L. Bassinet

发表

Follow-Up and Management of Chronic Rhinosinusitis in Adults with Primary Ciliary Dyskinesia: Review and Experience of Our Reference Centers

B. Crestani, J. Papon, É. Béquignon, 2019, Journal of clinical medicine.

Critical Evaluation of Sinonasal Disease in 64 Adults with Primary Ciliary Dyskinesia

B. Crestani, J. Papon, É. Béquignon, 2019, Journal of clinical medicine.

Quantitative analysis of ciliary beating in primary ciliary dyskinesia: a pilot study

B. Housset, S. Amselem, B. Crestani, 2012, Orphanet Journal of Rare Diseases.

Bordetella pertussis Adenylate Cyclase-Hemolysin Induces Interleukin-6 Secretion by Human Tracheal Epithelial Cells

B. Housset, J. Cavaillon, C. Fitting, 2004, Infection and Immunity.

[Pleuropneumonia due to Mycobacterium chelonae].

B. Housset, I. Monnet, B. Maître, 2011, Revue des maladies respiratoires.

Tuberculous aneurysms of the abdominal aorta.

P. Desgranges, J. Becquemin, J. Marzelle, 2008, Journal of vascular surgery.

Determinants of Refusal of A/H1N1 Pandemic Vaccination in a High Risk Population: A Qualitative Approach

I. Sermet-Gaudelus, O. Lortholary, O. Launay, 2012, PloS one.

Role of Adhesins and Toxins in Invasion of Human Tracheal Epithelial Cells by Bordetella pertussis

B. Housset, P. Gounon, P. Gueirard, 2000, Infection and Immunity.

Infertility in an adult cohort with primary ciliary dyskinesia: phenotype–gene association

S. Amselem, M. Boon, S. Christin‐Maitre, 2017, European Respiratory Journal.

Real-Life Safety and Effectiveness of Lumacaftor-Ivacaftor in Patients with Cystic Fibrosis.

D. Caimmi, A. Didier, S. Leroy, 2020, American journal of respiratory and critical care medicine.

Real-life initiation of lumacaftor/ivacaftor combination in adults with cystic fibrosis homozygous for the Phe508del CFTR mutation and severe lung disease.

S. Leroy, P. Burgel, D. Grenet, 2017, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Computed Tomography Description of the Uncinate Process Angulation in Patients With Cystic Fibrosis and Comparison With Primary Ciliary Dyskinesia, Nasal Polyposis, and Controls

J. Blondeau, F. Canoui-Poitrine, T. van den Abbeele, 2019, Ear, nose, & throat journal.

Loss-of-function mutations in RSPH1 cause primary ciliary dyskinesia with central-complex and radial-spoke defects.

B. Housset, S. Amselem, R. Epaud, 2013, American journal of human genetics.

A recurrent deep-intronic splicing CF mutation emphasizes the importance of mRNA studies in clinical practice.

M. Claustres, R. Epaud, E. Girodon, 2011, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Mutations in the amiloride‐sensitive epithelial sodium channel in patients with cystic fibrosis‐like disease

P. Lebecque, A. Azad, M. Schwartz, 2009, Human mutation.

Routine use of granulocyte colony-stimulating factor is not cost-effective and does not increase patient comfort in the treatment of small-cell lung cancer: an analysis using a Markov model.

B. Housset, C. Chouaid, C. Fuhrman, 1998, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Lessons from a French collaborative case–control study in cystic fibrosis patients during the 2009 A/H1N1 influenza pandemy

P. Boelle, I. Durieu, N. Stremler, 2015, BMC Infectious Diseases.

Nosocomial Pertussis Outbreak Among Adult Patients and Healthcare Workers

B. Housset, N. Guiso, E. Njamkepo, 2004, Infection Control & Hospital Epidemiology.

Health and Economic Consequences of an Outbreak of Pertussis Among Healthcare Workers in a Hospital in France

J. Caro, B. Housset, A. Ward, 2005, Infection Control & Hospital Epidemiology.

Nebulised liposomal amphotericin-B as maintenance therapy in allergic bronchopulmonary aspergillosis: a randomised, multicentre trial

D. Caillaud, F. Laurent, S. Ragot, 2021, European Respiratory Journal.

25 Unsolved severe chronic rhinosinusitis elucidated by extensive CFTR genotyping

S. Simon, I. Sermet-Gaudelus, I. Callebaut, 2017 .

Changes of CFTR functional measurements and clinical improvements in cystic fibrosis patients with non p.Gly551Asp gating mutations treated with ivacaftor.

I. Sermet-Gaudelus, M. Wilschanski, T. Nguyen-Khoa, 2017, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Ultrastructural analysis of the interactions between Bordetella pertussis, Bordetella parapertussis and Bordetella bronchiseptica and human tracheal epithelial cells.

M. Prevost, I. Bonne, P. Gueirard, 2005, Microbial pathogenesis.

Prospective evaluation of azole resistance in Aspergillus fumigatus clinical isolates in France.

J. Guillot, F. Botterel, E. Dannaoui, 2015, Medical mycology.

Clinical characteristics, functional respiratory decline and follow-up in adult patients with primary ciliary dyskinesia

B. Housset, P. Burgel, J. Papon, 2016, Thorax.

Cystic fibrosis transmembrane conductance regulator channel dysfunction in non-cystic fibrosis bronchiectasis.

P. Burgel, I. Sermet-Gaudelus, I. Fajac, 2010, American journal of respiratory and critical care medicine.

[Evaluation of occupational exposures in lung cancer].

B. Housset, F. Roos, F. Lebargy, 2000, Revue des maladies respiratoires.

Omalizumab treatment for allergic bronchopulmonary aspergillosis in young patients with cystic fibrosis.

A. Clément, I. Sermet-Gaudelus, J. Derelle, 2017, Respiratory medicine.

Automated computed tomographic scoring of lung disease in adults with primary ciliary dyskinesia

M. Revel, P. Burgel, G. Chassagnon, 2018, BMC Pulmonary Medicine.

Vaccine coverage in CF children: A French multicenter study.

I. Sermet-Gaudelus, O. Launay, H. Corvol, 2015, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Loss-of-function mutations in RSPH1 cause primary ciliary dyskinesia with central-complex and radial-spoke defects.

B. Housset, S. Amselem, R. Epaud, 2013, American journal of human genetics.

Real-life initiation of lumacaftor/ivacaftor combination in adults with cystic fibrosis homozygous for the Phe508del CFTR mutation and severe lung disease.

S. Leroy, P. Burgel, D. Grenet, 2017, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.