Results 161 to 170 of about 1,067 (198)
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La Presse Médicale, 2007
Wegener's granulomatosis is described by the Chapel Hill nomenclature (1994) as a systemic necrotizing vasculitis affecting small to medium-sized vessels. Cytoplasm-labeling antineutrophil cytoplasmic autoantibodies (cANCA) directed against proteinase 3 (PR3) are detected in the sera of approximately 90% of patients. Reported incidence varies from 2 to
Christian Pagnoux, Luis Teixeira
openaire +1 more source
Wegener's granulomatosis is described by the Chapel Hill nomenclature (1994) as a systemic necrotizing vasculitis affecting small to medium-sized vessels. Cytoplasm-labeling antineutrophil cytoplasmic autoantibodies (cANCA) directed against proteinase 3 (PR3) are detected in the sera of approximately 90% of patients. Reported incidence varies from 2 to
Christian Pagnoux, Luis Teixeira
openaire +1 more source
Acta Clinica Belgica, 1995
SummaryThe authors report an observation of Wegener’s granulomatosis with pulmonary, bronchial, renal, cutaneous and sinusal involvement. Five years ago, the patient was referred to us because of bilateral diffuse pulmonary infiltrates of unknown origin. A cortico therapy was introduced at that time and a complete clearance of the pulmonary infiltrates
M. Polus +5 more
openaire +1 more source
SummaryThe authors report an observation of Wegener’s granulomatosis with pulmonary, bronchial, renal, cutaneous and sinusal involvement. Five years ago, the patient was referred to us because of bilateral diffuse pulmonary infiltrates of unknown origin. A cortico therapy was introduced at that time and a complete clearance of the pulmonary infiltrates
M. Polus +5 more
openaire +1 more source

