Zobrazeno 1 - 10
of 173
pro vyhledávání: '"J. Wipff"'
Autor:
A. Combier, C. Frantz, J. Wipff, R. Bazeli, A. Feydy, P. Quartier, G. Touanga Ngoti, M. Thomas, C. Job Deslandre, M. Elhai, J. Avouac, Y. Allanore
Publikováno v:
Revue du Rhumatisme. 89:A54
Autor:
M. Thomas, G. Martinroche, A. Combier, J. Wipff, G. Touanga Ngoti, P. Quartier, C. Contin-Bordes, M.E. Truchetet, Y. Allanore
Publikováno v:
Revue du Rhumatisme. 89:A55
Autor:
Nicolas Dupin, Selim Aractingi, T. Bettuzzi, J. Wipff, Benjamin Terrier, Alban Deroux, Marie Jachiet, M.M. Farhat, M. Fabre
Publikováno v:
La Revue de Médecine Interne. 40:A72-A73
Introduction Les vascularites urticariennes (VU) sont des maladies systemiques rares caracterisees par une inflammation vasculaire dermique responsable de lesions urticariennes associees parfois a une atteinte d’organe. Elles sont separees en deux
Autor:
Anne Lohse, Valérie Devauchelle-Pensec, Christelle Sordet, Ta. Tran, Chantal Job Deslandre, C. Gaujoux-Viala, Irène Lemelle, Brigitte Bader-Meunier, Sylvain Breton, Pascal Pillet, Linda Rossi-Semerano, Elisabeth Solau-Gervais, M. De Bandt, J Wipff, Catherine Adamsbaum, Pauline Marteau
Publikováno v:
Oral Presentations.
Background Juvenile idiopathic arthritis (JIA) may lead to structural damage. Yet radiographic assessment is seldom considered in studies. Objectives To provide pragmatic guidelines concerning conventional radiography (CR) in each subtype of JIA (exc
Akademický článek
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Akademický článek
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Autor:
Magdalena Obarzanek-Fojt, P.-J. Wipff, Stephan Ryser, A.M. Moodycliffe, Bertrand Favre, Daniel Hohl, B. Hinz, Marcel Huber
Publikováno v:
British Journal of Dermatology. 164:125-134
Epidermolytic hyperkeratosis (bullous congenital ichthyosiform erythroderma), characterized by ichthyotic, rippled hyperkeratosis, erythroderma and skin blistering, is a rare autosomal dominant disease caused by mutations in keratin 1 or keratin 10 (
Autor:
D. Zerkak, Paul Legmann, Stanislas Chaussade, V. Abitbol, Yannick Allanore, Anh Tuan Dinh-Xuan, J Wipff, Daniel Dusser, M. Gilson, André Kahan
Publikováno v:
European Respiratory Journal. 35:112-117
The aims of the present study were to identify prognostic factors for systemic sclerosis (SSc)-related interstitial lung disease and to clarify the possible causative role of manometric oesophageal involvement. Consecutive SSc patients underwent pulm
Autor:
J, Wipff, F, Costantino, I, Lemelle, C, Pajot, A, Duquesne, M, Lorrot, A, Faye, B, Bader-Meunier, K, Brochard, V, Despert, S, Jean, M, Grall-Lerosey, Y, Marot, D, Nouar, A, Pagnier, P, Quartier, C, Job-Deslandre
Publikováno v:
Arthritisrheumatology (Hoboken, N.J.). 67(4)
To document more fully the characteristics of chronic recurrent multifocal osteomyelitis (CRMO) in pediatric patients, to collect data on the outcomes and management of the disease, and to define prognostic factors.One hundred seventy-eight patients
Publikováno v:
Pediatric Rheumatology
Pediatric Rheumatology, BioMed Central, 2013, 11 (Suppl 2), pp.P77
Pediatric Rheumatology Online Journal
Pediatric Rheumatology, 2013, 11 (Suppl 2), pp.P77
Pediatric Rheumatology, BioMed Central, 2013, 11 (Suppl 2), pp.P77
Pediatric Rheumatology Online Journal
Pediatric Rheumatology, 2013, 11 (Suppl 2), pp.P77
Oxidative damage caused by oxygen free radicals is generally considered a serious mechanism in the pathogenesis of many diseases as cardiovascular diseases, atherosclerosis, and inflammatory rheumatism. Increased oxidative stress has already been des
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42a57267a9e30db158f013e6f4b7aafa
https://www.hal.inserm.fr/inserm-00914645/file/1546-0096-11-S2-P77.pdf
https://www.hal.inserm.fr/inserm-00914645/file/1546-0096-11-S2-P77.pdf