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Journal Abstract Search

313 related items for PubMed ID: 8942027

  • 1. Cerebellar dysgenesis in infants and children: an experience of 22 cases.
    Yang MT, Chen CH, Chi CS, Mak SC.
    Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1996; 37(5):342-8. PubMed ID: 8942027
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  • 2. Dandy-Walker malformation: prenatal diagnosis and prognosis.
    Klein O, Pierre-Kahn A, Boddaert N, Parisot D, Brunelle F.
    Childs Nerv Syst; 2003 Aug; 19(7-8):484-9. PubMed ID: 12879343
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  • 3. [Holoprosencephaly accompanied with dysgenesis of the cerebellum].
    Yamashita N, Kamiya K, Nagai H.
    No Shinkei Geka; 1992 Oct; 20(10):1097-101. PubMed ID: 1407346
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  • 4. Neuroimaging of Dandy-Walker malformation: new concepts.
    Correa GG, Amaral LF, Vedolin LM.
    Top Magn Reson Imaging; 2011 Dec; 22(6):303-12. PubMed ID: 24132069
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  • 5. Joubert syndrome: a clinico-radiological study.
    Kendall B, Kingsley D, Lambert SR, Taylor D, Finn P.
    Neuroradiology; 1990 Dec; 31(6):502-6. PubMed ID: 2352633
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  • 7. Holoprosencephaly with cerebellar vermis hypoplasia in 13q deletion syndrome: Critical region for cerebellar dysgenesis within 13q32.2q34.
    Mimaki M, Shiihara T, Watanabe M, Hirakata K, Sakazume S, Ishiguro A, Shimojima K, Yamamoto T, Oka A, Mizuguchi M.
    Brain Dev; 2015 Aug; 37(7):714-8. PubMed ID: 25454392
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  • 8. Cerebellar vermis hypoplasia in a case of cri-du-chat syndrome.
    De Michele G, Presta M, Di Salle F, Serra L, Mazzaccara A, Della Rocca G, Ambrosio G, Filla A.
    Acta Neurol (Napoli); 1993 Apr; 15(2):92-6. PubMed ID: 8328329
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  • 9. Hypoplasia of the cerebellar vermis and corpus callosum in thrombocytopenia with absent radius syndrome on MRI studies.
    MacDonald MR, Schaefer GB, Olney AH, Patton DF.
    Am J Med Genet; 1994 Mar 01; 50(1):46-50. PubMed ID: 7512789
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  • 11. [Dandy-Walker complex with multiple anomalies: report of one case].
    Young HS, Liu YJ, Lee BF, Chen W, Wu KW, Tsang KT.
    Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1991 Mar 01; 32(2):128-33. PubMed ID: 2063687
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  • 14. Cerebellar cortical dysplasia: MR findings in a complex entity.
    Soto-Ares G, Delmaire C, Deries B, Vallee L, Pruvo JP.
    AJNR Am J Neuroradiol; 2000 Sep 01; 21(8):1511-9. PubMed ID: 11003288
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  • 15. Prenatal unilateral cerebellar hypoplasia in a series of 26 cases: significance and implications for prenatal diagnosis.
    Massoud M, Cagneaux M, Garel C, Varene N, Moutard ML, Billette T, Benezit A, Rougeot C, Jouannic JM, Massardier J, Gaucherand P, Desportes V, Guibaud L.
    Ultrasound Obstet Gynecol; 2014 Oct 01; 44(4):447-54. PubMed ID: 24185815
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  • 17. Isolated Unilateral Cerebellar Hemispheric Dysplasia: A Rare Entity.
    Chatur C, Balani A, Vadapalli R, Murthy MG.
    Can J Neurol Sci; 2019 Nov 01; 46(6):760-761. PubMed ID: 31352912
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  • 18. Ritscher-Schinzel (3C) syndrome: documentation of the phenotype.
    Kosaki K, Curry CJ, Roeder E, Jones KL.
    Am J Med Genet; 1997 Feb 11; 68(4):421-7. PubMed ID: 9021015
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  • 19. Intellectual prognosis of the Dandy-Walker malformation in children: the importance of vermian lobulation.
    Boddaert N, Klein O, Ferguson N, Sonigo P, Parisot D, Hertz-Pannier L, Baraton J, Emond S, Simon I, Chigot V, Schmit P, Pierre-Kahn A, Brunelle F.
    Neuroradiology; 2003 May 11; 45(5):320-4. PubMed ID: 12682795
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  • 20. Lissencephaly with brainstem and cerebellar hypoplasia and congenital cataracts.
    Abumansour IS, Wrogemann J, Chudley AE, Chodirker BN, Salman MS.
    J Child Neurol; 2014 Jun 11; 29(6):860-4. PubMed ID: 23625088
    [Abstract] [Full Text] [Related]

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