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Journal Abstract Search

137 related items for PubMed ID: 8971750

  • 1. Lissencephaly with extreme cerebral and cerebellar hypoplasia. A magnetic resonance imaging study.
    Kroon AA, Smit BJ, Barth PG, Hennekam RC.
    Neuropediatrics; 1996 Oct; 27(5):273-6. PubMed ID: 8971750
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  • 4. Early fatal pontocerebellar hypoplasia with simplified cerebral gyration and pseudolissencephaly. A neuroradiological pitfall.
    Hoffmann A, Weber P, Fallet-Bianco C, Radu EW, Probst A.
    Fetal Diagn Ther; 2006 Oct; 21(2):161-7. PubMed ID: 16490996
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  • 5. Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations.
    Hong SE, Shugart YY, Huang DT, Shahwan SA, Grant PE, Hourihane JO, Martin ND, Walsh CA.
    Nat Genet; 2000 Sep; 26(1):93-6. PubMed ID: 10973257
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  • 6. Lissencephaly and mild cerebellar vermis hypoplasia in a case of microcephaly and chorioretinal dysplasia.
    Lee BJ, Kim JH, Yu YS.
    Ophthalmic Genet; 2010 Jun; 31(2):89-93. PubMed ID: 20450312
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  • 7. Genetic malformations of the cerebral cortex and epilepsy.
    Guerrini R.
    Epilepsia; 2005 Jun; 46 Suppl 1():32-7. PubMed ID: 15816977
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  • 8. Lissencephaly with agenesis of corpus callosum and rudimentary dysplastic cerebellum: a subtype of lissencephaly with cerebellar hypoplasia.
    Miyata H, Chute DJ, Fink J, Villablanca P, Vinters HV.
    Acta Neuropathol; 2004 Jan; 107(1):69-81. PubMed ID: 14566414
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  • 10. [Analysis of the clinical manifestations and magnetic resonance imaging features of 11 patients with lissencephaly].
    LI BX, GUO L, SONG YZ.
    Nan Fang Yi Ke Da Xue Xue Bao; 2011 Mar; 31(3):482-6. PubMed ID: 21421488
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  • 16. 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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  • 18. Microlissencephaly: a heterogeneous malformation of cortical development.
    Barkovich AJ, Ferriero DM, Barr RM, Gressens P, Dobyns WB, Truwit CL, Evrard P.
    Neuropediatrics; 1998 Jun 31; 29(3):113-9. PubMed ID: 9706619
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  • 19. [Brain abnormality within the scope of a VACTERL association].
    Nikischin W, Krolikowski I, Santer R.
    Monatsschr Kinderheilkd; 1991 Jun 31; 139(6):360-2. PubMed ID: 1896049
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