Autosomal recessive mutilating sensory neuropathy with spastic paraplegia maps to chromosome 5p15.31-14.1 von BOUHOUCHE, Ahmed, BENOMAR, Ali, BOUSLAM, Naima, OUAZZANI, Reda, CHKILI, Taieb, YAHYAOUI, Mohamed

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A PCR Amplification Method Reveals Instability of the Dodecamer Repeat in Progressive Myoclonus Epilepsy (EPM1) and No Correlation between the Size of the Repeat and Age at Onset von Lalioti, Maria D., Scott, Hamish S., Genton, Pierre, Grid, Djamel, Ouazzani, Réda, M'Rabet, Amel, Ibrahim, Sadi, Gouider, Riadh, Dravet, Charlotte, Chkili, Taieb, Bottani, Armand, Buresi, Catherine, Malafosse, Alain, Antonarakis, Stylianos E.

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Haplotype study of West European and North African Unverricht-Lundborg chromosomes: evidence for a few founder mutations von MOULARD, Bruno, GENTON, Pierre, UTERMANN, Barbara, BALDY-MOULINIER, Michel, BELAIDI, Halima, BERTRAN, Francoise, BIRABEN, Arnaud, CHERIF, André Ali, CHKILI, Taieb, CRESPEL, Arielle, DARCEL, Francoise, DULAC, Olivier, GRID, Djamel, GENY, Christian, HUMBERT-CLAUDE, Véronique, KASSIOTIS, Philippe, BURESI, Catherine, MALAFOSSE, Alain, JEANPIERRE, Marc, OUAZZANI, Réda, MRABET, Amel, MORRIS, Mike, LEGUEM, Eric, DRAVET, Charlotte, MAUGUIERE, Francois

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Molecular and Clinical Correlations in Autosomal Dominant Cerebellar Ataxia with Progressive Macular Dystrophy (SCA7) von David, Gilles, Dürr, Alexandra, Stevanin, Giovanni, Cancel, Géraldine, Abbas, Nacer, Benomar, Ali, Belal, Samir, Lebre, Anne-Sophie, Abada-Bendib, Myriem, Grid, Djamel, Holmberg, Monica, Yahyaoui, Mohamed, Hentati, Fayçal, Chkili, Taïeb, Agid, Yves, Brice, Alexis

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A Locus for an Axonal Form of Autosomal Recessive Charcot-Marie-Tooth Disease Maps to Chromosome 1q21.2-q21.3 von Bouhouche, Ahmed, Benomar, Ali, Birouk, Nazha, Mularoni, Angélique, Meggouh, Farid, Tassin, Johann, Grid, Djamal, Vandenberghe, Antoon, Yahyaoui, Mohamed, Chkili, Taïeb, Brice, Alexis, LeGuern, Eric

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Vitamin E deficiency ataxia associated with adenoma von Benomar, Ali, Yahyaoui, Mohammed, Marzouki, Naima, Birouk, Nezha, Bouslam, Naima, Belaidi, Halima, Amarti, Afaf, Ouazzani, Reda, Chkili, Taieb

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The first de novo mutation of the connexin 32 gene associated with X linked Charcot-Marie-Tooth disease von Meggouh, F, Benomar, A, Rouger, H, Tardieu, S, Birouk, N, Tassin, J, Barhoumi, C, Yahyaoui, M, Chkili, T, Brice, A, LeGuern, E

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Allelic heterogeneity of mediterranean myoclonus and the cystatin B gene von Labauge, Pierre, Ouazzani, RÉDa, M'Rabet, Amel, Grid, Djamel, Genton, Pierre, Dravet, Charlotte, Chkili, Taieb, Beck, Corrine, Buresi, Catherine, Baldy-Moulinier, Michel, Malafosse, Alain

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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 w... von 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.

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