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

David Shoseyov

Showing results (71-80 of 82) with videos related to

Pageof 9
Sort By:
Plos One|August 31, 2013
CCDC65 mutation causes primary ciliary dyskinesia with normal ultrastructure and hyperkinetic ciliaAmjad Horani, Steven L Brody, Thomas W Ferkol, et al.
Lancet (London, England)|August 30, 2008
Effectiveness of PTC124 treatment of cystic fibrosis caused by nonsense mutations: a prospective phase II trialEitan Kerem, Samit Hirawat, Shoshana Armoni, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|April 5, 2011
Ambulatory quantitative waking and sleeping cough assessment in patients with cystic fibrosisEitan Kerem, Michael Wilschanski, Nilsen L Miller, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|May 5, 2016
Eradication failure of newly acquired Pseudomonas aeruginosa isolates in cystic fibrosisMalena Cohen-Cymberknoh, Noa Gilead, Silvia Gartner, et al.
Annals of the American Thoracic Society|October 23, 2020
Ivacaftor in People with Cystic Fibrosis and a <i>3849+10kb C</i>→<i>T</i> or <i>D1152H</i> Residual Function MutationEitan Kerem, Malena Cohen-Cymberknoh, Reuven Tsabari, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|September 21, 2015
The impact of a national population carrier screening program on cystic fibrosis birth rate and age at diagnosis: Implications for newborn screeningPatrick Stafler, Meir Mei-Zahav, Michael Wilschanski, et al.
Respiratory Medicine|September 27, 2017
Clinical impact of Pseudomonas aeruginosa colonization in patients with Primary Ciliary DyskinesiaMalena Cohen-Cymberknoh, Nir Weigert, Alex Gileles-Hillel, et al.
Nature Medicine|July 14, 2015
Preconditioning allows engraftment of mouse and human embryonic lung cells, enabling lung repair in miceChava Rosen, Elias Shezen, Anna Aronovich, et al.
American Journal of Respiratory Cell and Molecular Biology|March 20, 2015
Immunofluorescence Analysis and Diagnosis of Primary Ciliary Dyskinesia with Radial Spoke DefectsAdrien Frommer, Rim Hjeij, Niki T Loges, et al.
Molecular Genetics & Genomic Medicine|May 27, 2017
Nationwide genetic analysis for molecularly unresolved cystic fibrosis patients in a multiethnic society: implications for preconception carrier screeningDoron M Behar, Ori Inbar, Michal Shteinberg, et al.
Pageof 9

Showing results (71-80 of 82) with videos related to

Sort By:
Pageof 9
Plos One|August 31, 2013
CCDC65 mutation causes primary ciliary dyskinesia with normal ultrastructure and hyperkinetic ciliaAmjad Horani, Steven L Brody, Thomas W Ferkol, et al.
Lancet (London, England)|August 30, 2008
Effectiveness of PTC124 treatment of cystic fibrosis caused by nonsense mutations: a prospective phase II trialEitan Kerem, Samit Hirawat, Shoshana Armoni, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|April 5, 2011
Ambulatory quantitative waking and sleeping cough assessment in patients with cystic fibrosisEitan Kerem, Michael Wilschanski, Nilsen L Miller, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|May 5, 2016
Eradication failure of newly acquired Pseudomonas aeruginosa isolates in cystic fibrosisMalena Cohen-Cymberknoh, Noa Gilead, Silvia Gartner, et al.
Annals of the American Thoracic Society|October 23, 2020
Ivacaftor in People with Cystic Fibrosis and a <i>3849+10kb C</i>→<i>T</i> or <i>D1152H</i> Residual Function MutationEitan Kerem, Malena Cohen-Cymberknoh, Reuven Tsabari, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|September 21, 2015
The impact of a national population carrier screening program on cystic fibrosis birth rate and age at diagnosis: Implications for newborn screeningPatrick Stafler, Meir Mei-Zahav, Michael Wilschanski, et al.
Respiratory Medicine|September 27, 2017
Clinical impact of Pseudomonas aeruginosa colonization in patients with Primary Ciliary DyskinesiaMalena Cohen-Cymberknoh, Nir Weigert, Alex Gileles-Hillel, et al.
Nature Medicine|July 14, 2015
Preconditioning allows engraftment of mouse and human embryonic lung cells, enabling lung repair in miceChava Rosen, Elias Shezen, Anna Aronovich, et al.
American Journal of Respiratory Cell and Molecular Biology|March 20, 2015
Immunofluorescence Analysis and Diagnosis of Primary Ciliary Dyskinesia with Radial Spoke DefectsAdrien Frommer, Rim Hjeij, Niki T Loges, et al.
Molecular Genetics & Genomic Medicine|May 27, 2017
Nationwide genetic analysis for molecularly unresolved cystic fibrosis patients in a multiethnic society: implications for preconception carrier screeningDoron M Behar, Ori Inbar, Michal Shteinberg, et al.
Pageof 9