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

M Ghorbel

Showing results (41-50 of 55) with videos related to

Pageof 6
Sort By:
Journal Francais D'Ophtalmologie|June 20, 2008
[Nasofrontal fistula and epidermoid cyst: a case study]L Harzallah, L Boughamoura, M Ghorbel, et al.
Bulletin Du Cancer|April 14, 2010
[Juvenile nasopharyngeal carcinoma: anatomoclinic, biologic, therapeutic and evolutive aspects]N Toumi, M Frikha, W Siala, et al.
Journal Francais D'Ophtalmologie|June 21, 2021
[Childhood strabismus secondary to posterior pole cavernous hemangioma of the retina]L Knani, A Mahjoub, H Nouri, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|October 29, 2000
Contrasted frequencies of p53 accumulation in the two age groups of North African nasopharyngeal carcinomasA Khabir, A Sellami, M Sakka, et al.
Journal Francais D'Ophtalmologie|November 16, 2020
[Acute macular outer retinopathy: Contribution of optical coherence tomography-angiography (OCT-A)]A Mahjoub, S Ben Mrad, N Ben Abdesslem, et al.
Journal Francais D'Ophtalmologie|November 10, 2021
[Bilateral central serous chorioretinopathy post-COVID-19]A Mahjoub, A Dlensi, A Romdhane, et al.
Andrologia|July 19, 2011
Screening of ΔF508 mutation and IVS8-poly T polymorphism in CFTR gene in Tunisian infertile men without CBAVDM Ghorbel, S Baklouti-Gargouri, R Keskes, et al.
American Journal of Medical Genetics|December 22, 1999
Pendred syndrome: phenotypic variability in two families carrying the same PDS missense mutationS Masmoudi, I Charfedine, M Hmani, et al.
Clinical Genetics|September 10, 2004
Refined mapping of the autosomal recessive non-syndromic deafness locus DFNB13 using eight novel microsatellite markersS Masmoudi, I Charfedine, I B Rebeh, et al.
Journal Francais D'Ophtalmologie|July 13, 2023
[Pyogenic granuloma: Clinical, etiological and therapeutic features. A series of five cases]A Mahjoub, N Zaafrane, R Chaabene, et al.
Pageof 6

Showing results (41-50 of 55) with videos related to

Sort By:
Pageof 6
Journal Francais D'Ophtalmologie|June 20, 2008
[Nasofrontal fistula and epidermoid cyst: a case study]L Harzallah, L Boughamoura, M Ghorbel, et al.
Bulletin Du Cancer|April 14, 2010
[Juvenile nasopharyngeal carcinoma: anatomoclinic, biologic, therapeutic and evolutive aspects]N Toumi, M Frikha, W Siala, et al.
Journal Francais D'Ophtalmologie|June 21, 2021
[Childhood strabismus secondary to posterior pole cavernous hemangioma of the retina]L Knani, A Mahjoub, H Nouri, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|October 29, 2000
Contrasted frequencies of p53 accumulation in the two age groups of North African nasopharyngeal carcinomasA Khabir, A Sellami, M Sakka, et al.
Journal Francais D'Ophtalmologie|November 16, 2020
[Acute macular outer retinopathy: Contribution of optical coherence tomography-angiography (OCT-A)]A Mahjoub, S Ben Mrad, N Ben Abdesslem, et al.
Journal Francais D'Ophtalmologie|November 10, 2021
[Bilateral central serous chorioretinopathy post-COVID-19]A Mahjoub, A Dlensi, A Romdhane, et al.
Andrologia|July 19, 2011
Screening of ΔF508 mutation and IVS8-poly T polymorphism in CFTR gene in Tunisian infertile men without CBAVDM Ghorbel, S Baklouti-Gargouri, R Keskes, et al.
American Journal of Medical Genetics|December 22, 1999
Pendred syndrome: phenotypic variability in two families carrying the same PDS missense mutationS Masmoudi, I Charfedine, M Hmani, et al.
Clinical Genetics|September 10, 2004
Refined mapping of the autosomal recessive non-syndromic deafness locus DFNB13 using eight novel microsatellite markersS Masmoudi, I Charfedine, I B Rebeh, et al.
Journal Francais D'Ophtalmologie|July 13, 2023
[Pyogenic granuloma: Clinical, etiological and therapeutic features. A series of five cases]A Mahjoub, N Zaafrane, R Chaabene, et al.
Pageof 6