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374 related items for PubMed ID: 17593378

  • 1. 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; 115(1):151-6. PubMed ID: 17593378
    [Abstract] [Full Text] [Related]

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

  • 3. [The acrocallosal syndrome. Report of an additional case].
    Wendisch J, Lorenz P, Kabus M, Rupprecht E, Walther S.
    Kinderarztl Prax; 1990 Jun; 58(6):315-21. PubMed ID: 2166860
    [Abstract] [Full Text] [Related]

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

  • 5. 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]

  • 6. 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]

  • 7. Hallux duplication, postaxial polydactyly, absence of the corpus callosum, severe mental retardation, and additional anomalies in two unrelated patients: a new syndrome.
    Schinzel A, Schmid W.
    Am J Med Genet; 1980 Dec 12; 6(3):241-9. PubMed ID: 7424976
    [Abstract] [Full Text] [Related]

  • 8. Rhombencephalosynapsis and related anomalies: a neuropathological study of 40 fetal cases.
    Pasquier L, Marcorelles P, Loget P, Pelluard F, Carles D, Perez MJ, Bendavid C, de La Rochebrochard C, Ferry M, David V, Odent S, Laquerrière A.
    Acta Neuropathol; 2009 Feb 12; 117(2):185-200. PubMed ID: 19057916
    [Abstract] [Full Text] [Related]

  • 9. A case of Joubert's syndrome with extensive cerebral malformations.
    ten Donkelaar HJ, Hoevenaars F, Wesseling P.
    Clin Neuropathol; 2000 Feb 12; 19(2):85-93. PubMed ID: 10749289
    [Abstract] [Full Text] [Related]

  • 10. Acrocallosal syndrome: association with cystic malformation of the brain and neurodevelopmental aspects.
    Thyen U, Aksu F, Bartsch O, Herb E.
    Neuropediatrics; 1992 Dec 12; 23(6):292-6. PubMed ID: 1491747
    [Abstract] [Full Text] [Related]

  • 11. Acrocallosal syndrome: additional manifestations.
    Casamassima AC, Beneck D, Gewitz MH, Horowitz MA, Woolf PK, Pettersen IM, Shapiro LR.
    Am J Med Genet; 1989 Mar 12; 32(3):311-7. PubMed ID: 2658584
    [Abstract] [Full Text] [Related]

  • 12. Acro-cardio-facial syndrome associated with neuroepithelial cyst: a case report.
    Sivasli O, Ozer EA, Ozer A, Aydinlioglu H, Helvaci M.
    Genet Couns; 2007 Mar 12; 18(2):247-50. PubMed ID: 17710878
    [Abstract] [Full Text] [Related]

  • 13. A and B preaxial polydactyly with syndactyly of feet and hands in the same person--a case report.
    Gawlikowska-Sroka A, Tudaj W, Czerwiński F.
    Adv Med Sci; 2009 Mar 12; 54(2):305-7. PubMed ID: 20053619
    [Abstract] [Full Text] [Related]

  • 14. Postaxial polydactyly, hallux duplication, absence of the corpus callosum, macrencephaly and severe mental retardation: a new syndrome?
    Schinzel A.
    Helv Paediatr Acta; 1979 May 12; 34(2):141-6. PubMed ID: 457430
    [Abstract] [Full Text] [Related]

  • 15. Acrocallosal syndrome in a girl born to consanguineous parents.
    Salgado LJ, Ali CA, Castilla EE.
    Am J Med Genet; 1989 Mar 12; 32(3):298-300. PubMed ID: 2729348
    [Abstract] [Full Text] [Related]

  • 16. A new case of megalencephaly and perisylvian polymicrogyria with post-axial polydactyly and hydrocephalus: MPPH syndrome.
    Colombani M, Chouchane M, Pitelet G, Morales L, Callier P, Pinard JP, Lion-François L, Thauvin-Robinet C, Mugneret F, Huet F, Guibaud L, Faivre L.
    Eur J Med Genet; 2006 Mar 12; 49(6):466-71. PubMed ID: 16807158
    [Abstract] [Full Text] [Related]

  • 17. Megalencephaly, polymicrogyria, and hydrocephalus (MPPH) syndrome: a new case with syndactyly.
    Pisano T, Meloni M, Cianchetti C, Falchi M, Nucaro A, Pruna D.
    J Child Neurol; 2008 Aug 12; 23(8):916-8. PubMed ID: 18474936
    [Abstract] [Full Text] [Related]

  • 18. Filippi syndrome: report of three additional cases.
    Williams MS, Williams JL, Wargowski DS, Pauli RM, Pletcher BA.
    Am J Med Genet; 1999 Nov 19; 87(2):128-33. PubMed ID: 10533026
    [Abstract] [Full Text] [Related]

  • 19. [Renal hypoplasia, polydactyly, cardiopathy: a new syndrome?].
    Bonnet J, Cordier MP, Ollagnon E, Guillaud MH, Raudrant D, Robert JM, Charvet F.
    J Genet Hum; 1987 Aug 19; 35(4):279-89. PubMed ID: 3309184
    [Abstract] [Full Text] [Related]

  • 20. Neuropathological analysis of an asymptomatic adult case with Dandy-Walker variant.
    Notaridis G, Ebbing K, Giannakopoulos P, Bouras C, Kövari E.
    Neuropathol Appl Neurobiol; 2006 Jun 19; 32(3):344-50. PubMed ID: 16640653
    [Abstract] [Full Text] [Related]

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