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Results: 1 to 20 of 553

1.

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]
2.

Segregation of hematuria in thin basement membrane disease with haplotypes at the loci for Alport syndrome.

Buzza M, Wilson D, Savige J.

Kidney Int. 2001 May;59(5):1670-6.

PMID:
11318937
[PubMed - indexed for MEDLINE]
Free Article
3.

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. Epub 2005 Oct 19.

PMID:
16235097
[PubMed - indexed for MEDLINE]
4.

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]
5.

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]
6.

COL4A4 mutation in thin basement membrane disease previously described in Alport syndrome.

Buzza M, Wang YY, Dagher H, Babon JJ, Cotton RG, Powell H, Dowling J, Savige J.

Kidney Int. 2001 Aug;60(2):480-3.

PMID:
11473630
[PubMed - indexed for MEDLINE]
Free Article
7.

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]
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. doi: 10.1016/j.mcp.2010.10.001. Epub 2010 Oct 14.

PMID:
20951199
[PubMed - indexed for MEDLINE]
9.

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]
10.

The clinical features of thin basement membrane nephropathy.

Gregory MC.

Semin Nephrol. 2005 May;25(3):140-5. Review.

PMID:
15880323
[PubMed - indexed for MEDLINE]
11.

COL4A3 mutations and their clinical consequences in thin basement membrane nephropathy (TBMN).

Wang YY, Rana K, Tonna S, Lin T, Sin L, Savige J.

Kidney Int. 2004 Mar;65(3):786-90.

PMID:
14871398
[PubMed - indexed for MEDLINE]
12.

COL4A3/COL4A4 mutations producing focal segmental glomerulosclerosis and renal failure in thin basement membrane nephropathy.

Voskarides K, Damianou L, Neocleous V, Zouvani I, Christodoulidou S, Hadjiconstantinou V, Ioannou K, Athanasiou Y, Patsias C, Alexopoulos E, Pierides A, Kyriacou K, Deltas C.

J Am Soc Nephrol. 2007 Nov;18(11):3004-16. Epub 2007 Oct 17.

PMID:
17942953
[PubMed - indexed for MEDLINE]
Free Article
13.

Do mutations in COL4A1 or COL4A2 cause thin basement membrane nephropathy (TBMN)?

Zhang KW, Tonna S, Wang YY, Rana K, Padavarat S, Savige J.

Pediatr Nephrol. 2007 May;22(5):645-51. Epub 2007 Jan 10.

PMID:
17216253
[PubMed - indexed for MEDLINE]
14.

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
15.

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]
16.

[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]
17.

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
18.

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]
19.

Clinico-pathological correlations in 127 patients in 11 large pedigrees, segregating one of three heterozygous mutations in the COL4A3/ COL4A4 genes associated with familial haematuria and significant late progression to proteinuria and chronic kidney disease from focal segmental glomerulosclerosis.

Pierides A, Voskarides K, Athanasiou Y, Ioannou K, Damianou L, Arsali M, Zavros M, Pierides M, Vargemezis V, Patsias C, Zouvani I, Elia A, Kyriacou K, Deltas C.

Nephrol Dial Transplant. 2009 Sep;24(9):2721-9. doi: 10.1093/ndt/gfp158. Epub 2009 Apr 8.

PMID:
19357112
[PubMed - indexed for MEDLINE]
Free Article
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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