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Journal Abstract Search

169 related items for PubMed ID: 23450485

  • 1. [Analysis of DCX gene mutation in a patient featuring X-linked subcortical laminar heterotopia and epilepsy].
    Li W, Zhang MP, Hou ZJ, Zeng T, Tang B, Liu XR.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Feb; 30(1):74-8. PubMed ID: 23450485
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  • 3. Identification of DCX gene mutation in lissencephaly spectrum with subcortical band heterotopia using whole exome sequencing.
    Jang MA, Woo HI, Kim JW, Lee J, Ki CS.
    Pediatr Neurol; 2013 May; 48(5):411-4. PubMed ID: 23583063
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  • 5. Novel DCX mutation-caused lissencephaly in a boy and very mild heterotopia in his mother.
    Takeshita S, Higuchi M, Suyama M, Koide W, Maki K, Ushijima K, Ban K, Saito M, Kato M, Saitoh S.
    Pediatr Int; 2015 Apr; 57(2):321-3. PubMed ID: 25868952
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  • 8. Paternal transmission of subcortical band heterotopia through DCX somatic mosaicism.
    Moreira I, Bastos-Ferreira R, Silva J, Ribeiro C, Alonso I, Chaves J.
    Seizure; 2015 Feb; 25():62-4. PubMed ID: 25645638
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  • 12. Genetic alteration of the DCX gene in Japanese patients with subcortical laminar heterotopia or isolated lissencephaly sequence.
    Sakamoto M, Ono J, Okada S, Nakamura Y, Kurahashi H.
    J Hum Genet; 2000 Feb; 45(3):167-70. PubMed ID: 10807542
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  • 15. Coexistence of mitochondrial and nuclear DNA mutations in a woman with mitochondrial encephalomyopathy and double cortex.
    Scuderi C, Borgione E, Castello F, Lo Giudice M, Fichera M, Elia M, Amato C, Savio M, Di Blasi FD, Vitello GA, Romano S, DiMauro S, Musumeci SA.
    Mitochondrion; 2010 Aug; 10(5):548-54. PubMed ID: 20433951
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  • 16. [Incontinentia pigmenti with subcortical band heterotopias].
    Aoun A, Goizet C, Arveiler B, Sarrazin E, Derancourt C.
    Arch Pediatr; 2015 Jan; 22(1):109-10. PubMed ID: 25435274
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  • 17. Listen carefully: LIS1 and DCX MLPA in lissencephaly and subcortical band heterotopia.
    Delatycki MB, Leventer RJ.
    Eur J Hum Genet; 2009 Jun; 17(6):701-2. PubMed ID: 19050725
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