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

Volltext

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

Volltext

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.

Volltext

Identification of seven novel mutations in the GAN gene von Bomont, P., Ioos, C., Yalcinkaya, C., Korinthenberg, R., Vallat, JM, Assami, S., Munnich, A., Chabrol, B., Kurlemann, G., Tazir, M., Koenig, M.

Volltext

G.P.10.09 Description of a family associating a calpainopathy and a Duchenne myopathy von Nouioua, S, Cobo, A.M, Benhassine, T, Urtizberea, A, Slimani, S, Terki, N, Assami, S, Tazir, M

Volltext

Primary results of the brazilian registry of atherothrombotic disease (NEAT) von de Barros e Silva, Pedro G. M., do Nascimento, Charlene Troiani, Pedrosa, Rodrigo Pinto, Nakazone, Marcelo Arruda, do Nascimento, Michel Ulloffo, de Araújo Melo, Leiliandry, Júnior, Osvaldo Lourenço Silva, Zimmermann, Sérgio Luiz, de Melo, Rodrigo Morel Vieira, Bergo, Ricardo Reinaldo, Precoma, Dalton Bertolim, Tramujas, Lucas, Lima, Eduardo Gomes, Dantas, João Miguel Malta, do Amaral Baruzzi, Antônio Cláudio, Flumignan, Ronald Luiz Gomes, de Oliveira Paiva, Maria Sanali Moura, Gowdak, Luís Henrique Wolff, de Carvalho, Priscila Nasser, de Figueiredo Neto, José Albuquerque, Silvestre, Odilson Marcos, Fioranelli, Alexandre, Vieira, Ricardo D.’Oliveira, Horak, Ana Clara Peneluppi, Miyada, Debora Harumi Kodama, Kojima, Flávia Cristina Soares, de Oliveira, Júlia Souza, de Oliveira Silva, Leila, Pavanello, Ricardo, Ramacciotti, Eduardo, Lopes, Renato D.

Volltext

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

Volltext

Charcot–Marie–Tooth 2-like presentation of an Algerian family with giant axonal neuropathy von Zemmouri, R., Azzedine, H., Assami, S., Kitouni, N., Vallat, J.M., Maisonobe, T., Hamadouche, T., Kessaci, M., Mansouri, B., Le Guern, E., Grid, D., Tazir, M.

Volltext

Decreases in Inflammatory and Coagulation Biomarkers Levels in HIV-Infected Patients Switching from Enfuvirtide to Raltegravir: ANRS 138 Substudy von Silva, Erika F., Charreau, Isabelle, Gourmel, Bernard, Mourah, Samia, Kalidi, Issa, Guillon, Brigitte, De Castro, Nathalie, Caron, François, Braun, Josephine, Molina, Jean-Michel

Volltext

The French national prospective cohort of patients co-infected with HIV and HCV (ANRS CO13 HEPAVIH): early findings, 2006-2010 von Loko, Marc-Arthur, Salmon, Dominique, Carrieri, Patrizia, Winnock, Maria, Mora, Marion, Merchadou, Laurence, Gillet, Stéphanie, Pambrun, Elodie, Delaune, Jean, Valantin, Marc-Antoine, Poizot-Martin, Isabelle, Neau, Didier, Bonnard, Philippe, Rosenthal, Eric, Barange, Karl, Morlat, Philippe, Lacombe, Karine, Gervais, Anne, Rouges, François, See, Alain Bicart, Lascoux-Combe, Caroline, Vittecoq, Daniel, Goujard, Cécile, Duvivier, Claudine, Spire, Bruno, Izopet, Jacques, Sogni, Philippe, Serfaty, Lawrence, Benhamou, Yves, Bani-Sadr, Firouzé, Dabis, François

Volltext

Efficacy and safety of raltegravir in treatment-experienced HIV-1-infected patients switching from enfuvirtide-based regimens: 48 week results of the randomized EASIER ANRS 138 tri... von Gallien, Sébastien, Braun, Joséphine, Delaugerre, Constance, Charreau, Isabelle, Reynes, Jacques, Jeanblanc, François, Verdon, Renaud, de Truchis, Pierre, May, Thierry, Madelaine-Chambrin, Isabelle, Aboulker, Jean-Pierre, Molina, Jean-Michel

Volltext

Congruence of terms between lists of problems and the ICNP®- Alpha Version von Cruz, D. M., Gutierrez, B. A. O., López, A. L., De Souza, T. T., Assami, S.

Volltext

Primary liver cancer is more aggressive in HIV-HCV coinfection than in HCV infection. A prospective study (ANRS CO13 Hepavih and CO12 Cirvir) von Bourcier, Valérie, Winnock, Maria, Ait Ahmed, Mohand, Sogni, Philippe, Pambrun, Elodie, Poizot-Martin, Isabelle, Chaffaut, Cendrine, Chevret, Sylvie, Trinchet, Jean-Claude, Salmon, Dominique

Volltext

HIV-1 tropism and liver fibrosis in HIV-HCV co-infected patients von Abravanel, Florence, Raymond, Stéphanie, Pambrun, Elodie, Winnock, Maria, Bonnard, Philippe, Sogni, Philippe, Trimoulet, Pascale, Dabis, François, Salmon-Ceron, Dominique, Izopet, Jacques

Volltext

Evaluation of the Frequency of Anaemia and Iron-Deficiency Anaemia in a Group of Algerian Menstruating Women by a Mixed Distribution Analysis: Contribution of Folate Deficiency and... von HERCBERG, S, GALAN, P, ASSAMI, M, ASSAMI, S

Volltext

Paraplégies spastiques familiales : étude d’une série de 70 familles et corrélations phénotype/génotype von Kediha, M.I., Nouioua, S., Brice, A., Assami, S., Stevanin, G., Tazir, M.

Volltext

P.P.1 04 Algerian FKRP mutations causing MDC1C congenital muscular dystrophy with mental retardation von Makri, S., Richard, P., Maugenre, S., Terki, N., Quijano-Roy, S., Assami, S., Romero, N.B., Ait-Kaci, M., Guicheney, P.

Volltext

P.P.1 03 A clinical, morphological and genetic study of congenital muscular dystrophies in Algeria von Makri, S., Terki, N., Belarbi, S., Assami, S., Maugenre, S., Gartioux, C., Allamand, V., Richard, P., Romero, N.B., Kaci-Ahmed, M. Ait, Grid, D., Guicheney, P., Tazir, M.

Volltext

Apport de la Teledetection dans l'Etude de la Relation entre Etats de Surface et Pedopaysages en Milieu Aride: Exemple de la Region d'el Outaya ( Biskra , Algerie ) von Halitim , Amor, Rouahana , Houria, Assami , Tarek, Hamdi-Aissa , Belhadj, Mostefaoui , Tawfik

Volltext

Identification of seven novel mutations in theGAN gene von Bomont, P., Ioos, C., Yalcinkaya, C., Korinthenberg, R., Vallat, JM, Assami, S., Munnich, A., Chabrol, B., Kurlemann, G., Tazir, M., Koenig, M.

Volltext