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128 results
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Malformations of cortical development and epilepsy.
Leventer RJ, Guerrini R, Dobyns WB. Leventer RJ, et al. Dialogues Clin Neurosci. 2008;10(1):47-62. Dialogues Clin Neurosci. 2008. PMID: 18472484 Free PMC article. Review.
Genetic abnormalities in a large cohort of Coffin-Siris syndrome patients.
Sekiguchi F, Tsurusaki Y, Okamoto N, Teik KW, Mizuno S, Suzumura H, Isidor B, Ong WP, Haniffa M, White SM, Matsuo M, Saito K, Phadke S, Kosho T, Yap P, Goyal M, Clarke LA, Sachdev R, McGillivray G, Leventer RJ, Patel C, Yamagata T, Osaka H, Hisaeda Y, Ohashi H, Shimizu K, Nagasaki K, Hamada J, Dateki S, Sato T, Chinen Y, Awaya T, Kato T, Iwanaga K, Kawai M, Matsuoka T, Shimoji Y, Tan TY, Kapoor S, Gregersen N, Rossi M, Marie-Laure M, McGregor L, Oishi K, Mehta L, Gillies G, Lockhart PJ, Pope K, Shukla A, Girisha KM, Abdel-Salam GMH, Mowat D, Coman D, Kim OH, Cordier MP, Gibson K, Milunsky J, Liebelt J, Cox H, El Chehadeh S, Toutain A, Saida K, Aoi H, Minase G, Tsuchida N, Iwama K, Uchiyama Y, Suzuki T, Hamanaka K, Azuma Y, Fujita A, Imagawa E, Koshimizu E, Takata A, Mitsuhashi S, Miyatake S, Mizuguchi T, Miyake N, Matsumoto N. Sekiguchi F, et al. Among authors: leventer rj. J Hum Genet. 2019 Dec;64(12):1173-1186. doi: 10.1038/s10038-019-0667-4. Epub 2019 Sep 17. J Hum Genet. 2019. PMID: 31530938
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
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
Polymicrogyria associated with scalp and limb defects: variant of Adams-Oliver syndrome.
Amor DJ, Leventer RJ, Hayllar S, Bankier A. Amor DJ, et al. Among authors: leventer rj. Am J Med Genet. 2000 Aug 14;93(4):328-34. doi: 10.1002/1096-8628(20000814)93:4<328::aid-ajmg13>;2-0. Am J Med Genet. 2000. PMID: 10946361
X-linked malformations of cortical development.
Leventer RJ, Mills PL, Dobyns WB. Leventer RJ, et al. Am J Med Genet. 2000 Fall;97(3):213-20. doi: 10.1002/1096-8628(200023)97:3<213::AID-AJMG1039>3.0.CO;2-W. Am J Med Genet. 2000. PMID: 11449490 Review.
Genotype-phenotype correlation in lissencephaly and subcortical band heterotopia: the key questions answered.
Leventer RJ. Leventer RJ. J Child Neurol. 2005 Apr;20(4):307-12. doi: 10.1177/08830738050200040701. J Child Neurol. 2005. PMID: 15921231 Review.
Neuropsychological profile of children with subcortical band heterotopia.
Spencer-Smith M, Leventer R, Jacobs R, Luca CD, Anderson V. Spencer-Smith M, et al. Dev Med Child Neurol. 2009 Nov;51(11):909-16. doi: 10.1111/j.1469-8749.2009.03309.x. Epub 2009 Mar 31. Dev Med Child Neurol. 2009. PMID: 19416314
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.
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
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