These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

269 related articles for article (PubMed ID: 7784975)

  • 1. [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]  

  • 2. Clinical and genetic mapping of X chromosome in the X-linked dominant inherited Alport's syndrome.
    Dai Y; Huang Y; He X; Wang S; Huang R; Tang M; Hu C
    Saudi J Kidney Dis Transpl; 2008 Sep; 19(5):767-74. PubMed ID: 18711293
    [TBL] [Abstract][Full Text] [Related]  

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

  • 4. 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]  

  • 5. [The modern concepts of hereditary nephritis].
    Fokeeva VV; Ignatova MS; Degtiareva EM; Rashidova GS
    Ter Arkh; 1992; 64(6):80-5. PubMed ID: 1440347
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. Alport syndrome. Molecular genetic aspects.
    Hertz JM
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Recent developments in hereditary nephritis (Alport's syndrome).
    Bubalo FS; Davidson DD
    Indiana Med; 1991 Dec; 84(12):860-6. PubMed ID: 1774457
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Renal prognosis in Alport's and related syndromes: influence of the mode of inheritance.
    Pochet JM; Bobrie G; Landais P; Goldfarb B; Grünfeld JP
    Nephrol Dial Transplant; 1989; 4(12):1016-21. PubMed ID: 2517321
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [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]  

  • 12. Detection of mutations in the COL4A5 gene in over 90% of male patients with X-linked Alport's syndrome by RT-PCR and direct sequencing.
    Inoue Y; Nishio H; Shirakawa T; Nakanishi K; Nakamura H; Sumino K; Nishiyama K; Iijima K; Yoshikawa N
    Am J Kidney Dis; 1999 Nov; 34(5):854-62. PubMed ID: 10561141
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A comparison of the clinical, histopathologic, and ultrastructural phenotypes in carriers of X-linked and autosomal recessive Alport's syndrome.
    Dagher H; Buzza M; Colville D; Jones C; Powell H; Fassett R; Wilson D; Agar J; Savige J
    Am J Kidney Dis; 2001 Dec; 38(6):1217-28. PubMed ID: 11728953
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. De-novo COL4A5 gene mutations in Alport's syndrome.
    Massella L; Rizzoni G; De Blasis R; Barsotti P; Faraggiana T; Renieri A; Seri M; Galli L; De Marchi M
    Nephrol Dial Transplant; 1994; 9(10):1408-11. PubMed ID: 7816253
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [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]  

  • 17. Contemporary diagnostic approach in Alport's syndrome.
    Grünfeld JP
    Ren Fail; 2000 Nov; 22(6):759-63. PubMed ID: 11104163
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Alport's-syndrome: diagnosis, light- and electronmicroscopic findings (author's transl)].
    Balzar E; Lubec G; Syŕe G; Weissenbacher G
    Padiatr Padol; 1976; 11(1):221-33. PubMed ID: 765939
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Hereditary nephritis (Alport's syndrome). Description of a family].
    Marcen Letosa R; Fdez Alonso J; Quereda Rguez navarro C; López Checa F; Castilla Jiménez J; Rodríguez Algarra G; Maceira Cruz B; Pereira Palomo P; Mateos Aguilar J
    Rev Clin Esp; 1977 Nov; 147(3):291-6. PubMed ID: 605240
    [No Abstract]   [Full Text] [Related]  

  • 20. [3 cases of Alport's syndrome with different clinical and morphologic manifestations].
    Bechcińska B; Danilewicz M; Kałuzyński A; Marek K; Wagrowska-Danilewicz M
    Patol Pol; 1989; 40(1):123-8. PubMed ID: 2477788
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.