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[PDF] from hindawi.comA Servy, T Clérici, C Malines… - diabetes, 2011 - downloads.hindawi.com
1 Service d'Anatomie et Cytologie Pathologiques, Hôpital Ambroise Paré, AP-HP, Université
de Versailles Saint-Quentin-en-Yvelines, 9 Avenue Charles de Gaulle, 92104 Boulogne-Billancourt
Cedex, France 2 Service de Rhumatologie, Hôpital Ambroise Paré, AP-HP, Université de ...
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CM Hedrich, B Fiebig, G Hahn, M Suttorp… - Clinical …, 2011 - cpj.sagepub.com
Abstract Juvenile scleroderma is a rare connective tissue disease that involves the skin and subcutaneous
tissue. Among all presentations of juvenile scleroderma, localized scleroderma (JLSc) is the
most frequent, followed by systemic disease (JSSc) and eosinophilic fasciitis (EF). In ...
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N Poliak, JS Orange, BR Pawel… - Annals of Allergy, Asthma …, 2011 - annallergy.org
... NEED REPRINTS? BOOKMARK ARTICLE. Eosinophilic fasciitis mimicking
angioedema and treatment response to infliximab in a pediatric patient. ...
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[HTML] from nih.govJH Chun, KH Lee, MS Sung… - Annals of Dermatology, 2011 - ncbi.nlm.nih.gov
Eosinophic fasciitis (EF) is an uncommon connective tissue disease characterized by
scleroderma-like cutaneous changes, peripheral eosinophilia, hypergammaglobulinemia, and
an elevated erythrocyte sedimentation rate (ESR). Typical histopathologic findings ...
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[HTML] from journalmc.orgD Valadares, J Neves, I Almeida… - Journal of Medical …, 2011 - journalmc.org
Eosinophilic Fasciitis is a rare rheumatologic disease usually characterized by erythema and
limbs pain, cutaneous induration and peripheral eosinophilia. However, it is important to consider
Eosinophilic Fasciitis in differential diagnosis of others scleroderma-like syndromes. The ...
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