NDLI: Présentation atypique d'une granulomatose avec polyangeite: à propos d'une observation pédiatrique

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Présentation atypique d'une granulomatose avec polyangeite: à propos d'une observation pédiatrique

Content Provider	Semantic Scholar
Author	Berriche, Olfa Younes, Samia Ammari, Wafa Alaya, Wafa Kessomtini, Wassia Hammami, Sonia
Copyright Year	2015
Abstract	La granulomatose avec polyangéite (GPA) est une vascularite nécrosante systémique, caractérisée par une inflammation granulomateuse, une nécrose tissulaire et une vascularite touchant les vaisseaux de moyen et, surtout, de petit calibre, elle touche rarement l'enfant. Pan African Medical Journal. 2015; 21:141 doi:10.11604/pamj.2015.21.141.7086 This article is available online at: http://www.panafrican-med-journal.com/content/article/21/141/full/ © Olfa Berriche et al. The Pan African Medical Journal ISSN 1937-8688. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Pan African Medical Journal – ISSN: 19378688 (www.panafrican-med-journal.com) Published in partnership with the African Field Epidemiology Network (AFENET). (www.afenet.net) Case report Open Access
File Format	PDF HTM / HTML
Alternate Webpage(s)	https://www.ajol.info/index.php/pamj/article/download/133647/123255
PubMed reference number	4546791
Volume Number	21
Language	English
Access Restriction	Open
Subject Keyword	Cholecystitis Diameter (qualifier value) Ephrin Type-B Receptor 1, human Gilles de la Tourette syndrome International Standard Serial Number License SECAM Scientific Publication pseudomembranous colitis
Content Type	Text
Resource Type	Article

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