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Ibtissem Chouchene. Chercheur, laboratoire de recherche clinique, épidémiologique et génétique des maladies oculaires héréditaires. الموقع الجغرافي
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Researchgate: Ibtissem Chouchene
Tunis, Tunisia
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Activités scientifiques d’Ibtissem Chouchene
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Books & Literature
authors:"Ibtissem Chouchene" - Search | Paperity
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Projet de fin d'études Plateforme de E-Insurance
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Institut des Hautes Etudes Commerciales République Tunisienne Carthage Ministè…
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Open Access . Cached. Download Links [ftp.ncbi.nlm.nih.gov] ... , Ibtissem Chouchene , Hamouda Boussen ...
Scientific Publications
Coexistence of mal de Meleda and congenital cataract in a...
jmedicalcasereports.biomedcentral.com
Ibtissem Chouchene 3, Hamouda Boussen 5, Mourad Mokni 2, 6, Amel Dhahri-Ben Osman 6, ... Leila Elmatri 3; Journal of Medical Case Reports :108. DOI: …
Publications
Coexistence of mal de Meleda and congenital cataract in a...
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Introduction Mal de Meleda is a rare form of palmoplantar keratoderma, with autosomal recessive transmission. It is characterized by diffuse erythema and...
Ibtissem Chouchene's Research | CureHunter
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Username: Password: Remember login. Login. Send password reminder... Ibtissem Chouchene Selected Research. Ibtissem Chouchene Research Topics ...
Coexistence of mal de Meleda and congenital cataract in a...
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A Tunisian family with two female siblings aged 45 and 30 years, presented with a clinical association of mal de Meleda and congenital cataract. The two...
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Reports & Statements
Central areolar choroidal dystrophy associated with inherited drusen...
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Original Article
Miscellaneous
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Article medicale Tunisie, Article medicale Rétinopathie pigmentaire à...
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... et de la rétinopathie pigmentaire à âge de début précoce. par Ibtissem Chouchene , Leila Largueche , Kaouther Derouiche , Souad Mabrouk , Sonia Abdelhak ...
Article medicale Tunisie, Article medicale Early ouset retinis...
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Ibtissem Chouchene, Leila Largueche, Kaouther Derouiche, Souad Mabrouk, Sonia Abdelhak, Leila El Matri. La tunisie Medicale ; Vol 93 ( n°07 ) :
Identification of a novel mutation in FOXL2 gene that leads to...
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Ibtissem Chouchene, Kaouthar Derouiche, +5 authors Leila El Matri; Published in Genetic testing and molecular biomarkers; DOI: gtmb
LOVD v Submitters registered to medgen.ugent.be/LOVD/
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Tunis, Ibtissem Chouchene . Hedi Rais Institute of Ophthalmology Department B Boulevard 9 Avril, Bab Saadoun, Tunis
THE DETERMINANTS OF THE PRESENCE OF INDEPENDENT (...)
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Abstract The purpose of this paper is to study the determinants of the presence of independent directors on boards of directors. Based on the
[Clinical characterization of the Stargardt disease and molecular...
hal-riip.archives-ouvertes.fr
... of the Stargardt disease and molecular exploration of the c.2041C>T mutation ( ABCA4 gene) in Tunisian patients]. Ibtissem Chouchene 1, * Leila Largueche
The Determinants of the Presence of Independent Directors in French...
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The Determinants of the Presence of Independent Directors in French Board Companies
Coexistence of mal de Meleda and congenital cataract in a...
hal.archives-ouvertes.fr
Mbarka Bchetnia 1, 2, Ahlem Merdassi 3, Cherine Charfeddine 1, Fatma Mgaieth 3, Selma Kassar 4, Farah Ouechtati 3, Ibtissem Chouchene 3, Hamouda ...
Macular Degeneration: Chouchene, I - Expertscape.com
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I Chouchene has special expertise in Macular Degeneration
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