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Rim Zainine

Showing results (11-20 of 27) with videos related to

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La Tunisie Medicale|March 28, 2015
[Wegener's granulomatosis revealed by an involvment of the lacrimal gland]Rim Zainine, Habib Jaafoura, Skander Kedous, et al.
La Tunisie Medicale|November 5, 2010
[Solitary plasmocytoma of the nasal cavity]Rim Zainine, Samia Sahtout, Ali Mardassi, et al.
Presse Medicale (Paris, France : 1983)|May 6, 2014
[Facial nerve paralysis secondary to acute otitis media]Houda Chahed, Afef Dhaouadi, Azza Mediouni, et al.
The Pan African Medical Journal|August 2, 2017
Ectopic thyroid tissue: unusual differential diagnosis of cervical paragangliomaHouda Chahed, Ghada Kharrat, Rim Bechraoui, et al.
La Tunisie Medicale|June 5, 2026
Correlation Between Computed Tomography and Endoscopy in the Characterization of Tracheal StenosisJihene Gharsalli, Houda Chahed, Wafa Atrous, et al.
International Journal of Pediatric Otorhinolaryngology|July 17, 2013
Compound heterozygosity for dominant and recessive GJB2 mutations in a Tunisian family and association with successful cochlear implant outcomeZied Riahi, Rim Zainine, Yosra Mellouli, et al.
La Tunisie Medicale|April 27, 2010
Chondrosarcoma of sinonasal cavity: a case report and brief literature reviewSalima Kharrat, Samia Sahtout, Sahbi Tababi, et al.
La Tunisie Medicale|October 5, 2010
[Allergic rhinitis]Afifa Charfi, Rim Zainine, Sourour Ben Ali, et al.
International Journal of Pediatric Otorhinolaryngology|July 17, 2013
A novel frameshift mutation (c.405delC) in the GJB2 gene associated with autosomal recessive hearing loss in two Tunisian familiesZied Riahi, Houda Chahed, Habib Jaafoura, et al.
Gene|May 18, 2013
Update of the spectrum of GJB2 gene mutations in Tunisian families with autosomal recessive nonsyndromic hearing lossZied Riahi, Hassen Hammami, Houyem Ouragini, et al.
Pageof 3

Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
La Tunisie Medicale|March 28, 2015
[Wegener's granulomatosis revealed by an involvment of the lacrimal gland]Rim Zainine, Habib Jaafoura, Skander Kedous, et al.
La Tunisie Medicale|November 5, 2010
[Solitary plasmocytoma of the nasal cavity]Rim Zainine, Samia Sahtout, Ali Mardassi, et al.
Presse Medicale (Paris, France : 1983)|May 6, 2014
[Facial nerve paralysis secondary to acute otitis media]Houda Chahed, Afef Dhaouadi, Azza Mediouni, et al.
The Pan African Medical Journal|August 2, 2017
Ectopic thyroid tissue: unusual differential diagnosis of cervical paragangliomaHouda Chahed, Ghada Kharrat, Rim Bechraoui, et al.
La Tunisie Medicale|June 5, 2026
Correlation Between Computed Tomography and Endoscopy in the Characterization of Tracheal StenosisJihene Gharsalli, Houda Chahed, Wafa Atrous, et al.
International Journal of Pediatric Otorhinolaryngology|July 17, 2013
Compound heterozygosity for dominant and recessive GJB2 mutations in a Tunisian family and association with successful cochlear implant outcomeZied Riahi, Rim Zainine, Yosra Mellouli, et al.
La Tunisie Medicale|April 27, 2010
Chondrosarcoma of sinonasal cavity: a case report and brief literature reviewSalima Kharrat, Samia Sahtout, Sahbi Tababi, et al.
La Tunisie Medicale|October 5, 2010
[Allergic rhinitis]Afifa Charfi, Rim Zainine, Sourour Ben Ali, et al.
International Journal of Pediatric Otorhinolaryngology|July 17, 2013
A novel frameshift mutation (c.405delC) in the GJB2 gene associated with autosomal recessive hearing loss in two Tunisian familiesZied Riahi, Houda Chahed, Habib Jaafoura, et al.
Gene|May 18, 2013
Update of the spectrum of GJB2 gene mutations in Tunisian families with autosomal recessive nonsyndromic hearing lossZied Riahi, Hassen Hammami, Houyem Ouragini, et al.
Pageof 3