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Journal Abstract Search

146 related items for PubMed ID: 10667295

  • 21. [A patient of Walker-Warburg syndrome with a haplotype different from that in Fukuyama-type congenital muscular dystrophy].
    Sasaki M, Kondo E, Yamashita Y, Toda T, Nonaka I.
    No To Hattatsu; 1999 Sep; 31(5):445-51. PubMed ID: 10487070
    [Abstract] [Full Text] [Related]

  • 22. Walker-Warburg syndrome.
    Rhodes RE, Hatten HP, Ellington KS.
    AJNR Am J Neuroradiol; 1992 Sep; 13(1):123-6. PubMed ID: 1595429
    [Abstract] [Full Text] [Related]

  • 23. Congenital muscular dystrophy with cerebral and ocular malformations (cerebro-oculo-muscular syndrome).
    Heyer R, Ehrich J, Goebel HH, Christen HJ, Hanefeld F.
    Brain Dev; 1986 Sep; 8(6):614-9. PubMed ID: 3103478
    [Abstract] [Full Text] [Related]

  • 24. Three siblings with Walker-Warburg Syndrome.
    Bornemann A, Pfeiffer R, Beinder E, Wenkel H, Schlicker U, Meyermann R, Kirchner T.
    Gen Diagn Pathol; 1996 May; 141(5-6):371-5. PubMed ID: 8780938
    [Abstract] [Full Text] [Related]

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

  • 26. Congenital muscular dystrophy: a review of the literature.
    Leyten QH, Gabreëls FJ, Renier WO, ter Laak HJ.
    Clin Neurol Neurosurg; 1996 Nov; 98(4):267-80. PubMed ID: 8930416
    [Abstract] [Full Text] [Related]

  • 27. Clinical spectrum and genetic studies of Fukuyama congenital muscular dystrophy.
    Yoshioka M, Kuroki S.
    Am J Med Genet; 1994 Nov 15; 53(3):245-50. PubMed ID: 7856660
    [Abstract] [Full Text] [Related]

  • 28. Genetic identity of Fukuyama-type congenital muscular dystrophy and Walker-Warburg syndrome.
    Toda T, Yoshioka M, Nakahori Y, Kanazawa I, Nakamura Y, Nakagome Y.
    Ann Neurol; 1995 Jan 15; 37(1):99-101. PubMed ID: 7818265
    [Abstract] [Full Text] [Related]

  • 29. Preserved merosin M-chain (or laminin-alpha 2) expression in skeletal muscle distinguishes Walker-Warburg syndrome from Fukuyama muscular dystrophy and merosin-deficient congenital muscular dystrophy.
    Voit T, Sewry CA, Meyer K, Hermann R, Straub V, Muntoni F, Kahn T, Unsöld R, Helliwell TR, Appleton R.
    Neuropediatrics; 1995 Jun 15; 26(3):148-55. PubMed ID: 7477753
    [Abstract] [Full Text] [Related]

  • 30. The prenatal diagnosis of the Walker-Warburg syndrome.
    Crowe C, Jassani M, Dickerman L.
    Prenat Diagn; 1986 Jun 15; 6(3):177-85. PubMed ID: 3523475
    [Abstract] [Full Text] [Related]

  • 31. Cobblestone lissencephaly with normal eyes and muscle.
    Dobyns WB, Patton MA, Stratton RF, Mastrobattista JM, Blanton SH, Northrup H.
    Neuropediatrics; 1996 Apr 15; 27(2):70-5. PubMed ID: 8737821
    [Abstract] [Full Text] [Related]

  • 32. A case study on Walker-Warburg syndrome.
    Kerr SL.
    Adv Neonatal Care; 2010 Feb 15; 10(1):21-4. PubMed ID: 20150777
    [Abstract] [Full Text] [Related]

  • 33. 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 15; 37(1):87-91. PubMed ID: 2240049
    [Abstract] [Full Text] [Related]

  • 34. [Congenital muscular dystrophy: report on 10 cases].
    Olivé M, Roig M, Bonaventura I, Navarro C.
    Neurologia; 1994 Nov 15; 9(9):387-92. PubMed ID: 7811489
    [Abstract] [Full Text] [Related]

  • 35. Difficulties with prenatal diagnosis of the Walker-Warburg syndrome.
    Low AS, Lee SL, Tan AS, Chan DK, Chan LL.
    Acta Radiol; 2005 Oct 15; 46(6):645-51. PubMed ID: 16334849
    [Abstract] [Full Text] [Related]

  • 36. Optical Coherence Tomography in an Infant with Walker-Warburg Syndrome.
    Mano N, Mitsutsuji T, Yoshikawa Y, Miyamoto M, Watanabe H, Shimizu K, Miki M, Mimura M, Ueki M, Ikeda T.
    Case Rep Ophthalmol; 2015 Oct 15; 6(2):210-5. PubMed ID: 26265907
    [Abstract] [Full Text] [Related]

  • 37. Analysis of genotype-phenotype correlation in Walker-Warburg syndrome with a novel CRPPA mutation in different clinical manifestations.
    Bayram N, Bayram AK, Per H, Gümüş H, Ozsaygili C, Doğan MS, Çağlayan AO.
    Eur J Ophthalmol; 2022 Sep 15; 32(5):NP71-NP76. PubMed ID: 33977792
    [Abstract] [Full Text] [Related]

  • 38. Lethal congenital muscular dystrophy in two sibs with arthrogryposis multiplex: new entity or variant of cobblestone lissencephaly syndrome?
    Seidahmed MZ, Sunada Y, Ozo CO, Hamid F, Campbell KP, Salih MA.
    Neuropediatrics; 1996 Dec 15; 27(6):305-10. PubMed ID: 9050048
    [Abstract] [Full Text] [Related]

  • 39. Fukuyama-type congenital muscular dystrophy and the Walker-Warburg syndrome. Commentary to Kimura's paper (pp. 182-91).
    Takada K.
    Brain Dev; 1993 Dec 15; 15(3):244-5. PubMed ID: 8214355
    [No Abstract] [Full Text] [Related]

  • 40. Cerebro-ocular dysplasia and muscular dystrophy: report of two cases.
    Federico A, Dotti MT, Malandrini A, Guazzi GC, Hayek G, Simonati A, Rizzuto N, Toti P.
    Neuropediatrics; 1988 May 15; 19(2):109-12. PubMed ID: 3374764
    [Abstract] [Full Text] [Related]

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