Leventer RJ - Search Results

1

Second-hit DEPDC5 mutation is limited to dysmorphic neurons in cortical dysplasia type IIA.

Lee WS, Stephenson SEM, Howell KB, Pope K, Gillies G, Wray A, Maixner W, Mandelstam SA, Berkovic SF, Scheffer IE, MacGregor D, Harvey AS, Lockhart PJ, Leventer RJ. Lee WS, et al. Among authors: leventer rj. Ann Clin Transl Neurol. 2019 Jul;6(7):1338-1344. doi: 10.1002/acn3.50815. Epub 2019 Jun 17. Ann Clin Transl Neurol. 2019. PMID: 31353856 Free PMC article.

2

Cortical malformations: a significant cause of paediatric neurological morbidity.

Leventer RJ, Harvey AS. Leventer RJ, et al. J Paediatr Child Health. 1998 Feb;34(1):6-8. doi: 10.1046/j.1440-1754.1998.00143.x. J Paediatr Child Health. 1998. PMID: 9568932

3

Clinical and imaging features of cortical malformations in childhood.

Leventer RJ, Phelan EM, Coleman LT, Kean MJ, Jackson GD, Harvey AS. Leventer RJ, et al. Neurology. 1999 Sep 11;53(4):715-22. doi: 10.1212/wnl.53.4.715. Neurology. 1999. PMID: 10489031

4

Bilateral generalized polymicrogyria (BGP): a distinct syndrome of cortical malformation.

Chang BS, Piao X, Giannini C, Cascino GD, Scheffer I, Woods CG, Topcu M, Tezcan K, Bodell A, Leventer RJ, Barkovich AJ, Grant PE, Walsh CA. Chang BS, et al. Among authors: leventer rj. Neurology. 2004 May 25;62(10):1722-8. doi: 10.1212/01.wnl.0000125187.52952.e9. Neurology. 2004. PMID: 15159468 Review.

5

Concomitant transverse myelitis and acute motor axonal neuropathy in an adolescent.

Howell KB, Wanigasinghe J, Leventer RJ, Ryan MM. Howell KB, et al. Among authors: leventer rj. Pediatr Neurol. 2007 Nov;37(5):378-81. doi: 10.1016/j.pediatrneurol.2007.05.020. Pediatr Neurol. 2007. PMID: 17950429

6

Malformations of cortical development and epilepsy.

Leventer RJ, Guerrini R, Dobyns WB. Leventer RJ, et al. Dialogues Clin Neurosci. 2008;10(1):47-62. doi: 10.31887/DCNS.2008.10.1/rjleventer. Dialogues Clin Neurosci. 2008. PMID: 18472484 Free PMC article. Review.

7

Clinical and imaging heterogeneity of polymicrogyria: a study of 328 patients.

Leventer RJ, Jansen A, Pilz DT, Stoodley N, Marini C, Dubeau F, Malone J, Mitchell LA, Mandelstam S, Scheffer IE, Berkovic SF, Andermann F, Andermann E, Guerrini R, Dobyns WB. Leventer RJ, et al. Brain. 2010 May;133(Pt 5):1415-27. doi: 10.1093/brain/awq078. Epub 2010 Apr 19. Brain. 2010. PMID: 20403963 Free PMC article.

8

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. Among authors: leventer rj. Epilepsia. 2010 Sep;51(9):1902-5. doi: 10.1111/j.1528-1167.2010.02694.x. Epilepsia. 2010. PMID: 20726879 Free article.

9

Reducing the exome search space for mendelian diseases using genetic linkage analysis of exome genotypes.

Smith KR, Bromhead CJ, Hildebrand MS, Shearer AE, Lockhart PJ, Najmabadi H, Leventer RJ, McGillivray G, Amor DJ, Smith RJ, Bahlo M. Smith KR, et al. Among authors: leventer rj. Genome Biol. 2011 Sep 14;12(9):R85. doi: 10.1186/gb-2011-12-9-r85. Genome Biol. 2011. PMID: 21917141 Free PMC article.

10

Febrile infection-related epilepsy syndrome is not caused by SCN1A mutations.

Carranza Rojo D, Harvey AS, Iona X, Dibbens LM, Damiano JA, Arsov T, Gill D, Freeman JL, Leventer RJ, Vincent A, Berkovic SF, McMahon JM, Scheffer IE. Carranza Rojo D, et al. Among authors: leventer rj. Epilepsy Res. 2012 Jun;100(1-2):194-8. doi: 10.1016/j.eplepsyres.2012.02.007. Epub 2012 Mar 3. Epilepsy Res. 2012. PMID: 22386634

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