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Journal Abstract Search

286 related items for PubMed ID: 18991192

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  • 2. Characterization of language and reading skills in familial polymicrogyria.
    Oliveira EP, Hage SR, Guimarães CA, Brandão-Almeida I, Lopes-Cendes I, Guerreiro CA, Teixeira KC, Montenegro MA, Cendes F, Guerreiro MM.
    Brain Dev; 2008 Apr; 30(4):254-60. PubMed ID: 17920799
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  • 3. Pediatric congenital bilateral perisylvian syndrome: clinical and MRI features in 12 patients.
    Gropman AL, Barkovich AJ, Vezina LG, Conry JA, Dubovsky EC, Packer RJ.
    Neuropediatrics; 1997 Aug; 28(4):198-203. PubMed ID: 9309709
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  • 9. Malformations of cortical development: clinical spectrum in a series of 101 patients and review of the literature (Part I).
    Güngör S, Yalnizoğlu D, Turanli G, Saatçi I, Erdoğan-Bakar E, Topçu M.
    Turk J Pediatr; 2007 Aug; 49(2):120-30. PubMed ID: 17907510
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  • 10. Malformations of cortical development and epilepsy: evaluation of 101 cases (part II).
    Güngör S, Yalnizoğlu D, Turanli G, Saatçi I, Erdoğan-Bakar E, Topçu M.
    Turk J Pediatr; 2007 Aug; 49(2):131-40. PubMed ID: 17907511
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  • 11. Congenital bilateral perisylvian syndrome: a case study.
    Donders J, Mullarkey SK, Allchin J.
    Clin Neuropsychol; 2009 Feb; 23(2):276-85. PubMed ID: 18618376
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  • 13. Familial perisylvian polymicrogyria: a new familial syndrome of cortical maldevelopment.
    Guerreiro MM, Andermann E, Guerrini R, Dobyns WB, Kuzniecky R, Silver K, Van Bogaert P, Gillain C, David P, Ambrosetto G, Rosati A, Bartolomei F, Parmeggiani A, Paetau R, Salonen O, Ignatius J, Borgatti R, Zucca C, Bastos AC, Palmini A, Fernandes W, Montenegro MA, Cendes F, Andermann F.
    Ann Neurol; 2000 Jul; 48(1):39-48. PubMed ID: 10894214
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  • 17. Agenesis of the arcuate fasciculi in congenital bilateral perisylvian syndrome: a diffusion tensor imaging and tractography study.
    Bernal B, Rey G, Dunoyer C, Shanbhag H, Altman N.
    Arch Neurol; 2010 Apr; 67(4):501-5. PubMed ID: 20385920
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  • 18. Bilateral polymicrogyria as the indicative feature in a child with a 22q11.2 deletion.
    Gerkes EH, Hordijk R, Dijkhuizen T, Sival DA, Meiners LC, Sikkema-Raddatz B, van Ravenswaaij-Arts CM.
    Eur J Med Genet; 2010 Apr; 53(5):344-6. PubMed ID: 20553986
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  • 20. [Characterization of the linguistic profile of a family with Perisylvian Syndrome].
    de Oliveira EP, Guerreiro MM, Guimarães CA, Brandão-Almeida IL, Montenegro MA, Cendes F, Hage SR.
    Pro Fono; 2005 Apr; 17(3):393-402. PubMed ID: 16389796
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