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Rim Amouri

Showing results (1-10 of 42) with videos related to

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Handbook of Clinical Neurology|August 13, 2013
Giant axonal neuropathyFayçal Hentati, Emna Hentati, Rim Amouri
Parkinsonism & Related Disorders|April 1, 2011
Autosomal recessive spastic ataxia of Charlevoix-Saguenay: an overviewYosr Bouhlal, Rim Amouri, Ghada El Euch-Fayeche, et al.
Journal of Molecular Neuroscience : MN|June 17, 2009
A novel SACS gene mutation in a Tunisian familyYosr Bouhlal, Ghada El Euch-Fayeche, Fayçal Hentati, et al.
Brain : a Journal of Neurology|December 27, 2013
Molecular, clinical and peripheral neuropathy study of Tunisian patients with ataxia with vitamin E deficiencyGhada El Euch-Fayache, Yosr Bouhlal, Rim Amouri, et al.
Journal of Molecular Neuroscience : MN|July 28, 2009
Allelic ROBO3 heterogeneity in Tunisian patients with horizontal gaze palsy with progressive scoliosisRim Amouri, Houda Nehdi, Yosr Bouhlal, et al.
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|February 27, 2010
A novel heteroplasmic tRNA Ser(UCN) mtDNA point mutation associated with progressive ophthalmoplegia and dysphagiaSihem Souilem, Mounir Kefi, Michelangelo Mancuso, et al.
Journal of Neurogenetics|June 24, 2008
Autosomal recessive ataxia caused by three distinct gene defects in a single consanguineous familyYosr Bouhlal, Mourad Zouari, Mounir Kefi, et al.
Genes|July 27, 2024
The Evolution of Genetic Variability at the <i>LRRK2</i> LocusDylan T Guenther, Jordan Follett, Rim Amouri, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 10, 2014
Motor phenotype of LRRK2-associated Parkinson's disease: a Tunisian longitudinal studyFatma Nabli, Samia Ben Sassi, Rim Amouri, et al.
Journal of the Neurological Sciences|October 2, 2010
A novel mitochondrial tRNA(Ile) point mutation associated with chronic progressive external ophthalmoplegia and hyperCKemiaSihem Souilem, Saber Chebel, Michelangelo Mancuso, et al.
Pageof 5

Showing results (1-10 of 42) with videos related to

Sort By:
Pageof 5
Handbook of Clinical Neurology|August 13, 2013
Giant axonal neuropathyFayçal Hentati, Emna Hentati, Rim Amouri
Parkinsonism & Related Disorders|April 1, 2011
Autosomal recessive spastic ataxia of Charlevoix-Saguenay: an overviewYosr Bouhlal, Rim Amouri, Ghada El Euch-Fayeche, et al.
Journal of Molecular Neuroscience : MN|June 17, 2009
A novel SACS gene mutation in a Tunisian familyYosr Bouhlal, Ghada El Euch-Fayeche, Fayçal Hentati, et al.
Brain : a Journal of Neurology|December 27, 2013
Molecular, clinical and peripheral neuropathy study of Tunisian patients with ataxia with vitamin E deficiencyGhada El Euch-Fayache, Yosr Bouhlal, Rim Amouri, et al.
Journal of Molecular Neuroscience : MN|July 28, 2009
Allelic ROBO3 heterogeneity in Tunisian patients with horizontal gaze palsy with progressive scoliosisRim Amouri, Houda Nehdi, Yosr Bouhlal, et al.
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|February 27, 2010
A novel heteroplasmic tRNA Ser(UCN) mtDNA point mutation associated with progressive ophthalmoplegia and dysphagiaSihem Souilem, Mounir Kefi, Michelangelo Mancuso, et al.
Journal of Neurogenetics|June 24, 2008
Autosomal recessive ataxia caused by three distinct gene defects in a single consanguineous familyYosr Bouhlal, Mourad Zouari, Mounir Kefi, et al.
Genes|July 27, 2024
The Evolution of Genetic Variability at the <i>LRRK2</i> LocusDylan T Guenther, Jordan Follett, Rim Amouri, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 10, 2014
Motor phenotype of LRRK2-associated Parkinson's disease: a Tunisian longitudinal studyFatma Nabli, Samia Ben Sassi, Rim Amouri, et al.
Journal of the Neurological Sciences|October 2, 2010
A novel mitochondrial tRNA(Ile) point mutation associated with chronic progressive external ophthalmoplegia and hyperCKemiaSihem Souilem, Saber Chebel, Michelangelo Mancuso, et al.
Pageof 5