Granulomatosis with polyangiitis (GPA) and microscopic polyangiitis (MPA) belong to a group of rare autoimmune diseases called anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis, characterized by inflammatory cell infiltration leading to necrosis of the blood vessels. ,
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Medicine by Alexandros G. Sfakianakis,Anapafseos 5 Agios Nikolaos 72100 Crete Greece,00302841026182,00306932607174,alsfakia@gmail.com,
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Παρασκευή 23 Φεβρουαρίου 2018
Rituximab for Granulomatosis with Polyangiitis or Microscopic Polyangiitis: A Review of the Clinical effectiveness, Cost-effectiveness, and Guidelines [Internet].
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Publication date: September 2017 Source: European Journal of Surgical Oncology (EJSO), Volume 43, Issue 9 http://ift.tt/2gezJ2D
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Publication date: January–February 2018 Source: Materials Today, Volume 21, Issue 1 Author(s): David Bradley http://ift.tt/2BP...
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