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Journal Abstract Search

279 related items for PubMed ID: 23622213

  • 1. Diffuse malformations of cortical development.
    Bahi-Buisson N, Guerrini R.
    Handb Clin Neurol; 2013; 111():653-65. PubMed ID: 23622213
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  • 2. [Epileptogenic brain malformations: radiological and clinical presentation and indications for genetic testing].
    Bahi-Buisson N, Boddaert N, Saillour Y, Souville I, Poirier K, Léger PL, Castelnau L, Plouin P, Carion N, Beldjord C, Chelly J.
    Rev Neurol (Paris); 2008 Dec; 164(12):995-1009. PubMed ID: 18808783
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  • 3. Genetic malformations of cortical development.
    Guerrini R, Marini C.
    Exp Brain Res; 2006 Aug; 173(2):322-33. PubMed ID: 16724181
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  • 7. Epilepsy and genetic malformations of the cerebral cortex.
    Guerrini R, Carrozzo R.
    Am J Med Genet; 2001 Aug; 106(2):160-73. PubMed ID: 11579436
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  • 8. Epileptogenic brain malformations: clinical presentation, malformative patterns and indications for genetic testing.
    Guerrini R, Carrozzo R.
    Seizure; 2002 Apr; 11 Suppl A():532-43; quiz 544-7. PubMed ID: 12185771
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  • 9. Epilepsy and malformations of the cerebral cortex.
    Guerrini R, Sicca F, Parmeggiani L.
    Epileptic Disord; 2003 Sep; 5 Suppl 2():S9-26. PubMed ID: 14617417
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  • 10. Periventricular heterotopia: phenotypic heterogeneity and correlation with Filamin A mutations.
    Parrini E, Ramazzotti A, Dobyns WB, Mei D, Moro F, Veggiotti P, Marini C, Brilstra EH, Dalla Bernardina B, Goodwin L, Bodell A, Jones MC, Nangeroni M, Palmeri S, Said E, Sander JW, Striano P, Takahashi Y, Van Maldergem L, Leonardi G, Wright M, Walsh CA, Guerrini R.
    Brain; 2006 Jul; 129(Pt 7):1892-906. PubMed ID: 16684786
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  • 16. Overlapping cortical malformations and mutations in TUBB2B and TUBA1A.
    Cushion TD, Dobyns WB, Mullins JG, Stoodley N, Chung SK, Fry AE, Hehr U, Gunny R, Aylsworth AS, Prabhakar P, Uyanik G, Rankin J, Rees MI, Pilz DT.
    Brain; 2013 Feb; 136(Pt 2):536-48. PubMed ID: 23361065
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  • 19. X-linked malformations of cortical development.
    Leventer RJ, Mills PL, Dobyns WB.
    Am J Med Genet; 2000 Feb; 97(3):213-20. PubMed ID: 11449490
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  • 20. Lissencephaly and band heterotopia: LIS1, TUBA1A, and DCX mutations in Hungary.
    Mokánszki A, Körhegyi I, Szabó N, Bereg E, Gergev G, Balogh E, Bessenyei B, Sümegi A, Morris-Rosendahl DJ, Sztriha L, Oláh E.
    J Child Neurol; 2012 Dec; 27(12):1534-40. PubMed ID: 22408144
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