Ataxia with oculomotor apraxia type 2: A clinical and genetic study of 19 patients
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
Published in Journal of the neurological sciences (15.03.2009)
Published in Journal of the neurological sciences (15.03.2009)
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Journal Article
Autosomal recessive cerebellar ataxia: A clinical and genetic study
Hamza, W, Nouioua, S, Lagier-Tourenne, C, Assami, S, Benhassine, T, Koenig, M, Tazir, M
Published in Journal of the neurological sciences (15.10.2013)
Published in Journal of the neurological sciences (15.10.2013)
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Journal Article
Phenotypic variability in autosomal recessive axonal Charcot–Marie–Tooth disease due to the R298C mutation in lamin A/C
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.
Published in Brain (London, England : 1878) (01.01.2004)
Published in Brain (London, England : 1878) (01.01.2004)
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Journal Article
Identification of seven novel mutations in the GAN gene
Bomont, P., Ioos, C., Yalcinkaya, C., Korinthenberg, R., Vallat, JM, Assami, S., Munnich, A., Chabrol, B., Kurlemann, G., Tazir, M., Koenig, M.
Published in Human mutation (01.04.2003)
Published in Human mutation (01.04.2003)
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Journal Article
G.P.10.09 Description of a family associating a calpainopathy and a Duchenne myopathy
Nouioua, S, Cobo, A.M, Benhassine, T, Urtizberea, A, Slimani, S, Terki, N, Assami, S, Tazir, M
Published in Neuromuscular disorders : NMD (01.09.2009)
Published in Neuromuscular disorders : NMD (01.09.2009)
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Journal Article
Genetic heterogeneity in giant axonal neuropathy: an Algerian family not linked to chromosome 16q24.1
Tazir, M, Vallat, J.M, Bomont, P, Zemmouri, R, Sindou, P, Assami, S, Nouioua, S, Hammadouche, T, Grid, D, Koenig, M
Published in Neuromuscular disorders : NMD (01.11.2002)
Published in Neuromuscular disorders : NMD (01.11.2002)
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Journal Article
Charcot–Marie–Tooth 2-like presentation of an Algerian family with giant axonal neuropathy
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.
Published in Neuromuscular disorders : NMD (01.12.2000)
Published in Neuromuscular disorders : NMD (01.12.2000)
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Journal Article
Congruence of terms between lists of problems and the ICNP®- Alpha Version
Cruz, D. M., Gutierrez, B. A. O., López, A. L., De Souza, T. T., Assami, S.
Published in International nursing review (01.06.2000)
Published in International nursing review (01.06.2000)
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Journal Article
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 inflammatory processes in the determination of anaemia
Hercberg, S, Galan, P, Assami, M, Assami, S
Published in International journal of epidemiology (01.03.1988)
Published in International journal of epidemiology (01.03.1988)
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Journal Article
Paraplégies spastiques familiales : étude d’une série de 70 familles et corrélations phénotype/génotype
Kediha, M.I., Nouioua, S., Brice, A., Assami, S., Stevanin, G., Tazir, M.
Published in Revue neurologique (01.04.2014)
Published in Revue neurologique (01.04.2014)
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Journal Article
P.P.1 04 Algerian FKRP mutations causing MDC1C congenital muscular dystrophy with mental retardation
Makri, S., Richard, P., Maugenre, S., Terki, N., Quijano-Roy, S., Assami, S., Romero, N.B., Ait-Kaci, M., Guicheney, P.
Published in Neuromuscular disorders : NMD (01.10.2006)
Published in Neuromuscular disorders : NMD (01.10.2006)
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Journal Article
P.P.1 03 A clinical, morphological and genetic study of congenital muscular dystrophies in Algeria
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.
Published in Neuromuscular disorders : NMD (01.10.2006)
Published in Neuromuscular disorders : NMD (01.10.2006)
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Journal Article
Identification of seven novel mutations in theGAN gene
Bomont, P., Ioos, C., Yalcinkaya, C., Korinthenberg, R., Vallat, JM, Assami, S., Munnich, A., Chabrol, B., Kurlemann, G., Tazir, M., Koenig, M.
Published in Human mutation (01.04.2003)
Published in Human mutation (01.04.2003)
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Journal Article
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 inflammatory processes in the determination of anaemia
Hercberg, S, Galan, P, Assami, M, Assami, S. (Centre de Recherche sur les Anemies Nutritionnelles, Paris Cedex (France). Inst. Scientifique et Technique de l'Alimentation)
Published in International Journal of Epidemiology (United Kingdom) (1988)
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Published in International Journal of Epidemiology (United Kingdom) (1988)
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