I. Sermet

发表

Recommendations for the classification of diseases as CFTR-related disorders.

B. Kerem, J. Zieleński, P. Pignatti, 2011, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Comparing Mycobacterium massiliense and Mycobacterium abscessus lung infections in cystic fibrosis patients.

I. Pin, J. Gaillard, J. Herrmann, 2015, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Nasal polyposis and cystic fibrosis(CF): review of the literature.

C. Elie, B. Lacour, I. Sermet, 2011, Rhinology.

Follow-up of 452 totally implantable vascular devices in cystic fibrosis patients

F. Brémont, I. Sermet, A. Munck, 2004, European Respiratory Journal.

New clinical diagnostic procedures for cystic fibrosis in Europe.

N. Derichs, F. Vermeulen, I. Fajac, 2011, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Phenotypic characterisation of patients with intermediate sweat chloride values: towards validation of the European diagnostic algorithm for cystic fibrosis

P. Lebecque, N. Derichs, K. De Boeck, 2009, Thorax.

Effectiveness of bacteriophages in the sputum of cystic fibrosis patients.

I. Vachier, N. Molinari, I. Sermet, 2014, Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases.

Glutathione S-transferases related to P. aeruginosa lung infection in cystic fibrosis children: preliminary study.

M. Loriot, P. Beaune, B. Lacour, 2009, Clinical biochemistry.

Clinimetric properties of bronchoalveolar lavage inflammatory markers in cystic fibrosis

L. Kent, L. Dupont, I. Sermet, 2013, European Respiratory Journal.

Urgent lung transplantation in cystic fibrosis patients: experience of a French center.

I. Sermet, R. Souilamas, M. Saueressig, 2011, European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery.

Glucose tolerance and insulin secretion, morbidity, and death in patients with cystic fibrosis.

G. Velho, I. Sermet, E. Bismuth, 2008, The Journal of pediatrics.

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.

Standards of care for CFTR variant-specific therapy (including modulators) for people with cystic fibrosis.

Karen L. Robinson, C. Castellani, K. Raraigh, 2022, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Pharmacokinetics and Diffusion into Sputum of Oseltamivir and Oseltamivir Carboxylate in Adults with Cystic Fibrosis

I. Sermet, O. Lortholary, O. Launay, 2011, Antimicrobial Agents and Chemotherapy.

Prior infection by seasonal coronaviruses does not prevent SARS-CoV-2 infection and associated Multisystem Inflammatory Syndrome in children

D. Kariyawasam, C. Huon, B. Bader-Meunier, 2020, medRxiv.

A new large CFTR rearrangement illustrates the importance of searching for complex alleles

P. Ruszniewski, E. Girodon, I. Sermet, 2006, Human mutation.

Clinical variability and genetic homogeneity of the camptodactyly-arthropathy-coxa vara-pericarditis syndrome.

A. Munnich, A. Prieur, P. Woo, 2000, American journal of medical genetics.

SLC34A3 mutations in patients with hereditary hypophosphatemic rickets with hypercalciuria predict a key role for the sodium-phosphate cotransporter NaPi-IIc in maintaining phosphate homeostasis.

M. Bastepe, I. Sermet, J. Loredo-Osti, 2006, American journal of human genetics.

Therapeutic Approaches for Patients with Cystic Fibrosis Not Eligible for Current CFTR Modulators

I. Fajac, I. Sermet, 2021, Cells.

A European consensus for the evaluation and management of infants with an equivocal diagnosis following newborn screening for cystic fibrosis.

A Munck, K G Brownlee, C Castellani, 2009, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Defining DIOS and Constipation in Cystic Fibrosis With a Multicentre Study on the Incidence, Characteristics, and Treatment of DIOS

R. Houwen, I. Sermet, M. Wilschanski, 2010, Journal of pediatric gastroenterology and nutrition.

Lung transplantation in childhood and adolescence: unicentric 14-year experience with sex matching as the main prognosticator.

F. Le Pimpec Barthès, M. Riquet, B. Cholley, 2016, European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery.

Isolation, cultivation, and application of primary respiratory epithelial cells obtained by nasal brushing, polyp samples, or lung explants

I. Sermet, D. Downey, L. Galietta, 2022, STAR protocols.

Novel CFTR mutations in black cystic fibrosis patients

J. Steffann, I. Sermet, G. Lenoir, 2004, Clinical genetics.

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.

Suboptimal Ciprofloxacin Dosing as a Potential Cause of Decreased Pseudomonas aeruginosa Susceptibility in Children with Cystic Fibrosis

Isabelle Sermet, Gérard Pons, J. Zahar, 2010, Pharmacotherapy.

Exhaled nitric oxide in cystic fibrosis: relationships with airway and lung vascular impairments

L. Trinquart, C. Delclaux, A. Clément, 2009, European Respiratory Journal.

Exhaled nitric oxide in cystic fibrosis: relationships with airway and lung vascular impairments

L. Trinquart, C. Delclaux, A. Clément, 2009, European Respiratory Journal.

Recommendations for the classification of diseases as CFTR-related disorders.

B. Kerem, J. Zieleński, P. Pignatti, 2011, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

New clinical diagnostic procedures for cystic fibrosis in Europe.

N. Derichs, F. Vermeulen, P. Melotti, 2011, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Influence of perfusate temperature on nasal potential difference

F. Vermeulen, P. Melotti, K. De Boeck, 2012, European Respiratory Journal.

Phenotypic characterisation of patients with intermediate sweat chloride values: towards validation of the European diagnostic algorithm for cystic fibrosis

P. Lebecque, N. Derichs, I. Sermet, 2009, Thorax.

A European consensus for the evaluation and management of infants with an equivocal diagnosis following newborn screening for cystic fibrosis.

C. Castellani, I. Sermet, M. Schwarz, 2009, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Guideline on the design and conduct of cystic fibrosis clinical trials: the European Cystic Fibrosis Society-Clinical Trials Network (ECFS-CTN).

H. Tiddens, I. Sermet, V. Bulteel, 2011, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.