P-R Burgel
Overview
Explore the profile of P-R Burgel including associated specialties, affiliations and a list of published articles.
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Articles
60
Citations
666
Followers
0
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Recent Articles
1.
Ancel J, Guecamburu M, Marques Da Silva V, Schilfarth P, Boyer L, Pilette C, et al.
Rev Mal Respir
. 2022 May;
39(5):427-441.
PMID: 35568574
Introduction: The first COPD biennial organized by the French Society of Respiratory Diseases (SPLF) took place on 17 December 2021. State Of The Art: The objective of the biennial was...
2.
Martin C, Burnet E, Ronayette-Preira A, De Carli P, Martin J, Delmas L, et al.
Respir Med Res
. 2021 Jun;
80:100829.
PMID: 34091202
Backgound: Elexacaftor-tezacaftor-ivacaftor partially restores cystic fibrosis transmembrane conductance regulator function, and has been shown to induce significant clinical improvement in patients with at least one Phe508del allele. Yet little data...
3.
Joumaa H, Regard L, Carlier N, Chassagnon G, Alabadan E, Canoui E, et al.
Respir Med Res
. 2020 Aug;
78:100780.
PMID: 32759053
No abstract available.
4.
Deslee G, Zysman M, Burgel P, Perez T, Boyer L, Gonzalez J, et al.
Respir Med Res
. 2020 Jun;
78:100764.
PMID: 32498023
No abstract available.
5.
Ehret N, Carlier N, Marey J, Rabbat A, Burgel P, Roche N
Rev Mal Respir
. 2020 Apr;
37(4):308-319.
PMID: 32284206
Introduction: The relations between chronic obstructive pulmonary disease (COPD) and respiratory diseases due to Aspergillus spp. are not well understood. Methods: We analysed a retrospective series of patients hospitalized with...
6.
Pagin A, Sermet-Gaudelus I, Burgel P
Arch Pediatr
. 2020 Mar;
27 Suppl 1:eS25-eS29.
PMID: 32172933
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...
7.
Burgel P, Montani D, Blanc F, Pigearias B, Roche N
Respir Med Res
. 2019 Jul;
75:A1-A2.
PMID: 31256850
No abstract available.
8.
Fitton I, Revel M, Burgel P, Hernigou A, Boussaud V, Guillemain R, et al.
Diagn Interv Imaging
. 2019 Feb;
100(5):287-294.
PMID: 30711497
Purpose: The purpose of this study was first to evaluate the imaging-related cumulative post-transplantation radiation dose in cystic fibrosis (CF) lung transplantation (LT) recipients and second, to identify the occurrence...
9.
Burgel P, Montani D, Pigearias B, Blanc F, Roche N
Rev Pneumol Clin
. 2018 Dec;
74(6):367-368.
PMID: 30527221
No abstract available.
10.
Lafoeste H, Regard L, Martin C, Chassagnon G, Burgel P
Rev Pneumol Clin
. 2018 Oct;
74(5):267-278.
PMID: 30343944
Introduction: Cystic fibrosis (CF) is a genetic disease primarily affecting the lungs, which could lead to chronic respiratory failure and premature death. CF patients are usually followed in specialized centers,...