Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Pierre-Régis Burgel"'
Autor:
Matthew S. Edwards, Deborah J. Morris-Rosendahl, Robert Wilson, Guillaume Thouvenin, Siobhán B. Carr, Claire Hogg, Amelia Shoemark, Mary P. Carroll, Bruna Rubbo, Eric G. Haarman, Bernard Maitre, Estelle Escudier, Gregory Jouvion, Mahmood R. Fassad, Marie Legendre, Michel R. Loebinger, Gunnar E. Carlsson, Camille Parsons, Irma C.M. Bon, Pierre-Régis Burgel, Sunayna Best, Joost Brandsma, Isabelle Honoré, David Hunt, Jean-François Papon, Woolf T. Walker, Hannah M. Mitchison, Jane S. Lucas, Simon N. Thomas, Mitali P. Patel
Publikováno v:
The European respiratory journal, 58(2):2002359. European Respiratory Society
European Respiratory Journal
European Respiratory Journal, 2021, 58 (2), pp.2002359. ⟨10.1183/13993003.02359-2020⟩
Shoemark, A, Rubbo, B, Legendre, M, Fassad, M R, Haarman, E G, Best, S, Bon, I C M, Brandsma, J, Burgel, P-R, Carlsson, G, Carr, S B, Carroll, M, Edwards, M, Escudier, E, Honoré, I, Hunt, D, Jouvion, G, Loebinger, M R, Maitre, B, Morris-Rosendahl, D, Papon, J-F, Parsons, C M, Patel, M P, Thomas, N S, Thouvenin, G, Walker, W T, Wilson, R, Hogg, C, Mitchison, H M & Lucas, J S 2021, ' Topological data analysis reveals genotype-phenotype relationships in primary ciliary dyskinesia ', The European respiratory journal, vol. 58, no. 2, 2002359 . https://doi.org/10.1183/13993003.02359-2020
European Respiratory Journal, European Respiratory Society, 2021, 58 (2), pp.2002359. ⟨10.1183/13993003.02359-2020⟩
European Respiratory Journal
European Respiratory Journal, 2021, 58 (2), pp.2002359. ⟨10.1183/13993003.02359-2020⟩
Shoemark, A, Rubbo, B, Legendre, M, Fassad, M R, Haarman, E G, Best, S, Bon, I C M, Brandsma, J, Burgel, P-R, Carlsson, G, Carr, S B, Carroll, M, Edwards, M, Escudier, E, Honoré, I, Hunt, D, Jouvion, G, Loebinger, M R, Maitre, B, Morris-Rosendahl, D, Papon, J-F, Parsons, C M, Patel, M P, Thomas, N S, Thouvenin, G, Walker, W T, Wilson, R, Hogg, C, Mitchison, H M & Lucas, J S 2021, ' Topological data analysis reveals genotype-phenotype relationships in primary ciliary dyskinesia ', The European respiratory journal, vol. 58, no. 2, 2002359 . https://doi.org/10.1183/13993003.02359-2020
European Respiratory Journal, European Respiratory Society, 2021, 58 (2), pp.2002359. ⟨10.1183/13993003.02359-2020⟩
BackgroundPrimary ciliary dyskinesia (PCD) is a heterogeneous inherited disorder caused by mutations in approximately 50 cilia-related genes. PCD genotype–phenotype relationships have mostly arisen from small case series because existing statistica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fae0266988495c6128a73a76aa8b5ed4
https://eprints.soton.ac.uk/446244/
https://eprints.soton.ac.uk/446244/
Autor:
Neil J. Greening, Iwein Gyselinck, Lowie Van Fleteren, Timm Greulich, Sanjay Ramakrishnan, Henrik Watz, Frits M.E. Franssen, Jennifer K Quint, Arturo Huerta, Marco Contoli, Pierre-Régis Burgel, Wim Janssens, Mona Bafadhel
Publikováno v:
Monitoring airway disease.
Introduction: Despite being a high-risk event for morbidity and mortality, there is little consensus globally regarding the assessment and management of hospitalised exacerbations of COPD. Objectives: To find a consensus list of symptoms, physiologic
Publikováno v:
Diabetes. 69
Cystic fibrosis related diabetes (CFRD) is found in 20 to 50% of adults with cystic fibrosis (CF). Repeated oral glucose tolerance tests are used to screen for CFRD, but are not perfect indicators and can be tiresome for patients who already undergo
Publikováno v:
Archives de Pédiatrie
Archives de Pédiatrie, 2020, Archives de Pédiatrie, 27 (1), pp.eS25-eS29. ⟨10.1016/S0929-693X(20)30047-6⟩
Archives de Pédiatrie, 2020, Archives de Pédiatrie, 27 (1), pp.eS25-eS29. ⟨10.1016/S0929-693X(20)30047-6⟩
International audience; Cystic fibrosis (CF) is a channelopathy caused by mutations in the gene encoding the CF transmembrane conductance regulator (CFTR) protein. Diagnosis of CF has long relied on a combination of clinical (including gastrointestin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f489805f60e108f60e8231b10fe2ba8c
https://hal.univ-lille.fr/hal-03798142
https://hal.univ-lille.fr/hal-03798142
Autor:
Amandine Collin, Marjorie Vermeersch, Virginia De Rose, Frank Aboubakar Nana, Antoine Froidure, Clémence Martin, François M. Carlier, Teresinha Leal, Charles Pilette, Sophie Gohy, Marylène Lecocq, Delphine Hoton, Bruno Detry, Stijn E. Verleden, Lucile Regard, Pierre-Régis Burgel, Caroline Bouzin, Sabrina Noël
Publikováno v:
EBioMedicine, Vol. 60, p. 102974 [1-16] (2020)
EBioMedicine
EBioMedicine, 60
EBioMedicine, Vol 60, Iss, Pp 102974-(2020)
EBioMedicine
EBioMedicine, 60
EBioMedicine, Vol 60, Iss, Pp 102974-(2020)
Background: In cystic fibrosis (CF), recurrent infections suggest impaired mucosal immunity but whether production of secretory immunoglobulin A (S-IgA) is impaired remains elusive. S-IgA is generated following polymeric immunoglobulin receptor (pIgR
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60b5f01a30f2c51e62b4bb0fdbe69634
https://hdl.handle.net/2078.1/237427
https://hdl.handle.net/2078.1/237427
Autor:
Dominique Hubert, Joël Coste, Paul Legmann, Clémence Martin, Guillaume Chassagnon, Marie-Pierre Revel, Evangelia I. Zacharaki, Isabelle Fajac, Pierre-Régis Burgel, Nikos Paragios
Publikováno v:
European Radiology. 28:5111-5120
To develop an automated density-based computed tomography (CT) score evaluating high-attenuating lung structural abnormalities in patients with cystic fibrosis (CF). Seventy adult CF patients were evaluated. The development cohort comprised 17 patien
Autor:
Florence Niedergang, Kshanti Africano-Gomez, Nisha Kurian, Gaell Mayer, Elisabeth Israelsson, Floriane Herit, Jamil Jubrail, Kristofer Thörn, Lisa Öberg, Pierre-Régis Burgel, Danen Cunoosamy
Publikováno v:
Airway Cell Biology and Immunopathology.
Introduction & Hypothesis: Alveolar macrophages (AM) are critical to chronic obstructive pulmonary disease (COPD) pathogenesis. Evidence suggests they are defective in internalisation which could drive exacerbations where human rhinovirus (HRV) is fr
Autor:
Claus Vogelmeier, Rob Janssen, Christel Haenebalcke, Marko Topalovic, Nilakash Das, Emiel F.M. Wouters, Huib A. M. Kerstjens, Pierre-Régis Burgel, Christophe Pison, Renaud Louis, Marc Schlesser, Piet Vercauter, Giuseppe Liistro, Eric Derom, Wim Janssens, Vincent Ninane, Jokke Wynants, Marc Daenen
Publikováno v:
Clinical Problems.
Introduction: The use of pulmonary function tests (PFT) is built on an expert opinion. PFT interpretation relies on the recognition of patterns but scarcely leads to a specific respiratory disease diagnosis. We aimed to explore the accuracy and inter
Autor:
L. Bassinet, Marie-Pierre Revel, Bernard Maitre, Charlotte Martin, Trieu-Nghi Hoang-Thi, Thong Hua-Huy, Isabelle Honoré, Pierre-Régis Burgel, Guillaume Chassagnon
Publikováno v:
BMC Pulmonary Medicine
BMC Pulmonary Medicine, Vol 18, Iss 1, Pp 1-8 (2018)
BMC Pulmonary Medicine, Vol 18, Iss 1, Pp 1-8 (2018)
Background The present study aimed to develop an automated computed tomography (CT) score based on the CT quantification of high-attenuating lung structures, in order to provide a quantitative assessment of lung structural abnormalities in patients w
Autor:
Pierre-Régis Burgel
Publikováno v:
La Presse Médicale. 43:1337-1343
COPD is characterized by incompletely reversible airflow limitation (FEV1/FVC < 70%). The historical classification of COPD, which was based on the severity of airflow limitation assessed by the level of FEV1, did not take into account the various as