1. A. Boukhris, G. Stevanin, I. Feki, P. Denora, N. Elleuch, M. I. Miladi, C. Goizet, J. Truchetto, S. Belal, A. Brice, and C. Mhiri. Tunisian hereditary spastic paraplegias: clinical variability supported by genetic heterogeneity. Clin Genet, 75(6):527-36, 2009. Note: Journal ArticleResearch Support, Non-U.S. Gov'tDenmark. [WWW] Keyword(s): Adolescent, Adult, Aged, Aged, 80 and over, Brain/pathology, Child, Consanguinity, Female, Genes, Recessive, *Genetic Heterogeneity, Humans, Male, Middle Aged, Mutation, *Phenotype, Spastic Paraplegia, Hereditary/*epidemiology/*genetics/pathology, Sural Nerve/pathology, Tunisia/epidemiology.



2. A. Boukhris, I. Feki, E. Denis, M. I. Miladi, A. Brice, C. Mhiri, and G. Stevanin. Spastic paraplegia 15: linkage and clinical description of three Tunisian families. Mov Disord, 23(3):429-33, 2008. Note: Journal ArticleResearch Support, Non-U.S. Gov'tUnited Statesofficial journal of the Movement Disorder Society. [WWW]



3. A. Boukhris, G. Stevanin, I. Feki, E. Denis, N. Elleuch, M. I. Miladi, J. Truchetto, P. Denora, S. Belal, C. Mhiri, and A. Brice. Hereditary Spastic Paraplegia With Mental Impairment and Thin Corpus Callosum in Tunisia: SPG11, SPG15, and Further Genetic Heterogeneity. Arch Neurol, 65(3):393-402, 2008. Note: Journal article. [WWW]



4. I. Feki, M. I. Miladi, N. Elleuch, A. Boukhris, G. Stevanin, A. Brice, and C. Mhiri. [Familial spastic paraplegia with severe amyotrophy of the hands. (Silver syndrome?)]. Rev Neurol (Paris), 163(4):476-9, 2007. Note: Case ReportsEnglish AbstractJournal ArticleFrance. [WWW] Keyword(s): Adult, Brachial Plexus Neuritis/genetics/*pathology, Electric Stimulation, Electromyography, Evoked Potentials, Somatosensory/physiology, Female, Foot/pathology, Hand/*pathology, Humans, Magnetic Resonance Imaging, Male, Neurologic Examination, Paraplegia/genetics/*pathology, Pedigree, Syndrome.

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