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Journal Abstract Search

342 related items for PubMed ID: 18798594

  • 1. Galloway-Mowat syndrome.
    Akhtar N, Kiran S, Hafeez F.
    J Coll Physicians Surg Pak; 2008 Aug; 18(8):520-1. PubMed ID: 18798594
    [Abstract] [Full Text] [Related]

  • 2. Perinatal imaging findings of Galloway-Mowat syndrome.
    Chen CP, Lin SP, Tsai JD, Huang JK, Yen JL, Tseng CC, Wang W.
    Genet Couns; 2007 Aug; 18(3):353-5. PubMed ID: 18019379
    [No Abstract] [Full Text] [Related]

  • 3. Collapsing glomerulopathy in Galloway-Mowat syndrome: a case report and review of the literature.
    Sartelet H, Pietrement C, Noel LH, Sabouraud P, Birembaut P, Oligny LL, Roussel B, Doco-Fenzy M.
    Pathol Res Pract; 2008 Aug; 204(6):401-6. PubMed ID: 18276083
    [Abstract] [Full Text] [Related]

  • 4. Galloway-Mowat syndrome of abnormal gyral patterns and glomerulopathy.
    Cooperstone BG, Friedman A, Kaplan BS.
    Am J Med Genet; 1993 Aug 15; 47(2):250-4. PubMed ID: 8213914
    [Abstract] [Full Text] [Related]

  • 5. Galloway-mowat syndrome - unusual form of nephrotic syndrome in adolescent.
    Naidu GD, Deepthi P, RajaKarthik K, Sriram S, Swarnalatha G, Gangadhar T.
    Saudi J Kidney Dis Transpl; 2017 Aug 15; 28(5):1188-1191. PubMed ID: 28937085
    [Abstract] [Full Text] [Related]

  • 6. Recurrent Galloway Mowat syndrome associated with abnormal prenatal sonographic findings.
    Chen CP, Lin SP, Chang TY, Tsai JD, Huang JK, Wang W.
    Genet Couns; 2006 Aug 15; 17(1):87-9. PubMed ID: 16719284
    [No Abstract] [Full Text] [Related]

  • 7. Late-onset nephrotic syndrome and severe cerebellar atrophy in Galloway-Mowat syndrome.
    Steiss JO, Gross S, Neubauer BA, Hahn A.
    Neuropediatrics; 2005 Oct 15; 36(5):332-5. PubMed ID: 16217710
    [Abstract] [Full Text] [Related]

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  • 9. [Genetic-morphologic fatal syndromes. Cerebro-oculo-facioskeletal syndrome (Pena-Shokeir syndrome II)].
    Henkel KE, Pfeiffer RA, Stöss H.
    Pathologe; 1993 Jul 15; 14(4):219-20. PubMed ID: 8367388
    [No Abstract] [Full Text] [Related]

  • 10. Nephrotic syndrome, microcephaly, and developmental delay: three separate syndromes.
    Meyers KE, Kaplan P, Kaplan BS.
    Am J Med Genet; 1999 Jan 29; 82(3):257-60. PubMed ID: 10215551
    [Abstract] [Full Text] [Related]

  • 11. Galloway-Mowat syndrome: neurologic features in two sibling pairs.
    Ekstrand JJ, Friedman AL, Stafstrom CE.
    Pediatr Neurol; 2012 Aug 29; 47(2):129-32. PubMed ID: 22759691
    [Abstract] [Full Text] [Related]

  • 12. The Dubowitz syndrome.
    Wilroy RS, Tipton RE, Summitt RL.
    Am J Med Genet; 1978 Aug 29; 2(3):275-84. PubMed ID: 263660
    [Abstract] [Full Text] [Related]

  • 13. Late-onset growth restriction in Galloway-Mowat syndrome: a case report.
    Kang L, Kuo PL, Lee KH, Liu YC, Chang CH, Chang FM, Lin SJ.
    Prenat Diagn; 2005 Feb 29; 25(2):159-62. PubMed ID: 15712336
    [Abstract] [Full Text] [Related]

  • 14. Galloway-Mowat syndrome in Taiwan: OSGEP mutation and unique clinical phenotype.
    Lin PY, Tseng MH, Zenker M, Rao J, Hildebrandt F, Lin SH, Lin CC, Chang JH, Hsu CH, Lee MD, Lin SP, Tsai JD.
    Orphanet J Rare Dis; 2018 Dec 17; 13(1):226. PubMed ID: 30558655
    [Abstract] [Full Text] [Related]

  • 15. Recurrence of Galloway Mowat syndrome and associated prenatal imaging findings.
    Horton AL, Smith JK, Strauss RA.
    Prenat Diagn; 2009 Mar 17; 29(3):280-2. PubMed ID: 19177459
    [No Abstract] [Full Text] [Related]

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  • 17. Prenatal and postnatal growth retardation, microcephaly, developmental delay, and pigmentation abnormalities: Naegeli syndrome, dyskeratosis congenita, poikiloderma Clericuzio type, or separate entity?
    Belligni EF, Dokal I, Hennekam RC.
    Eur J Med Genet; 2011 Mar 17; 54(3):231-5. PubMed ID: 21252004
    [Abstract] [Full Text] [Related]

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  • 19. Late-onset nephrotic syndrome in galloway-mowat syndrome: a case report.
    Hazza I, Najada AH.
    Saudi J Kidney Dis Transpl; 1999 Mar 17; 10(2):171-4. PubMed ID: 18212429
    [Abstract] [Full Text] [Related]

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