MEFV gene variants in children with Henoch-Schönlein purpura and association with clinical manifestations: a single-center Mediterranean experience-Reference-Cited by-同舟云学术

MEFV gene variants in children with Henoch-Schönlein purpura and association with clinical manifestations: a single-center Mediterranean experience

Published:2018-12-12 Issue:1 Volume:131 Page:68-72
ISSN:0032-5481
Container-title:Postgraduate Medicine
language:en
Short-container-title:Postgraduate Medicine

Author:

Ekinci Rabia Miray Kisla¹^ORCID,Balci Sibel¹^ORCID,Bisgin Atil²^ORCID,Atmis Bahriye³^ORCID,Dogruel Dilek⁴^ORCID,Altintas Derya Ufuk⁴^ORCID,Yilmaz Mustafa¹^ORCID

Affiliation:

1. Department of Pediatric Rheumatology, Cukurova University Faculty of Medicine, Adana, Turkey

2. Department of Medical Genetics, Cukurova University Faculty of Medicine, Adana, Turkey

3. Department of Pediatric Nephrology, Cukurova University Faculty of Medicine, Adana, Turkey

4. Department of Pediatric Allergy and Immunology, Cukurova University Faculty of Medicine, Adana, Turkey

Funder

Cukurova University Scientific Research Unit

Publisher

Informa UK Limited

Subject

General Medicine

Link

https://www.tandfonline.com/doi/pdf/10.1080/00325481.2019.1552479

Reference26 articles.

1. 2012 Revised International Chapel Hill Consensus Conference Nomenclature of Vasculitides

2. Incidence of Henoch-Schonlein purpura, Kawasaki disease, and rare vasculitides in children of different ethnic origins

3. Clinical update: Henoch-Schönlein purpura

4. Vasculitis in siblings with familial Mediterranean fever: a report of three cases and review of the literature

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