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

Imen Chabchoub

Showing results (51-60 of 55) with videos related to

Pageof 6
Sort By:
You have reached the last page of results.This site can display upto 55 results.
Molecular Neurobiology|March 10, 2016
Molecular Diagnostic and Prognostic Subtyping of Gliomas in Tunisian PopulationSaoussen Trabelsi, Imen Chabchoub, Iadh Ksira, et al.
Genetic Testing and Molecular Biomarkers|October 7, 2014
Molecular investigation of distal renal tubular acidosis in Tunisia, evidence for founder mutationsMajdi Nagara, Konstantinos Voskarides, Sonia Nouira, et al.
Annales D'Endocrinologie|October 10, 2025
Rare causes of pediatric primary adrenal insufficiency: Data from a large nationwide Tunisian cohortRania Khalfallah, Fakhri Kallabi, Delphine Mallet, et al.
Journal of Clinical Immunology|October 15, 2015
Report of the Tunisian Registry of Primary Immunodeficiencies: 25-Years of Experience (1988-2012)Fethi Mellouli, Imen Ben Mustapha, Monia Ben Khaled, et al.
Pediatric Nephrology (Berlin, Germany)|October 24, 2017
Clinical and genetic heterogeneity in familial steroid-sensitive nephrotic syndromeGuillaume Dorval, Olivier Gribouval, Vanesa Martinez-Barquero, et al.
Pageof 6

Showing results (51-60 of 55) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 55 results.
Molecular Neurobiology|March 10, 2016
Molecular Diagnostic and Prognostic Subtyping of Gliomas in Tunisian PopulationSaoussen Trabelsi, Imen Chabchoub, Iadh Ksira, et al.
Genetic Testing and Molecular Biomarkers|October 7, 2014
Molecular investigation of distal renal tubular acidosis in Tunisia, evidence for founder mutationsMajdi Nagara, Konstantinos Voskarides, Sonia Nouira, et al.
Annales D'Endocrinologie|October 10, 2025
Rare causes of pediatric primary adrenal insufficiency: Data from a large nationwide Tunisian cohortRania Khalfallah, Fakhri Kallabi, Delphine Mallet, et al.
Journal of Clinical Immunology|October 15, 2015
Report of the Tunisian Registry of Primary Immunodeficiencies: 25-Years of Experience (1988-2012)Fethi Mellouli, Imen Ben Mustapha, Monia Ben Khaled, et al.
Pediatric Nephrology (Berlin, Germany)|October 24, 2017
Clinical and genetic heterogeneity in familial steroid-sensitive nephrotic syndromeGuillaume Dorval, Olivier Gribouval, Vanesa Martinez-Barquero, et al.
Pageof 6