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Volume 15 Supplement 2

French recommendations for the management of systemic necrotizing vasculitides (polyarteritis nodosa and ANCA-associated vasculitides)

Reviews

Publication costs were funded by The French Rare Diseases Healthcare Network: auto-immune and auto-inflammatory rare diseases (FAI2R). The articles have undergone the journal's standard peer review process for supplements. The supplement editor declares no competing interests.

  1. Systemic necrotizing vasculitis comprises a group of diseases resembling polyarteritis nodosa and anti-neutrophil cytoplasmic antibody-associated vasculitis (ANCA): granulomatosis with polyangiitis, eosinophil...

    Authors: Benjamin Terrier, Raphaël Darbon, Cécile-Audrey Durel, Eric Hachulla, Alexandre Karras, Hélène Maillard, Thomas Papo, Xavier Puechal, Grégory Pugnet, Thomas Quemeneur, Maxime Samson, Camille Taille and Loïc Guillevin
    Citation: Orphanet Journal of Rare Diseases 2020 15(Suppl 2):351
    Content type: Position statement Published on:

    The Correction to this article has been published in Orphanet Journal of Rare Diseases 2021 16:155

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  • ISSN: 1750-1172 (electronic)

Orphanet Journal of Rare Diseases

ISSN: 1750-1172