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Items: 1 to 20 of 82

1.

Challenge in pathologic diagnosis of Alport syndrome: evidence from correction of previous misdiagnosis.

Yao XD, Chen X, Huang GY, Yu YT, Xu ST, Hu YL, Wang QW, Chen HP, Zeng CH, Ji DX, Hu WX, Tang Z, Liu ZH.

Orphanet J Rare Dis. 2012 Dec 21;7:100. doi: 10.1186/1750-1172-7-100.

2.

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
3.

Characterization of the peripheral retinopathy in X-linked and autosomal recessive Alport syndrome.

Shaw EA, Colville D, Wang YY, Zhang KW, Dagher H, Fassett R, Guymer R, Savige J.

Nephrol Dial Transplant. 2007 Jan;22(1):104-8. Epub 2006 Oct 27.

4.

Spectrum of clinical features and type IV collagen alpha-chain distribution in Chinese patients with Alport syndrome.

Wei G, Zhihong L, Huiping C, Caihong Z, Zhaohong C, Leishi L.

Nephrol Dial Transplant. 2006 Nov;21(11):3146-54. Epub 2006 Aug 29.

5.

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

Kashtan CE.

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

6.

[Clinical and pathological features of Alport syndrome in children].

Zhu CH, Huang SM, Wu HM, Bao HY, Chen Y, Han Y, Zhao F, Zhang AH, Zhang WZ.

Zhongguo Dang Dai Er Ke Za Zhi. 2010 Mar;12(3):188-91. Chinese.

7.

A clinicopathological study of Alport syndrome and detection of type IV collagen chains in Alport patients.

Chen N, Pan X, Ren H, Dong D.

Chin Med J (Engl). 1998 Sep;111(9):797-802.

PMID:
11155669
8.

[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
9.

Delayed diagnosis of Alport syndrome without hematuria.

Yin-Yin C, You-Ming P, Yu-Mei L.

Iran J Kidney Dis. 2014 May;8(3):250-1. Erratum in: Iran J Kidney Dis. 2014 Jul;8(4):350.

10.

Clinical and molecular diagnosis of Alport syndrome.

Kashtan CE.

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

PMID:
8608415
11.

Pregnancy complicated with Alport syndrome: a good obstetric outcome and failure to diagnose an infant born to a mother with Alport syndrome by umbilical cord immunofluorescence staining.

Matsubara S, Ueda Y, Takahashi H, Nagai T, Kuwata T, Muto S, Yamaguchi T, Takizawa T, Suzuki M.

J Obstet Gynaecol Res. 2009 Dec;35(6):1109-14. doi: 10.1111/j.1447-0756.2009.01069.x.

PMID:
20144175
12.
13.

Alport syndrome. Molecular genetic aspects.

Hertz JM.

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

PMID:
19728970
14.

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
15.

Alport syndrome: from bedside to genome to bedside.

Kashtan CE, Michael AF.

Am J Kidney Dis. 1993 Nov;22(5):627-40. Review.

PMID:
8238007
16.

Alport syndrome. A review of the ocular manifestations.

Colville DJ, Savige J.

Ophthalmic Genet. 1997 Dec;18(4):161-73. Review.

PMID:
9457747
17.

Antigen retrieval with protease digestion applied in immunohistochemical diagnosis of Alport syndrome.

Guan N, Yu LX, Wu GH, Xing Y, Ding J.

Nephrol Dial Transplant. 2008 Nov;23(11):3509-13. doi: 10.1093/ndt/gfn305. Epub 2008 Jun 3.

18.

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.

19.

Histopathology, ultrastructure, and clinical phenotypes in thin glomerular basement membrane disease variants.

Liapis H, Gökden N, Hmiel P, Miner JH.

Hum Pathol. 2002 Aug;33(8):836-45.

PMID:
12203217
20.

[Clinical and genetic features of the Alport 'syndromes'].

Pescucci C, Longo I, Mari F, Scala E, Bruttini M, Caselli R, Renieri A.

G Ital Nefrol. 2005 Sep-Oct;22(5):466-76. Review. Italian.

PMID:
16267804
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