140 related articles for article (PubMed ID: 16641919)
41. Type IV collagen alpha 5 chain. Normal distribution and abnormalities in X-linked Alport syndrome revealed by monoclonal antibody.
Yoshioka K; Hino S; Takemura T; Maki S; Wieslander J; Takekoshi Y; Makino H; Kagawa M; Sado Y; Kashtan CE
Am J Pathol; 1994 May; 144(5):986-96. PubMed ID: 8178947
[TBL] [Abstract][Full Text] [Related]
42. Basement membranes and human disease.
Van Agtmael T; Bruckner-Tuderman L
Cell Tissue Res; 2010 Jan; 339(1):167-88. PubMed ID: 19756754
[TBL] [Abstract][Full Text] [Related]
43. Benign hereditary nephritis.
Peterson AS; Schubert JJ
J Fam Pract; 1977 Mar; 4(3):437-41. PubMed ID: 845562
[TBL] [Abstract][Full Text] [Related]
44. 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]
45. [From Alport syndrome to benign familial hematuria: clinical and genetic aspect].
Maziers N; Dahan K; Pirson Y
Nephrol Ther; 2005 May; 1(2):90-100. PubMed ID: 16895672
[TBL] [Abstract][Full Text] [Related]
46. A novel Cys1638Tyr NC1 domain substitution in alpha5(IV) collagen causes Alport syndrome with late onset renal failure without hearing loss or eye abnormalities.
Wilson JC; Yoon HS; Walker RJ; Eccles MR
Nephrol Dial Transplant; 2007 May; 22(5):1338-46. PubMed ID: 17277342
[TBL] [Abstract][Full Text] [Related]
47. Confocal microscopy of the skin in the diagnosis of X-linked Alport syndrome.
Muda AO; Massella L; Giannakakis K; Renieri A; Rizzoni G; Faraggiana T
J Invest Dermatol; 2003 Jul; 121(1):208-11. PubMed ID: 12839584
[No Abstract] [Full Text] [Related]
48. Understanding renal disorders as systemic diseases: the fascinating world of basement membranes beyond the glomerulus.
Gross O
Nephrol Dial Transplant; 2008 Jun; 23(6):1823-5. PubMed ID: 18385387
[No Abstract] [Full Text] [Related]
49. 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]
50. 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]
51. Poststreptococcal acute glomerulonephritis can be a risk factor for accelerating kidney dysfunction in Alport syndrome: a case experience.
Araki Y; Kawaguchi A; Sakakibara N; Nagaoka Y; Yamamura T; Horinouchi T; Nagano C; Morisada N; Iijima K; Nozu K
CEN Case Rep; 2020 Nov; 9(4):418-422. PubMed ID: 32592137
[TBL] [Abstract][Full Text] [Related]
52. [Familial hematuric nephropathies].
Gubler MC
Rev Prat; 1997 Sep; 47(14):1545-9. PubMed ID: 9366112
[TBL] [Abstract][Full Text] [Related]
53. [From the molecular genetics of Alport's syndrome to principles of organo-protection in chronic renal diseases].
Gross O; Weber M
Med Klin (Munich); 2005 Dec; 100(12):826-31. PubMed ID: 16453099
[TBL] [Abstract][Full Text] [Related]
54. Hematuria and decreased kidney function as initial signs of acute B-cell lymphoblastic leukemia.
Seo-Mayer P; Kenney B; McNamara J; Stein J; Moeckel GW
Am J Kidney Dis; 2010 Nov; 56(5):1001-5. PubMed ID: 20599308
[TBL] [Abstract][Full Text] [Related]
55. 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]
56. Thin-glomerular-basement-membrane nephropathy: is it a benign cause of isolated hematuria?
Gandhi S; Kalantar-Zadeh K; Don BR
South Med J; 2002 Jul; 95(7):768-71. PubMed ID: 12144088
[TBL] [Abstract][Full Text] [Related]
57. [Significance of family studies and kidney biopsies in children with renal hematuria].
Pistor K; Bachmann H; Rumpelt HJ; Olbing H
Monatsschr Kinderheilkd; 1985 May; 133(5):269-73. PubMed ID: 4010678
[TBL] [Abstract][Full Text] [Related]
58. [Alport syndrome in 23-year-old woman].
Finke D; Bilińska W; Kałuzyński A; Nowicki M
Pol Merkur Lekarski; 2008; 24 Suppl 4():22-4. PubMed ID: 18924495
[TBL] [Abstract][Full Text] [Related]
59. Immunohistochemical diagnosis of Alport's syndrome in paraffin-embedded renal sections: antigen retrieval with autoclave heating.
Naito I; Ninomiya Y; Nomura S
Med Electron Microsc; 2003 Mar; 36(1):1-7. PubMed ID: 12658346
[TBL] [Abstract][Full Text] [Related]
60. Familial hematuria: a clinical, ultrastructural and morphometric study.
Schärer K; Waldherr R; Müller-Möhlis TC; Tariverdian G
Prog Clin Biol Res; 1989; 305():173-7. PubMed ID: 2762351
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
