BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

139 related articles for article (PubMed ID: 7634524)

  • 21. Hereditary nephritis (Alport's syndrome)--clinical profile and inheritance in 28 kindreds.
    Chugh KS; Sakhuja V; Agarwal A; Jha V; Joshi K; Datta BN; Gupta A; Gupta KL
    Nephrol Dial Transplant; 1993; 8(8):690-5. PubMed ID: 8414153
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Late hereditary degenerative sensorineural hearing loss associated with IgA mesangial glomerulonephritis of probable autosomal dominant heredity].
    de Serdio JL; Chahin J; Gil-Curbelo JA; Perera A; Saavedra JA
    Acta Otorrinolaringol Esp; 1993; 44(6):447-54. PubMed ID: 8155361
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Chronic hereditary nephritis with hearing loss (Alport's syndrome)].
    Zientalska-Rumińska E; Stankiewicz-Szymczak W; Moszyński B
    Otolaryngol Pol; 1989; 43(5-6):401-8. PubMed ID: 2640496
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Making the diagnosis of Alport's syndrome.
    Pirson Y
    Kidney Int; 1999 Aug; 56(2):760-75. PubMed ID: 10432421
    [No Abstract]   [Full Text] [Related]  

  • 25. [Retinal flecks in Alport's syndrome].
    Mili-Boussen I; Ghattas M; Ben Romdhane B; Ouertani A
    Arch Pediatr; 2000 Dec; 7(12):1304-6. PubMed ID: 11147065
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Genetics of classic Alport's syndrome.
    Flinter FA; Cameron JS; Chantler C; Houston I; Bobrow M
    Lancet; 1988 Oct; 2(8618):1005-7. PubMed ID: 2902439
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Hereditary nephritis with bearing loss of the receiver type (Alport's syndrome) with a description of 2 cases].
    Zhelev N; Astrug A; Konstantinova B; Henov D
    Vutr Boles; 1974; 13(6):137-44. PubMed ID: 4467473
    [TBL] [Abstract][Full Text] [Related]  

  • 28. The gene corresponding to the putative Goodpasture antigen is present in Alport's syndrome.
    Savige JA
    Clin Exp Immunol; 1991 Aug; 85(2):236-9. PubMed ID: 1864003
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Alport's syndrome.
    Oni AO; Eweka AO; Otuaga PO; Odia JO
    Saudi J Kidney Dis Transpl; 2009 Nov; 20(6):1087-9. PubMed ID: 19861880
    [No Abstract]   [Full Text] [Related]  

  • 30. The brainstem auditory evoked responses in Alport's syndrome.
    Di Paolo B; Di Marco T; Palmieri PF; Spisni C; Albertazzi A
    Nephrol Dial Transplant; 1987; 2(5):323-6. PubMed ID: 3122109
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [X chromosome dominant hereditary nephritis: characterization by pedigree analysis and simple studies in general practice].
    Wälchli P
    Praxis (Bern 1994); 1999 Oct; 88(44):1811-4. PubMed ID: 10584551
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Effects of renal transplantation on hearing and ocular changes in a monozygotic twin with Alport's syndrome: comparison with other twin on hemodialysis.
    Sefer S; Trotić R; Lacmanović V; Degoricija V; Ratković-Gusić I; Kes P
    Croat Med J; 2000 Jun; 41(2):203-6. PubMed ID: 10853053
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [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]  

  • 34. Auditory manifestations of Alport's disease syndrome.
    Rintelmann W
    Trans Sect Otolaryngol Am Acad Ophthalmol Otolaryngol; 1976; 82(3 Pt 1):375-87. PubMed ID: 960411
    [No Abstract]   [Full Text] [Related]  

  • 35. [Alport's syndrome: apropos of 2 families].
    Grünfeld JP
    Nephrologie; 2000; 21(6):295-8. PubMed ID: 11117109
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Lenticonus in Alport's syndrome. A family study.
    Singh DS; Bisht DB; Kapoor S; Sharma RN; Sankaran K; Majumdar NK
    Acta Ophthalmol (Copenh); 1977 Feb; 55(1):164-9. PubMed ID: 576544
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. Genetic features of Alport's syndrome.
    Schröder CH; Brunner H; Monnens LA
    Contrib Nephrol; 1990; 80():3-8. PubMed ID: 2282819
    [No Abstract]   [Full Text] [Related]  

  • 39. X-linked recessive nephritis with mental retardation, sensorineural hearing loss, and macrocephaly.
    Lane W; Robson M; Lowry RB; Leung AK
    Clin Genet; 1994 Jun; 45(6):314-7. PubMed ID: 7923864
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Alport's syndrome].
    Papajík T; Zadrazil J; Bachleda P
    Vnitr Lek; 1993 Nov; 39(11):1102-7. PubMed ID: 8284910
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.