Lynch syndrome in Tunisia: first description of clinical features and germline mutations von Moussa, Sana Aissi-Ben, Moussa, Amel, Kourda, Nadia, Mezlini, Amel, Abdelli, Nabil, Zerimech, Farid, Najjar, Taoufik, Jilani, Sarah Ben, Porchet, Nicole, Ayed, Farhat Ben, Manai, Mohamed, Buisine, Marie-Pierre

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Frequent mutations of the CA simple sequence repeat in intron 1 of EGFR in mismatch repair-deficient colorectal cancers von Buisine, Marie-Pierre, Wacrenier, Agnes, Mariette, Christophe, Leteurtre, Emmanuelle, Escande, Fabienne, Aissi, Sana, Ketele, Amandine, Leclercq, Annette, Porchet, Nicole, Lesuffleur, Thecla

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IGF1 polymorphisms and colon cancer risk in Tunisian population von Dhifallah, Haifa, Aissi, Sana, Njima, Manel, Zakhama, Abdelfatteh, Kenani, Abderraouf

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IGF1 polymorphisms and colon cancer risk in Tunisian population von Dhifallah, Haifa, Aissi, Sana, Njima, Manel, Zakhama, Abdelfatteh, Kenani, Abderraouf

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Somatic molecular changes and histo-pathological features of colorectal cancer in Tunisia von Aissi, Sana, Buisine, Marie Pierre, Zerimech, Farid, Kourda, Nadia, Moussa, Amel, Manai, Mohamed, Porchet, Nicole

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KRAS mutations in colorectal cancer from Tunisia: relationships with clinicopathologic variables and data on TP53 mutations and microsatellite instability von Aissi, Sana, Buisine, Marie-Pierre, Zerimech, Farid, Kourda, Nadia, Moussa, Amel, Manai, Mohamed, Porchet, Nicole

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TP53 mutations in colorectal cancer from Tunisia: relationships with site of tumor origin, microsatellite instability and KRAS mutations von Aissi, Sana, Buisine, Marie-Pierre, Zerimech, Farid, Kourda, Nadia, Moussa, Amel, Manai, Mohamed, Porchet, Nicole

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Molecular characterization of Lynch syndrome in Tunisia von Sana, Aissi, Farid, Zérimech, Amel, Moussa, Nadia, Kourda, Amel, Mezlini, Nabil, Abdelli, Taoufik, Najjar, Farhat, Ben Ayed, Sarah, Ben Jilani, Mohamed, Manai, Marie-Pierre, Buisine

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Frequent mutations of the CA simple sequence repeat in intron 1 of EGFR in mismatch repair-defi cient colorectal cancers von Buisine, Marie-Pierre, Wacrenier, Agnès, Mariette, Christophe, Leteurtre, Emmanuelle, Escande, Fabienne, Aissi, Sana, Ketele, Amandine, Leclercq, Annette, Porchet, Nicole, Lesuffleur, Thécla

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Identification and characterization of a novel MLH1 genomic rearrangement as the cause of HNPCC in a Tunisian family: evidence for a homologous Alu-mediated recombination von Aissi-Ben Moussa, Sana, Moussa, Amel, Lovecchio, Tonio, Kourda, Nadia, Najjar, Taoufik, Ben Jilani, Sarra, El Gaaied, Amel, Porchet, Nicole, Manai, Mohamed, Buisine, Marie-Pierre

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Les domaines de la mémoire épisodique verbale dans la sclérose en plaques : approche cognitive pour le dépistage précoce von Dhia, Rihab Ben, Aissi, Mouna, Sana, Haddad, Daoussi, Nizar, Frih-Ayed, Mahbouba

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Dépistage de la détérioration cognitive dans la maladie de Parkinson par le score de Moca version arabisée von Sana, Haddad, Aissi, Mouna, Dhia, Rihab Ben, Daoussi, Nizar, Frih, Ayed Mahbouba

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