Ventricular septal defect in a child with Alport syndrome: a case report-Reference-Cited by-同舟云学术

Ventricular septal defect in a child with Alport syndrome: a case report

Published:2010-10-05 Issue:1 Volume:10 Page:
ISSN:1471-2261
Container-title:BMC Cardiovascular Disorders
language:en
Short-container-title:BMC Cardiovasc Disord

Author:

Bassareo Pier Paolo,Marras Andrea Raffaele,Mercuro Giuseppe

Publisher

Springer Science and Business Media LLC

Subject

Cardiology and Cardiovascular Medicine

Link

http://link.springer.com/article/10.1186/1471-2261-10-48/fulltext.html

Reference26 articles.

1. Alport AC: Hereditary familial congenital haemorrhagic nephritis. BMJ. 1927, i: 504-506. 10.1136/bmj.1.3454.504.

2. Williamson DAJ: Alport's syndrome of hereditary nephritis with deafness. Lancet. 1961, ii: 1321-1323. 10.1016/S0140-6736(61)90899-6.

3. Heidet L, Gubler MC: The renal lesions of Alport syndrome. J Am Soc Nephrol. 2009, 20: 1210-1215. 10.1681/ASN.2008090984.

4. Heikkilä P, Soininen R: The type IV collagen family. Molecular Pathology and Genetics of Alport Syndrome. Edited by: Tryggvason K. 1996, Basel: Karger, 105-129. 1

5. Kashtan CE, Kim Y: Distribution of the alpha 1 and alpha 2 chains of collagen IV and of collagens V and VI in Alport syndrome. Kidney Int. 1992, 42: 115-126. 10.1038/ki.1992.269.

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3. Identification of a novel COL4A5 mutation in a Chinese family with X-linked Alport syndrome using exome sequencing;Molecular Biology Reports;2014-02-13

4. Alport syndrome—insights from basic and clinical research;Nature Reviews Nephrology;2012-11-20

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