BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

179 related articles for article (PubMed ID: 27410722)

  • 1. The Transition from Thin Basement Membranes to Typical Alport Syndrome Morphology in Children.
    Baek H; Lee SI; Park T; Cho M
    Fetal Pediatr Pathol; 2016; 35(6):369-375. PubMed ID: 27410722
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Collagen type IV nephropathy: from thin basement membrane nephropathy to Alport syndrome].
    Endreffy E; Ondrik Z; Kemény E; Vas Z; Maróti Z; Lencse G; Bereczki C; Haszon I; Túri S; Iványi B
    Orv Hetil; 2005 Dec; 146(52):2647-53. PubMed ID: 16468607
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A unique evolution of the kidney phenotype in a patient with autosomal recessive Alport syndrome.
    Vischini G; Kapp ME; Wheeler FC; Hopp L; Fogo AB
    Hum Pathol; 2018 Nov; 81():229-234. PubMed ID: 29530752
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Alport syndrome and thin glomerular basement membrane nephropathy: a practical approach to diagnosis.
    Haas M
    Arch Pathol Lab Med; 2009 Feb; 133(2):224-32. PubMed ID: 19195966
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Temporal retinal thinning and the diagnosis of Alport syndrome and Thin basement membrane nephropathy.
    Chen Y; Colville D; Ierino F; Symons A; Savige J
    Ophthalmic Genet; 2018 Apr; 39(2):208-214. PubMed ID: 29172845
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Spectrum of collagen type IV nephropathies: from thin basement membrane nephropathy to Alport syndrome.
    Vizjak A; Ferluga D
    Srp Arh Celok Lek; 2008 Dec; 136 Suppl 4():323-6. PubMed ID: 20804103
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Familial hematuria: A review.
    Plevová P; Gut J; Janda J
    Medicina (Kaunas); 2017; 53(1):1-10. PubMed ID: 28236514
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Collagen type IV nephropathy: genetic heterogeneity examinations in affected Hungarian families.
    Endreffy E; Ondrik Z; Iványi B; Maróti Z; Bereczki C; Haszon I; Györke Z; Worum E; Németh K; Rikker C; Ökrös Z; Túri S
    Mol Cell Probes; 2011 Feb; 25(1):28-34. PubMed ID: 20951199
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Chronic renal failure and shortened lifespan in COL4A3+/- mice: an animal model for thin basement membrane nephropathy.
    Beirowski B; Weber M; Gross O
    J Am Soc Nephrol; 2006 Jul; 17(7):1986-94. PubMed ID: 16775036
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Somatic mosaicism for a mutation of the COL4A5 gene is a cause of mild phenotype male Alport syndrome.
    Krol RP; Nozu K; Nakanishi K; Iijima K; Takeshima Y; Fu XJ; Nozu Y; Kaito H; Kanda K; Matsuo M; Yoshikawa N
    Nephrol Dial Transplant; 2008 Aug; 23(8):2525-30. PubMed ID: 18332068
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Carriers of Autosomal Recessive Alport Syndrome with Thin Basement Membrane Nephropathy Presenting as Focal Segmental Glomerulosclerosis in Later Life.
    Deltas C; Savva I; Voskarides K; Papazachariou L; Pierides A
    Nephron; 2015; 130(4):271-80. PubMed ID: 26201269
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Quantitative analysis of glomerular type IV collagen alpha3-5 chain expression in children with thin basement membrane disease.
    Ueda T; Nakajima M; Akazawa H; Maruhashi Y; Shimoyama H; Sakagami Y; Takagawa K; Kamitsuji H; Naito I; Sado Y; Yoshioka A
    Nephron; 2002 Oct; 92(2):271-8. PubMed ID: 12218303
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Inherited diseases of the glomerular basement membrane.
    Gubler MC
    Nat Clin Pract Nephrol; 2008 Jan; 4(1):24-37. PubMed ID: 18094725
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Persistent familial hematuria in children and the locus for thin basement membrane nephropathy.
    Rana K; Wang YY; Powell H; Jones C; McCredie D; Buzza M; Udawela M; Savige J
    Pediatr Nephrol; 2005 Dec; 20(12):1729-37. PubMed ID: 16235097
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Clinical and pathological study of 47 cases with Alport syndrome].
    He X; Liu GL; Xia ZK; Ren XG; Gao YF; Fan ZM; Fu YF; Fu J; Gao CL; Mao S; Chen R
    Zhonghua Er Ke Za Zhi; 2008 Dec; 46(12):914-8. PubMed ID: 19134254
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Familial hematuric syndromes--Alport syndrome, thin glomerular basement membrane disease and Fechtner/Epstein syndromes.
    Kashtan CE
    Contrib Nephrol; 2001; (136):79-99. PubMed ID: 11688406
    [No Abstract]   [Full Text] [Related]  

  • 18. Thin Basement Membrane: An Underrated Cause of End-Stage Renal Disease.
    Uzzo M; Moroni G; Ponticelli C
    Nephron; 2023; 147(7):383-391. PubMed ID: 36882005
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Three Novel Heterozygous COL4A4 Mutations Result in Three Different Collagen Type IV Kidney Disease Phenotypes.
    Li A; Gao EZ; Cui YX; Liu JH; Lv X; Wei XX; Xia XY; Gao CL; Liu FX; Xia ZK; Asan ; Liu ZH; Li XJ
    Cytogenet Genome Res; 2018; 154(1):30-36. PubMed ID: 29669314
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 9.