Creatine deficiency syndrome. A treatable myopathy due to arginine–glycine amidinotransferase (AGAT) deficiency
Nouioua, S, Cheillan, D, Zaouidi, S, Salomons, G.S, Amedjout, N, Kessaci, F, Boulahdour, N, Hamadouche, T, Tazir, M
Published in Neuromuscular disorders : NMD (01.08.2013)
Published in Neuromuscular disorders : NMD (01.08.2013)
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PP207-MON: Which Drinks Consume the Algerian Students?
Mekhancha-Dahel, C.C, Nouioua, S, Adjali-Hassani, W, Mekhancha, D.-E
Published in Clinical nutrition (Edinburgh, Scotland) (01.09.2014)
Published in Clinical nutrition (Edinburgh, Scotland) (01.09.2014)
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Spine deformities in Charcot-Marie-Tooth 4C caused by SH3TC2 gene mutations
Azzedine, H, Ravisé, N, Verny, C, Gabrëels-Festen, A, Lammens, M, Grid, D, Vallat, J M, Durosier, G, Senderek, J, Nouioua, S, Hamadouche, T, Bouhouche, A, Guilbot, A, Stendel, C, Ruberg, M, Brice, A, Birouk, N, Dubourg, O, Tazir, M, LeGuern, E
Published in Neurology (22.08.2006)
Published in Neurology (22.08.2006)
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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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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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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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The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North Africa
Richard, P, Gaudon, K, Haddad, H, Ammar, A Ben, Genin, E, Bauché, S, Paturneau-Jouas, M, Müller, J S, Lochmüller, H, Grid, D, Hamri, A, Nouioua, S, Tazir, M, Mayer, M, Desnuelle, C, Barois, A, Chabrol, B, Pouget, J, Koenig, J, Gouider-Khouja, N, Hentati, F, Eymard, B, Hantaï, D
Published in Neurology (09.12.2008)
Published in Neurology (09.12.2008)
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Founder Effect and Estimation of the Age of the c.892C>T (p.Arg298Cys) Mutation in LMNA Associated to Charcot‐Marie‐Tooth Subtype CMT2B1 in Families from North Western Africa
Hamadouche, T., Poitelon, Y., Genin, E., Chaouch, M., Tazir, M., Kassouri, N., Nouioua, S., Chaouch, A., Boccaccio, I., Benhassine, T., De Sandre‐Giovannoli, A., Grid, D., Lévy, N., Delague, V.
Published in Annals of human genetics (01.09.2008)
Published in Annals of human genetics (01.09.2008)
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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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191P Characterization of patients SMA diagnosed in Algeria
Hallal, S., Benchaabi, O., Nouioua, S., Yargui, L.
Published in Neuromuscular disorders : NMD (01.10.2024)
Published in Neuromuscular disorders : NMD (01.10.2024)
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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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260P NEUROMYODredger – 3 billion megaproject: expanding the accessibility of exome sequencing for the diagnosis of neurodevelopmental and neuromuscular disorders in nine countries
Malfatti, E., Caramizaru, A., Lee, H., Kim, J., Shoaito, H., Pennisi, A., Fahmi, N., Escobar-Cedillo, R., Miranda-Duarte, A., Nouioua, S., Benchaabi, O., Martinez, P., Castiglioni, C., Dobrescu, A., Tajsharghi, H.
Published in Neuromuscular disorders : NMD (01.10.2024)
Published in Neuromuscular disorders : NMD (01.10.2024)
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Journal Article
Creatine deficiency syndrome. A treatable myopathy due to arginineaglycine amidinotransferase (AGAT) deficiency
Nouioua, S, Cheillan, D, Zaouidi, S, Salomons, G S, Amedjout, N, Kessaci, F, Boulahdour, N, Hamadouche, T, Tazir, M
Published in Neuromuscular disorders : NMD (01.08.2013)
Published in Neuromuscular disorders : NMD (01.08.2013)
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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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