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159 related items for PubMed ID: 1491747

  • 1. Acrocallosal syndrome: association with cystic malformation of the brain and neurodevelopmental aspects.
    Thyen U, Aksu F, Bartsch O, Herb E.
    Neuropediatrics; 1992 Dec; 23(6):292-6. PubMed ID: 1491747
    [Abstract] [Full Text] [Related]

  • 2. Greig cephalopolysyndactyly syndrome with dysgenesis of the corpus callosum in a Bedouin family.
    Marafie MJ, Temtamy SA, Rajaram U, al-Awadi SA, el-Badramany MH, Farag TI.
    Am J Med Genet; 1996 Dec 18; 66(3):261-4. PubMed ID: 8985483
    [Abstract] [Full Text] [Related]

  • 3. Acrocallosal syndrome: additional manifestations.
    Casamassima AC, Beneck D, Gewitz MH, Horowitz MA, Woolf PK, Pettersen IM, Shapiro LR.
    Am J Med Genet; 1989 Mar 18; 32(3):311-7. PubMed ID: 2658584
    [Abstract] [Full Text] [Related]

  • 4. Agenesis of the corpus callosum and Dandy-Walker malformation associated with hemimegalencephaly in the sebaceous nevus syndrome.
    Dodge NN, Dobyns WB.
    Am J Med Genet; 1995 Mar 27; 56(2):147-50. PubMed ID: 7625436
    [Abstract] [Full Text] [Related]

  • 5. Seckel syndrome with asymptomatic tonsillar herniation and congenital mirror movements.
    Thapa R, Mukherjee K.
    J Child Neurol; 2010 Feb 27; 25(2):231-3. PubMed ID: 19372093
    [Abstract] [Full Text] [Related]

  • 6. Hypogenitalism in the acrocallosal syndrome.
    Temtamy SA, Meguid NA.
    Am J Med Genet; 1989 Mar 27; 32(3):301-5. PubMed ID: 2658583
    [Abstract] [Full Text] [Related]

  • 7. An additional manifestation in acrocallosal syndrome: temporal lobe hypoplasia.
    Aykut A, Cogulu O, Ekmekci AY, Ozkinay F.
    Genet Couns; 2008 Mar 27; 19(2):237-40. PubMed ID: 18618999
    [Abstract] [Full Text] [Related]

  • 8. Acrocallosal syndrome in a girl born to consanguineous parents.
    Salgado LJ, Ali CA, Castilla EE.
    Am J Med Genet; 1989 Mar 27; 32(3):298-300. PubMed ID: 2729348
    [Abstract] [Full Text] [Related]

  • 9. Possible new autosomal recessive syndrome of partial agenesis of the corpus callosum, pontine hypoplasia, focal white matter changes, hypotonia, mental retardation, and minor anomalies.
    Jonas RE, Kimonis VE, Morales A.
    Am J Med Genet; 1997 Dec 12; 73(2):184-8. PubMed ID: 9409870
    [Abstract] [Full Text] [Related]

  • 10. [Agenesis of the corpus callosum].
    Nielsen LH.
    Ugeskr Laeger; 1995 Feb 06; 157(6):737-9. PubMed ID: 7701633
    [Abstract] [Full Text] [Related]

  • 11. [Familial agenesis of the corpus callosum: a new form].
    Castro-Gago M, Rodriguez-Nuñez A, Eiris J, Peña J, Tojo R, Novo-Rodriguez I.
    Arch Fr Pediatr; 1993 Apr 06; 50(4):327-30. PubMed ID: 8379821
    [Abstract] [Full Text] [Related]

  • 12. Common congenital brain anomalies.
    Byrd SE, Naidich TP.
    Radiol Clin North Am; 1988 Jul 06; 26(4):755-72. PubMed ID: 3289074
    [Abstract] [Full Text] [Related]

  • 13. Acrocallosal syndrome in fetus: focus on additional brain abnormalities.
    Fernandez C, Soulier M, Coulibaly B, Liprandi A, Benoit B, Giuliano F, Sigaudy S, Figarella-Branger D, Fallet-Bianco C.
    Acta Neuropathol; 2008 Jan 06; 115(1):151-6. PubMed ID: 17593378
    [Abstract] [Full Text] [Related]

  • 14. Fryns syndrome survivors and neurologic outcome.
    Van Hove JL, Spiridigliozzi GA, Heinz R, McConkie-Rosell A, Iafolla AK, Kahler SG.
    Am J Med Genet; 1995 Nov 20; 59(3):334-40. PubMed ID: 8599357
    [Abstract] [Full Text] [Related]

  • 15. Acrocallosal syndrome: new findings.
    Moeschler JB, Pober BR, Holmes LB, Graham JM.
    Am J Med Genet; 1989 Mar 20; 32(3):306-10. PubMed ID: 2729349
    [Abstract] [Full Text] [Related]

  • 16. Acrocallosal syndrome in a child with de novo inverted tandem duplication of 12p11.2-p13.3.
    Pfeiffer RA, Legat G, Trautmann U.
    Ann Genet; 1992 Mar 20; 35(1):41-6. PubMed ID: 1610119
    [Abstract] [Full Text] [Related]

  • 17. Corpus callosum agenesis, facial anomalies, Robin sequence, and other anomalies: a new autosomal recessive syndrome?
    Toriello HV, Carey JC.
    Am J Med Genet; 1988 Sep 20; 31(1):17-23. PubMed ID: 3223497
    [Abstract] [Full Text] [Related]

  • 18. 6q terminal deletion syndrome associated with a distinctive EEG and clinical pattern: a report of five cases.
    Elia M, Striano P, Fichera M, Gaggero R, Castiglia L, Galesi O, Malacarne M, Pierluigi M, Amato C, Musumeci SA, Romano C, Majore S, Grammatico P, Zara F, Striano S, Faravelli F.
    Epilepsia; 2006 May 20; 47(5):830-8. PubMed ID: 16686647
    [Abstract] [Full Text] [Related]

  • 19. Peters'-Plus syndrome with agenesis of the corpus callosum: report of a case and confirmation of autosomal recessive inheritance.
    Camera G, Centa A, Pozzolo S, Camera A.
    Clin Dysmorphol; 1993 Oct 20; 2(4):317-21. PubMed ID: 8305962
    [Abstract] [Full Text] [Related]

  • 20. Spectrum of the acrocallosal syndrome.
    Koenig R, Bach A, Woelki U, Grzeschik KH, Fuchs S.
    Am J Med Genet; 2002 Feb 15; 108(1):7-11. PubMed ID: 11857542
    [Abstract] [Full Text] [Related]

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