Mutations in MTMR13, a New Pseudophosphatase Homologue of MTMR2 and Sbf1, in Two Families with an Autosomal Recessive Demyelinating Form of Charcot-Marie-Tooth Disease Associated w... von Azzedine, H., Bolino, A., Taïeb, T., Birouk, N., Di Duca, M., Bouhouche, A., Benamou, S., Mrabet, A., Hammadouche, T., Chkili, T., Gouider, R., Ravazzolo, R., Brice, A., Laporte, J., LeGuern, E.

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The phenotypic manifestations of autosomal recessive axonal Charcot-Marie-Tooth due to a mutation in Lamin A/C gene von Chaouch, M, Allal, Y, De Sandre-Giovannoli, A, Vallat, J M, Amer-el-Khedoud, A, Kassouri, N, Chaouch, A, Sindou, P, Hammadouche, T, Tazir, M, Lévy, N, Grid, D

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Homozygous Defects in LMNA, Encoding Lamin A/C Nuclear-Envelope Proteins, Cause Autosomal Recessive Axonal Neuropathy in Human (Charcot-Marie-Tooth Disorder Type 2) and Mouse von De Sandre-Giovannoli, Annachiara, Chaouch, Malika, Kozlov, Serguei, Vallat, Jean-Michel, Tazir, Meriem, Kassouri, Nadia, Szepetowski, Pierre, Hammadouche, Tarik, Vandenberghe, Antoon, Stewart, Colin L., Grid, Djamel, Lévy, Nicolas

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Genetic heterogeneity in giant axonal neuropathy: an Algerian family not linked to chromosome 16q24.1 von Tazir, M, Vallat, J.M, Bomont, P, Zemmouri, R, Sindou, P, Assami, S, Nouioua, S, Hammadouche, T, Grid, D, Koenig, M

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The Autosomal Recessive Form of CMT Disease Linked to 5q31-q33 von GUILBOT, A., KESSALI, M., RAVISÉ, N., HAMMADOUCHE, T., BOUHOUCHE, A., MAISONOBE, T., GRID, D., BRICE, A., LEGUERN, E.

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The Autosomal Recessive Form of CMT Disease Linked to 5q31-q33 von GUILBOT, A., KESSALI, M., RAVISÉ, N., HAMMADOUCHE, T., BOUHOUCHE, A., MAISONOBE, T., GRID, D., BRICE, A., LeGUERN, E.

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Variations in the pre-operative status of patients coming to primary hip replacement for osteoarthritis in European orthopaedic centres von Dieppe, Paul, Judge, Andrew, Williams, Susan, Ikwueke, Ifeoma, Guenther, Klaus-Peter, Floeren, Markus, Huber, Joerg, Ingvarsson, Thorvaldur, Learmonth, Ian, Lohmander, L Stefan, Nilsdotter, Anna, Puhl, Wofhart, Rowley, David, Thieler, Robert, Dreinhoefer, Karsten

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Le profil clinique, évolutif, électrophysiologique et anatomopathologique de la maladie de Charcot-Marie-Tooth (CMT) à transmission autosomale récessive liée aux gènes GDAP1, MTMR2... von Kassouri, N., Vallat, J.M., Lévy, N., Belamri, L., Hammadouche, T., Chaouch, A., Chaouch, M.

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The Autosomal Recessive Form of CMT Disease Linked to 5q31-q33 von Guilbot, A, Kessali, M, Ravisé, N, Hammadouche, T, Bouhouche, A, Maisonobe, T, Grid, D, Brice, A, LeGUERN, E

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The Autosomal Recessive Form of CMT Disease Linked to 5q31-q33 von Guilbot, A, Kessali, M, Ravisé, N, Hammadouche, T, Bouhouche, A, Maisonobe, T, Grid, D, Brice, A, Leguern, E

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The phenotypic manifestations of autosomal recessive axonalCharcot–Marie–Tooth due to a mutation in Lamin A/C gene von Chaouch, M., Allal, Y., De Sandre-Giovannoli, A., Vallat, J.M., Amer-el-Khedoud, A., Kassouri, N., Chaouch, A., Sindou, P., Hammadouche, T., Tazir, M., Lévy, N., Grid, D.

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Homozygous Defects In Lmna, Encoding Lamin A/C Nuclear-Envelope Proteins, Cause Autosomal Recessive Axonal Neuropathy In Human (Charcot-Marie-Tooth Disorder Type 2) And Mouse von De Sandre-Giovannoli, A, Chaouch, M, Kozlov, S, Vallat, JM, Tazir, M, Kassouri, N, Szepetowski, P, Hammadouche, T, Vandenberghe, A, Stewart, CL, Grid, D, Levy, N.

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The phenotypes of autosomal recessive HSMN linked to chromosomes 5q and 11q von Salih, M.A., Kessali, M., Hammadouche, T., Kabira, M., Tahan, A., Al Rayes, M., Maisonobe, T., Le Guern, E., Urtizberea, J.A., Grid, D.

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Access to Care and Therapy for Kawasaki Disease in the Arab Countries: A Kawasaki Disease Arab Initiative (Kawarabi) Multicenter Survey von Alzyoud, Raed, El-Kholy, Nermeen, Arab, Yousra, Choueiter, Nadine, Harahsheh, Ashraf S., Aselan, Adnan Salem, Kotby, Alyaa, Bouaziz, Asma, Salih, Aso F., Abushhaiwia, Awatif, Alahmadi, Fahad, Agha, Hala M., Elmarsafawy, Hala M., Alrabte, Hanifa, Al-Saloos, Hesham, Boudiaf, Houda, Hijazi, Issa, Bouayed, Kenza, Al Senaidi, Khalfan Salim, Boughammoura, Lamia, Jalal, Maryam, Ladj, Mohamed S., Abu-Shukair, Mohammed E., ElGanzoury, Mona M., Hammadouche, Nacera, Elsamman, Nora, Mouawad, Pierre, Boukari, Rachida, Benalikhoudja, Nassiba, Jdour, Salima, Abu Al-Saoud, Sima Y., Touri, Soued Nabila, Kammoun, Thouraya, Fitouri, Zohra, Dahdah, Nagib

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Temps ductiles von Hammadouche, Lyes

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300 COMPARISON OF PATIENT AND SURGEON EXPECTATIONS FOR TOTAL HIP ARTHROPLASTY von Jourdan, C, Poiraudeau, S, Descamps, S, Nizard, R, Hammadouche, M, Anract, P, Ravaud, P

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Long term clinical results of total joint replacement with alumina/alumina articulation von Sedel, Laurent, Bizot, P, Nizard, R, Hammadouche, M, Hannouche, D

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Long Term Clinical Results of Total Joint Replacement with Alumina/Alumina Articulation von Nizard, Remy, Hannouche, Didier, Sedel, Laurent, Hammadouche, M., Bizot, P.

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