Revue de la littérature récente sur les neuropathies héréditaires
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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 with Early-Onset Glaucoma
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.
Published in American journal of human genetics (01.05.2003)
Published in American journal of human genetics (01.05.2003)
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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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Demyelinating disease affecting both the central nervous system (CNS) and peripheral nervous system (PNS): Study of 2 cases
Benaaboud, B, Birouk, N, Aidi, S, Belaidi, H, Kably, B, El Alaoui Faris, M, Ouazzani, R
Published in Journal of the neurological sciences (15.10.2013)
Published in Journal of the neurological sciences (15.10.2013)
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Motor form of chronic inflammatory demyelinating polyradiculoneuropathy with conduction block: Clinical, electrophysiological and outcome study of 6 cases
Birouk, N, Belaidi, H, Kably, B, Aidi, S, El Alaoui Faris, M, Yahyaoui, M, Ouazzani, R
Published in Journal of the neurological sciences (15.10.2013)
Published in Journal of the neurological sciences (15.10.2013)
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Clinical, electrophysiological and molecular genetic characteristics of 93 patients with X-linked Charcot–Marie–Tooth disease
Dubourg, O., Tardieu, S., Birouk, N., Gouider, R., Léger, J. M., Maisonobe, T., Brice, A., Bouche, P., LeGuern, E.
Published in Brain (London, England : 1878) (01.10.2001)
Published in Brain (London, England : 1878) (01.10.2001)
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Spectrum of clinical and electrophysiologic features in HNPP patients with the 17p11.2 deletion
Mouton, P, Tardieu, S, Gouider, R, Birouk, N, Maisonobe, T, Dubourg, O, Brice, A, LeGuern, E, Bouche, P
Published in Neurology (22.04.1999)
Published in Neurology (22.04.1999)
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Autosomal-recessive forms of demyelinating Charcot-Marie-Tooth disease
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
Published in Neuromolecular medicine (01.03.2006)
Published in Neuromolecular medicine (01.03.2006)
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Autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2): phenotype-genotype correlations in 13 Moroccan families
Bouhouche, Ahmed, Birouk, Nazha, Azzedine, Hamid, Benomar, Ali, Durosier, Garry, Ente, Dorothée, Muriel, Marie-Paule, Ruberg, Merle, Slassi, Ilham, Yahyaoui, Mohamed, Dubourg, Odile, Ouazzani, Reda, LeGuern, Eric
Published in Brain (London, England : 1878) (01.04.2007)
Published in Brain (London, England : 1878) (01.04.2007)
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X-linked Charcot-Marie-Tooth disease with connexin 32 mutations: clinical and electrophysiologic study
Birouk, N, LeGuern, E, Maisonobe, T, Rouger, H, Gouider, R, Tardieu, S, Gugenheim, M, Routon, M C, Léger, J M, Agid, Y, Brice, A, Bouche, P
Published in Neurology (01.04.1998)
Published in Neurology (01.04.1998)
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P5.48 Infantile-onset permanent weakness in muscle phosphofructokinase deficiency
Laforet, P, Piraud, M, Petit, F, Hogrel, J.Y, Romero, N.B, Eymard, B, Birouk, N
Published in Neuromuscular disorders : NMD (01.10.2011)
Published in Neuromuscular disorders : NMD (01.10.2011)
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The frequency of 17p11.2 duplication and Connexin 32 mutations in 282 Charcot-Marie-Tooth families in relation to the mode of inheritance and motor nerve conduction velocity
Dubourg, O, Tardieu, S, Birouk, N, Gouider, R, Léger, J.M, Maisonobe, T, Brice, A, Bouche, P, LeGuern, E
Published in Neuromuscular disorders : NMD (01.07.2001)
Published in Neuromuscular disorders : NMD (01.07.2001)
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High incidence of SMN1 gene deletion in Moroccan adult-onset spinal muscular atrophy patients
BOUHOUCHE, A, BENOMAR, A, BIROUK, N, BOUSLAM, N, OUAZZANI, R, YAHYAOUI, M, CHKILI, T
Published in Journal of neurology (01.10.2003)
Published in Journal of neurology (01.10.2003)
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