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Search Results - Rim, Bechraoui
Search Results - Rim, Bechraoui
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MR imaging of endolymphatic hydrops in Ménière's disease: feasibility at 1.5 T
by
Ben Lakhal, Amine
,
Boukriba, Seif
,
Bechraoui, Rim
,
Mannoubi, Sondes
,
Mizouni, Habiba
Published in
Egyptian journal of radiology and nuclear medicine
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Epidemiology and predictive factors of fungal malignant otitis externa
by
Bechraoui, Rim
,
Dhaha, Mohamed
,
Chahed, Houda
,
Ksentini, Amal
,
Zainine, Rim
,
Amor, Mohamed
,
Beltaief, Najeh
,
Besbes, Ghazi
Published in
Indian journal of otology
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Ectopic thyroid tissue: unusual differential diagnosis of cervical paraganglioma
by
Chahed, Houda
,
Kharrat, Ghada
,
Bechraoui, Rim
,
Marrakchi, Jihene
,
Mediouni, Azza
,
Amor, Mohamed Ben
,
Zainine, Rim
,
Beltaief, Nejeh
,
Besbes, Ghazi
Published in
The Pan African medical journal
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Paraganglioma of the carotid body: Report of 26 patients and review of the literature
by
Rim, Zainine
,
Rim, Bechraoui
,
Houda, Chahed
,
Souheil, Jbali
,
Najeh, Beltaief
,
Ghazi, Besbes
Published in
Egyptian journal of ear, nose, throat and allied sciences
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Whole exome sequencing identifies mutations in Usher syndrome genes in profoundly deaf Tunisian patients
by
Riahi, Zied
,
Bonnet, Crystel
,
Zainine, Rim
,
Lahbib, Saida
,
Bouyacoub, Yosra
,
Bechraoui, Rym
,
Marrakchi, Jihène
,
Hardelin, Jean-Pierre
,
Louha, Malek
,
Largueche, Leila
,
Ben Yahia, Salim
,
Kheirallah, Moncef
,
Elmatri, Leila
,
Besbes, Ghazi
,
Abdelhak, Sonia
,
Petit, Christine
Published in
PloS one
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Whole Exome Sequencing Identifies Mutations in Usher Syndrome Genes in Profoundly Deaf Tunisian Patients: e0120584
by
Riahi, Zied
,
Bonnet, Crystel
,
Zainine, Rim
,
Lahbib, Saida
,
Bouyacoub, Yosra
,
Bechraoui, Rym
,
Marrakchi, Jihene
,
Hardelin, Jean-Pierre
,
Louha, Malek
,
Largueche, Leila
Published in
PloS one
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Egyptian Journal Of Ear Nose Throat And Allied Sciences
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Egyptian Journal Of Radiology And Nuclear Medicine
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