BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

262 related articles for article (PubMed ID: 7398144)

  • 1. Hereditary nephropathy (Alport syndrome): correlation of clinical data with glomerular basement membrane alterations.
    Rumpelt HJ
    Clin Nephrol; 1980 May; 13(5):203-7. PubMed ID: 7398144
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Evolution of glomerular basement membrane lesions in a male patient with Alport syndrome: ultrastructural and morphometric study.
    Cangiotti AM; Sessa A; Meroni M; Montironi R; Ragaiolo M; Mambelli V; Cinti S
    Nephrol Dial Transplant; 1996 Sep; 11(9):1829-34. PubMed ID: 8918631
    [No Abstract]   [Full Text] [Related]  

  • 3. Correlation of glomerular basement membrane alterations with clinical data in progressive hereditary nephritis (Alport's syndrome).
    Basta-Jovanovic G; Venkataseshan VS; Churg J
    Am J Kidney Dis; 1990 Jul; 16(1):51-6. PubMed ID: 2195878
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Samoyed hereditary glomerulopathy (SHG). Evolution of splitting of glomerular capillary basement membranes.
    Jansen B; Thorner P; Baumal R; Valli V; Maxie MG; Singh A
    Am J Pathol; 1986 Dec; 125(3):536-45. PubMed ID: 3799818
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Alport-type glomerulopathy: evidence for diminished capillary loop size.
    Rumpelt HJ; Steinke A; Thoenes W
    Clin Nephrol; 1992 Feb; 37(2):57-64. PubMed ID: 1372542
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Samoyed hereditary glomerulopathy. Immunohistochemical staining of basement membranes of kidney for laminin, collagen type IV, fibronectin, and Goodpasture antigen, and correlation with electron microscopy of glomerular capillary basement membranes.
    Thorner P; Jansen B; Baumal R; Valli VE; Goldberger A
    Lab Invest; 1987 Apr; 56(4):435-43. PubMed ID: 3550289
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Alport's syndrome (progressive hereditary nephritis).
    Gaboardi F; Edefonti A; Imbasciati E; Tarantino A; Mihatsch MJ; Zollinger HU
    Clin Nephrol; 1974; 2(4):143-56. PubMed ID: 4603152
    [No 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; 30(3):122-7. PubMed ID: 3180520
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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; 142(4):253-7. PubMed ID: 6716210
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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;
    Nephrol Dial Transplant; 2005 Mar; 20(3):545-51. PubMed ID: 15618242
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. [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; 146(52):2647-53. PubMed ID: 16468607
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Alport syndrome-like basement membrane changes in Frasier syndrome: an electron microscopy study.
    Ito S; Hataya H; Ikeda M; Takata A; Kikuchi H; Hata J; Morikawa Y; Kawamura S; Honda M
    Am J Kidney Dis; 2003 May; 41(5):1110-5. PubMed ID: 12722046
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Alport syndrome: 15-year follow-up in 28 cases].
    Genova R; Polisseni E; Agazzani E; Maffei S
    Pediatr Med Chir; 1986; 8(3):331-40. PubMed ID: 3786195
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The pathology of the kidney in the Alport syndrome.
    Spear GS
    Birth Defects Orig Artic Ser; 1974; 10(4):109-13. PubMed ID: 4470885
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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; 15(3-4):325. PubMed ID: 11149132
    [No Abstract]   [Full Text] [Related]  

  • 17. Hereditary nephritis and hypoplastic dysplastic nephropathy: hydroxylysine glycoside excretion and the glomerular basement membrane.
    Veltischev Y; Ignatova M; Ananenko A; Klembovsky A; Daihin E; Brydun A; Degtyareva E
    Int J Pediatr Nephrol; 1983 Sep; 4(3):149-54. PubMed ID: 6642868
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Ultrastructural lesions of the glomerular basement membrane in hereditary chronic nephritis.
    Hinglais N; Grünfeld JP; Troconis L; Bois E
    Adv Nephrol Necker Hosp; 1974; 3():133-52. PubMed ID: 4219701
    [No Abstract]   [Full Text] [Related]  

  • 19. Electron microscopic studies in hereditary nephritis.
    Churg J; Strauss L; Sherman RL
    Birth Defects Orig Artic Ser; 1974; 10(4):89-92. PubMed ID: 4470915
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Clinicopathological study on progressive hereditary nephritis: observations of ultrastructural lesions in the glomerular basement membrane].
    Yoshida R
    Nihon Jinzo Gakkai Shi; 1992 Nov; 34(11):1135-48. PubMed ID: 1294768
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.