1. B. O. Ben Cheikh, S. Baulac, F. Lahjouji, A. Bouhouche, P. Couarch, N. Khalili, W. Regragui, S. Lehericy, M. Ruberg, A. Benomar, S. Heath, T. Chkili, M. Yahyaoui, M. Jiddane, R. Ouazzani, and E. LeGuern. A locus for bilateral occipital polymicrogyria maps to chromosome 6q16-q22. Neurogenetics, 10(1):35-42, 2009. Note: Journal ArticleResearch Support, Non-U.S. Gov'tUnited States. [WWW] Keyword(s): Adult, Chromosome Mapping, *Chromosomes, Human, Pair 6, Consanguinity, DNA Mutational Analysis, Family, Female, Genetic Predisposition to Disease, Humans, Lod Score, Magnetic Resonance Imaging, Male, Malformations of Cortical Development/*genetics/pathology/physiopathology, Middle Aged, Morocco, Polymorphism, Single Nucleotide, Young Adult.



2. S. Hanein, E. Martin, A. Boukhris, P. Byrne, C. Goizet, A. Hamri, A. Benomar, A. Lossos, P. Denora, J. Fernandez, N. Elleuch, S. Forlani, A. Durr, I. Feki, M. Hutchinson, F. M. Santorelli, C. Mhiri, A. Brice, and G. Stevanin. Identification of the SPG15 gene, encoding spastizin, as a frequent cause of complicated autosomal-recessive spastic paraplegia, including Kjellin syndrome. Am J Hum Genet, 82(4):992-1002, 2008. Note: Journal ArticleResearch Support, Non-U.S. Gov'tUnited States. [WWW]



3. B. Ouled Amar Ben Cheikh, S. Baulac, F. Lahjouji, A. Bouhouche, P. Couarch, N. Khalili, W. Regragui, S. Lehericy, M. Ruberg, A. Benomar, S. Heath, T. Chkili, M. Yahyaoui, M. Jiddane, R. Ouazzani, and E. Leguern. A locus for bilateral occipital polymicrogyria maps to chromosome 6q16-q22. Neurogenetics, 2008. Note: Journal article. [WWW]



4. A. Bouhouche, N. Birouk, H. Azzedine, A. Benomar, G. Durosier, D. Ente, M. P. Muriel, M. Ruberg, I. Slassi, M. Yahyaoui, O. Dubourg, R. Ouazzani, and E. LeGuern. Autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2): phenotype-genotype correlations in 13 Moroccan families. Brain, 130:1062-1075, 2007. Note: Part 4. [WWW]



5. N. Bouslam, A. Bouhouche, A. Benomar, S. Hanein, S. Klebe, H. Azzedine, S. Di Giandomenico, A. Boland-Auge, F. M. Santorelli, A. Durr, A. Brice, M. Yahyaoui, and G. Stevanin. A novel locus for autosomal recessive spastic ataxia on chromosome 17p. Hum Genet, 121(3-4):413-20, 2007. Note: Journal ArticleResearch Support, Non-U.S. Gov'tGermany. [WWW] Keyword(s): Adult, Age of Onset, Cerebellar Ataxia/*genetics, Chromosome Mapping, *Chromosomes, Human, Pair 17, Consanguinity, Female, *Genes, Recessive, Haplotypes, Humans, Male, Microsatellite Repeats, Pedigree, Spastic Paraplegia, Hereditary/*genetics.



6. N. Elleuch, N. Bouslam, S. Hanein, A. Lossos, A. Hamri, S. Klebe, V. Meiner, N. Birouk, I. Lerer, D. Grid, D. Bacq, M. Tazir, D. Zelenika, Z. Argov, A. Durr, M. Yahyaoui, A. Benomar, A. Brice, and G. Stevanin. Refinement of the SPG15 candidate interval and phenotypic heterogeneity in three large Arab families. Neurogenetics, 8(4):307-15., 2007. Note: Journal article. [WWW]



7. N. Elleuch, C. Depienne, A. Benomar, A. M. Hernandez, X. Ferrer, B. Fontaine, D. Grid, C. M. Tallaksen, R. Zemmouri, G. Stevanin, A. Durr, and A. Brice. Mutation analysis of the paraplegin gene (SPG7) in patients with hereditary spastic paraplegia. Neurology, 66(5):654-9, 2006. Note: Journal ArticleResearch Support, Non-U.S. Gov'tUnited States. [WWW] Keyword(s): Brain/pathology, DNA Mutational Analysis, Europe, Exons, Humans, Metalloendopeptidases/*genetics, *Mutation, Polymorphism, Genetic, Reverse Transcriptase Polymerase Chain Reaction, Spastic Paraplegia, Hereditary/*genetics/pathology, Variation (Genetics).



8. N. Bouslam, A. Benomar, H. Azzedine, A. Bouhouche, M. Namekawa, S. Klebe, C. Charon, A. Durr, M. Ruberg, A. Brice, M. Yahyaoui, and G. Stevanin. Mapping of a new form of pure autosomal recessive spastic paraplegia (SPG28). Ann Neurol, 57(4):567-71, 2005. Note: Journal ArticleResearch Support, Non-U.S. Gov'tUnited States. [WWW] Keyword(s): Adult, *Chromosome Mapping, *Chromosomes, Human, Pair 14, Female, Humans, Lod Score, Male, Microsatellite Repeats, Middle Aged, Morocco, Pedigree, Polymerase Chain Reaction, Spastic Paraplegia, Hereditary/*genetics.



9. I. Le Ber, N. Bouslam, S. Rivaud-Pechoux, J. Guimaraes, A. Benomar, C. Chamayou, C. Goizet, M. C. Moreira, S. Klur, M. Yahyaoui, Y. Agid, M. Koenig, G. Stevanin, A. Brice, and A. Durr. Frequency and phenotypic spectrum of ataxia with oculomotor apraxia 2: a clinical and genetic study in 18 patients. Brain, 127(Pt 4):759-67, 2004. Note: Journal ArticleResearch Support, Non-U.S. Gov'tEnglanda journal of neurology. [WWW] Keyword(s): Adolescent, Adult, Age of Onset, Apraxias/*genetics/physiopathology, Biological Markers/blood, Child, Child, Preschool, Disease Progression, Gait Ataxia/*genetics/physiopathology, Haplotypes, Humans, Linkage (Genetics), Lod Score, Middle Aged, Neuropsychological Tests, Ocular Motility Disorders/*genetics/physiopathology, Pedigree, Phenotype, alpha-Fetoproteins/analysis.



10. N. Birouk, H. Azzedine, O. Dubourg, M. P. Muriel, A. Benomar, T. Hamadouche, T. Maisonobe, R. Ouazzani, A. Brice, M. Yahyaoui, T. Chkili, and E. Le Guern. Phenotypical features of a Moroccan family with autosomal recessive Charcot-Marie-Tooth disease associated with the S194X mutation in the GDAP1 gene. Arch Neurol, 60(4):598-604, 2003. Note: Journal ArticleResearch Support, Non-U.S. Gov'tUnited States. [WWW] Keyword(s): Adolescent, Adult, Charcot-Marie-Tooth Disease/*ethnology/*genetics/pathology, Child, Preschool, Consanguinity, DNA Mutational Analysis, Electrophysiology, Female, Genes, Recessive/*genetics, Humans, Infant, Lod Score, Male, Morocco/ethnology, *Mutation, Pedigree, Phenotype, Serine/genetics.

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