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Results: 1 to 20 of 220

1.

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. doi: 10.1043/1543-2165-133.2.224. Review.

PMID:
19195966
[PubMed - indexed for MEDLINE]
2.

Thin basement membrane nephropathy.

Savige J, Rana K, Tonna S, Buzza M, Dagher H, Wang YY.

Kidney Int. 2003 Oct;64(4):1169-78. Review.

PMID:
12969134
[PubMed - indexed for MEDLINE]
3.

[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 25;146(52):2647-53. Hungarian.

PMID:
16468607
[PubMed - indexed for MEDLINE]
4.

Alport syndrome and thin basement membrane nephropathy.

Thorner PS.

Nephron Clin Pract. 2007;106(2):c82-8. Epub 2007 Jun 6. Review.

PMID:
17570934
[PubMed - indexed for MEDLINE]
5.

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. Review.

PMID:
20804103
[PubMed - indexed for MEDLINE]
6.

A novel mutation of COL4A3 presents a different contribution to Alport syndrome and thin basement membrane nephropathy.

Hou P, Chen Y, Ding J, Li G, Zhang H.

Am J Nephrol. 2007;27(5):538-44. Epub 2007 Aug 24.

PMID:
17726307
[PubMed - indexed for MEDLINE]
7.

The genetics of thin basement membrane nephropathy.

Rana K, Wang YY, Buzza M, Tonna S, Zhang KW, Lin T, Sin L, Padavarat S, Savige J.

Semin Nephrol. 2005 May;25(3):163-70. Review.

PMID:
15880327
[PubMed - indexed for MEDLINE]
8.

Alport syndrome. Molecular genetic aspects.

Hertz JM.

Dan Med Bull. 2009 Aug;56(3):105-52.

PMID:
19728970
[PubMed - indexed for MEDLINE]
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. Epub 2006 Jun 14.

PMID:
16775036
[PubMed - indexed for MEDLINE]
Free Article
10.

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. doi: 10.1080/03008200802148280.

PMID:
18661361
[PubMed - indexed for MEDLINE]
11.

Alport Syndrome and Thin Basement Membrane Nephropathy.

Kashtan CE.

In: Pagon RA, Adam MP, Ardinger HH, Bird TD, Dolan CR, Fong CT, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2014.
2001 Aug 28 [updated 2013 Feb 28].

PMID:
20301386
[PubMed]
Books & Documents
12.

[Thin glomerular basement membrane disease].

Frascà GM, Balestra E, Fanciulli E, Freddi P, Mazzucchelli R, Montironi R, D'Arezzo M, Sagripanti S.

G Ital Nefrol. 2008 Jan-Feb;25(1):49-56. Review. Italian.

PMID:
18264918
[PubMed - indexed for MEDLINE]
13.

Familial hematuria due to type IV collagen mutations: Alport syndrome and thin basement membrane nephropathy.

Kashtan CE.

Curr Opin Pediatr. 2004 Apr;16(2):177-81. Review.

PMID:
15021198
[PubMed - indexed for MEDLINE]
14.

Novel heterozygous COL4A3 mutation in a family with late-onset ESRD.

Hoefele J, Lange-Sperandio B, Ruessmann D, Glöckner-Pagel J, Alberer M, Benz MR, Nagel M, Weber LT.

Pediatr Nephrol. 2010 Aug;25(8):1539-42. doi: 10.1007/s00467-010-1467-4. Epub 2010 Feb 23.

PMID:
20177710
[PubMed - indexed for MEDLINE]
15.

Clinical and molecular diagnosis of Alport syndrome.

Kashtan CE.

Proc Assoc Am Physicians. 1995 Oct;107(3):306-13. Review.

PMID:
8608415
[PubMed - indexed for MEDLINE]
16.

Nine novel COL4A3 and COL4A4 mutations and polymorphisms identified in inherited membrane diseases.

Rana K, Tonna S, Wang YY, Sin L, Lin T, Shaw E, Mookerjee I, Savige J.

Pediatr Nephrol. 2007 May;22(5):652-7. Epub 2007 Jan 10.

PMID:
17216251
[PubMed - indexed for MEDLINE]
17.

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.

PMID:
8178947
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

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. doi: 10.1093/ndt/gfn681. Epub 2009 Jan 7.

PMID:
19129241
[PubMed - indexed for MEDLINE]
Free Article
19.

A COL4A3 gene mutation and post-transplant anti-alpha 3(IV) collagen alloantibodies in Alport syndrome.

Kalluri R, van den Heuvel LP, Smeets HJ, Schroder CH, Lemmink HH, Boutaud A, Neilson EG, Hudson BG.

Kidney Int. 1995 Apr;47(4):1199-204.

PMID:
7783419
[PubMed - indexed for MEDLINE]
20.

Alport syndrome. An inherited disorder of renal, ocular, and cochlear basement membranes.

Kashtan CE.

Medicine (Baltimore). 1999 Sep;78(5):338-60. Review.

PMID:
10499074
[PubMed - indexed for MEDLINE]

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