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Harriet Corvol

Showing results (121-130 of 146) with videos related to

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BMC Medical Genomics|March 8, 2018
Whole exome sequencing in three families segregating a pediatric case of sarcoidosisAlain Calender, Pierre Antoine Rollat Farnier, Adrien Buisson, et al.
American Journal of Human Genetics|June 16, 2015
RSPH3 Mutations Cause Primary Ciliary Dyskinesia with Central-Complex Defects and a Near Absence of Radial SpokesLudovic Jeanson, Bruno Copin, Jean-François Papon, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 28, 2020
Clinical response to lumacaftor-ivacaftor in patients with cystic fibrosis according to baseline lung functionPierre-Régis Burgel, Isabelle Durieu, Raphaël Chiron, et al.
Human Molecular Genetics|February 8, 2017
Cystic fibrosis gene modifier SLC26A9 modulates airway response to CFTR-directed therapeuticsLisa J Strug, Tanja Gonska, Gengming He, et al.
The Lancet. Respiratory Medicine|October 25, 2025
Effect of elexacaftor-tezacaftor-ivacaftor on bronchial dilatations in adolescents with cystic fibrosis: a multicentre prospective observational studyIsabelle Sermet-Gaudelus, Alexia Letierce, Laureline Berteloot, et al.
Orphanet Journal of Rare Diseases|April 22, 2018
Pulmonary hemosiderosis in children with Down syndrome: a national experienceAurelia Alimi, Jessica Taytard, Rola Abou Taam, et al.
Plos Genetics|February 27, 2019
Genetic association and transcriptome integration identify contributing genes and tissues at cystic fibrosis modifier lociJiafen Gong, Fan Wang, Bowei Xiao, et al.
HGG Advances|February 7, 2022
Leveraging TOPMed imputation server and constructing a cohort-specific imputation reference panel to enhance genotype imputation among cystic fibrosis patientsQuan Sun, Weifang Liu, Jonathan D Rosen, et al.
American Journal of Respiratory and Critical Care Medicine|August 31, 2017
Airway Mucosal Host Defense Is Key to Genomic Regulation of Cystic Fibrosis Lung Disease SeverityDeepika Polineni, Hong Dang, Paul J Gallins, et al.
Clinical and Translational Science|May 10, 2025
Elexacaftor/Tezacaftor/Ivacaftor Population Pharmacokinetics in Pediatric Patients With Cystic FibrosisNgoc Hoa Truong, Sihem Benaboud, Naïm Bouazza, et al.
Pageof 15

Showing results (121-130 of 146) with videos related to

Sort By:
Pageof 15
BMC Medical Genomics|March 8, 2018
Whole exome sequencing in three families segregating a pediatric case of sarcoidosisAlain Calender, Pierre Antoine Rollat Farnier, Adrien Buisson, et al.
American Journal of Human Genetics|June 16, 2015
RSPH3 Mutations Cause Primary Ciliary Dyskinesia with Central-Complex Defects and a Near Absence of Radial SpokesLudovic Jeanson, Bruno Copin, Jean-François Papon, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 28, 2020
Clinical response to lumacaftor-ivacaftor in patients with cystic fibrosis according to baseline lung functionPierre-Régis Burgel, Isabelle Durieu, Raphaël Chiron, et al.
Human Molecular Genetics|February 8, 2017
Cystic fibrosis gene modifier SLC26A9 modulates airway response to CFTR-directed therapeuticsLisa J Strug, Tanja Gonska, Gengming He, et al.
The Lancet. Respiratory Medicine|October 25, 2025
Effect of elexacaftor-tezacaftor-ivacaftor on bronchial dilatations in adolescents with cystic fibrosis: a multicentre prospective observational studyIsabelle Sermet-Gaudelus, Alexia Letierce, Laureline Berteloot, et al.
Orphanet Journal of Rare Diseases|April 22, 2018
Pulmonary hemosiderosis in children with Down syndrome: a national experienceAurelia Alimi, Jessica Taytard, Rola Abou Taam, et al.
Plos Genetics|February 27, 2019
Genetic association and transcriptome integration identify contributing genes and tissues at cystic fibrosis modifier lociJiafen Gong, Fan Wang, Bowei Xiao, et al.
HGG Advances|February 7, 2022
Leveraging TOPMed imputation server and constructing a cohort-specific imputation reference panel to enhance genotype imputation among cystic fibrosis patientsQuan Sun, Weifang Liu, Jonathan D Rosen, et al.
American Journal of Respiratory and Critical Care Medicine|August 31, 2017
Airway Mucosal Host Defense Is Key to Genomic Regulation of Cystic Fibrosis Lung Disease SeverityDeepika Polineni, Hong Dang, Paul J Gallins, et al.
Clinical and Translational Science|May 10, 2025
Elexacaftor/Tezacaftor/Ivacaftor Population Pharmacokinetics in Pediatric Patients With Cystic FibrosisNgoc Hoa Truong, Sihem Benaboud, Naïm Bouazza, et al.
Pageof 15