High frequency of the V548A fs X572 XPC mutation in Tunisia: implication for molecular diagnosis
Ben Rekaya, M, Messaoud, O, Talmoudi, F, Nouira, S, Ouragini, H, Amouri, A, Boussen, H, Boubaker, S, Mokni, M, Mokthar, I, Abdelhak, S, Zghal, M
Published in Journal of human genetics (01.07.2009)
Published in Journal of human genetics (01.07.2009)
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Genetic basis of dominant dystrophic epidermolysis bullosa in tunisian families and co-occurrence of dominant and recessive mutations
Ben Brick, A.S., Laroussi, N., Mesrati, H., Kefi, R., Ouragini, H., Bchetnia, M., Romdhane, L., Marrakchi, S., Boubaker, M.S., Castiglia, D., Hovnanian, A., Abdelhak, S., Turki, H., Kharfi, M.
Published in Journal of the European Academy of Dermatology and Venereology (01.01.2016)
Published in Journal of the European Academy of Dermatology and Venereology (01.01.2016)
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Severe phenotypes in two Tunisian families with novel XPA mutations: evidence for a correlation between mutation location and disease severity
Messaoud, O., Ben Rekaya, M., Ouragini, H., Benfadhel, S., Azaiez, H., Kefi, R., Gouider-Khouja, N., Mokhtar, I., Amouri, A., Boubaker, M. S., Zghal, M., Abdelhak, S.
Published in Archives of Dermatological Research (01.03.2012)
Published in Archives of Dermatological Research (01.03.2012)
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Identification of two novel variants in PRKAG2 gene in Tunisian type 2 diabetic patients with family history of cardiovascular disease
Nouira, S, Arfa, I, Kammoun, I, Abid, A, Ouragini, H, Dorboz, I, Ghazouani, W, Fadhel, S. Ben, Zorgati, M.M, Ammar, S. Ben, Blousa-Chabchoub, S, Kachboura, S, Abdelhak, S
Published in Diabetes research and clinical practice (01.02.2010)
Published in Diabetes research and clinical practice (01.02.2010)
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HELLP syndrome: analysis of 23 cases
Kaddour, C, Laamourou, M, Souissi, R, Haddad, Z, Chaaoua, T, Ouragini, H, Gdoura, W
Published in Critical care (London, England) (2005)
Published in Critical care (London, England) (2005)
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Épidermolyse bulleuse dystrophique d’Hallopeau-Siemens dans la ville de Sfax (étude de 43 patients)
Mesrati, H., Chaabane, H., Amouri, M., Bchetnia, M., Ben Brick, S., Ouragini, H., Mseddi, M., Abelhak, S., Turki, H.
Published in Annales de dermatologie et de vénéréologie (01.04.2013)
Published in Annales de dermatologie et de vénéréologie (01.04.2013)
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P191 - Identification de porteurs sains au sein de familles tunisiennes atteintes d’épidermolyse bulleuse dystrophique : intérêt pour le conseil génétique
Daoud, W., Ouragini, H., Cherif, F., Boubaker, S., Abdelhak, S., Ben Osman Dhahri, A.
Published in Annales de dermatologie et de vénéréologie (01.10.2005)
Published in Annales de dermatologie et de vénéréologie (01.10.2005)
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P190 - Variabilité phénotypique au sein de 10 familles atteintes d’épidermolyse bulleuse dystrophique récessive de type non hallopeau-siemens
Daoud, W., Cherif, F., Ouragini, H., Boubaker, S., Abdelhak, S., Ben Osman Dhahri, A.
Published in Annales de dermatologie et de vénéréologie (01.10.2005)
Published in Annales de dermatologie et de vénéréologie (01.10.2005)
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