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 *

151 related articles for article (PubMed ID: 31630709)

  • 1. Alport's syndrome.
    Bruni V; Petrisano M; Tarsitano F; Falvo F; Parisi F; Cucinotta U; Betta P; Di Benedetto V; Scuderi MG; Pensabene L; Sestito S; Cuppari C; Fede C; Chimenz R; Concolino D
    J Biol Regul Homeost Agents; 2019; 33(5 Suppl. 1):19-24. Special Issue: Focus on Pediatric Nephrology. PubMed ID: 31630709
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Autosomal recessive Alport's syndrome and benign familial hematuria are collagen type IV diseases.
    Tazón Vega B; Badenas C; Ars E; Lens X; Milà M; Darnell A; Torra R
    Am J Kidney Dis; 2003 Nov; 42(5):952-9. PubMed ID: 14582039
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Ultrastructural and immunohistochemical findings in Alport's syndrome: a study of 108 patients from 97 Italian families with particular emphasis on COL4A5 gene mutation correlations.
    Mazzucco G; Barsotti P; Muda AO; Fortunato M; Mihatsch M; Torri-Tarelli L; Renieri A; Faraggiana T; De Marchi M; Monga G
    J Am Soc Nephrol; 1998 Jun; 9(6):1023-31. PubMed ID: 9621285
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

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

  • 8. 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]  

  • 9. 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]  

  • 10. Improving recognition of inherited renal disease.
    Masengu A; Courtney AE
    Practitioner; 2012 Feb; 256(1748):17-20, 2-3. PubMed ID: 22497104
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Autosomal dominant form of type IV collagen nephropathy exists among patients with hereditary nephritis difficult to diagnose clinicopathologically.
    Imafuku A; Nozu K; Sawa N; Hasegawa E; Hiramatsu R; Kawada M; Hoshino J; Tanaka K; Ishii Y; Takaichi K; Fujii T; Ohashi K; Iijima K; Ubara Y
    Nephrology (Carlton); 2018 Oct; 23(10):940-947. PubMed ID: 28704582
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Rapid DNA-based prenatal diagnosis by genetic linkage in three families with Alport's syndrome.
    Turco AE; Bresin E; Rossetti S; Peterlin B; Morandi R; Pignatti PF
    Am J Kidney Dis; 1997 Aug; 30(2):174-9. PubMed ID: 9261027
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Molecular aspects of Alport's syndrome.
    Weber M; Netzer KO; Pullig O
    Clin Investig; 1992 Sep; 70(9):809-15. PubMed ID: 1450636
    [TBL] [Abstract][Full Text] [Related]  

  • 15. COL4A4-related nephropathy caused by a novel mutation in a large consanguineous Saudi family.
    Ramzan K; Imtiaz F; Taibah K; Alnufiee S; Akhtar M; Al-Hazzaa SA; Al-Owain M
    Int J Pediatr Otorhinolaryngol; 2014 Mar; 78(3):427-32. PubMed ID: 24398087
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [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]  

  • 17. X-Linked and Autosomal Recessive Alport Syndrome: Pathogenic Variant Features and Further Genotype-Phenotype Correlations.
    Savige J; Storey H; Il Cheong H; Gyung Kang H; Park E; Hilbert P; Persikov A; Torres-Fernandez C; Ars E; Torra R; Hertz JM; Thomassen M; Shagam L; Wang D; Wang Y; Flinter F; Nagel M
    PLoS One; 2016; 11(9):e0161802. PubMed ID: 27627812
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Autosomal-dominant Alport syndrome: natural history of a disease due to COL4A3 or COL4A4 gene.
    Pescucci C; Mari F; Longo I; Vogiatzi P; Caselli R; Scala E; Abaterusso C; Gusmano R; Seri M; Miglietti N; Bresin E; Renieri A
    Kidney Int; 2004 May; 65(5):1598-603. PubMed ID: 15086897
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Revision about hearing loss in the Alport's syndrome, analyzing the clinical, genetic and bio-molecular aspects.
    Alves FR; de A Quintanilha Ribeiro F
    Braz J Otorhinolaryngol; 2005; 71(6):813-9. PubMed ID: 16878253
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Siblings with Alport's syndrome showing unique staining patterns for alpha5(IV) and alpha6(IV) chains of collagen type IV.
    Tsuji T; Fujigaki Y; Sakakima M; Sado Y; Hishida A
    Clin Exp Nephrol; 2010 Jun; 14(3):283-7. PubMed ID: 20213338
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.