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Journal Abstract Search

153 related items for PubMed ID: 6426737

  • 21. Alport syndrome. Molecular genetic aspects.
    Hertz JM.
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
    [Abstract] [Full Text] [Related]

  • 22. [Hereditary nephropathy in children].
    Mongeau JG.
    Union Med Can; 1967 Nov; 96(11):1394-401. PubMed ID: 5604030
    [No Abstract] [Full Text] [Related]

  • 23. [Alport's syndrome and associated congenital malformations of the kidney and ear].
    Bérard F, Morand R.
    Ann Otolaryngol Chir Cervicofac; 1967 Nov; 84(7):555-60. PubMed ID: 6073014
    [No Abstract] [Full Text] [Related]

  • 24. [Pedigree analysis of two families with Alport's syndrome].
    Wässer S, Theile H, Schöne D, Lemme B.
    Padiatr Grenzgeb; 1980 Nov; 19(3):167-71. PubMed ID: 7454376
    [No Abstract] [Full Text] [Related]

  • 25. [Familial hereditary nephritis].
    Urbańczyk J.
    Wiad Lek; 1969 Oct; 22(20):1881-4. PubMed ID: 5368500
    [No Abstract] [Full Text] [Related]

  • 26. [Muckle-Wells' syndrome. Study of a family].
    Marcen Letosa R, Fernández-Alonso J, Quereda Rodriguez-Navarro C, Periera Palomo P, Rodríguez Algarra G, Castilla Jiménez J, Montes Delgado R, Mendoza Llera M.
    Rev Clin Esp; 1978 Apr 15; 149(1):93-6. PubMed ID: 674761
    [No Abstract] [Full Text] [Related]

  • 27. Hereditary nephropathy without deafness.
    Dockhorn RJ.
    Am J Dis Child; 1967 Aug 15; 114(2):135-8. PubMed ID: 4951535
    [No Abstract] [Full Text] [Related]

  • 28. [Congenital and hereditary hearing disorders in population of the Nakhichevan Autonomous Republic].
    Panakhiian VM.
    Vestn Otorinolaringol; 2004 Aug 15; (6):22-4. PubMed ID: 15699983
    [Abstract] [Full Text] [Related]

  • 29. Hereditary nephritis: clinical evaluation of a pediatric series.
    Piaggio G, Degl'Innocenti ML, Perfumo F, Gusmano R.
    Contrib Nephrol; 1990 Aug 15; 80():157-61. PubMed ID: 2282816
    [No Abstract] [Full Text] [Related]

  • 30. Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA mutation in 16 Chinese families: implication for early detection and prevention of deafness.
    Dai P, Liu X, Han D, Qian Y, Huang D, Yuan H, Li W, Yu F, Zhang R, Lin H, He Y, Yu Y, Sun Q, Qin H, Li R, Zhang X, Kang D, Cao J, Young WY, Guan MX.
    Biochem Biophys Res Commun; 2006 Feb 03; 340(1):194-9. PubMed ID: 16375862
    [Abstract] [Full Text] [Related]

  • 31. [Hereditary deafness (a review)].
    Brunecký Z.
    Cesk Otolaryngol; 1979 Oct 03; 28(5):304-7. PubMed ID: 389463
    [No Abstract] [Full Text] [Related]

  • 32. Sensorineural deafness in the FG syndrome: report on four new cases.
    Neri G, Blumberg B, Miles PV, Opitz JM.
    Am J Med Genet; 1984 Oct 03; 19(2):369-77. PubMed ID: 6542310
    [Abstract] [Full Text] [Related]

  • 33. [Renal lesions in Alpert's syndrome].
    Bettez P, Babai F.
    Ann Anat Pathol (Paris); 1968 Oct 03; 13(3):277-88. PubMed ID: 5727102
    [No Abstract] [Full Text] [Related]

  • 34. Waardenburg syndrome type II: phenotypic findings and diagnostic criteria.
    Liu XZ, Newton VE, Read AP.
    Am J Med Genet; 1995 Jan 02; 55(1):95-100. PubMed ID: 7702105
    [Abstract] [Full Text] [Related]

  • 35. [Chronic hereditary nephropathy with deafness and eye involvment].
    Hauser J.
    Schweiz Med Wochenschr; 1974 May 25; 104(21):767-72. PubMed ID: 4829025
    [No Abstract] [Full Text] [Related]

  • 36. [Hereditary progressive nephritis with report of 11 families and data of renal biopsy in 2 patients].
    Chen YP.
    Zhonghua Nei Ke Za Zhi; 1982 Oct 25; 21(10):587-91. PubMed ID: 7151546
    [No Abstract] [Full Text] [Related]

  • 37. [Alport's syndrome].
    Huberman ED, Szylman P, Pequenera JC, Cooperberg L, Schuseim I.
    Arch Fund Roux Ocefa; 1967 Oct 25; 1(2):173-8. PubMed ID: 6073019
    [No Abstract] [Full Text] [Related]

  • 38. Hereditary nephritis, deafness and thrombocytopenia. Case report and review.
    Thomas HS, Bauer JH.
    Mo Med; 1984 Jun 25; 81(6):305-7, 311. PubMed ID: 6377037
    [No Abstract] [Full Text] [Related]

  • 39. Association of familial nephritis without deafness and multiple sclerosis.
    Czeizel AE, Uri-Szabó K.
    Clin Nephrol; 1994 Oct 25; 42(4):277-8. PubMed ID: 7834925
    [No Abstract] [Full Text] [Related]

  • 40. Hereditary glomerulonephritis of non-Alport type.
    Doherty CC, Middleton DT, Hill CM.
    Proc Eur Dial Transplant Assoc; 1983 Oct 25; 19():575-81. PubMed ID: 6878256
    [Abstract] [Full Text] [Related]

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