Amir Boukhris

Summary

Country: France

Publications

  1. pmc Deletion analysis of SMN and NAIP genes in Tunisian patients with spinal muscular atrophy
    Imen Rekik
    Department of Neurology, HabibBourguiba University Hospital, Faculte de Medecine de Sfax, Sfax, Tunisia
    Ann Indian Acad Neurol 16:57-61. 2013
  2. doi request reprint A new locus (SPG46) maps to 9p21.2-q21.12 in a Tunisian family with a complicated autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum
    Amir Boukhris
    Department of Neurology, Habib Bourguiba University Hospital, Sfax, Tunisia
    Neurogenetics 11:441-8. 2010
  3. doi request reprint Hereditary spastic paraplegia with mental impairment and thin corpus callosum in Tunisia: SPG11, SPG15, and further genetic heterogeneity
    Amir Boukhris
    Department of Neurology, Habib Bourguiba University Hospital, Tunis, Tunisia
    Arch Neurol 65:393-402. 2008
  4. ncbi request reprint Spastic paraplegia 15: linkage and clinical description of three Tunisian families
    Amir Boukhris
    Department of Neurology, Habib Bourguiba University Hospital, Sfax, Tunisia
    Mov Disord 23:429-33. 2008

Collaborators

  • Giovanni Stevanin
  • Imen Rekik
  • Imed Feki
  • Sourour Ketata
  • Nourhene Essid
  • Chokri Mhiri
  • Mohamed Amri

Detail Information

Publications4

  1. pmc Deletion analysis of SMN and NAIP genes in Tunisian patients with spinal muscular atrophy
    Imen Rekik
    Department of Neurology, HabibBourguiba University Hospital, Faculte de Medecine de Sfax, Sfax, Tunisia
    Ann Indian Acad Neurol 16:57-61. 2013
    ..Spinal muscular atrophy (SMA) is an autosomal recessive neuromuscular disorder involving degeneration of anterior horn cells of spinal cord, resulting in progressive muscle weakness and atrophy...
  2. doi request reprint A new locus (SPG46) maps to 9p21.2-q21.12 in a Tunisian family with a complicated autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum
    Amir Boukhris
    Department of Neurology, Habib Bourguiba University Hospital, Sfax, Tunisia
    Neurogenetics 11:441-8. 2010
    ..We propose that testing for this locus should be performed, after exclusion of mutations in SPG11 and SPG15 genes, in AR-HSP-TCC families, especially when cerebellar ataxia and cataract are present...
  3. doi request reprint Hereditary spastic paraplegia with mental impairment and thin corpus callosum in Tunisia: SPG11, SPG15, and further genetic heterogeneity
    Amir Boukhris
    Department of Neurology, Habib Bourguiba University Hospital, Tunis, Tunisia
    Arch Neurol 65:393-402. 2008
    ..To perform a clinical and genetic study of Tunisian families with autosomal recessive (AR) hereditary spastic paraplegia with thin corpus callosum (HSP-TCC)...
  4. ncbi request reprint Spastic paraplegia 15: linkage and clinical description of three Tunisian families
    Amir Boukhris
    Department of Neurology, Habib Bourguiba University Hospital, Sfax, Tunisia
    Mov Disord 23:429-33. 2008
    ..Interestingly, like retinal degeneration, thin corpus callosum is not a constant feature in this entity...