CICP: Cluster Iterative Closest Point for sparse–dense point cloud registration von Lamine Tazir, M., Gokhool, Tawsif, Checchin, Paul, Malaterre, Laurent, Trassoudaine, Laurent

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COMPARISON OF UAV LIDAR ODOMETRY OF ROTATING AND FIXED VELODYNE PLATFORMS von Tazir, M. L., Seube, N.

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Congenital myasthenic syndromes by Epsilon subunit mutations: Phenotypic profiles of 17 Algerian families von Kediha, M.I., Tazir, M., Sternberg, D., Eymard, B., Ali Pacha, L.

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Congenital myasthenic syndrome by mutation of the ColQ gene: Phenotypic and evolutionary profile of three Algerian families von Kediha, M.I., Tazir, M., Magnouche, C., Sternberg, D., Belarbi, S., Eymard, B., Ali Pacha, L.

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High prevalence of methicillin-resistant Staphylococcus aureus clone ST80-IV in hospital and community settings in Algiers von Antri, K., Rouzic, N., Dauwalder, O., Boubekri, I., Bes, M., Lina, G., Vandenesch, F., Tazir, M., Ramdani-Bouguessa, N., Etienne, J.

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Ataxia with oculomotor apraxia type 2: clinical, biological and genotype/phenotype correlation study of a cohort of 90 patients von Anheim, M., Monga, B., Fleury, M., Charles, P., Barbot, C., Salih, M., Delaunoy, J. P., Fritsch, M., Arning, L., Synofzik, M., Schöls, L., Sequeiros, J., Goizet, C., Marelli, C., Le Ber, I., Koht, J., Gazulla, J., De Bleecker, J., Mukhtar, M., Drouot, N., Ali-Pacha, L., Benhassine, T., Chbicheb, M., M’Zahem, A., Hamri, A., Chabrol, B., Pouget, J., Murphy, R., Watanabe, M., Coutinho, P., Tazir, M., Durr, A., Brice, A., Tranchant, C., Koenig, M.

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P118 Évolution de la flore microbienne et de l’antibiorésistance chez le diabétique von Ouerdane, K, Aouiche, S, Azzouz, M, Hannachi, R, Meftah, A, Djennane, F, Tazir, M, Boudiba, A

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Classifications of neurogenetic diseases: An increasingly complex problem von Vallat, J.-M., Goizet, C., Tazir, M., Couratier, P., Magy, L., Mathis, S.

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MUTATIONS IN THE GLUCOCEREBROSIDASE GENE CONFER A RISK FOR PARKINSON DISEASE IN NORTH AFRICA von LESAGE, S, CONDROYER, C, TAZIR, M, BRICE, A, HECHAM, N, ANHEIM, M, BELARBI, S, LOHMAN, E, VIALLET, F, POLLAK, P, ABADA, M, DÜRR, A

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Creatine deficiency syndrome. A treatable myopathy due to arginine–glycine amidinotransferase (AGAT) deficiency von Nouioua, S, Cheillan, D, Zaouidi, S, Salomons, G.S, Amedjout, N, Kessaci, F, Boulahdour, N, Hamadouche, T, Tazir, M

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Spine deformities in Charcot-Marie-Tooth 4C caused by SH3TC2 gene mutations von AZZEDINE, H, RAVISE, N, HAMADOUCHE, T, BOUHOUCHE, A, GUILBOT, A, STENDEL, C, RUBERG, M, BRICE, A, BIROUK, N, DUBOURG, O, TAZIR, M, LEGUERN, E, VERNY, C, GABRËELS-FESTEN, A, LAMMENS, M, GRID, D, VALLAT, J. M, DUROSIER, G, SENDEREK, J, NOUIOUA, S

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Ataxia with oculomotor apraxia type 2: A clinical and genetic study of 19 patients von Tazir, M, Ali-Pacha, L, M'Zahem, A, Delaunoy, J.P, Fritsch, M, Nouioua, S, Benhassine, T, Assami, S, Grid, D, Vallat, J.M, Hamri, A, Koenig, M

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IS THE COMMON LRRK2 G2019S MUTATION RELATED TO DYSKINESIAS IN NORTH AFRICAN PARKINSON DISEASE? von LESAGE, S, BELARBI, S, TAZIR, M, BRICE, A, TROIANO, A, CONDROYER, C, HECHAM, N, POLLAK, P, LOHMAN, E, BENHASSINE, T, YSMAIL-DAHLOUK, F, DÜRR, A

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Evolution of antimicrobial resistance and serotype distribution of Streptococcus pneumoniae isolated from children with invasive and noninvasive pneumococcal diseases in Algeria fr... von Ramdani-Bouguessa, N, Ziane, H, Bekhoucha, S, Guechi, Z, Azzam, A, Touati, D, Naim, M, Azrou, S, Hamidi, M, Mertani, A, Laraba, A, Annane, T, Kermani, S, Tazir, M

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Autosomal recessive cerebellar ataxia: A clinical and genetic study von Hamza, W, Nouioua, S, Lagier-Tourenne, C, Assami, S, Benhassine, T, Koenig, M, Tazir, M

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Autosomal-recessive forms of demyelinating Charcot-Marie-Tooth disease von Dubourg, O, Azzedine, H, Verny, C, Durosier, G, Birouk, N, Gouider, R, Salih, M, Bouhouche, A, Thiam, A, Grid, D, Mayer, M, Ruberg, M, Tazir, M, Brice, A, LeGuern, E

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Phenotypic variability in autosomal recessive axonal Charcot–Marie–Tooth disease due to the R298C mutation in lamin A/C von Tazir, M., Azzedine, H., Assami, S., Sindou, P., Nouioua, S., Zemmouri, R., Hamadouche, T., Chaouch, M., Feingold, J., Vallat, J. M., Leguern, E., Grid, D.

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Low disease risk in relatives of north african lrrk2 Parkinson disease patients von Troiano, A R, Elbaz, A, Lohmann, E, Belarbi, S, Vidailhet, M, Bonnet, A-M, Lesage, S, Pollak, P, Cazeneuve, C, Borg, M, Feingold, J, Dürr, A, Tazir, M, Brice, A

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DETECTING AND ANALYZING CORROSION SPOTS ON THE HULL OF LARGE MARINE VESSELS USING COLORED 3D LIDAR POINT CLOUDS von Aijazi, A. K., Malaterre, L., Tazir, M. L., Trassoudaine, L., Checchin, P.

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The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North Africa von RICHARD, P, GAUDON, K, HAMRI, A, NOUIOUA, S, TAZIR, M, MAYER, M, DESNUELLE, C, BAROIS, A, CHABROL, B, POUGET, J, KOENIG, J, GOUIDER-KHOUJA, N, HADDAD, H, HENTATI, F, EYMARD, B, HANTAÏ, D, BEN AMMAR, A, GENIN, E, BAUCHE, S, PATURNEAU-JOUAS, M, MÜLLER, J. S, LOCHMÜLLER, H, GRID, D

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