Le syndrome de la traversée thoracobrachiale. Association entre anomalies osseuses et dilatation anévrismale de l’artère sous-clavière : à propos de 12 cas von Gouider, T. Ben Hadj, Böge, G., Marty-Ané, C.-H., Alric, P.

Volltext

Novel presenilin 1 mutation (p.I83T) in Tunisian family with early-onset Alzheimer's disease von Achouri-Rassas, Afef, Ben Ali, Nadia, Fray, Saloua, Hadj Fredj, Sondes, Kechaou, Meriem, Zakraoui, Nouria Oudiaa, Cherif, Aroua, Chabbi, Slim, Anane, Nadia, Messaoud, Taieb, Gouider, Riadh, Belal, Samir

Volltext

Identification of a primarily neurological phenotypic expression of xeroderma pigmentosum complementation group A in a Tunisian family von Messaoud, O., Ben Rekaya, M., Kefi, R., Chebel, S., Boughammoura‐Bouatay, A., Bel Hadj Ali, H., Gouider‐Khouja, N., Zili, J., Frih‐Ayed, M., Mokhtar, I., Abdelhak, S., Zghal, M.

Volltext

Design and Rationale of the National Tunisian Registry of Percutaneous Coronary Intervention: Protocol for a Prospective Multicenter Observational Study von Hammami, Rania, Boudiche, Selim, Rami, Tlili, Ben Halima, Nejeh, Jamel, Ahmed, Rekik, Bassem, Gribaa, Rym, Imtinene, Ben Mrad, Charfeddine, Salma, Ellouze, Tarek, Bahloul, Amine, Hédi, Ben Slima, Langar, Jamel, Ben Ahmed, Habib, Ibn Elhadj, Zied, Hmam, Mohamed, Ben Abdessalem, Mohamed Aymen, Maaoui, Sabri, Fennira, Sana, Lobna, Laroussi, Hassine, Majed, Ouanes, Sami, Mohamed Faouzi, Drissi, Mallek, Souad, Mahdhaoui, Abdallah, Meriem, Dghim, Jomaa, Walid, Zayed, Sofien, Kateb, Tawfik, Bouchahda, Nidhal, Azaiez, Fares, Ben Salem, Helmi, Marouen, Morched, Noamen, Aymen, Abdesselem, Salem, Hichem, Denguir, Ibn Hadj Amor, Hassen, Abdeljelil, Farhati, Amara, Amine, Bejar, Karim, Khaldoun, Ben Hamda, Hamza, Chiheb, Ben Jamaa, Mohsen, Fourati, Sami, Elleuch, Faycal, Grati, Zeineb, Chtourou, Slim, Marouene, Sami, Sahnoun, Mohamed, Hadrich, Morched, Mohamed Abdelkader, Maalej, Bouraoui, Hatem, Kamoun, Kamel, Hadrich, Moufid, Ben Chedli, Tarek, Drissa, Mohamed Akrem, Charfeddine, Hanene, Saadaoui, Nizar, Achraf, Gargouri, Ahmed, Siala, Ayari, Mokdad, Nabil, Marsit, Mnif, Sabeur, Sahnoun, Maher, Kammoun, Helmi, Ben Jemaa, Khaled, Mostari, Gharbi, Hamrouni, Nebil, Yamen, Maazoun, Ellouz, Yassine, Smiri, Zahreddine, Hdiji, Amine, Bassem, Jerbi, Ayadi, Wacef, Zouari, Amir, Abbassi, Chedly, Fatma, Boujelben Masmoudi, Battikh, Kais, Kharrat, Elyes, Gtif, Imen, Sami, Milouchi, Bezdah, Leila, Kachboura, Salem, Maatouk, Mohamed Faouzi, Kraiem, Sondes, Jeridi, Gouider, Neffati, Elyes, Kammoun, Samir, Ben Ameur, Youssef, Fehri, Wafa, Gamra, Habib, Zakhama, Lilia, Addad, Faouzi, Mohamed Sami, Mourali, Abid, Leila

Volltext

Identification of a primarily neurological phenotypic expression of xeroderma pigmentosum complementation group A in a Tunisian family: Primarily neurological XP-A clinical form von Messaoud, O., Ben Rekaya, M., Kefi, R., Chebel, S., Boughammoura-Bouatay, A., Bel Hadj Ali, H., Gouider-Khouja, N., Zili, J., Frih-Ayed, M., Mokhtar, I., Abdelhak, S., Zghal, M.

Volltext

Identification of a primarily neurological phenotypic expression of xeroderma pigmentosum complementation group A in a Tunisian family von Messaoud, O., Ben Rekaya, M., Kefi, R., Chebel, S., Boughammoura-Bouatay, A., Bel Hadj Ali, H., Gouider-Khouja, N., Zili, J., Frih-Ayed, M., Mokhtar, I., Abdelhak, S., Zghal, M.

Volltext