BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

358 related articles for article (PubMed ID: 11007700)

  • 1. Familial interstitial nephritis with progressive renal failure.
    Zhang H; Wada J; Nanba K; Kunitomi M; Hida K; Nagake Y; Shikata K; Makino H
    Am J Kidney Dis; 2000 Oct; 36(4):E25. PubMed ID: 11007700
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 3(7):488-91. PubMed ID: 11791413
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hereditary nephritis in the bull terrier: evidence for inheritance by an autosomal dominant gene.
    Hood JC; Robinson WF; Huxtable CR; Bradley JS; Sutherland RJ; Thomas MA
    Vet Rec; 1990 May; 126(18):456-9. PubMed ID: 2356601
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Hereditary nephritis associated with low-tone sensorineural hearing difficulty: a case report.
    Motoyama O; Ohshima M; Shigetomi Y; Ohara T; Nagai Y; Kawamura S; Iitaka K
    Nihon Jinzo Gakkai Shi; 1996 May; 38(5):233-7. PubMed ID: 8699614
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [A case of idiopathic chronic interstitial nephritis progressed to renal failure without proteinuria nor hematuria].
    Mukai H; Shimamoto K; Nakagawa M; Miyazaki Y; Fujisawa J; Minase T; Nakamura Y; Takada M; Iimura O
    Nihon Jinzo Gakkai Shi; 1992 Feb; 34(2):223-9. PubMed ID: 1588774
    [TBL] [Abstract][Full Text] [Related]  

  • 6. End-stage renal failure due to familial hypokalaemic interstitial nephritis with identical HLA tissue types.
    Wallace MR; Bruton D; North A; Wild DJ
    N Z Med J; 1985 Jan; 98(771):5-7. PubMed ID: 3855525
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Renal apolipoprotein A-I amyloidosis: a rare and usually ignored cause of hereditary tubulointerstitial nephritis.
    Gregorini G; Izzi C; Obici L; Tardanico R; Röcken C; Viola BF; Capistrano M; Donadei S; Biasi L; Scalvini T; Merlini G; Scolari F
    J Am Soc Nephrol; 2005 Dec; 16(12):3680-6. PubMed ID: 16221867
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Familial interstitial nephritis.
    Richmond JM; Whitworth JA; Kincaid-Smith PS
    Clin Nephrol; 1981 Sep; 16(3):109-13. PubMed ID: 7296967
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Hereditary interstitial nephritis without basement membrane changes.
    Levy NT; Meyers AM; Margolius LP; Verhaart S; Wadee WA
    Nephron; 1995; 69(4):418-23. PubMed ID: 7777106
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Recent developments in hereditary nephritis (Alport's syndrome).
    Bubalo FS; Davidson DD
    Indiana Med; 1991 Dec; 84(12):860-6. PubMed ID: 1774457
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clinical and genetic mapping of X chromosome in the X-linked dominant inherited Alport's syndrome.
    Dai Y; Huang Y; He X; Wang S; Huang R; Tang M; Hu C
    Saudi J Kidney Dis Transpl; 2008 Sep; 19(5):767-74. PubMed ID: 18711293
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Nephronophtisis].
    Niaudet P; Salomon R
    Nephrol Ther; 2006 Sep; 2(4):200-6. PubMed ID: 16966065
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Alport syndrome or progressive hereditary nephritis with hearing loss].
    Gubler MC; Heidet L; Antignac C
    Nephrol Ther; 2007 Jun; 3(3):113-20. PubMed ID: 17540313
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Familial interstitial nephritis.
    Coles GA; Robinson K; Branch RA
    Clin Nephrol; 1976 Dec; 6(6):513-7. PubMed ID: 1009697
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Renal prognosis in women with hereditary nephritis.
    Grünfeld JP; Noël LH; Hafez S; Droz D
    Clin Nephrol; 1985 Jun; 23(6):267-71. PubMed ID: 4028523
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Familial hematuric nephropathies].
    Gubler MC
    Rev Prat; 1997 Sep; 47(14):1545-9. PubMed ID: 9366112
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Characteristic ultrastructural lesion of the glomerular basement membrane in progressive hereditary nephritis (Alport's syndrome).
    Hinglais N; Grünfeld JP; Bois E
    Lab Invest; 1972 Nov; 27(5):473-87. PubMed ID: 4653971
    [No Abstract]   [Full Text] [Related]  

  • 18. [Nephronophthisis: study of 10 cases. Incidence, natural history and associated pathology (author's transl)].
    Gómez Campderá FJ; Niembro E; López Gómez JM; Canals MJ; Bárcenas MC; Gómez JA; Rengel MA; Luque de Pablos A
    Med Clin (Barc); 1981 Oct; 77(6):230-5. PubMed ID: 7321636
    [TBL] [Abstract][Full Text] [Related]  

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

  • 20. Absence of ocular manifestations in autosomal dominant Alport syndrome associated with haematological abnormalties.
    Colville D; Wang YY; Jamieson R; Collins F; Hood J; Savige J
    Ophthalmic Genet; 2000 Dec; 21(4):217-25. PubMed ID: 11135492
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 18.