Lawrence KM - Search Results

1

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. Crompton DE, et al. Among authors: lawrence km. Brain. 2010 Nov;133(11):3221-31. doi: 10.1093/brain/awq251. Epub 2010 Sep 23. Brain. 2010. PMID: 20864493

2

Evidence for genetic factors in vasovagal syncope: a twin-family study.

Klein KM, Xu SS, Lawrence K, Fischer A, Berkovic SF. Klein KM, et al. Among authors: lawrence k. Neurology. 2012 Aug 7;79(6):561-5. doi: 10.1212/WNL.0b013e3182635789. Neurology. 2012. PMID: 22869686

3

Genetics of epilepsy: The testimony of twins in the molecular era.

Vadlamudi L, Milne RL, Lawrence K, Heron SE, Eckhaus J, Keay D, Connellan M, Torn-Broers Y, Howell RA, Mulley JC, Scheffer IE, Dibbens LM, Hopper JL, Berkovic SF. Vadlamudi L, et al. Neurology. 2014 Sep 16;83(12):1042-8. doi: 10.1212/WNL.0000000000000790. Epub 2014 Aug 8. Neurology. 2014. PMID: 25107880 Free PMC article.

4

Autosomal dominant vasovagal syncope: clinical features and linkage to chromosome 15q26.

Klein KM, Bromhead CJ, Smith KR, O'Callaghan CJ, Corcoran SJ, Heron SE, Iona X, Hodgson BL, McMahon JM, Lawrence KM, Scheffer IE, Dibbens LM, Bahlo M, Berkovic SF. Klein KM, et al. Among authors: lawrence km. Neurology. 2013 Apr 16;80(16):1485-93. doi: 10.1212/WNL.0b013e31828cfad0. Neurology. 2013. PMID: 23589636

5

Glucose transporter 1 deficiency as a treatable cause of myoclonic astatic epilepsy.

Mullen SA, Marini C, Suls A, Mei D, Della Giustina E, Buti D, Arsov T, Damiano J, Lawrence K, De Jonghe P, Berkovic SF, Scheffer IE, Guerrini R. Mullen SA, et al. Arch Neurol. 2011 Sep;68(9):1152-5. doi: 10.1001/archneurol.2011.102. Epub 2011 May 9. Arch Neurol. 2011. PMID: 21555602

6

Gene expression analysis in absence epilepsy using a monozygotic twin design.

Helbig I, Matigian NA, Vadlamudi L, Lawrence KM, Bayly MA, Bain SM, Diyagama D, Scheffer IE, Mulley JC, Holloway AJ, Dibbens LM, Berkovic SF, Hayward NK. Helbig I, et al. Among authors: lawrence km. Epilepsia. 2008 Sep;49(9):1546-54. doi: 10.1111/j.1528-1167.2008.01630.x. Epub 2008 Apr 24. Epilepsia. 2008. PMID: 18435749 Free article.

7

Familial Lennox-Gastaut syndrome in male siblings with a novel DCX mutation and anterior pachygyria.

Lawrence KM, Mei D, Newton MR, Leventer RJ, Guerrini R, Berkovic SF. Lawrence KM, et al. Epilepsia. 2010 Sep;51(9):1902-5. doi: 10.1111/j.1528-1167.2010.02694.x. Epilepsia. 2010. PMID: 20726879 Free article.

8

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. Arsov T, et al. Among authors: lawrence km. Epilepsia. 2012 Dec;53(12):e204-7. doi: 10.1111/epi.12007. Epub 2012 Oct 25. Epilepsia. 2012. PMID: 23106342 Free article.

9

Glucose transporter 1 deficiency in the idiopathic generalized epilepsies.

Arsov T, Mullen SA, Rogers S, Phillips AM, Lawrence KM, Damiano JA, Goldberg-Stern H, Afawi Z, Kivity S, Trager C, Petrou S, Berkovic SF, Scheffer IE. Arsov T, et al. Among authors: lawrence km. Ann Neurol. 2012 Nov;72(5):807-15. doi: 10.1002/ana.23702. Ann Neurol. 2012. PMID: 23280796

10

Genetics of febrile seizure subtypes and syndromes: a twin study.

Eckhaus J, Lawrence KM, Helbig I, Bui M, Vadlamudi L, Hopper JL, Scheffer IE, Berkovic SF. Eckhaus J, et al. Among authors: lawrence km. Epilepsy Res. 2013 Jul;105(1-2):103-9. doi: 10.1016/j.eplepsyres.2013.02.011. Epub 2013 Mar 21. Epilepsy Res. 2013. PMID: 23522981

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