Reix Philippe

Glucose trajectories in cystic fibrosis and their association with pulmonary function

Quitterie Reynaud, Muriel Rabilloud, Sylvain Roche, Stéphanie Poupon-Bourdy, Jean Iwaz, Raphaële Nové-Josserand...

Journal of Cystic Fibrosis . 17 ( 3 ) : 400 - 406

DOI: 10.1016/j.jcf.2017.09.010

2018

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

Aurélie Labaste, Camille Ohlmann, Catherine Mainguy, Virginie Jubin, Marie Perceval, Laurianne Coutier...

Journal of Cystic Fibrosis . 16 ( 6 ) : 709-712

DOI: 10.1016/j.jcf.2017.05.002

2017

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Health related quality of life in infants and children with interstitial lung disease: a national pilot survey in France.

Clara Lauby, Pierre-Yves Boëlle, Ralph Epaud, Jacques de Blic, Rola Abou Taam, Philippe Reix...

Congrès Francophone Pédiatrique de Pneumologie et d’Allergologie .

2017

Poster

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Hémosidérose idiopathique pulmonaire de l’enfant et trisomie 21: une étude nationale.

Aurélia Alimi, Jessica Taytard, Rola Abou Taam, Véronique Houdouin, Aude Forgeron, Marc Lubrano Lavadera...

Congrès Francophone Pédiatrique de Pneumologie et d’Allergologie .

2017

Poster

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

Hiba Dowaikh, Florence Morfin-Sherpa, Philippe Reix

Pediatric Pulmonology . 52 ( 10 ) : E70-E72

DOI: 10.1002/ppul.23746

2017

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

Magali Saguintaah, Yann Cabon, Rémi Gauthier, Cécile Duboibaudry, Laure Couderc, Muriel Le Bourgeois...

Journal of Cystic Fibrosis . 16 ( 1 ) : 151 - 157

DOI: 10.1016/j.jcf.2016.10.014

2017

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

Laurence Pages-Monteiro, Romain Martin, Carine Commun, Nolwenn Alliot, Claire Bardel, Hélène Meugnier...

PLoS ONE . 12 ( 3 ) : 1-19

DOI: 10.1371/journal.pone.0173022

2017

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

Cécile Picard, Guillaume Thouvenin, Caroline Kannengiesser, Jean-Christophe Dubus, Nadia Jeremiah, Frédéric Rieux-Laucat...

Chest . 150 ( 3 ) : E65-E71

DOI: 10.1016/j.chest.2016.02.682

2016

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

Evelyne Véricel, Stéphane Mazur, Romain Colas, Véronique Delaup, Catherine Calzada, Philippe Reix...

Prostaglandins, Leukotrienes and Essential Fatty Acids . 115 : 41 - 47

DOI: 10.1016/j.plefa.2016.10.008

2016

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

Marie-Louise Frémond, Mathieu Paul Rodero, Nadia Jeremiah, Alexandre Belot, Eric Jeziorski, Darragh Duffy...

Journal of Allergy and Clinical Immunology . 138 ( 6 ) : 1752-1755

DOI: 10.1016/j.jaci.2016.07.015

2016

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

Stefan Matecki, Lisa Kent, Kris de Boeck, Muriel Le Bourgeois, Stefan Zielen, Cesare Braggion...

Journal of Cystic Fibrosis . 15 ( 1 ) : 10 - 20

DOI: 10.1016/j.jcf.2015.03.015

2016

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

Céline Grimaldi, François Brémont, Michèle Berlioz-Baudoin, Jacques Brouard, Harriet Corvol, Laure Couderc...

European Journal of Pediatrics . 174 ( 12 ) : 1613 - 1620

DOI: 10.1007/s00431-015-2579-4

2015

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

Clélia Buchs, Laurianne Coutier, Stéphanie Vrielynck, Virginie Jubin, Catherine Mainguy, Philippe Reix

Pediatric Pulmonology . 50 ( 11 ) : 1073 - 1081

DOI: 10.1002/ppul.23301

2015

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A French multicentric study and review of pulmonary Nocardia spp. in cystic fibrosis patients

Véronica Rodriguez-Nava, Stéphane Durupt, Sandra Chyderiotis, Anne-Marie Freydiere, Judith Karsenty, Michèle de Montclos...

Medical Microbiology and Immunology . 204 ( 4 ) : 493-504

DOI: 10.1007/s00430-014-0360-3

2015

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Exposure of Staphylococcus aureus to subinhibitory concentrations of β-lactam antibiotics induces heterogeneous vancomycin-intermediate Staphylococcus aureus

Mélanie Roch, Perrine Clair, Adriana Renzoni, Marie-Elisabeth Reverdy, Olivier Dauwalder, Michèle Bes...

Antimicrobial Agents and Chemotherapy . 58 ( 9 ) : 5306-5314

DOI: 10.1128/AAC.02574-14

2014

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Impact of Scedosporium apiospermum complex seroprevalence in patients with cystic fibrosis

Perrine Parize, Sandrine Nail-Billaud, Anne-Lise Bienvenu, Stéphanie Bourdy, Marie Le Pogam, Philippe Reix...

Journal of Cystic Fibrosis . 13 ( 6 ) : 667-673

DOI: 10.1016/j.jcf.2014.01.011

2014

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New insights into pediatric idiopathic pulmonary hemosiderosis: the French RespiRare(R) cohort.

Jessica Taytard, Nadia Nathan, Jacques de Blic, Mickael Fayon, Ralph Epaud, Antoine Deschildre...

Orphanet Journal of Rare Diseases . 8 ( 1 ) : 161

DOI: 10.1186/1750-1172-8-161

2013

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Late onset Ondine syndrome: literature review on a case report

M. Butin, G. Labbe, S. Vrielynck, P. Franco, B. Massenavette, G. Bellon...

Archives de Pédiatrie . 19 : 1205--7

DOI: 10.1016/j.arcped.2012.08.015

2012

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

Nadia Nathan, Rola Abou Taam, Ralph Epaud, Christophe Delacourt, Antoine Deschildre, Philippe Reix...

Orphanet Journal of Rare Diseases . 7 ( 1 ) : 40

DOI: 10.1186/1750-1172-7-40

2012

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Successful management of severe infant bullous pemphigoid with omalizumab

C. Dufour, A. L. Souillet, C. Chaneliere, F. Jouen, C. Bodemer, D. Jullien...

British Journal of Dermatology . 166 : 1140--2

DOI: 10.1111/j.1365-2133.2011.10748.x

2012

Article dans une revue

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A New Animal Model of Obstructive Sleep Apnea Responding to Continuous Positive Airway Pressure

Pc. Neuzeret, F. Gormand, Philippe Reix, S. Parrot, Jp. Sastre, C. Buda...

Sleep . 34 : 541-548

2011

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Intrafamilial transmission of Staphylococcus aureus Panton-Valentine leukocidin responsible for two cases of neonatal necrotizing pneumonia

G. Catho, Y. Gillet, O. Dumitrescu, G. Lina, G. Labbé, G. Bellon...

Archives de Pédiatrie . 18 : 1090-1094

DOI: 10.1016/j.arcped.2011.07.019

2011

Article dans une revue

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Combined pulmonary fibrosis and emphysema syndrome associated with familial SFTPC mutation

V. Cottin, Philippe Reix, C. Khouatra, F. Thivolet-Bejui, D. Feldmann, J. F. Cordier

Thorax . 66 ( 10 ) : 918-9

DOI: 10.1136/thx.2010.151407

2011

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Hyperpolarized 3He MR for sensitive imaging of ventilation function and treatment efficiency in young cystic fibrosis patients with normal lung function.

Elise Bannier, Katarzyna Cieslar, Karim Mosbah, Françoise Aubert, François Duboeuf, Zahir Salhi...

Radiology . 255 ( 1 ) : 225-32

DOI: 10.1148/radiol.09090039

2010

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New surfactant protein C gene mutations associated with diffuse lung disease

Loïc Guillot, Ralph Epaud, Guillaume Thouvenin, Laurence Jonard, Amira Mohsni, Remy Couderc...

Journal of Medical Genetics . 46 ( 7 ) : 490

DOI: 10.1136/jmg.2009.066829

2009

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

Anne Termoz, Sandrine Touzet, Stéphanie Bourdy, Evelyne Decullier, Laeticia Bouveret, Cyrille Colin...

Pediatric Pulmonology . 43 ( 9 ) : 908-15

DOI: 10.1002/ppul.20878

2008

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The CF-CIRC study: a French collaborative study to assess the accuracy of cystic fibrosis diagnosis in neonatal screening.

Isabelle Sermet-Gaudelus, Delphine Roussel, Stéphanie Bui, Eric Deneuville, Frédéric Huet, Philippe Reix...

BMC Pediatrics . 6 : 25

DOI: 10.1186/1471-2431-6-25

2006

Article dans une revue

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Publications

Glucose trajectories in cystic fibrosis and their association with pulmonary function

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

Health related quality of life in infants and children with interstitial lung disease: a national pilot survey in France.

Hémosidérose idiopathique pulmonaire de l’enfant et trisomie 21: une étude nationale.

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

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

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

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

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

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

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

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

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

A French multicentric study and review of pulmonary Nocardia spp. in cystic fibrosis patients

Exposure of Staphylococcus aureus to subinhibitory concentrations of β-lactam antibiotics induces heterogeneous vancomycin-intermediate Staphylococcus aureus

Impact of Scedosporium apiospermum complex seroprevalence in patients with cystic fibrosis

New insights into pediatric idiopathic pulmonary hemosiderosis: the French RespiRare(R) cohort.

Late onset Ondine syndrome: literature review on a case report

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

Successful management of severe infant bullous pemphigoid with omalizumab

A New Animal Model of Obstructive Sleep Apnea Responding to Continuous Positive Airway Pressure

Intrafamilial transmission of Staphylococcus aureus Panton-Valentine leukocidin responsible for two cases of neonatal necrotizing pneumonia

Combined pulmonary fibrosis and emphysema syndrome associated with familial SFTPC mutation

Hyperpolarized 3He MR for sensitive imaging of ventilation function and treatment efficiency in young cystic fibrosis patients with normal lung function.

New surfactant protein C gene mutations associated with diffuse lung disease

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

The CF-CIRC study: a French collaborative study to assess the accuracy of cystic fibrosis diagnosis in neonatal screening.