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2010, ISBN 9781849962469, xxii, 193
Systemic vasculitides are an increasingly important group of disorders, many of which present significant diagnostic challenges. Including full-color... 
diagnosis | therapy | Vasculitis | Vasculitis - therapy
Book
Therapeutics and clinical risk management, ISSN 1176-6336, 01/2014, Volume 10, Issue default, pp. 279 - 293
Granulomatosis with polyangiitis (GPA, formerly Wegener's granulomatosis) is a multisystem autoimmune condition associated with anti-neutrophil cytoplasm antibodies... 
Life Sciences & Biomedicine | Health Care Sciences & Services | Science & Technology | Care and treatment | Forecasts and trends | Wegener's granulomatosis | Spleen | Lupus | Antigens | Enzymes | Immunoglobulins | Psoriasis | Cytokines | Pathogenesis | Mortality | Rheumatology | Neutrophils | Genomes | Inflammation | Hemorrhage | Lungs | Rheumatoid arthritis | immunosuppression | biologics | vasculitis | anti-neutrophil cytoplasm antibody
Journal Article
Journal Article
ANCA: SEROLOGY IN WEGENER'S GRANULOMATOSIS, 12/2005
BACKGROUND AND OBJECTIVES: Wegener′s granulomatosis (WG) is being increasingly diagnosed in India, which exists in two forms, the ′limited Wegener′s granulomatosis′ (LWG... 
cytoplasmic ANCA | Wegener′s granulomatosis | anti-neutrophil cytoplasmic antibodies | indirect immunofluorescence | anti-Proteinase3 | enzyme linked immunosorbent assay
Journal
Journal Article
Journal Article
Pituitary, ISSN 1386-341X, 3/2008, Volume 11, Issue 1, pp. 77 - 84
Journal Article
Journal Article