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Journal Abstract Search

201 related items for PubMed ID: 803883

  • 1. A familial syndrome of central nervous system and ocular malformations.
    Chemke J, Czernobilsky B, Mundel G, Barishak YR.
    Clin Genet; 1975 Jan; 7(1):1-7. PubMed ID: 803883
    [Abstract] [Full Text] [Related]

  • 2. [Oculocerebral anomalies in Walker's lissencephaly].
    Robain O, Dhermy P, Dufier JL, Blanck MF, Dulac O, Bursztyn J.
    J Fr Ophtalmol; 1985 Jan; 8(1):59-72. PubMed ID: 3923093
    [Abstract] [Full Text] [Related]

  • 3. Multiple congenital malformations including severe eye anomalies and abnormal cerebellar development with Dandy-Walker malformation in a girl with partial trisomy 3q.
    de Azevedo Moreira LM, Neri FB, de Quadros Uzeda S, de Carvalho AF, Santana GC, Souza FR, Rollemberg JC.
    Ophthalmic Genet; 2005 Mar; 26(1):37-43. PubMed ID: 15823924
    [Abstract] [Full Text] [Related]

  • 4. Dandy-Walker(like) malformation, atrio-ventricular septal defect and a similar pattern of minor anomalies in 2 sisters: a new syndrome?
    Ritscher D, Schinzel A, Boltshauser E, Briner J, Arbenz U, Sigg P.
    Am J Med Genet; 1987 Feb; 26(2):481-91. PubMed ID: 3812597
    [Abstract] [Full Text] [Related]

  • 5. Report on a patient with congenital muscular dystrophy, hydrocephalus, Dandy-Walker malformation and leukodystrophy.
    Di Rocco M, Leveratto L, Cama A, Bado M, Tortori Donati P, Andreussi L, Borrone C.
    Genet Couns; 1993 Feb; 4(4):295-8. PubMed ID: 8110418
    [Abstract] [Full Text] [Related]

  • 6. Diagnostic criteria for Walker-Warburg syndrome.
    Dobyns WB, Pagon RA, Armstrong D, Curry CJ, Greenberg F, Grix A, Holmes LB, Laxova R, Michels VV, Robinow M.
    Am J Med Genet; 1989 Feb; 32(2):195-210. PubMed ID: 2494887
    [Abstract] [Full Text] [Related]

  • 7. Dandy-Walker syndrome in consecutive siblings: familial hindbrain malformation.
    Lehman RM.
    Neurosurgery; 1981 Jun; 8(6):717-9. PubMed ID: 7279160
    [No Abstract] [Full Text] [Related]

  • 8. Sagittal craniosynostosis, Dandy-Walker malformation, and hydrocephalus: a unique multiple malformation syndrome.
    Braddock SR, Jones KL, Superneau DW, Jones MC.
    Am J Med Genet; 1993 Oct 01; 47(5):640-3; discussion 644. PubMed ID: 8266990
    [Abstract] [Full Text] [Related]

  • 9. Autosomal recessive eye and brain anomalies: Warburg syndrome.
    Pagon RA, Clarren SK, Milam DF, Hendrickson AE.
    J Pediatr; 1983 Apr 01; 102(4):542-6. PubMed ID: 6403688
    [Abstract] [Full Text] [Related]

  • 10. Hydrocephalus, lissencephaly, ocular abnormalities and congenital muscular dystrophy. A Warburg syndrome variant?
    Pavone L, Gullotta F, Grasso S, Vannucchi C.
    Neuropediatrics; 1986 Nov 01; 17(4):206-11. PubMed ID: 3100980
    [Abstract] [Full Text] [Related]

  • 11. Walker-Warburg syndrome with microtia and absent auditory canals.
    Gershoni-Baruch R, Mandel H, Miller B, Sujov P, Braun J.
    Am J Med Genet; 1990 Sep 01; 37(1):87-91. PubMed ID: 2240049
    [Abstract] [Full Text] [Related]

  • 12. A new lethal chondrodysplasia with spondylocostal dysostosis, multiple internal anomalies and Dandy-Walker cyst.
    Moerman P, Vandenberghe K, Fryns JP, Haspeslagh M, Lauweryns JM.
    Clin Genet; 1985 Feb 01; 27(2):160-4. PubMed ID: 3884191
    [Abstract] [Full Text] [Related]

  • 13. Neuroimaging of Dandy-Walker malformation: new concepts.
    Correa GG, Amaral LF, Vedolin LM.
    Top Magn Reson Imaging; 2011 Dec 01; 22(6):303-12. PubMed ID: 24132069
    [Abstract] [Full Text] [Related]

  • 14. Prenatal diagnosis of trisomy 9 mosaic presenting as a case of Dandy-Walker malformation.
    Bureau YA, Fraser W, Fouquet B.
    Prenat Diagn; 1993 Feb 01; 13(2):79-85. PubMed ID: 8464839
    [Abstract] [Full Text] [Related]

  • 15. Walker-Warburg syndrome: report of three affected sibs.
    Rodgers BL, Vanner LV, Pai GS, Sens MA.
    Am J Med Genet; 1994 Jan 15; 49(2):198-201. PubMed ID: 8116667
    [Abstract] [Full Text] [Related]

  • 16. Ritscher-Schinzel cranio-cerebello-cardiac (3C) syndrome: report of four new cases and review.
    Leonardi ML, Pai GS, Wilkes B, Lebel RR.
    Am J Med Genet; 2001 Aug 15; 102(3):237-42. PubMed ID: 11484200
    [Abstract] [Full Text] [Related]

  • 17. Goldston syndrome: report of a case.
    Gulcan YH, Duman N, Kumral A, Sağol, Lebe B, Kavukçu S, Erçal D, Celiloğlu M, Ozkan H.
    Genet Couns; 2001 Aug 15; 12(3):263-7. PubMed ID: 11693790
    [Abstract] [Full Text] [Related]

  • 18. Ocular malformations and lissencephaly.
    Warburg M.
    Eur J Pediatr; 1987 Sep 15; 146(5):450-2. PubMed ID: 3119342
    [Abstract] [Full Text] [Related]

  • 19. Sibs with Ritscher-Schinzel (3C) syndrome and anal malformations.
    Orstavik KH, Bechensteen AG, Fugelseth D, Orderud W.
    Am J Med Genet; 1998 Jan 23; 75(3):300-3. PubMed ID: 9475602
    [Abstract] [Full Text] [Related]

  • 20. Dandy-Walker malformation in Ellis-van Creveld syndrome.
    Zangwill KM, Boal DK, Ladda RL.
    Am J Med Genet; 1988 Sep 23; 31(1):123-9. PubMed ID: 3223493
    [Abstract] [Full Text] [Related]

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