Ultrasonographic screening for cystic echinococcosis in sheep in Tunisia by Lahmar, S., Chéhida, F. Ben, Pétavy, A.F., Hammou, A., Lahmar, J., Ghannay, A., Gharbi, H.A., Sarciron, M.E.

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Spondylocarpotarsal synostosis syndrome (with a posterior midline unsegmented bar) by AL KAISSI, A, BEN GHACHEM, M, NASSIB, N, BEN CHEHIDA, F, KOZLOWSKI, K

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Cystic Hydatic Disease in Sheep: Treatment with Percutaneous Aspiration and Injection with Dipeptide Methyl Ester by Lahmar, S, Sarciron, M.E, Ben Chehida, F, Hammou, A, Gharbi, H.A, Gherardi, A, Lahmar, J, Ghannay, A, Pétavy, A.F

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Ultrasonographic screening for cystic echinococcosis in sheep in Tunisia by Lahmar, S, Ben Chéhida, F, Pétavy, A.F, Hammou, A, Lahmar, J, Ghannay, A, Gharbi, H.A, Sarciron, M.E

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Progressive congenital torticollis in VATER association syndrome by Al Kaissi, Ali, Ben Chehida, Farid, Safi, Hatem, Nassib, Nabil, Ben Ghachem, Maher, Gharbi, Hassan, Grill, Franz

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Familial vertebral segmentation defects, Sprengel anomaly, and omovertebral bone with variable expressivity by Kaissi, Ali Al, Chehida, Farid Ben, Gharbi, Hassan, Ghachem, Maher Ben, Hendaoui, Lotfi, Hennekam, Raoul C.M.

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Toxoplasmose congénitale simulant une tumeur cérébrale á propos d'une observation by Aloui, N., Maarouf, M., Felah, S., Chehida, F.Ben, Bellagha, I., Khaldi, F., Hammou, A.

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Percutaneous treatment of hydatid cysts (Echinococcus granulosus) by GARGOURI, M, NEJET BEN AMOR, FERI BEN CHEHIDA, AZZA HAMMOU, GHARBI, H. A, MOHAMED BEN CHEIKH, HEFDI KCHOUK, KAMEL AYACHI, GOLVAN, J.-Y

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Douleurs osseuses fébriles chez l’enfant drépanocytaire : apport de l’IRM by Aloui, N., Nessib, N., Jalel, C., Ben Chehida, F., Zidi, A., Bellagha, I., Hendaoui, L., Abdallah, N.B., Railhac, J.J., Ghachem, M., Hammou, A.

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Acute osteomyelitis in children: early MRI diagnosis by Aloui, N, Nessib, N, Jalel, C, Ellouze, S, Ben Chehida, F, Sayed, M, Bellagha, I, Ghachem, M, Hammou, A

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Febrile osseous pain in children with sickle cell disease: MRI findings by Aloui, N, Nessib, N, Jalel, C, Ben Chehida, F, Zidi, A, Bellagha, I, Hendaoui, L, Abdallah, N B, Railhac, J J, Ghachem, M, Hammou, A

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Douleurs osseuses fébriles chez l’enfant by Aloui, N., Nessib, N., Jalel, C., Ellouze, S., Ben Chehida, F., Sayed, M., Bellagha, I., Ghachem, M., Hammou, A.

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Douleurs osseuses fébriles chez l'enfant : Apport de l'IRM by ALOUI, N, NESSIB, N, JALEL, C, ELLOUZE, S, BEN CHEHIDA, F, SAYED, M, BELLAGHA, I, GHACHEM, M, HAMMOU, A

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Towards an Automatic Co-generator for Manycores’ Architecture and Runtime: STHORM case-study by Bechara, Charly, Chehida, Karim Ben, Thabet, Farhat

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Glycogen storage disease type I in Tunisia: An epidemiological analysis by Chehida, A. Ben, Tebib, N., Cherif, W., Turkia, H. Ben, Abdelmoula, S., Azzouz, H., Ben Dridi, M. F.

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HARS: A hardware-assisted runtime software for embedded many-core architectures by Lhuillier, Yves, Ojail, Maroun, Guerre, Alexandre, Philippe, Jean-Marc, Chehida, Karim Ben, Thabet, Farhat, Andriamisaina, Caaliph, Jaber, Chafic, David, Raphaël

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Adrénoleucodystrophie liée à l’X : étude clinique et génétique d’une série de patients tunisiens by Kallabi, F., Essalah, W., Guirat, M., Affes, L., Gharbi, N., Ben Khalifa, S., Kammoun, T., Ben Chehida, A., Boudabous, H., Abdelmoula, M.S., Kraoua, I., Feki, M., Ben Ayed, I., Kamoun, H.

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Les maladies héréditaires du métabolisme en Tunisie: défis, acquis, espoirs by Ben Dridi, M.-F., Ben Turkia, H., Azzouz, H., Ben Chehida, A., Ben Abdelaziz, R., Tebib, N.

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Mutation spectrum of glycogen storage disease type Ia in Tunisia: Implication for molecular diagnosis by Barkaoui, E, Cherif, W, Tebib, N, Charfeddine, C, Ben Rhouma, F, Azzouz, H, Ben Chehida, A, Monastiri, K, Chemli, J, Amri, F, Ben Turkia, H, Abdelmoula, M. S, Kaabachi, N, Abdelhak, S, Ben Dridi, M. F

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P-405 – Étude de 10 cas pédiatriques de Maladie de Wilson: Quelles difficultés? by Ben Chehida, A., Besbes, T., Bouslah, M., Ben Abdelaziz, R., Ben Rehouma, F., Azzouz, H., Boudabous, H., Abdelmoula, M.S., Abdelhak, S., Ben Turkia, H., Tebib, N.

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