Spastic paraplegia 15: linkage and clinical description of three Tunisian families.

Journal: Movement disorders : official journal of the Movement Disorder Society

Publication Year: 2008

Authors & Co-authors:  Boukhris Amir A Feki Imed I Denis Elodie E Miladi Mohamed Imed MI Brice Alexis A Mhiri Chokri C Stevanin Giovanni G

Hereditary spastic paraplegia with mental impairment and thin corpus callosum in Tunisia: SPG11, SPG15, and further genetic heterogeneity.

Journal: Archives of neurology

Publication Year: 2008

Authors & Co-authors:  Boukhris Amir A Stevanin Giovanni G Feki Imed I Denis Elodie E Elleuch Nizar N Miladi Mohamed Imed MI Truchetto Jérémy J Denora Paola P Belal Samir S Mhiri Chokri C

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.

Journal: Neurogenetics

Publication Year: 2011

Authors & Co-authors:  Boukhris Amir A Feki Imed I Elleuch Nizar N Miladi Mohamed Imed MI Boland-Augé Anne A Truchetto Jérémy J Mundwiller Emeline E Jezequel Nadia N Zelenika Diana D Mhiri Chokri C

Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders.

Journal: Science (New York, N.Y.)

Publication Year: 2014

Authors & Co-authors:  Novarino Gaia G Fenstermaker Ali G AG Zaki Maha S MS Hofree Matan M Silhavy Jennifer L JL Heiberg Andrew D AD Abdellateef Mostafa M Rosti Basak B Scott Eric E Mansour Lobna L

Clinically approved immunomodulators ameliorate behavioral changes in a mouse model of hereditary spastic paraplegia type 11.

Journal: Frontiers in neuroscience

Publication Year: 

Authors & Co-authors:  Hörner Popp Branchu Stevanin Darios Klebe Groh Martini