N. Stremler

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Genomic analysis of an emerging multiresistant Staphylococcus aureus strain rapidly spreading in cystic fibrosis patients revealed the presence of an antibiotic inducible bacteriophage

J. Sarles, David Hernández, P. François, 2009, Biology Direct.

Non‐classic cystic fibrosis associated with D1152H CFTR mutation

P. Burgel, N. Stremler, M. Reynaud‐Gaubert, 2010, Clinical genetics.

Mycobacterium chimaera pulmonary infection complicating cystic fibrosis: a case report

M. Drancourt, J. Rolain, N. Stremler, 2011, Journal of medical case reports.

[Value of continuous glucose monitoring in screening for diabetes in cystic fibrosis].

J. Sarles, N. Stremler, J. Dubus, 2009, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

AGER -429T/C Is Associated with an Increased Lung Disease Severity in Cystic Fibrosis

P. Böelle, P. Reix, J. Dalphin, 2012, PloS one.

Respiratory management of children with spinal muscular atrophy (SMA).

N. Stremler, B. Fauroux, A. Amaddeo, 2020, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Paediatric long term continuous positive airway pressure and noninvasive ventilation in France: A cross-sectional study.

S. Matecki, I. Pin, M. Ollivier, 2021, Respiratory medicine.

Long-Term Mechanical Ventilation Equipment for Neuromuscular Patients: Meeting the Expectations of Patients and Prescribers

J. Pépin, D. Orlikowski, I. Pin, 2014, Respiratory Care.

Outbreak of Corynebacterium pseudodiphtheriticum Infection in Cystic Fibrosis Patients, France

J. Sarles, D. Raoult, J. Rolain, 2010, Emerging infectious diseases.

ISPa46, a novel insertion sequence in the oprD porin gene of an imipenem-resistant Pseudomonas aeruginosa isolate from a cystic fibrosis patient in Marseille, France.

S. Leroy, J. Rolain, S. Diene, 2013, International journal of antimicrobial agents.

Soluble squalamine tablets for the rapid disinfection of home nebulizers of cystic fibrosis patients.

D. Raoult, J. Rolain, N. Stremler, 2012, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Long term noninvasive ventilation and continuous positive airway pressure in children with neuromuscular diseases in France

S. Matecki, M. Ollivier, P. Bokov, 2022, Neuromuscular Disorders.

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.

Inquilinus limosus and Cystic Fibrosis

J. Sarles, D. Raoult, J. Rolain, 2008, Emerging infectious diseases.

Nocardia farcinica lung infection in a patient with cystic fibrosis: a case report

J. Sarles, D. Raoult, J. Rolain, 2010, Journal of medical case reports.

First isolation of two colistin-resistant emerging pathogens, Brevundimonas diminuta and Ochrobactrum anthropi, in a woman with cystic fibrosis: a case report

J. Sarles, D. Raoult, J. Rolain, 2008, Journal of medical case reports.

Molecular Detection of Multiple Emerging Pathogens in Sputa from Cystic Fibrosis Patients

J. Sarles, D. Raoult, J. Rolain, 2008, PloS one.

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.

Pulmonary acceleration time to optimize the timing of lung transplant in cystic fibrosis

J. Pépin, P. Boelle, P. Burgel, 2012, Pulmonary circulation.

E. Bosdure, N. Stremler, P. Petit, 2018, Pediatric blood & cancer.

Sleep quality and nocturnal hypoxaemia and hypercapnia in children and young adults with cystic fibrosis

J. Pépin, P. Boelle, P. Burgel, 2012, Archives of Disease in Childhood.

Evaluation of colistin susceptibility in multidrug-resistant clinical isolates from cystic fibrosis, France

J. Rolain, N. Stremler, J. Dubus, 2013, European Journal of Clinical Microbiology & Infectious Diseases.

Evaluation of colistin susceptibility in multidrug-resistant clinical isolates from cystic fibrosis, France

J. Rolain, N. Stremler, J. Dubus, 2013, European Journal of Clinical Microbiology & Infectious Diseases.

Screening strategies for glucose tolerance abnormalities and diabetes in people with cystic fibrosis.

P. Reix, P. Burgel, N. Stremler, 2023, Diabetes & metabolism.

Inquilinus limosus: an easily missed emerging resistant respiratory pathogen in cystic fibrosis patients

J. Sarles, D. Raoult, J. Rolain, 2008 .

Author's response to reviews Title: First isolation of Two colistin-resistant Emerging Pathogens, Brevundimonas diminuta and Ochrobactrum anthropi, in a Cystic Fibrosis Patient

J. Sarles, D. Raoult, F. Bittar, 2008 .

Microbial diversity in the sputum of a cystic fibrosis patient studied with 16S rDNA pyrosequencing

J. Sarles, C. Robert, D. Raoult, 2009, European Journal of Clinical Microbiology & Infectious Diseases.

[Recommendations for pediatric oxygen therapy in acute and chronic settings: needs assessment, implementation criteria, prescription practices and follow-up].

C. Delacourt, I. Pin, N. Stremler, 2012, Archives de pédiatrie.

Genomic analysis of an emerging multiresistant Staphylococcus aureus strain rapidly spreading in cystic fibrosis patients revealed the presence of an antibiotic inducible bacteriophage

J. Sarles, David Hernández, P. François, 2009, Biology Direct.

Infantile form of carnitine palmitoyltransferase II deficiency in a girl with rapid fatal onset

P. Divry, N. Stremler, O. Paut, 1995, Journal of Inherited Metabolic Disease.

Practice of noninvasive ventilation for cystic fibrosis: a nationwide survey in France.

P. Boelle, P. Burgel, A. Clément, 2008, Respiratory care.