Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Sylvain, Blanchon"'
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
In the last 10 years, the care of patients with cystic fibrosis (CF) has been revolutionized with the introduction of cystic fibrosis transmembrane conductance regulator (CFTR) modulator drugs, with a major impact on symptoms and life expectancy, esp
Externí odkaz:
https://doaj.org/article/3278978b4cc241f68a3865bbcff6e915
Autor:
Georgia Mitropoulou, Angela Koutsokera, Chantal Csajka, Sylvain Blanchon, Alain Sauty, Jean-Francois Brunet, Christophe von Garnier, Grégory Resch, Benoit Guery
Publikováno v:
European Respiratory Review, Vol 31, Iss 166 (2022)
Lower respiratory tract infections lead to significant morbidity and mortality. They are increasingly caused by multidrug-resistant pathogens, notably in individuals with cystic fibrosis, hospital-acquired pneumonia and lung transplantation. The use
Externí odkaz:
https://doaj.org/article/de2e561e43614de5a9f439481863ab50
Autor:
Mirjam Nussbaumer, Elisabeth Kieninger, Stefan A. Tschanz, Sibel T. Savas, Carmen Casaulta, Myrofora Goutaki, Sylvain Blanchon, Andreas Jung, Nicolas Regamey, Claudia E. Kuehni, Philipp Latzin, Loretta Müller
Publikováno v:
ERJ Open Research, Vol 7, Iss 4 (2021)
Background Diagnosis of primary ciliary dyskinesia (PCD) is challenging since there is no gold standard test. The European Respiratory (ERS) and American Thoracic (ATS) Societies developed evidence-based diagnostic guidelines with considerable differ
Externí odkaz:
https://doaj.org/article/89e1d3c576d84fa5ba240a58f29a6e82
Autor:
Eva Choong, Alain Sauty, Angela Koutsokera, Sylvain Blanchon, Pascal André, Laurent Decosterd
Publikováno v:
Pharmaceutics, Vol 14, Iss 8, p 1674 (2022)
Drugs modulating the cystic fibrosis transmembrane conductance regulator (CFTR) protein, namely ivacaftor, lumacaftor, tezacaftor, and elexacaftor, are currently revolutionizing the management of patients with cystic fibrosis (CF), particularly those
Externí odkaz:
https://doaj.org/article/c39febd2b9914d9b9cd7389ea3d26fc2
Bronchial Remodeling-based Latent Class Analysis Predicts Exacerbations in Severe Preschool Wheezers
Autor:
Michael Fayon, Fabien Beaufils, Pauline Esteves, Maryline Campagnac, Elise Maurat, Marine Michelet, Valerie Siao-Him-Fa, Frederic Lavrand, Guillaume Simon, Hugues Begueret, Patrick Berger, Françoise Auriol, Sylvain Blanchon, Dominique Carles, Vincent Boisserie-Lacroix, François Brémont, Stéphanie Bui, Marie-Luce Choukroun, Stéphane Debelleix, Hala Feghali, Géraldine Labouret, Audrey Martin Blondel, Sébastien Marais, Marie Mittaine, Fabienne Nacka, Olga Ousova, Isabelle Rouquette, François Semjen, Frédérique Sgoifo, Thomas Trian
Publikováno v:
American Journal of Respiratory and Critical Care Medicine. 207:416-426
Children with preschool wheezing represent a very heterogeneous population with wide variability regarding their clinical, inflammatory, obstructive, and/or remodeling patterns. We hypothesized that assessing bronchial remodeling would help clinician
Autor:
Clara Fernandez Elviro, Sylvain Blanchon, Sylke Hoehnel, Urs Schumacher, Alain Sauty, Nathalie Brandenberg, Nicolas Regamey
Publikováno v:
Swiss Medical Weekly, Vol 151, Iss 1516 (2021)
Cystic fibrosis (CF) is a genetic disease caused by a bi-allelic mutation of the cystic fibrosis transmembrane conductance regulator (CFTR) gene. When the diagnosis cannot be confirmed by a positive sweat test or/and the identification of two CF-caus
Externí odkaz:
https://doaj.org/article/9a31cba8737845acaa57ae083e3e1446
Autor:
Loretta Müller, Sibel T. Savas, Stefan A. Tschanz, Andrea Stokes, Anaïs Escher, Mirjam Nussbaumer, Marina Bullo, Claudia E. Kuehni, Sylvain Blanchon, Andreas Jung, Nicolas Regamey, Beat Haenni, Martin Schneiter, Jonas Ingold, Elisabeth Kieninger, Carmen Casaulta, Philipp Latzin, on behalf of the Swiss PCD Research Group
Publikováno v:
Diagnostics, Vol 11, Iss 9, p 1540 (2021)
Primary ciliary dyskinesia (PCD) is a rare genetic disease characterized by dyskinetic cilia. Respiratory symptoms usually start at birth. The lack of diagnostic gold standard tests is challenging, as PCD diagnostics requires different methods with h
Externí odkaz:
https://doaj.org/article/0512b868d0cd464db36b4b55548cf843
Autor:
Georgia Mitropoulou, Pieter-Jan Gijs, Angela Koutsokera, Alain Sauty, Sylvain Blanchon, Chantal Csajka, Jean-François Brunet, Grégory Resch, Benoit Guery, Christophe Von Garnier
Publikováno v:
Revue Médicale Suisse. 18:2150-2156
Autor:
Georgia, Mitropoulou, Pieter-Jan, Gijs, Angela, Koutsokera, Alain, Sauty, Sylvain, Blanchon, Chantal, Csajka, Jean-François, Brunet, Grégory, Resch, Benoit, Guery, Christophe, Von Garnier
Publikováno v:
Revue medicale suisse. 18(804)
The crisis of antibiotic resistance represents a global public health challenge, affecting particularly patients with respiratory infections. The use of (bacterio)phages for the treatment of bacterial infections (phage therapy) seems safe but its eff
Publikováno v:
Revue Médicale Suisse. 19:351-352