Elleuch, Nizar

Top Publications

Top Publications Authored or Co-Authored by "Elleuch, Nizar"

• Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum

  Nature Genetics, Volume 39, No. 3, Year 2007, Citations 309
• Identification of the SPG15 Gene, Encoding Spastizin, as a Frequent Cause of Complicated Autosomal-Recessive Spastic Paraplegia, Including Kjellin Syndrome

  American Journal of Human Genetics, Volume 82, No. 4, Year 2008, Citations 199
• Mutation analysis of the paraplegin gene (SPG7) in patients with hereditary spastic paraplegia

  Neurology, Volume 66, No. 5, Year 2006, Citations 102
• Autosomal recessive spastic paraplegia (SPG30) with mild ataxia and sensory neuropathy maps to chromosome 2q37.3

  Brain, Volume 129, No. 6, Year 2006, Citations 62
• Hereditary spastic paraplegia with mental impairment and thin corpus callosum in Tunisia: SPG11, SPG15, and further genetic heterogeneity

  Archives of Neurology, Volume 65, No. 3, Year 2008, Citations 58