Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

I Sermet

Showing results (31-40 of 71) with videos related to

Pageof 8
Sort By:
European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology|December 10, 1999
Rapid improvement of intracranial tuberculomas after addition of ofloxacin to first-line antituberculosis treatmentI Sermet-Gaudelus, F Stambouli, V Abadie, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|October 11, 2022
ECFS standards of care on CFTR-related disorders: Updated diagnostic criteriaC Castellani, K De Boeck, E De Wachter, et al.
The American Journal of Clinical Nutrition|June 29, 2000
Simple pediatric nutritional risk score to identify children at risk of malnutritionI Sermet-Gaudelus, A S Poisson-Salomon, V Colomb, et al.
Clinical Genetics|March 18, 2004
Novel CFTR mutations in black cystic fibrosis patientsM N Feuillet-Fieux, M Ferrec, N Gigarel, et al.
The Journal of Infectious Diseases|December 8, 1998
Priming of blood neutrophils in children with cystic fibrosis: correlation between functional and phenotypic expression of opsonin receptors before and after platelet-activating factor primingV Witko-Sarsat, L Halbwachs-Mecarelli, I Sermet-Gaudelus, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|April 23, 2015
Persistent Bordetella bronchiseptica infection in a child with cystic fibrosis: Relationship to bacterial phenotypeNevine El Khatib, Agnes Ferroni, Muriel Le Bourgeois, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 14, 2020
Guidelines for the management of children at risk of secondary bone fragility: Expert opinion of a French working groupT Edouard, S Guillaume-Czitrom, J Bacchetta, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|October 30, 2008
A European consensus for the evaluation and management of infants with an equivocal diagnosis following newborn screening for cystic fibrosisS J Mayell, A Munck, J V Craig, et al.
Human Mutation|June 30, 2000
Identification of a novel mutation, 1087delT, in exon 7 of the CFTR gene in a patient with cystic fibrosisM N Feuillet-Fieux, I Sermet, A Edelman, et al.
The European Respiratory Journal|April 7, 2004
Follow-up of 452 totally implantable vascular devices in cystic fibrosis patientsA Munck, S Malbezin, J Bloch, et al.
Pageof 8

Showing results (31-40 of 71) with videos related to

Sort By:
Pageof 8
European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology|December 10, 1999
Rapid improvement of intracranial tuberculomas after addition of ofloxacin to first-line antituberculosis treatmentI Sermet-Gaudelus, F Stambouli, V Abadie, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|October 11, 2022
ECFS standards of care on CFTR-related disorders: Updated diagnostic criteriaC Castellani, K De Boeck, E De Wachter, et al.
The American Journal of Clinical Nutrition|June 29, 2000
Simple pediatric nutritional risk score to identify children at risk of malnutritionI Sermet-Gaudelus, A S Poisson-Salomon, V Colomb, et al.
Clinical Genetics|March 18, 2004
Novel CFTR mutations in black cystic fibrosis patientsM N Feuillet-Fieux, M Ferrec, N Gigarel, et al.
The Journal of Infectious Diseases|December 8, 1998
Priming of blood neutrophils in children with cystic fibrosis: correlation between functional and phenotypic expression of opsonin receptors before and after platelet-activating factor primingV Witko-Sarsat, L Halbwachs-Mecarelli, I Sermet-Gaudelus, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|April 23, 2015
Persistent Bordetella bronchiseptica infection in a child with cystic fibrosis: Relationship to bacterial phenotypeNevine El Khatib, Agnes Ferroni, Muriel Le Bourgeois, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 14, 2020
Guidelines for the management of children at risk of secondary bone fragility: Expert opinion of a French working groupT Edouard, S Guillaume-Czitrom, J Bacchetta, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|October 30, 2008
A European consensus for the evaluation and management of infants with an equivocal diagnosis following newborn screening for cystic fibrosisS J Mayell, A Munck, J V Craig, et al.
Human Mutation|June 30, 2000
Identification of a novel mutation, 1087delT, in exon 7 of the CFTR gene in a patient with cystic fibrosisM N Feuillet-Fieux, I Sermet, A Edelman, et al.
The European Respiratory Journal|April 7, 2004
Follow-up of 452 totally implantable vascular devices in cystic fibrosis patientsA Munck, S Malbezin, J Bloch, et al.
Pageof 8