Lista de obras -

A CFTR potentiator in patients with cystic fibrosis and the G551D mutation

artículo científico publicado en 2011

A novel lipidomic strategy reveals plasma phospholipid signatures associated with respiratory disease severity in cystic fibrosis patients.

artículo científico publicado en 2009

Age-related prevalence and distribution of nontuberculous mycobacterial species among patients with cystic fibrosis

artículo científico publicado en 2005

An international randomized multicenter comparison of nasal potential difference techniques

artículo científico publicado en 2010

An unexpected effect of TNF-α on F508del-CFTR maturation and function

artículo científico publicado en 2015

Analysis of nasal potential in murine cystic fibrosis models

artículo científico publicado en 2016

Ataluren for the treatment of nonsense-mutation cystic fibrosis: a randomised, double-blind, placebo-controlled phase 3 trial

artículo científico publicado en 2014

Basic protocol for transepithelial nasal potential difference measurements

artículo científico publicado en 2004

Biosynthesis of cystic fibrosis transmembrane conductance regulator

artículo científico

Body temperature measurement in daily practice

artículo científico publicado en 2005

CFTR functional measurements in human models for diagnosis, prognosis and personalized therapy: Report on the pre-conference meeting to the 11th ECFS Basic Science Conference, Malta, 26-29 March 2014

artículo científico publicado en 2014

Characterization of nasal potential difference in cftr knockout and F508del-CFTR mice

artículo científico publicado en 2013

Chloride transport in nasal ciliated cells of cystic fibrosis heterozygotes

artículo científico publicado en 2005

Cis variants identified in F508del complex alleles modulate CFTR channel rescue by small molecules

artículo científico publicado en 2017

Clonal relationship and differentiation among Mycobacterium abscessus isolates as determined using the semiautomated repetitive extragenic palindromic sequence PCR-based DiversiLab system

artículo científico publicado en 2014

Continuous versus intermittent infusions of ceftazidime for treating exacerbation of cystic fibrosis

artículo científico publicado en 2009

Coronin-1 is associated with neutrophil survival and is cleaved during apoptosis: potential implication in neutrophils from cystic fibrosis patients

artículo científico publicado en 2009

Correction of CFTR function in nasal epithelial cells from cystic fibrosis patients predicts improvement of respiratory function by CFTR modulators

artículo científico publicado en 2017

Determinants of refusal of A/H1N1 pandemic vaccination in a high risk population: a qualitative approach

artículo científico publicado en 2012

Diagnosis of Cystic Fibrosis in Screened Populations.

artículo científico publicado en 2017

Diagnosis of Cystic Fibrosis: Consensus Guidelines from the Cystic Fibrosis Foundation

artículo científico publicado en 2017

Disruption of cytokeratin-8 interaction with F508del-CFTR corrects its functional defect

artículo científico publicado en 2012

Effect of ivacaftor treatment in patients with cystic fibrosis and the G551D-CFTR mutation: patient-reported outcomes in the STRIVE randomized, controlled trial

artículo científico publicado en 2015

European Cystic Fibrosis Society Standards of Care: Best Practice guidelines

artículo científico publicado en 2014

European best practice guidelines for cystic fibrosis neonatal screening

scholarly article by Carlo Castellani et al published May 2009 in Journal of Cystic Fibrosis

European cystic fibrosis bone mineralisation guidelines

artículo científico publicado en 2011

Evaluation of MRP1-5 gene expression in cystic fibrosis patients homozygous for the delta F508 mutation

artículo científico publicado en 2003

French law: what about a reasoned reimbursement of serum vitamin D assays?

artículo científico publicado en 2016

Genotypic and phenotypic variation in Pseudomonas aeruginosa reveals signatures of secondary infection and mutator activity in certain cystic fibrosis patients with chronic lung infections

artículo científico publicado en 2011

Guidelines on the early management of infants diagnosed with cystic fibrosis following newborn screening

scientific article published on September 2010

Haemophagocytic syndrome in Plasmodium falciparum malaria

artículo científico publicado en 2000

In vitro prediction of stop-codon suppression by intravenous gentamicin in patients with cystic fibrosis: a pilot study

artículo científico publicado en 2007

Infections caused by Mycobacterium abscessus: epidemiology, diagnostic tools and treatment

artículo científico publicado en 2016

Inflammation and CFTR: might neutrophils be the key in cystic fibrosis?

artículo científico publicado en 1999

Insulin-like growth factor I correlates with lean body mass in cystic fibrosis patients ⬇️

artículo científico publicado el 1 de noviembre de 2003

Interest of colchicine for the treatment of cystic fibrosis patients. Preliminary report

artículo científico publicado en 1999

Ivacaftor treatment in patients with cystic fibrosis and theG551D-CFTRmutation ⬇️

artículo científico publicado el 1 de marzo de 2013

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

artículo científico publicado en 2016

Long-Term Rasamsonia argillacea Complex Species Colonization Revealed by PCR Amplification of Repetitive DNA Sequences in Cystic Fibrosis Patients

artículo científico publicado en 2016

Long-term safety and efficacy of ivacaftor in patients with cystic fibrosis who have the Gly551Asp-CFTR mutation: a phase 3, open-label extension study (PERSIST).

artículo científico publicado en 2014

Matrix-assisted laser desorption ionization-time of flight mass spectrometry for identification of nonfermenting gram-negative bacilli isolated from cystic fibrosis patients

artículo científico publicado en 2008

Measurement of temperature and fever in children

artículo científico publicado en 1999

Mutations in GAS8, a Gene Encoding a Nexin-Dynein Regulatory Complex Subunit, Cause Primary Ciliary Dyskinesia with Axonemal Disorganization.

artículo científico publicado en 2016

Mycobacterium abscessus and children with cystic fibrosis

artículo científico publicado en 2003

Myeloperoxidase promoter polymorphism -463G is associated with more severe clinical expression of cystic fibrosis pulmonary disease.

artículo científico publicado en 2006

NUTRITIONAL STATUS ASSESSMENT IN PATIENTS WITH CYSTIC FIBROSIS

artículo científico publicado en 2015

Nebulized antibiotics in cystic fibrosis

artículo científico publicado en 2002

Normal function of the cystic fibrosis conductance regulator protein can be associated with homozygous (Delta)F508 mutation

artículo científico publicado en 2002

Pain in children and adults with cystic fibrosis: a comparative study

artículo científico publicado en 2009

Plasma lipidomics reveals potential prognostic signatures within a cohort of cystic fibrosis patients.

artículo científico publicado en 2011

Priming of blood neutrophils in children with cystic fibrosis: correlation between functional and phenotypic expression of opsonin receptors before and after platelet-activating factor priming

artículo científico publicado en 1999

Prior infection by seasonal coronaviruses, as assessed by serology, does not prevent SARS-CoV-2 infection and disease in children, France, April to June 2020 ⬇️

artículo científico publicado en 2021

Pseudomonas aeruginosa LasB protease impairs innate immunity in mice and humans by targeting a lung epithelial cystic fibrosis transmembrane regulator-IL-6-antimicrobial-repair pathway

artículo científico

Rapid improvement of intracranial tuberculomas after addition of ofloxacin to first-line antituberculosis treatment

artículo científico publicado en 1999

Rattlesnake Phospholipase A2 Increases CFTR-Chloride Channel Current and Corrects ∆F508CFTR Dysfunction: Impact in Cystic Fibrosis

artículo científico publicado en 2016

Sputum itraconazole concentrations in cystic fibrosis patients

artículo científico publicado en 2001

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

artículo científico publicado en 2006

The hsa-miR-125a/hsa-let-7e/hsa-miR-99b cluster is potentially implicated in Cystic Fibrosis pathogenesis

artículo científico publicado en 2015

US Cystic Fibrosis Foundation and European Cystic Fibrosis Society consensus recommendations for the management of non-tuberculous mycobacteria in individuals with cystic fibrosis

artículo científico publicado en 2016

US Cystic Fibrosis Foundation and European Cystic Fibrosis Society consensus recommendations for the management of non-tuberculous mycobacteria in individuals with cystic fibrosis: executive summary

artículo científico publicado en 2016

Un test de la sueur normal n'exclut pas le diagnostic de mucoviscidose

artículo científico publicado en 2000

Update on cystic fibrosis-related bone disease: a special focus on children

artículo científico publicado en 2009

Use of 16S rRNA gene sequencing for identification of nonfermenting gram-negative bacilli recovered from patients attending a single cystic fibrosis center.

artículo científico publicado en 2002

Value of the chlorhexidine decontamination method for recovery of nontuberculous mycobacteria from sputum samples of patients with cystic fibrosis

artículo científico publicado en 2006

[Antibiotic therapy in cystic fibrosis. II Antibiotic strategy]

artículo científico publicado en 2000

[Phenotypic and genotypic characteristics of non fermenting atypical strains recovered from cystic fibrosis patients]

artículo científico publicado en 2003

[Weakening osteopathies, chronic kidney disease, malabsorption, biological anomalies of calium/phosphorus metabolism: appropriate indications for a reasoned reimbursment of serum vitamin D measurement]

scientific article published on 01 July 2014

rAAV-CFTRΔR Rescues the Cystic Fibrosis Phenotype in Human Intestinal Organoids and Cystic Fibrosis Mice

artículo científico publicado en 2015

Lista de obras de

A CFTR potentiator in patients with cystic fibrosis and the G551D mutation

A novel lipidomic strategy reveals plasma phospholipid signatures associated with respiratory disease severity in cystic fibrosis patients.

Age-related prevalence and distribution of nontuberculous mycobacterial species among patients with cystic fibrosis

An international randomized multicenter comparison of nasal potential difference techniques

An unexpected effect of TNF-α on F508del-CFTR maturation and function

Analysis of nasal potential in murine cystic fibrosis models

Ataluren for the treatment of nonsense-mutation cystic fibrosis: a randomised, double-blind, placebo-controlled phase 3 trial

Basic protocol for transepithelial nasal potential difference measurements

Biosynthesis of cystic fibrosis transmembrane conductance regulator

Body temperature measurement in daily practice

CFTR functional measurements in human models for diagnosis, prognosis and personalized therapy: Report on the pre-conference meeting to the 11th ECFS Basic Science Conference, Malta, 26-29 March 2014

Characterization of nasal potential difference in cftr knockout and F508del-CFTR mice

Chloride transport in nasal ciliated cells of cystic fibrosis heterozygotes

Cis variants identified in F508del complex alleles modulate CFTR channel rescue by small molecules

Clonal relationship and differentiation among Mycobacterium abscessus isolates as determined using the semiautomated repetitive extragenic palindromic sequence PCR-based DiversiLab system

Continuous versus intermittent infusions of ceftazidime for treating exacerbation of cystic fibrosis

Coronin-1 is associated with neutrophil survival and is cleaved during apoptosis: potential implication in neutrophils from cystic fibrosis patients

Correction of CFTR function in nasal epithelial cells from cystic fibrosis patients predicts improvement of respiratory function by CFTR modulators

Determinants of refusal of A/H1N1 pandemic vaccination in a high risk population: a qualitative approach

Diagnosis of Cystic Fibrosis in Screened Populations.

Diagnosis of Cystic Fibrosis: Consensus Guidelines from the Cystic Fibrosis Foundation

Disruption of cytokeratin-8 interaction with F508del-CFTR corrects its functional defect

Effect of ivacaftor treatment in patients with cystic fibrosis and the G551D-CFTR mutation: patient-reported outcomes in the STRIVE randomized, controlled trial

European Cystic Fibrosis Society Standards of Care: Best Practice guidelines

European best practice guidelines for cystic fibrosis neonatal screening

European cystic fibrosis bone mineralisation guidelines

Evaluation of MRP1-5 gene expression in cystic fibrosis patients homozygous for the delta F508 mutation

French law: what about a reasoned reimbursement of serum vitamin D assays?

Genotypic and phenotypic variation in Pseudomonas aeruginosa reveals signatures of secondary infection and mutator activity in certain cystic fibrosis patients with chronic lung infections

Guidelines on the early management of infants diagnosed with cystic fibrosis following newborn screening

Haemophagocytic syndrome in Plasmodium falciparum malaria

In vitro prediction of stop-codon suppression by intravenous gentamicin in patients with cystic fibrosis: a pilot study

Infections caused by Mycobacterium abscessus: epidemiology, diagnostic tools and treatment

Inflammation and CFTR: might neutrophils be the key in cystic fibrosis?

Insulin-like growth factor I correlates with lean body mass in cystic fibrosis patients ⬇️

Interest of colchicine for the treatment of cystic fibrosis patients. Preliminary report

Ivacaftor treatment in patients with cystic fibrosis and theG551D-CFTRmutation ⬇️

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

Long-Term Rasamsonia argillacea Complex Species Colonization Revealed by PCR Amplification of Repetitive DNA Sequences in Cystic Fibrosis Patients

Long-term safety and efficacy of ivacaftor in patients with cystic fibrosis who have the Gly551Asp-CFTR mutation: a phase 3, open-label extension study (PERSIST).

Matrix-assisted laser desorption ionization-time of flight mass spectrometry for identification of nonfermenting gram-negative bacilli isolated from cystic fibrosis patients

Measurement of temperature and fever in children

Mutations in GAS8, a Gene Encoding a Nexin-Dynein Regulatory Complex Subunit, Cause Primary Ciliary Dyskinesia with Axonemal Disorganization.

Mycobacterium abscessus and children with cystic fibrosis

Myeloperoxidase promoter polymorphism -463G is associated with more severe clinical expression of cystic fibrosis pulmonary disease.

NUTRITIONAL STATUS ASSESSMENT IN PATIENTS WITH CYSTIC FIBROSIS

Nebulized antibiotics in cystic fibrosis

Normal function of the cystic fibrosis conductance regulator protein can be associated with homozygous (Delta)F508 mutation

Pain in children and adults with cystic fibrosis: a comparative study

Plasma lipidomics reveals potential prognostic signatures within a cohort of cystic fibrosis patients.

Priming of blood neutrophils in children with cystic fibrosis: correlation between functional and phenotypic expression of opsonin receptors before and after platelet-activating factor priming

Prior infection by seasonal coronaviruses, as assessed by serology, does not prevent SARS-CoV-2 infection and disease in children, France, April to June 2020 ⬇️

Pseudomonas aeruginosa LasB protease impairs innate immunity in mice and humans by targeting a lung epithelial cystic fibrosis transmembrane regulator-IL-6-antimicrobial-repair pathway

Rapid improvement of intracranial tuberculomas after addition of ofloxacin to first-line antituberculosis treatment

Rattlesnake Phospholipase A2 Increases CFTR-Chloride Channel Current and Corrects ∆F508CFTR Dysfunction: Impact in Cystic Fibrosis

Sputum itraconazole concentrations in cystic fibrosis patients

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

The hsa-miR-125a/hsa-let-7e/hsa-miR-99b cluster is potentially implicated in Cystic Fibrosis pathogenesis

US Cystic Fibrosis Foundation and European Cystic Fibrosis Society consensus recommendations for the management of non-tuberculous mycobacteria in individuals with cystic fibrosis

US Cystic Fibrosis Foundation and European Cystic Fibrosis Society consensus recommendations for the management of non-tuberculous mycobacteria in individuals with cystic fibrosis: executive summary

Un test de la sueur normal n'exclut pas le diagnostic de mucoviscidose

Update on cystic fibrosis-related bone disease: a special focus on children

Use of 16S rRNA gene sequencing for identification of nonfermenting gram-negative bacilli recovered from patients attending a single cystic fibrosis center.

Value of the chlorhexidine decontamination method for recovery of nontuberculous mycobacteria from sputum samples of patients with cystic fibrosis

[Antibiotic therapy in cystic fibrosis. II Antibiotic strategy]

[Phenotypic and genotypic characteristics of non fermenting atypical strains recovered from cystic fibrosis patients]

[Weakening osteopathies, chronic kidney disease, malabsorption, biological anomalies of calium/phosphorus metabolism: appropriate indications for a reasoned reimbursment of serum vitamin D measurement]

rAAV-CFTRΔR Rescues the Cystic Fibrosis Phenotype in Human Intestinal Organoids and Cystic Fibrosis Mice