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authFullName_s : Houyem Ouragini

Haplotypic classification of dystrophic epidermolysis bullosa in Tunisian consanguineous families: implication for diagnosis

Houyem Ouragini , Faïka Cherif , Wafa Daoud , Selma Kassar , Chérine Charfeddine , et al.
Archives of Dermatological Research, 2008, 300 (7), pp.365 - 370. ⟨10.1007/s00403-008-0861-2⟩
Journal articles istex pasteur-01375212v1

Genetic analysis of hereditary multiple exostoses in Tunisian families: a novel frame-shift mutation in the EXT1 gene

Sana Sfar , Abderrazak Abid , Wijden Mahfoudh , Houyem Ouragini , Farah Ouechtati , et al.
Molecular Biology Reports, 2009, 36 (4), pp.661-667. ⟨10.1007/s11033-008-9226-3⟩
Journal articles istex pasteur-01375178v1
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Dystrophic epidermolysis bullosa phenotypes in a large consanguineous Tunisian family

Houyem Ouragini , Faika Cherif , Selma Kassar , Giovanna Floriddia , Monica Pascucci , et al.
Journal of Dermatological Science, 2009, 54 (2), pp.114-120. ⟨10.1016/j.jdermsci.2009.01.006⟩
Journal articles pasteur-01375196v1

Clinical and genetic investigation of a large Tunisian family with complete achromatopsia: identification of a new nonsense mutation in GNAT2 gene.

Farah Ouechtati , Ahlem Merdassi , Yosra Bouyacoub , Leila Largueche , Kaouther Derouiche , et al.
Journal of Human Genetics, 2011, 56 (1), pp.22-8. ⟨10.1038/jhg.2010.128⟩
Journal articles pasteur-00604858v1

Clinical and genetic investigation of pediatric cases of Wolff-Parkinson-White syndrome in Tunisian families.

Sonia Nouira , Fatma Ouarda , Cherine Charfeddine , Imen Arfa , Houyem Ouragini , et al.
Heart & Lung, 2010, 39 (5), pp.432-6. ⟨10.1016/j.hrtlng.2009.10.012⟩
Journal articles istex pasteur-00612166v1

Rapid and inexpensive detection of common HBB gene mutations in Tunisian population by high-resolution melting analysis: Implication for molecular diagnosis

Houyem Ouragini , Fayrouz. Haddad , Imen Darragi , Salem Abbes
Hematology, 2014, 19 (2), pp.80 - 84. ⟨10.1179/1607845413Y.0000000096⟩
Journal articles pasteur-01375110v1

Mutational founder effect in recessive dystrophic epidermolysis bullosa families from Southern Tunisia.

Ahlem Sabrine Ben Brick , Nadia Laroussi , Hela Mesrati , Rym Kefi , Mbarka Bchetnia , et al.
Archives of Dermatological Research, 2014, 306 (4), pp.405-11. ⟨10.1007/s00403-013-1421-y⟩
Journal articles pasteur-01061249v1
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Differential impact of consanguineous marriages on autosomal recessive diseases in Tunisia

Nizar Ben Halim , Sana Hsouna , Khaled Lasram , Insaf Rejeb , Asma Walha , et al.
American Journal of Human Biology, 2016, 28 (2), pp.171 - 180. ⟨10.1002/ajhb.22764⟩
Journal articles pasteur-01374977v1

rs11886868 and rs4671393 of BCL11A associated with HbF level variation and modulate clinical events among sickle cell anemia patients

Leila Chaouch , Imen Moumni , Houyem Ouragini , Imen Darragi , Miniar Kalai , et al.
Hematology, 2016, 21 (7), pp.425-429. ⟨10.1080/10245332.2015.1107275⟩
Journal articles pasteur-01374983v1
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Clinical and Genetic Investigation of Atrial Septal Defect with Atrioventricular Conduction Defect in a Large Consanguineous Tunisian Family

Sonia Nouira , Ikram Kamoun , Houyem Ouragini , Cherine Charfeddine , Haifa Mahjoub , et al.
Archives of Medical Research, 2008, 39 (4), pp.429 - 433. ⟨10.1016/j.arcmed.2008.01.002⟩
Journal articles pasteur-01375202v1

The role of rs1984112_G at CD36 gene in increasing reticulocyte level among sickle cell disease patients

Miniar Kalai , Marwa Dridi , Leila Chaouch , Imen Moumni , Houyem Ouragini , et al.
Hematology, 2017, 22 (3), pp.178-182. ⟨10.1080/10245332.2016.1253253⟩
Journal articles hal-01513653v1

Update of the spectrum of GJB2 gene mutations in Tunisian families with autosomal recessive nonsyndromic hearing loss.

Zied Riahi , Hassen Hammami , Houyem Ouragini , Habib Messai , Rim Zainine , et al.
Gene, 2013, 525 (1), pp.1-4. ⟨10.1016/j.gene.2013.04.078⟩
Journal articles pasteur-00861409v1