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Journal Abstract Search

265 related items for PubMed ID: 22333901

  • 1. Symmetric polymicrogyria and pachygyria associated with TUBB2B gene mutations.
    Guerrini R, Mei D, Cordelli DM, Pucatti D, Franzoni E, Parrini E.
    Eur J Hum Genet; 2012 Sep; 20(9):995-8. PubMed ID: 22333901
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  • 2. Mutations in the beta-tubulin gene TUBB2B result in asymmetrical polymicrogyria.
    Jaglin XH, Poirier K, Saillour Y, Buhler E, Tian G, Bahi-Buisson N, Fallet-Bianco C, Phan-Dinh-Tuy F, Kong XP, Bomont P, Castelnau-Ptakhine L, Odent S, Loget P, Kossorotoff M, Snoeck I, Plessis G, Parent P, Beldjord C, Cardoso C, Represa A, Flint J, Keays DA, Cowan NJ, Chelly J.
    Nat Genet; 2009 Jun; 41(6):746-52. PubMed ID: 19465910
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  • 3. 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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  • 8. TUBA1A mutations: from isolated lissencephaly to familial polymicrogyria.
    Jansen AC, Oostra A, Desprechins B, De Vlaeminck Y, Verhelst H, Régal L, Verloo P, Bockaert N, Keymolen K, Seneca S, De Meirleir L, Lissens W.
    Neurology; 2011 Mar 15; 76(11):988-92. PubMed ID: 21403111
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  • 10. Somatic mutations in cerebral cortical malformations.
    Jamuar SS, Lam AT, Kircher M, D'Gama AM, Wang J, Barry BJ, Zhang X, Hill RS, Partlow JN, Rozzo A, Servattalab S, Mehta BK, Topcu M, Amrom D, Andermann E, Dan B, Parrini E, Guerrini R, Scheffer IE, Berkovic SF, Leventer RJ, Shen Y, Wu BL, Barkovich AJ, Sahin M, Chang BS, Bamshad M, Nickerson DA, Shendure J, Poduri A, Yu TW, Walsh CA.
    N Engl J Med; 2014 Aug 21; 371(8):733-43. PubMed ID: 25140959
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  • 11. Polymicrogyria with dysmorphic basal ganglia? Think tubulin!
    Amrom D, Tanyalçin I, Verhelst H, Deconinck N, Brouhard GJ, Décarie JC, Vanderhasselt T, Das S, Hamdan FF, Lissens W, Michaud JL, Jansen AC.
    Clin Genet; 2014 Feb 21; 85(2):178-83. PubMed ID: 23495813
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  • 13. β-Tubulinopathy caused by a mutation of the TUBB2B gene: magnetic resonance imaging findings of the brain.
    Jimenez J, Herrera DA, Vargas SA, Montoya J, Castillo M.
    Neuroradiol J; 2019 Apr 21; 32(2):148-150. PubMed ID: 30704335
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