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Journal Abstract Search

213 related items for PubMed ID: 11688406

  • 1. Familial hematuric syndromes--Alport syndrome, thin glomerular basement membrane disease and Fechtner/Epstein syndromes.
    Kashtan CE.
    Contrib Nephrol; 2001; (136):79-99. PubMed ID: 11688406
    [No Abstract] [Full Text] [Related]

  • 2. Quantitative analysis of glomerular type IV collagen alpha3-5 chain expression in children with thin basement membrane disease.
    Ueda T, Nakajima M, Akazawa H, Maruhashi Y, Shimoyama H, Sakagami Y, Takagawa K, Kamitsuji H, Naito I, Sado Y, Yoshioka A.
    Nephron; 2002 Oct; 92(2):271-8. PubMed ID: 12218303
    [Abstract] [Full Text] [Related]

  • 3. Persistent familial hematuria in children and the locus for thin basement membrane nephropathy.
    Rana K, Wang YY, Powell H, Jones C, McCredie D, Buzza M, Udawela M, Savige J.
    Pediatr Nephrol; 2005 Dec; 20(12):1729-37. PubMed ID: 16235097
    [Abstract] [Full Text] [Related]

  • 4. [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
    [Abstract] [Full Text] [Related]

  • 5. 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; 13(9):778-81. PubMed ID: 10603120
    [Abstract] [Full Text] [Related]

  • 6. Spectrum of collagen type IV nephropathies: from thin basement membrane nephropathy to Alport syndrome.
    Vizjak A, Ferluga D.
    Srp Arh Celok Lek; 2008 Dec; 136 Suppl 4():323-6. PubMed ID: 20804103
    [Abstract] [Full Text] [Related]

  • 7. [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]

  • 8. Alpha 5 COLIV chain distribution in glomerular basement membrane in a male with X-linked Alport syndrome and thin basement membrane.
    Rizzoni G, Massella L, Muda AO.
    Pediatr Nephrol; 2000 Dec 25; 15(3-4):325. PubMed ID: 11149132
    [No Abstract] [Full Text] [Related]

  • 9. On the methodology for measuring thickness of glomerular basement membranes.
    Tungekar MF, Pickett TM.
    Nephrol Dial Transplant; 2005 Oct 25; 20(10):2287; author reply 2287. PubMed ID: 16166751
    [No Abstract] [Full Text] [Related]

  • 10. Benign familial hematuria due to mutation of the type IV collagen alpha4 gene.
    Lemmink HH, Nillesen WN, Mochizuki T, Schröder CH, Brunner HG, van Oost BA, Monnens LA, Smeets HJ.
    J Clin Invest; 1996 Sep 01; 98(5):1114-8. PubMed ID: 8787673
    [Abstract] [Full Text] [Related]

  • 11. Thin basement membrane--do we have a window for understanding the molecular pathogenesis?
    Netzer KO, Seibold S, Weber M.
    Nephrol Dial Transplant; 1999 May 01; 14(5):1060-1. PubMed ID: 10344333
    [No Abstract] [Full Text] [Related]

  • 12. Alport syndrome and benign familial hematuria (thin basement membrane disease) in two brothers of a family with hematuria.
    Takemura T, Yanagida H, Yagi K, Moriwaki K, Okada M.
    Clin Nephrol; 2003 Sep 01; 60(3):195-200. PubMed ID: 14524583
    [Abstract] [Full Text] [Related]

  • 13. Collagen IV diseases: A focus on the glomerular basement membrane in Alport syndrome.
    Cosgrove D, Liu S.
    Matrix Biol; 2017 Jan 01; 57-58():45-54. PubMed ID: 27576055
    [Abstract] [Full Text] [Related]

  • 14. Thin GBM nephropathy: premature glomerular obsolescence is associated with hypertension and late onset renal failure.
    Nieuwhof CM, de Heer F, de Leeuw P, van Breda Vriesman PJ.
    Kidney Int; 1997 May 01; 51(5):1596-601. PubMed ID: 9150478
    [Abstract] [Full Text] [Related]

  • 15. [Hereditary nephropathies].
    Yoshikawa N, Ito H, Nakamura N.
    Pediatrie; 1990 May 01; 45(1):5-11. PubMed ID: 2158049
    [Abstract] [Full Text] [Related]

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  • 17. Alport syndrome diagnosed by immunofluorescence using a new monoclonal antibody.
    Kiyatake I, Tomino Y, Shirato I, Nakayama S, Koide H.
    Intern Med; 1993 Jan 01; 32(1):26-30. PubMed ID: 8495040
    [Abstract] [Full Text] [Related]

  • 18. Familial hematuria: a clinical, ultrastructural and morphometric study.
    Schärer K, Waldherr R, Müller-Möhlis TC, Tariverdian G.
    Prog Clin Biol Res; 1989 Jan 01; 305():173-7. PubMed ID: 2762351
    [No Abstract] [Full Text] [Related]

  • 19. An 18-year-old male with hematuria, renal insufficiency, and defective synthesis of type IV collagen.
    Markowitz GS, Gelber C, D'agati VD.
    Kidney Int; 2006 Jun 01; 69(12):2278-82. PubMed ID: 16641919
    [No Abstract] [Full Text] [Related]

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