Results 171 to 180 of about 1,092 (215)
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Granulomatose de Wegener du sujet âgé

Revue De Medecine Interne, 2001
Resume Propos. – Determiner les differences cliniques, biologiques ou evolutives de la granulomatose de Wegener survenant chez le sujet âge de plus de 60 ans. Methode. – Etude retrospective de cohorte. Patients. – Nous avons apprecie les caracteristiques cliniques, biologiques et evolutives de la granulomatose de Wegener chez 11 sujets de plus de ...
A.L Fauchais   +10 more
exaly   +2 more sources

La granulomatose de Wegener

Annales De Pathologie, 2005
Faouzi El Mezni   +6 more
exaly   +2 more sources

Granulomatose de Wegener

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

La Granulomatose De Wegener:

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

Hémoptysies récidivantes au cours dˈune granulomatose de Wegener

Revue De Medecine Interne, 2001
P Corne   +5 more
exaly   +2 more sources

Granulomatose avec polyangéite (maladie de Wegener)

La Presse Médicale, 2012
Granulomatosis with polyangiitis (GPA), is the recently proposed, new alternative name for Wegener's granulomatosis. It defines a systemic small-vessels vasculitis, characterized by frequent involvement of upper and lower respiratory tract. The presence of cytoplasmic-type ANCA with anti-proteinase 3 specificity is observed in more than 90% of patients
Alexandre Karras   +3 more
openaire   +1 more source

Granulomatose de wegener et grossesseune observation

La Revue de Médecine Interne, 1989
Resume Les observations de grossesse au cours de la granulomatose de Wegener sont tres rares quatre seulement ont ete decrites. Les auteurs rapportent un cinquieme cas au cours duquel la maladie s'est declaree dans le post-partum, ce qui a ete deja note deux fois dans la litterature.
S. M'Rad   +8 more
openaire   +1 more source

Atteintes hypophysaires de la granulomatose de Wegener

La Presse Médicale, 2004
Resume Introduction La granulomatose de Wegener est une vascularite necrosante, avec atteinte preferentielle des voies aeriennes superieures, des poumons et des reins. Moins de 20 cas de localisation hypophysaire ont ete decrits et il s’agit le plus souvent d’atteintes posthypophysaires, revelees par un diabete insipide. Observation Il s’agit de
Laurence Vittaz   +6 more
openaire   +1 more source

Présentation inhabituelle d’une granulomatose de Wegener

La Revue de Médecine Interne, 2010
We report an unusual case of Wegener's granulomatosis revealed by spleen infarction and complicated by reno-vascular hypertension. A 33-year-old man with a history of spleen infraction and cerebral venous thrombosis was admitted for malignant hypertension, renal failure and nephritic syndrome.
S. Ketari Jamoussi   +7 more
openaire   +1 more source

Atteintes cutanées révélatrices d'une granulomatose de Wegener

La Presse Médicale, 2007
Summary Introduction Wegener's granulomatosis is a rare systemic vasculitis, characterized by involvement of the upper airways, lungs and kidneys; other organs may also be affected. Cutaneous lesions occur frequently during the disease course but seldom as its initial presentation.
Imed Ben Ghorbel   +3 more
openaire   +1 more source

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