Coexistence of Fabry disease and IgA nephropathy: a report of two cases-Reference-Cited by-同舟云学术

Coexistence of Fabry disease and IgA nephropathy: a report of two cases

Published:2014-06-10 Issue:4 Volume:183 Page:671-675
ISSN:0021-1265
Container-title:Irish Journal of Medical Science (1971 -)
language:en
Short-container-title:Ir J Med Sci

Author:

Yin G.,Wu Y.,Zeng C.-H.,Chen H.-P.,Liu Z.-H.

Publisher

Springer Science and Business Media LLC

Subject

General Medicine

Link

http://link.springer.com/content/pdf/10.1007/s11845-014-1161-9.pdf

Reference17 articles.

1. Germain DP (2010) Fabry disease. Orphanet J Rare Dis 5:30. doi: 10.1186/1750-1172-5-30

2. Cai ZY, Zhang YK, Wang SX et al (2011) Diffuse thin glomerular basement membrane in association with Fabry disease in a Chinese female patient. Nephrol Dial Transplant 26(11):3813–3816. doi: 10.1093/ndt/gfr455

3. Singh HK, Nickeleit V, Kriegsmann J et al (2001) Coexistence of Fabry’s disease and necrotizing and crescentic glomerulonephritis. Clin Nephrol 55(1):73–79

4. D’Amico G (2000) Natural history of idiopathic IgA nephropathy: role of clinical and histological prognostic factors. Am J Kidney Dis 36(2):227–237. doi: 10.1053/ajkd.2000.8966

5. Chao CT, Lin WC, Kao TW (2012) Fabry disease and immunoglobulin A nephropathy. Nephrology (Carlton) 17(8):782–783. doi: 10.1111/j.1440-1797.2012.01594.x

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