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

Heart rate variability and sympathetic skin response for the assessment of autonomic dysfunction in leucine-rich repeat kinase 2 associated Parkinson's disease.

Journal: Neurophysiologie clinique = Clinical neurophysiology

Publication Year: 2022

Authors & Co-authors:  Nasri Amina A Kacem Imen I Farhat Nouha N Gharbi Alya A Sakka Selma S Souissi Amira A Zidi Sabrina S Damak Mariem M Bendjebara Mouna M Gargouri Amina A

Validation of the Arabic Version of the Movement Disorder Society-Unified Parkinson's Disease Rating Scale.

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

Publication Year: 2022

Authors & Co-authors:  Khalil Hanan H Aldaajani Zakiyah F ZF Aldughmi Mayis M Al-Sharman Alham A Mohammad Tareq T Mehanna Raja R El-Jaafary Shaimaa I SI Dahshan Ahmed A Ben Djebara Mouna M Kamel Walaa A WA