BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

202 related articles for article (PubMed ID: 2659195)

  • 21. [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]  

  • 22. Establishing the diagnosis of benign familial hematuria. The importance of examining the urine sediment of family members.
    Blumenthal SS; Fritsche C; Lemann J
    JAMA; 1988 Apr; 259(15):2263-6. PubMed ID: 3352118
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [A case of familial hematuria. (A contribution to Alport's syndrome)].
    Jończyk K; Kobierska-Szczepańska A
    Wiad Lek; 1970 Dec; 23(23):2139-42. PubMed ID: 5496021
    [No Abstract]   [Full Text] [Related]  

  • 24. [Familial esophageal leiomyomatosis associated with Alport's syndrome in a 9-year-old boy].
    Roussel B; Birembaut P; Gaillard D; Puchelle JC; D'Albignac G; Pennaforte F; Fandre M
    Helv Paediatr Acta; 1986 Oct; 41(4):359-68. PubMed ID: 3793512
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Glomerular morphometry II: familial and nonfamilial haematuria.
    Yoshikawa N; Cameron AH; White RH
    Histopathology; 1981 May; 5(3):251-6. PubMed ID: 7239446
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Familial IgA nephropathy associated with bilateral sensorineural deafness.
    Chahin J; Ortiz A; Mendez L; Gallego E; Garcia-Perez J; Garcia-Castro G; Julian BA; Egido J
    Am J Kidney Dis; 1992 Jun; 19(6):592-6. PubMed ID: 1595709
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Contribution of an ophthalmologic test to the diagnosis of familial nephropathies. Apropos of 10 cases].
    Marrakchi S; Lasram L; Bouguila H; Barbirou I; Ouertani A; Ayed S
    J Fr Ophtalmol; 1994; 17(4):238-41. PubMed ID: 8089404
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. Autosomal dominant Alport's syndrome: study of a large Tunisian family.
    Kharrat M; Makni S; Makni K; Kammoun K; Charfeddine K; Azaeiz H; Jarraya F; Ben Hmida M; Gubler MC; Ayadi H; Hachicha J
    Saudi J Kidney Dis Transpl; 2006 Sep; 17(3):320-5. PubMed ID: 16970251
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [The first experience in Russia of using DNA diagnosis in Alport's syndrome in a family with a unique morphological picture of the kidney lesion].
    Tsalikova FD; Ignatova MS; Krasnopol'skaia KD; Tverskaia SM; Brydun AV
    Ter Arkh; 1995; 67(4):45-7. PubMed ID: 7784975
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Autosomal dominant Alport syndrome: molecular analysis of the COL4A4 gene and clinical outcome.
    Marcocci E; Uliana V; Bruttini M; Artuso R; Silengo MC; Zerial M; Bergesio F; Amoroso A; Savoldi S; Pennesi M; Giachino D; Rombolà G; Fogazzi GB; Rosatelli C; Martinhago CD; Carmellini M; Mancini R; Di Costanzo G; Longo I; Renieri A; Mari F
    Nephrol Dial Transplant; 2009 May; 24(5):1464-71. PubMed ID: 19129241
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Alport's syndrome representing as crescentic glomerulonephritis: a report of two siblings.
    Harris JP; Rakowski TA; Argy WP; Schreiner GE
    Clin Nephrol; 1978 Dec; 10(6):245-9. PubMed ID: 729217
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Diagnosis of Alport's syndrome].
    Rasenack U
    Dtsch Med Wochenschr; 1975 Jan; 100(3):109-10. PubMed ID: 1112225
    [No Abstract]   [Full Text] [Related]  

  • 34. [Borderline indications for renal biopsy].
    Barbiano Di Belgiojoso G; Ferrario F; Genderini A
    G Ital Nefrol; 2002; 19(3):335-49. PubMed ID: 12195403
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Alport's syndrome: new findings].
    García-Torres R; Orozco L
    Bol Med Hosp Infant Mex; 1993 Aug; 50(8):596-602. PubMed ID: 8357522
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Anterior lenticonus--an unusual feature of Alport's syndrome.
    Kapoor S; Kapoor MS
    J Laryngol Otol; 1977 Sep; 91(9):819-22. PubMed ID: 915382
    [TBL] [Abstract][Full Text] [Related]  

  • 37. COL4A3/COL4A4 mutations link familial hematuria and focal segmental glomerulosclerosis. glomerular epithelium destruction via basement membrane thinning?
    Voskarides K; Pierides A; Deltas C
    Connect Tissue Res; 2008; 49(3):283-8. PubMed ID: 18661361
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Alport's syndrome--case report].
    Słowik M; Popiela G; Kazimierczak K; Szelepin L; Szaliński M
    Klin Oczna; 2004; 106(3):332-4. PubMed ID: 15515320
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Alport's syndrome in twins].
    Syrenicz A; Czekalski S; Majkowska L
    Pol Tyg Lek; 1991 Oct 28-Nov 4; 46(43-44):844-6. PubMed ID: 1669176
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Use of a monoclonal antibody in differential diagnosis of children with haematuria and hereditary nephritis.
    Savage CO; Reed A; Kershaw M; Pincott J; Pusey CD; Dillon MJ; Barratt TM; Lockwood CM
    Lancet; 1986 Jun; 1(8496):1459-61. PubMed ID: 2873277
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.