Results 71 to 80 of about 5,453 (193)

Infections respiratoires fongiques et mucoviscidose : focus sur Scedosporium apiospermum [PDF]

, 2012
National ...
J.P. Bouchara
core   +1 more source

Mucoviscidose: apresentação de um caso. [PDF]

, 1982
Trabalho de Conclusão de Curso - Universidade Federal de Santa Catarina, Centro de Ciências da Saúde, Departamento de Pediatria, Curso de Medicina, Florianópolis ...
Maresch, Bruno A
core  

Social support for the chronically ill during lockdown. Qualitative research in the COVID‐19 pandemic

Sociology of Health &Illness, Volume 47, Issue 1, January 2025.
Abstract Chronic illness requires a web of actors, both professional and familiar, who constitute the support network of the chronically ill. This article aims to analyse how the COVID‐19 pandemic has impacted on the delicate balance of these supports. Qualitative research was conducted among people with four types of chronic diseases in France: cystic
Louise Virole, Céline Gabarro, Elise Ricadat   +2 more
wiley   +1 more source

Glucose tolerance in Canadian and French cystic fibrosis adult patients

Scientific Reports, 2019
Cystic fibrosis (CF)-related diabetes is associated with increased mortality. We analysed the clinical and glycemic profiles of two cohorts of patients treated according to the same guidelines in France and Canada. To investigate incidence differences in
Quitterie Reynaud, Valérie Boudreau, Sandrine Touzet, Katherine Desjardins, Stéphanie Poupon Bourdy, Emilie Blond, Yves Berthiaume, Rémi Rabasa-Lhoret, Isabelle Durieu   +8 more
doaj   +1 more source

Pseudomonas aeruginosa prise en flagrant délit de casse ! Pseudomonas aeruginosa caught in the act ! [PDF]

, 2013
International audienceDes armes qui attaquent le génome eucaryote de façon encore mystérieuse Pseudomonas aeruginosa est une bactérie pathogène opportuniste infectant principalement les individus aux défenses immunitaires affaiblies, les patients ayant ...
Elsen, Sylvie, Lemercier, Claudie
core   +3 more sources

Surfactant protein a in cystic fibrosis: supratrimeric structure and pulmonary outcome. [PDF]

, 2012
The state of oligomerization of surfactant associated protein-A (SP-A) monomers differs between individuals. This likely affects SP-A's functional properties and could thereby influence clinical status in patients with lung diseases.
Ballmann, Manfred, Griese, Matthias, Heinrich, Stephanie, Kabesch, Michael, Kappler, Matthias, Paul, Karl, Ratjen, Felix, Rietschel, Ernst   +7 more
core   +8 more sources

An Efficient Low‐Cost Device for Sampling Exhaled Breath Condensate EBC

Advanced Sensor Research, Volume 3, Issue 7, July 2024.
Exhaled breath condensate (EBC) is not simply distilled water but contains molecular biomarkers that are indicators for the health status of a person, typically in the case of lung diseases. A user‐friendly collection device has been designed that samples up to 2 mL of EBC in just 5 min thanks to utilizing materials with task‐specific thermo‐physical ...
Mehran Khorshid, Soroush Bakhshi Sichani, Dimna L. Barbosa Estrada, Werner Neefs, Alexander Clement, Gerhard Pohlmann, Ralph Epaud, Sophie Lanone, Patrick Wagner   +8 more
wiley   +1 more source

COBRAPed cohort: Do sensitization patterns differentiate children with severe asthma from those with a milder disease?

Pediatric Allergy and Immunology, Volume 35, Issue 3, March 2024.
IgE sensitization patterns in severe recurrent wheeze/school‐age asthma. Abstract Background It is unclear whether sensitization patterns differentiate children with severe recurrent wheeze (SRW)/severe asthma (SA) from those with non‐severe recurrent wheeze (NSRW)/non‐severe asthma (NSA).
Stéphanie Lejeune, Naïm Bouazza, Pascale Roland Nicaise, Valérie Jolaine, Léa Roditis, Christophe Marguet, Flore Amat, Patrick Berger, Michael Fayon, Jean‐Christophe Dubus, Sophie Valois, Philippe Reix, Mathieu Pellan, Jacques Brouard, Raphael Chiron, Lisa Giovannini‐Chami, Jacques de Blic, Antoine Deschildre, Guillaume Lezmi, the COBRAPed Study Group, Rola Abou‐Taam, Muriel Le Bourgeois, Alice Hadchouel‐Duvergé, David Drummond, Christophe Delacourt, Marie‐Alexandra Alyanakian, Lucienne Chatennoud, Caroline Thumerelle, Clémence Mordacq, Irina Badiu‐Decleyre, Cécile Bonnel, Laure Delbecque, Laurent Beghin, Graziella Mingardi, Caroline Tournegros, Sylvain Blanchon, Léa Roditis, Véronique Houdoin, Stéphanie Wanin, Marie Noelle Lebras, Stéphane Debelleix, Valérie Siao, Marine Servat, Guillaume Simon, Patricia El Boustany, Emmanuelle Bosdure, Julie Mazenq, Isabelle Cabon, Camille Ohlmann, Stéphanie Vrielynck, Virginie Jubin, Sylvie‐Anne André Gomez, Marie‐Christine Werck Gallois, Priscille Biermé, Isabelle Pin, Sylvie Chollet‐Martin   +55 more
wiley   +1 more source

Traitement de la fibrose kystique en physiothérapie : les meilleures pratiques [PDF]

, 2014
Travail d'intégration présenté à la Faculté de médecine en vue de l’obtention du grade de maîtrise et sciences de la santé - PhysiothérapieProblématique : La fibrose kystique est une maladie génétique incurable affectant les systèmes respiratoire et ...
Charbonneau-Corbeil, Léa, Charbonneau-Dufresne, Florence, Circé, Annick, Côté, Amélie   +3 more
core   +1 more source

CSN5 binds to misfolded CFTR and promotes its degradation [PDF]

, 2008
Cystic fibrosis is mainly caused by mutations that interfere with the biosynthetic folding of the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The aim of this study was to find cellular proteins interacting with CFTR and regulating
Tanguy, Gaëlle, Drévillon, Loïc, Arous, Nicole, Hasnain, Afia, Hinzpeter, Alexandre, Fritsch, Janine, Goossens, Michel, Fanen, Pascale   +7 more
core   +1 more source