Role of PAX2 gene polymorphisms in Henoch-Schonlein purpura nephritis
Author:
Publisher
Wiley
Subject
Nephrology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1440-1797.2006.00537.x/fullpdf
Reference21 articles.
1. Deletion polymorphism of the angiotensin converting enzyme gene predicts persistent proteinuria in Henoch-Schonlein purpura nephritis
2. The role of PAX2 in normal and abnormal development of the urinary tract
3. Mapping of Pax-2 Transcription Activation Domains
4. Prognosis of Henoch-Schonlein nephritis in children.
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2. Potential of Serum and Urinary Matrix Metalloproteinase-9 Levels for the Early Detection of Renal Involvement in Children With Henoch-Schönlein Purpura;Iranian Journal of Pediatrics;2016-06-05
3. Association of the paired box 2 gene polymorphism with the susceptibility and pathogenesis of Henoch-Schönlein purpura in children;Molecular Medicine Reports;2014-11-10
4. The genetics of Henoch–Schönlein purpura: a systematic review and meta-analysis;Rheumatology International;2013-01-17
5. Association Between Graves’ Disease and Renal Coloboma Syndrome: A Case Report;Clinical Pediatric Endocrinology;2013
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