BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

122 related articles for article (PubMed ID: 752943)

  • 1. [Hereditary nephritis (Alport). II. Clinical and morphological correlations].
    Popović-Rolović M; Sindjić M; Smiljanić S; Calić-Perisić N; Stefanović Z
    Srp Arh Celok Lek; 1978 Oct; 106(10):883-96. PubMed ID: 752943
    [No Abstract]   [Full Text] [Related]  

  • 2. [Alport-Perkoff syndrome. Clinical and ultramicroscopic study of a family].
    López Sánchez A; López Campos JL; Montagut Sánchez M; Delgado Yanes JC; Pérez Gúzman E; Pérez Cresco J; Bernaldo de Quirós J
    Rev Clin Esp; 1974 Mar; 132(5):435-44. PubMed ID: 4831274
    [No Abstract]   [Full Text] [Related]  

  • 3. 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]  

  • 4. [Hereditary nephritis (Alport)].
    Popović-Rolović M; Smiljanić S
    Srp Arh Celok Lek; 1978 Apr; 106(4):353-68. PubMed ID: 751225
    [No Abstract]   [Full Text] [Related]  

  • 5. Hereditary nephritis and deafness. Report of a family.
    Shani M; Fine LG
    Isr J Med Sci; 1970; 6(4):544-8. PubMed ID: 5472337
    [No Abstract]   [Full Text] [Related]  

  • 6. [Clinico-morphological study of nephritis-like forms of renal dysplasia in children].
    Ignatova MS; Degtiareva EM; Klembovskiĭ AI; Korovina NA; Bosin VIu
    Vopr Okhr Materin Det; 1978 Apr; 23(4):13-8. PubMed ID: 664492
    [No Abstract]   [Full Text] [Related]  

  • 7. [Contribution to the study of Alport's syndrome. Apropos of a case].
    Schneegans E; Rohmer A; Levy-Silagy J; el-Mejjati A; Sengel A; Stoebner P; Laforgue D
    Ann Pediatr (Paris); 1971 Dec; 18(12):757-69. PubMed ID: 5004890
    [No Abstract]   [Full Text] [Related]  

  • 8. [Diagnosis of Alport syndrome by immunohistochemical staining of type IV collagen alpha chains in paraffin-embedded renal sections].
    Yu LX; Guan N; Wu GH
    Zhonghua Er Ke Za Zhi; 2008 Apr; 46(4):301. PubMed ID: 19099735
    [No Abstract]   [Full Text] [Related]  

  • 9. [Alport's Syndrome. Hereditary nephritis, perceptive deafness and lens anomalies].
    Norrelund N
    Ugeskr Laeger; 1971 Mar; 133(11):503-5. PubMed ID: 5092560
    [No Abstract]   [Full Text] [Related]  

  • 10. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. [Hereditary hematuric nephropathy].
    Prekop R; Mydlík M; Jurkovic I
    Cesk Pediatr; 1970 Mar; 25(3):125-7. PubMed ID: 5440263
    [No Abstract]   [Full Text] [Related]  

  • 13. Characterization of the peripheral retinopathy in X-linked and autosomal recessive Alport syndrome.
    Shaw EA; Colville D; Wang YY; Zhang KW; Dagher H; Fassett R; Guymer R; Savige J
    Nephrol Dial Transplant; 2007 Jan; 22(1):104-8. PubMed ID: 17071739
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 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. [Alport's syndrome in Eastern Slovakia].
    Kluka V; Tischler V; Vereb J
    Cesk Pediatr; 1986 Oct; 41(10):569-73. PubMed ID: 3502944
    [No Abstract]   [Full Text] [Related]  

  • 17. Consultation with the specialist. Familial nephritis/Alport syndrome.
    Fouser L
    Pediatr Rev; 1998 Aug; 19(8):265-7. PubMed ID: 9707716
    [No Abstract]   [Full Text] [Related]  

  • 18. [Alport syndrome in 23-year-old woman].
    Finke D; Bilińska W; Kałuzyński A; Nowicki M
    Pol Merkur Lekarski; 2008; 24 Suppl 4():22-4. PubMed ID: 18924495
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clinical and molecular diagnosis of Alport syndrome.
    Kashtan CE
    Proc Assoc Am Physicians; 1995 Oct; 107(3):306-13. PubMed ID: 8608415
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Hereditary nephropathy.
    Bĕlobrádková J; Herout V; Kubes L
    Sb Ved Pr Lek Fak Karlovy Univerzity Hradci Kralove; 1978; 21(5):487-98. PubMed ID: 292128
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.