P. Reix

P. Reix, I. Durieu, J. Nicolas, 2019, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

Cumulative Incidence and Risk Factors for Severe COVID-19 in French People with Cystic Fibrosis

P. Reix, P. Burgel, C. Marguet, 2022, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

Clinical response to lumacaftor-ivacaftor in patients with cystic fibrosis according to baseline lung function.

P. Reix, P. Burgel, J. Paillasseur, 2020, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Severe Pulmonary Fibrosis as the First Manifestation of Interferonopathy (TMEM173 Mutation).

F. Rieux-Laucat, P. Reix, J. Dubus, 2016, Chest.

Chest physiotherapy enhances detection of Pseudomonas aeruginosa in nonexpectorating children with cystic fibrosis

P. Reix, I. Pin, C. Marguet, 2021, ERJ Open Research.

A new animal model of obstructive sleep apnea responding to continuous positive airway pressure.

P. Reix, S. Parrot, Jian-Sheng Lin, 2011, Sleep.

Optimized approach for the identification of highly efficient correctors of nonsense mutations in human diseases

P. Reix, S. Rebuffat, E. Adriaenssens, 2017, PloS one.

Proceedings of the 23rd Paediatric Rheumatology European Society Congress: part one

J. Stinson, J. Jaremko, A. Goris, 2017, Pediatric Rheumatology.

New surfactant protein C gene mutations associated with diffuse lung disease

P. Reix, L. Guillot, R. Epaud, 2009, Journal of Medical Genetics.

178 Glucose tolerance in cystic fibrosis patients over a 3-year period (DIAMUCO study)

P. Reix, I. Pin, M. Laville, 2015 .

The CF-CIRC study: a French collaborative study to assess the accuracy of Cystic Fibrosis diagnosis in neonatal screening

P. Reix, G. Bellon, I. Sermet-Gaudelus, 2006, BMC pediatrics.

Case series of omalizumab for allergic bronchopulmonary aspergillosis in cystic fibrosis patients

P. Reix, P. Burgel, I. Durieu, 2017, Pediatric pulmonology.

Successful management of severe infant bullous pemphigoid with omalizumab

C. Bodemer, P. Reix, F. Cambazard, 2012, The British journal of dermatology.

preterm and full-term lambs Postnatal maturation of vagal respiratory reflexes in

Fadi Xu, P. Reix, J. Arsenault, 2015 .

Nutritional Status in the First 2 Years of Life in Cystic Fibrosis Diagnosed by Newborn Screening

P. Reix, F. Brémont, A. Munck, 2018, Journal of pediatric gastroenterology and nutrition.

Exposure of Staphylococcus aureus to Subinhibitory Concentrations of β-Lactam Antibiotics Induces Heterogeneous Vancomycin-Intermediate Staphylococcus aureus

F. Vandenesch, P. Reix, M. Reverdy, 2014, Antimicrobial Agents and Chemotherapy.

Acute chest pain in an adolescent with cystic fibrosis in September: Would you have thought about this?

P. Reix, Hiba Dowaikh, F. Morfin-Sherpa, 2017, Pediatric pulmonology.

Is the raised volume rapid thoracic compression technique ready for use in clinical trials in infants with cystic fibrosis?

S. Matecki, P. Reix, L. Kent, 2016, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Influence of Prematurity on Postnatal Maturation of Heart Rate and Arterial Pressure Responses to Hypoxia in Lambs

P. Reix, J. Arsenault, François Moreau-Bussière, 2007, Neonatology.

Effects of C fiber blockade on cardiorespiratory responses to laryngeal stimulation in concious lambs

P. Reix, J. Arsenault, D. Dorion, 2003, Respiratory Physiology & Neurobiology.

Real-world assessment of LCI following lumacaftor-ivacaftor initiation in adolescents and adults with cystic fibrosis.

P. Reix, P. Burgel, J. Paillasseur, 2021, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

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.

Profiling the response to lumacaftor‐ivacaftor in children with cystic between fibrosis and new insight from a French‐Italian real‐life cohort

P. Reix, V. Lucidi, C. Marguet, 2022, Pediatric pulmonology.

Bronchiolitis obliterans and BOOP : what relevance in pediatric ?

P. Reix, 2008 .

Viral respiratory tract infections in young children with cystic fibrosis: a prospective full-year seasonal study

P. Reix, A. Doléans-Jordheim, F. Morfin, 2019, Virology Journal.

Palivizumab prophylaxis in infants with cystic fibrosis does not delay first isolation of Pseudomonas aeruginosa or Staphylococcus aureus

P. Reix, L. Coutier, M. Dalphin, 2017, European Journal of Pediatrics.

Efficacy and Safety of Elexacaftor/Tezacaftor/Ivacaftor in Children 6 Through 11 Years of Age with Cystic Fibrosis Heterozygous for F508del and a Minimal Function Mutation: A Phase 3b, Randomized, Placebo-controlled Study

D. Prais, P. Reix, H. Selvadurai, 2022, American journal of respiratory and critical care medicine.

French national cohort of neuroendocrine cell hyperplasia of infancy (FRENCHI) study: diagnosis and initial management

C. Delacourt, P. Reix, R. Epaud, 2022, European Journal of Pediatrics.

Effectiveness of palivizumab in children with childhood interstitial lung disease: The French experience

C. Delacourt, P. Reix, R. Epaud, 2016, Pediatric pulmonology.

Bronchiectasis in two pediatric patients with Rothmund–Thomson syndrome

P. Reix, G. Bellon, J. Derelle, 2007, Pediatrics international : official journal of the Japan Pediatric Society.

A formalized transition program for cystic fibrosis: A 10‐year retrospective analysis of 97 patients in Lyon

P. Reix, I. Durieu, Q. Reynaud, 2021, Pediatric pulmonology.

Impact of Scedosporium apiospermum complex seroprevalence in patients with cystic fibrosis.

P. Reix, I. Durieu, O. Lortholary, 2014, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Efficacy of the Janus kinase 1/2 inhibitor ruxolitinib in the treatment of vasculopathy associated with TMEM173-activating mutations in 3 children.

F. Rieux-Laucat, A. Fischer, C. Bodemer, 2016, The Journal of allergy and clinical immunology.

Effectiveness of home treatment for patients with cystic fibrosis: The intravenous administration of antibiotics to treat respiratory infections

P. Reix, E. Decullier, I. Pin, 2008, Pediatric pulmonology.

Moderate intake of docosahexaenoic acid raises plasma and platelet vitamin E levels in cystic fibrosis patients.

P. Reix, M. Lagarde, I. Durieu, 2016, Prostaglandins, leukotrienes, and essential fatty acids.

An impulse oscillometry system is less efficient than spirometry in tracking lung function improvements after intravenous antibiotic therapy in pediatric patients with cystic fibrosis

P. Reix, L. Coutier, C. Mainguy, 2015, Pediatric pulmonology.

Laryngeal sensitivity in the neonatal period: From bench to bedside

P. Reix, J. Praud, M. St-Hilaire, 2007, Pediatric pulmonology.

apneas in lambs is complete at the laryngeal level only Active upper airway closure during induced central

P. Micheau, P. Reix, J. Arsenault, 2015 .

Active upper airway closure during induced central apneas in lambs is complete at the laryngeal level only.

P. Reix, J. Arsenault, P. Fortier, 2003, Journal of applied physiology.

Upper airways and neonatal respiration

P. Reix, J. Praud, 2005, Respiratory Physiology & Neurobiology.

Diffuse chondroid malformation of the lung: Cases series of a hitherto undescribed congenital lung disease

P. Reix, R. Epaud, G. Bellon, 2010, Pediatric pulmonology.

A national internet-linked based database for pediatric interstitial lung diseases: the French network

C. Delacourt, J. Vibert, P. Reix, 2012, Orphanet Journal of Rare Diseases.

Hemothorax: an unusual complication of costal exostosis.

P. Reix, G. Bellon, J. Pracros, 2005, Journal of pediatric surgery.

Strong incidence of Pseudomonas aeruginosa on bacterial rrs and ITS genetic structures of cystic fibrosis sputa

F. Vandenesch, R. Marti, P. Reix, 2017, PloS one.

Impact of Coexistence Phenotype Between Staphylococcus aureus and Pseudomonas aeruginosa Isolates on Clinical Outcomes Among Cystic Fibrosis Patients

F. Vandenesch, P. Reix, K. Moreau, 2020, Frontiers in Cellular and Infection Microbiology.

Laryngeal response to nasal ventilation in nonsedated newborn lambs.

P. Reix, Joëlle Rouillard Lafond, François Moreau-Bussière, 2007, Journal of applied physiology.

Partial splenectomy for portal hypertension in cystic fibrosis related liver disease

P. Reix, I. Durieu, G. Bellon, 2007, Pediatric pulmonology.

[Allgrove syndrome].

P. Reix, A. Alakeel, D. Jullien, 2015, Annales de dermatologie et de venereologie.

[Allgrove syndrome].

P. Reix, A. Alakeel, D. Jullien, 2015, Annales de dermatologie et de venereologie.

The U UGA C sequence provides a favorable context to ELX-02 induced CFTR readthrough.

O. Namy, P. Reix, L. Bidou, 2022, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

The 2,6-diaminopurine as a highly potent corrector of UGA nonsense mutations in cancers and other genetic diseases

E. Westhof, M. Copin, P. Reix, 2020 .

Use of 2,6-diaminopurine as a potent suppressor of UGA premature stop codons in cystic fibrosis.

P. Reix, M. Chamaillard, N. Prevarskaya, 2023, Molecular therapy : the journal of the American Society of Gene Therapy.

Lumacaftor/ivacaftor initiation in two liver transplantation patients under tacrolimus and antifungal azoles

P. Reix, N. Stremler-Lebel, I. Chouchane, 2019, Clinical Case Reports.

Using chest computed tomography and unsupervised machine learning for predicting and evaluating response to lumacaftor–ivacaftor in people with cystic fibrosis

M. Revel, P. Reix, P. Burgel, 2021, European Respiratory Journal.

Clinical phenotype and genotype of children with borderline sweat test and abnormal nasal epithelial chloride transport.

Milan Macek, Gérard Lenoir, J. Sarles, 2010, American journal of respiratory and critical care medicine.

C. Delacourt, P. Reix, P. Boelle, 2019, Pediatric pulmonology.

goatsof spontaneous swallows on breathing in awake

P. Micheau, M. Kogo, P. Reix, 2015 .

Diaphragmatic paralysis in young children: A literature review

P. Reix, L. Coutier, T. Perrin, 2019, Pediatric pulmonology.

Nonnutritive swallowing and respiration relationships in preterm lambs.

P. Reix, J. Arsenault, J. Praud, 2004, Journal of applied physiology.

newborn lambs Laryngeal response to nasal ventilation in nonsedated

P. Reix, J. Praud, C. Moretti, 2015 .

Cricothyroid muscle electrical activity during respiration and apneas in lambs

P. Reix, Joëlle Rouillard Lafond, François Moreau-Bussière, 2007, Respiratory Physiology & Neurobiology.

Effect of nasal continuous or intermittent positive airway pressure on nonnutritive swallowing in the newborn lamb.

P. Reix, François Moreau-Bussière, J. Praud, 2005, Journal of applied physiology.

Most of Staphylococcus aureus and Pseudomonas aeruginosa co-infecting isolates coexist, a condition that may impact clinical outcomes in Cystic Fibrosis patients

F. Vandenesch, P. Reix, K. Moreau, 2020 .

Diffuse alveolar haemorrhage in children: an international multicentre study

P. Reix, A. Clément, N. Kiper, 2023, ERJ Open Research.

Factors associated with asthma severity in children: data from the French COBRAPed Cohort.

P. Reix, P. Berger, I. Pin, 2020, The journal of allergy and clinical immunology. In practice.

Lung clearance index: evidence for use in clinical trials in cystic fibrosis.

P. Reix, L. Kent, J. Bradley, 2014, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Usefulness of bronchoalveolar lavage in a French pediatric cohort with hypersensitivity pneumonitis

P. Reix, G. Reboux, A. Deschildre, 2020, Pediatric pulmonology.

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

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

A simplified, semi-quantitative structural lung disease computed tomography outcome during quiet breathing in infants with cystic fibrosis.

S. Matecki, P. Reix, N. Molinari, 2017, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Real-life acute lung function changes after lumacaftor/ivacaftor first administration in pediatric patients with cystic fibrosis.

P. Reix, L. Coutier, M. Perceval, 2017, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Implementation of Model-Based Dose Adjustment of Tobramycin in Adult Patients with Cystic Fibrosis

P. Reix, I. Durieu, S. Goutelle, 2022, Pharmaceutics.

P265 Real-life initiation of lumacaftor/ivacaftor in adolescents and adults homozygous for the F508del CFTR mutation: a French nationwide study

P. Reix, P. Burgel, I. Durieu, 2019, Journal of Cystic Fibrosis.

Viral respiratory tract infections in young children with cystic fibrosis: a prospective full-year seasonal study

P. Reix, A. Doléans-Jordheim, F. Morfin, 2019, Virology Journal.

Nonsense mutations accelerate lung disease and decrease survival of cystic fibrosis children.

B. Kerem, P. Reix, P. Burgel, 2023, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

49 Lumacaftor/ivacaftor (LUM/IVA) treatment in patients (pts) with cystic fibrosis (CF) aged ≥12 years homozygous for F508del-CFTR: description of a French Temporary Authorization for Use (ATU) cohort

P. Reix, P. Kiefer, R. Chiron, 2017 .

The role of sleep laboratory polygraphy in the evaluation of obstructive sleep apnea syndrome in Robin infants.

P. Reix, I. Ioan, L. Coutier, 2020, Sleep medicine.

Impact of prone positioning in infants with Pierre Robin sequence: a polysomnography study.

P. Reix, P. Franco, L. Coutier, 2019, Sleep medicine.

Rescue of Pap-Mas in Systemic JIA Using Janus Kinase Inhibitors, Case Report and Systematic Review

P. Reix, A. Belot, S. Collardeau-Frachon, 2023, Journal of clinical medicine.

C-fiber blockade influence on non-nutritive swallowing in full-term lambs

P. Reix, J. Praud, T. Niyonsenga, 2006, Respiratory Physiology & Neurobiology.

Postnatal maturation of vagal respiratory reflexes in preterm and full-term lambs.

P. Reix, François Moreau-Bussière, J. Praud, 2003, Journal of applied physiology.

Alpha1-antitrypsin deficiency: An updated review.

P. Reix, O. Guillaud, V. Cottin, 2023, Presse medicale.

Diffuse alveolar haemorrhage in children: an international multicentre study

P. Reix, A. Clément, N. Kiper, 2021, ERJ Open Research.

Genetic testing in idiopathic interstitial pneumonia

C. Delacourt, P. Reix, S. Amselem, 2015 .

Contribution Of Mutations In Genes Encoding Proteins Of The Surfactant Metabolism To Idiopathic Interstitial Pneumonia And Idiopathic Pulmonary Fibrosis In A Cohort Of 265 Families

C. Delacourt, P. Reix, S. Amselem, 2016 .

Moving the Dial on Airway Inflammation in Response to Trikafta in Adolescents with Cystic Fibrosis

P. Reix, E. Kerem, I. Sermet-Gaudelus, 2023, American journal of respiratory and critical care medicine.

Severe Pulmonary Fibrosis as the First Manifestation of Interferonopathy (TMEM173 Mutation).

F. Rieux-Laucat, P. Reix, J. Dubus, 2016, Chest.

Impact of Scedosporium apiospermum complex seroprevalence in patients with cystic fibrosis.

P. Reix, I. Durieu, O. Lortholary, 2014, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

airway pressure and flow Laryngeal muscle response to phasic and tonic upper

P. Reix, François Moreau-Bussière, D. Dorion, 2015 .

during periodic breathing in nonsedated lambs Laryngeal and abdominal muscle electrical activity

P. Reix, P. Fortier, D. Dorion, 2015 .

An impulse oscillometry system is less efficient than spirometry in tracking lung function improvements after intravenous antibiotic therapy in pediatric patients with cystic fibrosis

P. Reix, L. Coutier, C. Mainguy, 2015, Pediatric pulmonology.

Sweat test practice in pediatric pulmonology after introduction of cystic fibrosis newborn screening

P. Reix, I. Pin, J. Dubus, 2015, European Journal of Pediatrics.