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

Sleep medicine, 2019-02, Vol.54, p.257-261

2019

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

Sleep medicine, 2020-08, Vol.72, p.59-64

2020

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Children and adolescents with cystic fibrosis display moderate bone microarchitecture abnormalities: data from high-resolution peripheral quantitative computed tomography

Osteoporosis international, 2017-11, Vol.28 (11), p.3179-3188

2017

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Lung clearance index: Evidence for use in clinical trials in cystic fibrosis

Journal of cystic fibrosis, 2014-03, Vol.13 (2), p.123-138

2014

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Successful management of severe infant bullous pemphigoid with omalizumab

British journal of dermatology (1951), 2012-05, Vol.166 (5), p.1140-1142

2012

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New surfactant protein C gene mutations associated with diffuse lung disease

Journal of medical genetics, 2009-07, Vol.46 (7), p.490-494

2009

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Extracoronary echocardiographic findings as predictors of coronary artery lesions in the initial phase of Kawasaki disease

Archives of disease in childhood, 2013-02, Vol.98 (2), p.97-102

2013

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Neonatal low respiratory tract chlamydia trachomatis infection: Diagnostic and treatment management

Respiratory medicine case reports, 2019-01, Vol.28, p.100852, Article 100852

2019

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Insights into cystic fibrosis-related bone disease

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2016-08, Vol.23 (8), p.857-866

2016

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171 A chicken and egg situation

Journal of cystic fibrosis, 2017-06, Vol.16, p.S110-S110

2017

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Early lung disease in cystic fibrosis

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2016-12, Vol.23 (12S), p.12S9-12S14

2016

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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

Journal of cystic fibrosis, 2017-06, Vol.16, p.S76-S76

2017

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311 Are micronutrients nutritional status different according to glycemic profiles of cystic fibrosis supplemented adult patients?

Journal of cystic fibrosis, 2017-06, Vol.16, p.S142-S142

2017

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Early lung disease in infants with cystic fibrosis. Diagnostic tools and possible therapeutic pathways

Revue des maladies respiratoires, 2016-02, Vol.33 (2), p.102-116

2016

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51 Microbiological impact of palivizumab prophylaxis in infants with cystic fibrosis

Journal of cystic fibrosis, 2016-06, Vol.15, p.S64-S64

2016

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164 Are viral respiratory infections a real issue in infants with cystic fibrosis: preliminary results of a prospective cohort study

Journal of cystic fibrosis, 2017-06, Vol.16, p.S108-S108

2017

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IPD1.03 Risk of non tuberculous mycobacteria isolation according to different risk factors in adults CF patients: A systematic review and meta-analysis

Journal of cystic fibrosis, 2017-06, Vol.16, p.S56-S56

2017

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420 Report of 97 transitioning adolescents with cystic fibrosis from paediatric to adult care CF center

Journal of cystic fibrosis, 2017-06, Vol.16, p.S170-S170

2017

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WS14.5 What is happening when Pseudomonas aeruginosa grows in a cystic fibrosis lung microbiota?

Journal of cystic fibrosis, 2016-06, Vol.15, p.S24-S24

2016

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EPS1.4 Real life acute changes in spirometric indices after lumacaftor/ivacaftor first administration in pediatric patients with cystic fibrosis

Journal of cystic fibrosis, 2017-06, Vol.16, p.S36-S37

2017

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359 Use of radiological tools in French cystic fibrosis centers: A national survey

Journal of cystic fibrosis, 2013-06, Vol.12, p.S141-S141

2013

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New therapeutic developments in cystic fibrosis

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2016-12, Vol.23 (12S), p.12S47-12S53

2016

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Disseminated actinomycosis treated with clindamycin

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2017-05, Vol.24 (5), p.460-463

2017

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WS04.6 Children with cystic fibrosis: How compromised is bone?

Journal of cystic fibrosis, 2015-06, Vol.14, p.S8-S8

2015

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Allgrove syndrome

Annales de dermatologie et de vénéréologie, 2015-02, Vol.142 (2), p.121-124

2015

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

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

Children and adolescents with cystic fibrosis display moderate bone microarchitecture abnormalities: data from high-resolution peripheral quantitative computed tomography

Lung clearance index: Evidence for use in clinical trials in cystic fibrosis

Successful management of severe infant bullous pemphigoid with omalizumab

New surfactant protein C gene mutations associated with diffuse lung disease

Extracoronary echocardiographic findings as predictors of coronary artery lesions in the initial phase of Kawasaki disease

Neonatal low respiratory tract chlamydia trachomatis infection: Diagnostic and treatment management

Insights into cystic fibrosis-related bone disease

171 A chicken and egg situation

Early lung disease in cystic fibrosis

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

311 Are micronutrients nutritional status different according to glycemic profiles of cystic fibrosis supplemented adult patients?

Early lung disease in infants with cystic fibrosis. Diagnostic tools and possible therapeutic pathways

51 Microbiological impact of palivizumab prophylaxis in infants with cystic fibrosis

164 Are viral respiratory infections a real issue in infants with cystic fibrosis: preliminary results of a prospective cohort study

IPD1.03 Risk of non tuberculous mycobacteria isolation according to different risk factors in adults CF patients: A systematic review and meta-analysis

420 Report of 97 transitioning adolescents with cystic fibrosis from paediatric to adult care CF center

WS14.5 What is happening when Pseudomonas aeruginosa grows in a cystic fibrosis lung microbiota?

EPS1.4 Real life acute changes in spirometric indices after lumacaftor/ivacaftor first administration in pediatric patients with cystic fibrosis

359 Use of radiological tools in French cystic fibrosis centers: A national survey

New therapeutic developments in cystic fibrosis

Disseminated actinomycosis treated with clindamycin

WS04.6 Children with cystic fibrosis: How compromised is bone?

Allgrove syndrome

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