Clinical and mycological features of onychomycosis in central Tunisia: a 22 years retrospective study (1986-2007) von Dhib, I., Fathallah, A., Yaacoub, A., Zemni, R., Gaha, R., Said, M. B.

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Multiplex PCR assay for the detection of common dermatophyte nail infections von Dhib, I., Fathallah, A., Yaacoub, A., Hadj Slama, F., Said, M. B., Zemni, R.

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Clinical and mycological features of onychomycosis in central Tunisia: a 22years retrospective study (1986-2007) von Dhib, I, Fathallah, A, Yaacoub, A, Zemni, R, Gaha, R, Said, M B

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Relationship Between Phenotypic and Genotypic Characteristics of Trichophyton mentagrophytes Strains Isolated from Patients with Dermatophytosis von Dhib, I., Khammari, I., Yaacoub, A., Hadj Slama, F., Ben Saïd, M., Zemni, R., Fathallah, A.

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Evaluation of Chitine synthase (CHS1) polymerase chain reaction assay in diagnosis of dermatophyte onychomycosis von Dhib, I., Fathallah, A., Charfeddine, I.B., Meksi, S.G., Said, M.B., Slama, F., Zemni, R.

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Validation of the Distress Thermometer Questionnaire for Parents of Children with Down syndrome von Ben Cheikh, A, Bannour, R, Dardour, L, Tahri, O, Mhamed, A, Trabelsi, M, Zemni, R

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ARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardation von Bienvenu, Thierry, Poirier, Karine, Friocourt, Gaelle, Bahi, Nadia, Beaumont, Delphine, Fauchereau, Fabien, Ben Jeema, Lamia, Zemni, Ramzi, Vinet, Marie-Claude, Francis, Fiona, Couvert, Philippe, Gomot, Marie, Moraine, Claude, van Bokhoven, Hans, Kalscheuer, Vera, Frints, Suzanne, Gecz, Josef, Ohzaki, Kanae, Chaabouni, Habiba, Fryns, Jean-Pierre, Desportes, Vincent, Beldjord, Cherif, Chelly, Jamel

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A new member of the IL-1 receptor family highly expressed in hippocampus and involved in X-linked mental retardation von Moraine, Claude, Kahn, Axel, Fryns, Jean-Pierre, Cardona, Ana, Beldjord, Cherif, Zemni, Ramzi, Jun, Lin, Vinet, Marie-Claude, Frints, Suzanna, Whittaker, Adam, Couvert, Philippe, Hamel, Ben, Ross, Mark T, Howell, Gareth R, Carrié, Alain, Van Buggenhout, Griet, Marynen, Peter, McDonell, Nathalie, Chelly, Jamel, Bienvenu, Thierry, Strom, Tim, Ropers, Hans H

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Un variant du gène CD40 est associé avec la perte osseuse systémique au cours de la polyarthrite rhumatoïde von Sghiri, R., Benhassine, H., Baccouche, K., Jriri, S., Slama, F., Shakoor, Z., Almorgen, A., Elamri, N., Bouajina, E., Zemni, R.

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Oligophrenin-1 encodes a rhoGAP protein involved in X-linked mental retardation von Billuart, Pierre, Bienvenu, Thierry, Ronce, Nathalie, des Portes, Vincent, Vinet, Marie Claude, Zemni, Ramzi, Crollius, Hugues Roest, Carrié, Alain, Fauchereau, Fabien, Cherry, Michele, Briault, Sylvain, Hamel, Ben, Fryns, Jean-Pierre, Beldjord, Cherif, Kahn, Axel, Moraine, Claude, Chelly, Jamel

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A new gene involved in X-linked mental retardation identified by analysis of an X;2 balanced translocation von Friocourt, Gaelle, Carrié, Alain, Chafey, Philippe, Brandau, Oliver, Fryns, Jean P, Frints, Suzanna, Ropers, Hans H, Billuart, Pierre, McDonell, Nathalie, Vinet, Marie C, Portes, Vincent des, Cardona, Anna, Moraine, Claude, Fauchereau, Fabien, Couvert, Philippe, Meindl, Alfonse, Ronce, Nathalie, Chelly, Jamel, Beldjord, Cherif, Bokhoven, Han van, Zemni, Ramzi, Sudbrak, Ralf, Francis, Fiona, Sefiani, Aziz, Bienvenu, Thierry, Kahn, Axel

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Molecular cytogenetic analysis of a duplication Xp in a female with an abnormal phenotype and random X inactivation von Portnoï, Marie-France, Bouayed-Abdelmoula, Nouha, Mirc, Myriam, Zemni, Ramzi, Castaing, Henry, Stephann, Julie, Ardalan, Azarnouche, Vialard, François, Nouchy, Marc, Daoud, Patrick, Chelly, Jamel, Taillemite, Jean-Louis

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The Creatine Transporter Gene Paralogous at 16p11.2 Is Expressed in Human Brain von Bayou, Nadia, M'rad, Ridha, Belhadj, Ahlem, Daoud, Hussein, Zemni, Ramzi, Briault, Sylvain, Helayem, M. Béchir, Ben Jemaa, Lamia, Chaabouni, Habiba

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Missense mutation in PAK3, R67C, causes X-linked nonspecific mental retardation von Bienvenu, Thierry, des Portes, Vincent, McDonell, Nathalie, Carrié, Alain, Zemni, Ramzi, Couvert, Philippe, Ropers, Hilger H., Moraine, Claude, van Bokhoven, Hans, Fryns, Jean Pierre, Allen, Kristina, Walsh, Christopher A., Boué, Joelle, Kahn, Axel, Chelly, Jamel, Beldjord, Cherif

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TM4SF2 gene involvement reconsidered in an XLMR family after neuropsychological assessment von Gomot, Marie, Ronce, Nathalie, Dessay, Sabine, Zemni, Ramzi, Ayrault, Anne‐Dominique, Moizard, Marie‐Pierre, Nivelon, Annie, Gilgenkrantz, Simone, Dourlens, Julliette, Des Portes, Vincent, Chelly, Jamel, Moraine, Claude

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Determination of the gene structure of human oligophrenin-1 and identification of three novel polymorphisms by screening of DNA from 164 patients with non-specific X-linked mental... von Billuart, Pierre, Chelly, Jamel, Carrié, Alain, Vinet, Marie-Claude, Couvert, Philippe, McDonell, Nathalie, Zemni, Ramzi, Kahn, Axel, Moraine, Claude, Beldjord, Cherif, Bienvenu, Thierry

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Refined 2.7 centimorgan locus in Xp21.3-22.1 for a nonspecific X-linked mental retardation gene (MRX54): X-Linked Mental Retardation. Part III von BEN JEMAA, L, DES PORTES, V, ZEMNI, R, MRAD, R, MAAZOUL, F, BELDJORD, C, CHAABOUNI, H, CHELLY, J

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Refined 2.7 centimorgan locus in Xp21.3-22.1 for a nonspecific X-linked mental retardation gene (MRX54) von Jemaa, Lamia Ben, des Portes, Vincent, Zemni, Ramzi, Mrad, Ridha, Maazoul, Faouzi, Beldjord, Chérif, Chaabouni, Habiba, Chelly, Jamel

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Conduction mechanisms and complex impedance analysis in La0.6Sr0.4FeO3 ceramic von Lataoui, R., Triki, A., Hcini, S., Oueslati, A., Zemni, S., Kanoun, O.

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Structural, morphological and dielectric analyses of La1 − xSrxFeO3 solid solutions von Lataoui, R., Triki, A., Hcini, S., Zemni, S., Dhahri, J., Kanoun, O.

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