Zobrazeno 1 - 10
of 194
pro vyhledávání: '"S Durupt"'
Autor:
C. Rousset-Jablonski, Y. Mekki, A. Denis, Q. Reynaud, R. Nove-Josserand, S. Durupt, S. Touzet, M. Perceval, I. Ray-Coquard, F. Golfier, I. Durieu
Publikováno v:
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
A higher risk of human papillomavirus (HPV)-related cervical intra-epithelial neoplasia (CIN) is suspected among females with cystic fibrosis (CF).We conducted a single center prospective cohort study among females attending the Lyon adult CF center.
Publikováno v:
Journal of Cystic Fibrosis. 21:S79-S80
Publikováno v:
La Revue de medecine interne. 41(11)
Tryptase is the most abundant endopeptidase released by mast cells degranulation, involved in many pro and anti-inflammatory processes. Normal serum tryptase range is 0-11.4 μg/L. Tryptase is a useful diagnostic tool for anaphylaxis, systemic mastoc
Publikováno v:
La Revue de medecine interne. 41(11)
Aceruloplasminemia is a rare iron-overload disease that should be better known by physicians. It is an autosomal recessive disorder due to mutations in ceruloplasmin gene causing systemic iron overload, including cerebral and liver parenchyma. The im
Publikováno v:
Revue des Maladies Respiratoires. 35:592-603
Resume Introduction La majorite des femmes atteintes de mucoviscidose atteignent l’âge adulte et doivent beneficier d’un suivi gynecologique et d’une contraception adaptes. Etat des connaissances Il n’existe pas de contre-indication particul
Autor:
Catherine Mainguy, R. Nove-Josserand, C. Braun, V. Jubin, Jean-François Nicolas, Audrey Nosbaum, Isabelle Durieu, Camille Ohlmann, S. Durupt, P. Reix
Publikováno v:
Revue Française d'Allergologie. 61:270
Introduction Les patients atteints de mucoviscidose (MV) sont regulierement traites par antibiotiques (ATB) pour des infections respiratoires, et rapportent frequemment des reactions d’hypersensibilite (HSR). Le but de cette etude etait de mettre e
Publikováno v:
Revue de Pneumologie Clinique. 72:77-86
Resume Vingt-cinq ans apres l’identification du gene responsable de la mucoviscidose, les retombees de sa decouverte commencent (enfin) a profiter aux patients. La meilleure connaissance des anomalies genetiques et de leurs consequences, l’avenem
Akademický článek
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Autor:
P. Reix, R. Nove Josserand, O. Marchal, S. Durupt, Isabelle Durieu, M. Perceval, F. Magne, Q. Reynaud
Publikováno v:
Journal of Cystic Fibrosis
Journal of Cystic Fibrosis, Elsevier, 2017, 16, pp.S170. ⟨10.1016/S1569-1993(17)30750-6⟩
Journal of Cystic Fibrosis, Elsevier, 2017, 16, pp.S170. ⟨10.1016/S1569-1993(17)30750-6⟩
International audience
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48a47e7228af959ca9ac17a499600f16
https://hal.archives-ouvertes.fr/hal-01574398
https://hal.archives-ouvertes.fr/hal-01574398
Autor:
E. Chalayer, J Tebib, J Ninet, P Cathébras, Olivier Lambotte, B Asli, O Beyne-Rauzy, S Durupt, N Costedoat-Chalumeau, M. Ffrench, C. Vasselon
Publikováno v:
QJM: An International Journal of Medicine.
Background Besides peripheral cytopenias, bone marrow abnormalities, such as fibrosis, pure red cell aplasia and aplastic anemia have been reported in patients with systemic lupus erythematosus (SLE), suggesting that bone marrow may be a 25 target or