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

288 related items for PubMed ID: 4010678

  • 1. [Significance of family studies and kidney biopsies in children with renal hematuria].
    Pistor K, Bachmann H, Rumpelt HJ, Olbing H.
    Monatsschr Kinderheilkd; 1985 May; 133(5):269-73. PubMed ID: 4010678
    [Abstract] [Full Text] [Related]

  • 2. [Collagen type IV nephropathy: from thin basement membrane nephropathy to Alport syndrome].
    Endreffy E, Ondrik Z, Kemény E, Vas Z, Maróti Z, Lencse G, Bereczki C, Haszon I, Túri S, Iványi B.
    Orv Hetil; 2005 Dec 25; 146(52):2647-53. PubMed ID: 16468607
    [Abstract] [Full Text] [Related]

  • 3. A clinicopathological study of Alport syndrome and detection of type IV collagen chains in Alport patients.
    Chen N, Pan X, Ren H, Dong D.
    Chin Med J (Engl); 1998 Sep 25; 111(9):797-802. PubMed ID: 11155669
    [Abstract] [Full Text] [Related]

  • 4. [Clinical and pathological features of Alport syndrome in children].
    Zhu CH, Huang SM, Wu HM, Bao HY, Chen Y, Han Y, Zhao F, Zhang AH, Zhang WZ.
    Zhongguo Dang Dai Er Ke Za Zhi; 2010 Mar 25; 12(3):188-91. PubMed ID: 20350427
    [Abstract] [Full Text] [Related]

  • 5. Thin glomerular basement membrane disease: clinical significance of a morphological diagnosis--a collaborative study of the Italian Renal Immunopathology Group.
    Frascà GM, Onetti-Muda A, Mari F, Longo I, Scala E, Pescucci C, Roccatello D, Alpa M, Coppo R, Li Volti G, Feriozzi S, Bergesio F, Schena FP, Renieri A, Italian Renal Immunopathology Group.
    Nephrol Dial Transplant; 2005 Mar 25; 20(3):545-51. PubMed ID: 15618242
    [Abstract] [Full Text] [Related]

  • 6. Familial hematuria; clinico-pathological correlations.
    Yoshikawa N, White RH, Cameron AH.
    Clin Nephrol; 1982 Apr 25; 17(4):172-82. PubMed ID: 7042145
    [Abstract] [Full Text] [Related]

  • 7. The thin glomerular basement membrane in children with haematuria.
    Yoshikawa N, Hashimoto H, Katayama Y, Yamada Y, Matsuo T, Okada S.
    J Pathol; 1984 Apr 25; 142(4):253-7. PubMed ID: 6716210
    [Abstract] [Full Text] [Related]

  • 8. Hereditary nephritis in children with and without characteristic glomerular basement membrane alterations.
    Yoshikawa N, Ito H, Matsuyama S, Hazikano H, Okada S, Matsuo T.
    Clin Nephrol; 1988 Sep 25; 30(3):122-7. PubMed ID: 3180520
    [Abstract] [Full Text] [Related]

  • 9. Renal biopsy and family studies in 65 children with isolated hematuria.
    Schröder CH, Bontemps CM, Assmann KJ, Schuurmans Stekhoven JH, Foidart JM, Monnens LA, Veerkamp JH.
    Acta Paediatr Scand; 1990 Sep 25; 79(6-7):630-6. PubMed ID: 2386054
    [Abstract] [Full Text] [Related]

  • 10. [Renal biopsy in children with isolated microhematuria].
    Batinić D, Sćukanec-Spoljar M, Milosević D, Nizić L, Vrljicak K, Matković M.
    Acta Med Croatica; 2002 Sep 25; 56(4-5):163-6. PubMed ID: 12768895
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. [Alport's-syndrome: diagnosis, light- and electronmicroscopic findings (author's transl)].
    Balzar E, Lubec G, Syŕe G, Weissenbacher G.
    Padiatr Padol; 1976 Sep 25; 11(1):221-33. PubMed ID: 765939
    [Abstract] [Full Text] [Related]

  • 13. 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 25; 3(7):488-91. PubMed ID: 11791413
    [Abstract] [Full Text] [Related]

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

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. Coexistence of thin membrane and alport nephropathies in families with haematuria.
    Moghal NE, Milford DV, White RH, Raafat F, Higgins R.
    Pediatr Nephrol; 1999 Nov 25; 13(9):778-81. PubMed ID: 10603120
    [Abstract] [Full Text] [Related]

  • 17. COL4A4 mutation in thin basement membrane disease previously described in Alport syndrome.
    Buzza M, Wang YY, Dagher H, Babon JJ, Cotton RG, Powell H, Dowling J, Savige J.
    Kidney Int; 2001 Aug 25; 60(2):480-3. PubMed ID: 11473630
    [Abstract] [Full Text] [Related]

  • 18. Phenotypic and genotypic features of Alport syndrome in Chinese children.
    Wang F, Ding J, Guo S, Yang J.
    Pediatr Nephrol; 2002 Dec 25; 17(12):1013-20. PubMed ID: 12478350
    [Abstract] [Full Text] [Related]

  • 19. Alport syndrome. Molecular genetic aspects.
    Hertz JM.
    Dan Med Bull; 2009 Aug 25; 56(3):105-52. PubMed ID: 19728970
    [Abstract] [Full Text] [Related]

  • 20. Renal prognosis in women with hereditary nephritis.
    Grünfeld JP, Noël LH, Hafez S, Droz D.
    Clin Nephrol; 1985 Jun 25; 23(6):267-71. PubMed ID: 4028523
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 15.