Co-existence of renovascular hypertension, polyarteritis nodosa, antiphospholipid syndrome and methylenetetrahydrofolate reductase mutation
Author:
Affiliation:
1. Department of Pediatric Nephrology; Faculty of Medicine; Eskisehir Osmangazi University; Eskisehir; Turkey
Publisher
Wiley
Subject
Pediatrics, Perinatology, and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/ped.12135/fullpdf
Reference10 articles.
1. International consensus statement on an update of the classification criteria for definite antiphospholipid syndrome (APS);Miyakis;J. Thromb. Haemost.,2006
2. Cutaneous polyarteritis nodosa in a child with positive antiphospholipid and P-ANCA;Pereira;Scand. J. Rheumatol.,1995
3. Paediatric Rheumatology International Trials Organisation (PRINTO). EULAR/PRINTO/PRES criteria for Henoch-Schönlein purpura, childhood polyarteritis nodosa, childhood Wegener granulomatosis and childhood Takayasu arteritis: Ankara 2008. Part II: Final classification criteria;Ozen;Ann. Rheum. Dis.,2010
4. Polyarteritis nodosa complicated by catastrophic antiphospholipid syndrome;Han;J. Clin. Rheumatol.,2004
5. Antiphospholipid syndrome in children;Avcin;Curr. Opin. Rheumatol.,2008
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