These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

129 related items for PubMed ID: 2282812

  • 1. Hereditary progressive nephropathy with sensorineural deafness. Report on four kindreds.
    Ferrari L, Bonforte G, Brambilla P, Cairo G.
    Contrib Nephrol; 1990; 80():135-9. PubMed ID: 2282812
    [No Abstract] [Full Text] [Related]

  • 2. Three new kindreds affected with Alport's syndrome.
    Barbera G, Costanzi S, Sturniolo A, Passalacqua S, Splendiani G, Sangiorgi M, Attanasio A, Capria A, Federico F.
    Contrib Nephrol; 1990; 80():143-6. PubMed ID: 2282814
    [No Abstract] [Full Text] [Related]

  • 3. Heterogeneity of hereditary nephritis.
    Pecoraro C, Carbonaro L, Saravo MT, Manese M, Borgia G, Usberti M.
    Contrib Nephrol; 1990; 80():107-12. PubMed ID: 2282807
    [No Abstract] [Full Text] [Related]

  • 4. Chronic hereditary nephritis with nerve deafness. A Nebraska kindred.
    Patton RB.
    Ann Otol Rhinol Laryngol; 1970 Feb; 79(1):194-202. PubMed ID: 5415602
    [No Abstract] [Full Text] [Related]

  • 5. The inheritance of Alport's and related syndromes.
    Flinter FA, Bobrow M, Chantler C, Cameron JS.
    Nephrol Dial Transplant; 1990 Feb; 5(10):900. PubMed ID: 2128388
    [No Abstract] [Full Text] [Related]

  • 6. Renal prognosis in Alport's and related syndromes: influence of the mode of inheritance.
    Pochet JM, Bobrie G, Landais P, Goldfarb B, Grünfeld JP.
    Nephrol Dial Transplant; 1989 Feb; 4(12):1016-21. PubMed ID: 2517321
    [Abstract] [Full Text] [Related]

  • 7. [Chronic hereditary nephropathy with deafness and ocular lesions].
    Hauser J.
    Schweiz Med Wochenschr; 1974 May 18; 104(20):724-8. PubMed ID: 4829630
    [No Abstract] [Full Text] [Related]

  • 8. [Alport's syndrome: hereditary nephropathy with hematuria and deafness].
    Giger C, Guignard JP, Pelet B, Campiche M, Krstic R.
    Rev Med Suisse Romande; 1988 Apr 18; 108(4):349-55. PubMed ID: 3387770
    [No Abstract] [Full Text] [Related]

  • 9. Autosomal dominant progressive nephropathy with deafness: linkage to a new locus on chromosome 11q24.
    Prakash S, Chung KW, Sinha S, Barmada M, Ellis D, Ferrell RE, Finegold DN, Randhawa PS, Dinda A, Vats A.
    J Am Soc Nephrol; 2003 Jul 18; 14(7):1794-803. PubMed ID: 12819239
    [Abstract] [Full Text] [Related]

  • 10. Hereditary nephritis (Alport's syndrome)--clinical profile and inheritance in 28 kindreds.
    Chugh KS, Sakhuja V, Agarwal A, Jha V, Joshi K, Datta BN, Gupta A, Gupta KL.
    Nephrol Dial Transplant; 1993 Jul 18; 8(8):690-5. PubMed ID: 8414153
    [Abstract] [Full Text] [Related]

  • 11. Hereditary nephritis. Clinical spectrum and mode of inheritance in five new kindreds.
    Chazan JA, Zacks J, Cohen JJ, Garella S.
    Am J Med; 1971 Jun 18; 50(6):764-71. PubMed ID: 5089851
    [No Abstract] [Full Text] [Related]

  • 12. Autosomal dominant nephritis with renal failure of non-Alport type: clinical and molecular studies.
    Ilan T, Shohat T, Tobar A, Magal N, Yahav M, Halpern GJ, Rechavi G, Shohat M.
    Isr Med Assoc J; 2001 Jul 18; 3(7):488-91. PubMed ID: 11791413
    [Abstract] [Full Text] [Related]

  • 13. Hereditary macrothrombocytopenia, deafness, nephropathy.
    Catarini M.
    Haematologica; 1988 Jul 18; 73(1):43-7. PubMed ID: 3131204
    [No Abstract] [Full Text] [Related]

  • 14. Hereditary nephropathy without deafness.
    Dockhorn RJ.
    Am J Dis Child; 1967 Aug 18; 114(2):135-8. PubMed ID: 4951535
    [No Abstract] [Full Text] [Related]

  • 15. Autosomal dominant polycystic kidney disease associated with familial sensorineural deafness.
    Mora C, Navarro JF, García J, Gallego E, Macía M, Méndez ML, Chahin J, Rivero A.
    Scand J Urol Nephrol; 1999 Feb 18; 33(1):63-5. PubMed ID: 10100367
    [Abstract] [Full Text] [Related]

  • 16. Alport syndrome. Molecular genetic aspects.
    Hertz JM.
    Dan Med Bull; 2009 Aug 18; 56(3):105-52. PubMed ID: 19728970
    [Abstract] [Full Text] [Related]

  • 17. Familial IgA nephropathy associated with bilateral sensorineural deafness.
    Chahin J, Ortiz A, Mendez L, Gallego E, Garcia-Perez J, Garcia-Castro G, Julian BA, Egido J.
    Am J Kidney Dis; 1992 Jun 18; 19(6):592-6. PubMed ID: 1595709
    [Abstract] [Full Text] [Related]

  • 18. Linkage studies in X-linked Alport's syndrome.
    Szpiro-Tapia S, Bobrie G, Guilloud-Bataille M, Heuertz S, Julier C, Frézal J, Grünfeld JP, Hors-Cayla MC.
    Hum Genet; 1988 Dec 18; 81(1):85-7. PubMed ID: 2904407
    [Abstract] [Full Text] [Related]

  • 19. Familial hereditary nephropathy (Alport's syndrome).
    Purriel P, Drets M, Pascale E, Sánchez Cestau R, Borrás A, Ferreira WA, de Lucca A, Fernández L.
    Am J Med; 1970 Dec 18; 49(6):753-73. PubMed ID: 5006614
    [No Abstract] [Full Text] [Related]

  • 20. [Hereditary nephritis with deafness in one family].
    Golev GD.
    Klin Med (Mosk); 1989 Nov 18; 67(11):128-30. PubMed ID: 2625948
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 7.