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Publikováno v:
Die Pharmazie. 76(12)
Flow regulators are widely used in hospitals to assist with intravenous (IV) infusion of medication. The rupture of a flow regulator at the base of the clamp was observed during parenteral nutrition. This rupture resulted in fluid leakage and an inle
Autor:
R. Kanaan, N. Desmazes-Dufeu, B. Zuber, Dominique Hubert, Jeanne Chapron, Daniel Dusser, Jean-Paul Mira, P.-R. Burgel
Publikováno v:
Revue des Maladies Respiratoires. 28:503-516
The natural history of cystic fibrosis (CF) may be associated both with acute respiratory complications (respiratory exacerbations, haemoptysis, pneumothorax) and with non-respiratory complications (distal intestinal obstruction syndrome, dehydration
Autor:
Dominique Hubert, T. Bienvenu, N. Desmazes-Dufeu, R. Kanaan, Isabelle Fajac, T. Coman, Daniel Dusser, P.-R. Burgel
Publikováno v:
Revue des Maladies Respiratoires. 26:67-73
Introduction La mucoviscidose est habituellement diagnostiquee dans les premieres annees de vie. Observations Nous rapportons trois cas familiaux de mucoviscidose diagnostiques a l’âge adulte. Le premier patient, âge de 39 ans, a consulte pour un
Publikováno v:
Réanimation. 16:318-325
Resume La mucoviscidose est la plus frequente des maladies genetiques mettant en jeu le pronostic vital [1] chez les Caucasiens en conduisant a des defaillances respiratoires, pancreatiques et gastro-intestinales. Bien que cette maladie reste constam
Autor:
M. Abely, P. Bourget, R. Panzo, R. Nové-Josserand, C. Dupont, B.-L. Jouani, A. Amin, C. Merlette, F. Voge, N. Desmazes-Dufeu, F. Vidal, Dominique Hubert, J. Pages, Jean-Christophe Dubus
Ceftazidime is particularly efficient against Pseudomonas aeruginosa in cystic fibrosis patients. Thus, the spontaneous production of pyridine, which is a toxic product, raises some concern. Our aim was to examine the kinetics of degradation of cefta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8796d6195d8ed6eb2b9e5fa8e68b6d49
https://europepmc.org/articles/PMC3993216/
https://europepmc.org/articles/PMC3993216/
Autor:
J-C, Dubus, L, Bassinet, F, Chedevergne, B, Delaisi, N, Desmazes-Dufeu, G, Reychler, L, Vecellio
Publikováno v:
Revue des maladies respiratoires. 31(4)
In the past few years some new inhaled drugs and inhalation devices have been proposed for the treatment of cystic fibrosis. Breath-controlled nebulizers allow increased pulmonary deposition, with a lower variability and a shorter delivery time. The
Autor:
A. Amin, N. Desmazes-Dufeu, M. Abely, R. Panzo, C. Dupont, D. Hubert, P. Bourget, J. Pages, B.-L. Jaouani, R. Nové-Josserand, Jean-Christophe Dubus
Publikováno v:
Journal of Cystic Fibrosis. 12
Autor:
D. Dusser, R. Matran, A. Lockhart, Y. Aron, N. Desmazes-Dufeu, E. Swierczewski, Barbara S. Polla
Publikováno v:
Clinical & Experimental Allergy. 26:821-828
Summary Background Atopy, with or without associated asthma, provides a useful model for evaluating the genetic factors that control human immune responsiveness. HLA class II gene products are involved in the control of immune responses. Objectives W
Autor:
T. Bienvenu, R. Kanaan, D. Dusser, N. Desmazes-Dufeu, X Dray, Philippe Marteau, Dominique Hubert
Publikováno v:
European Journal of Clinical Nutrition. 59:152-154
Objective: To determine the prevalence and clinical features of malnutrition and its relationship with the CFTR genotype in a cystic fibrosis (CF) adult population. Design: Cross-sectional study. Setting: Department of Pulmonology, Cochin Hospital, P