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Journal Abstract Search

383 related items for PubMed ID: 18421985

  • 1. [Molecular genetics of lissencephaly and microcephaly].
    Mochida GH.
    Brain Nerve; 2008 Apr; 60(4):437-44. PubMed ID: 18421985
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  • 4. [Molecular mechanism of lissencephaly--how LIS1 and NDEL1 regulate cytoplasmic dynein?].
    Hirotsune S.
    Brain Nerve; 2008 Apr; 60(4):375-81. PubMed ID: 18421979
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  • 7. Molecular evolution of the brain size regulator genes CDK5RAP2 and CENPJ.
    Evans PD, Vallender EJ, Lahn BT.
    Gene; 2006 Jun 21; 375():75-9. PubMed ID: 16631324
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  • 8. Location and type of mutation in the LIS1 gene do not predict phenotypic severity.
    Uyanik G, Morris-Rosendahl DJ, Stiegler J, Klapecki J, Gross C, Berman Y, Martin P, Dey L, Spranger S, Korenke GC, Schreyer I, Hertzberg C, Neumann TE, Burkart P, Spaich C, Meng M, Holthausen H, Adès L, Seidel J, Mangold E, Buyse G, Meinecke P, Schara U, Zeschnigk C, Muller D, Helland G, Schulze B, Wright ML, Kortge-Jung S, Hehr A, Bogdahn U, Schuierer G, Kohlhase J, Aigner L, Wolff G, Hehr U, Winkler J.
    Neurology; 2007 Jul 31; 69(5):442-7. PubMed ID: 17664403
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  • 10. 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 31; 27(12):1534-40. PubMed ID: 22408144
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  • 11. A new paradigm for West syndrome based on molecular and cell biology.
    Kato M.
    Epilepsy Res; 2006 Aug 31; 70 Suppl 1():S87-95. PubMed ID: 16806828
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  • 12. Normal and abnormal neuronal migration in the developing cerebral cortex.
    Sun XZ, Takahashi S, Cui C, Zhang R, Sakata-Haga H, Sawada K, Fukui Y.
    J Med Invest; 2002 Aug 31; 49(3-4):97-110. PubMed ID: 12323012
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  • 16. Functional analyses of lissencephaly-related proteins in Dictyostelium.
    Meyer I, Kuhnert O, Gräf R.
    Semin Cell Dev Biol; 2011 Feb 31; 22(1):89-96. PubMed ID: 21034843
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  • 17. [Genetic and clinical aspects of lissencephaly].
    Verloes A, Elmaleh M, Gonzales M, Laquerrière A, Gressens P.
    Rev Neurol (Paris); 2007 May 31; 163(5):533-47. PubMed ID: 17571022
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  • 18. Neuropathological phenotype of a distinct form of lissencephaly associated with mutations in TUBA1A.
    Fallet-Bianco C, Loeuillet L, Poirier K, Loget P, Chapon F, Pasquier L, Saillour Y, Beldjord C, Chelly J, Francis F.
    Brain; 2008 Sep 31; 131(Pt 9):2304-20. PubMed ID: 18669490
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  • 19. LIS1-related isolated lissencephaly: spectrum of mutations and relationships with malformation severity.
    Saillour Y, Carion N, Quelin C, Leger PL, Boddaert N, Elie C, Toutain A, Mercier S, Barthez MA, Milh M, Joriot S, des Portes V, Philip N, Broglin D, Roubertie A, Pitelet G, Moutard ML, Pinard JM, Cances C, Kaminska A, Chelly J, Beldjord C, Bahi-Buisson N.
    Arch Neurol; 2009 Aug 31; 66(8):1007-15. PubMed ID: 19667223
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