton DE.

Contemp Adm Long Term Care. 1980 Oct;3(10):30, 32. No abstract available.

PMID:
10295036
27.

Confidentiality and the law.

Crompton DE.

Contemp Adm. 1980 Jun;3(6):10-3. No abstract available.

PMID:
10247123

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