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Handbook of Clinical Neurology
|
August 13, 2013
Giant axonal neuropathy
Fayçal Hentati, Emna Hentati, Rim Amouri
La Tunisie Medicale
|
August 29, 2007
[Acute polyradiculoneuropathy. Guillain-Barre syndrome]
Ilhem Turki, Salwa Djaïet, S Boukhris, et al.
Journal of Molecular Neuroscience : MN
|
June 17, 2009
A novel SACS gene mutation in a Tunisian family
Yosr Bouhlal, Ghada El Euch-Fayeche, Fayçal Hentati, et al.
Parkinsonism & Related Disorders
|
April 1, 2011
Autosomal recessive spastic ataxia of Charlevoix-Saguenay: an overview
Yosr Bouhlal, Rim Amouri, Ghada El Euch-Fayeche, et al.
Brain : a Journal of Neurology
|
December 27, 2013
Molecular, clinical and peripheral neuropathy study of Tunisian patients with ataxia with vitamin E deficiency
Ghada 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 scoliosis
Rim Amouri, Houda Nehdi, Yosr Bouhlal, et al.
Journal of Stroke and Cerebrovascular Diseases : the Official Journal of National Stroke Association
|
June 12, 2010
Cerebral venous thrombosis presenting with cerebellar ataxia and cortical blindness
Samia Ben Sassi, Habiba Mizouni, Fatma Nabli, et al.
Biological Research for Nursing
|
December 10, 2020
Association of <i>Bgl</i>II Polymorphism in <i>ITGA2</i> and (894G/T and -786T/C) Polymorphisms in eNOS Gene With Stroke Susceptibility in Tunisian Patients α2 Gene Polymorphism in α2β1 Integrin and eNOS Gene Variants and Stroke
Akrem Jalel, Fatma Midani, Sondess Hadj Fredj, et al.
Journal of Neurogenetics
|
June 24, 2008
Autosomal recessive ataxia caused by three distinct gene defects in a single consanguineous family
Yosr Bouhlal, Mourad Zouari, Mounir Kefi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
February 25, 2018
Disability progression in multiple sclerosis: a Tunisian prospective cohort study
Emna Hentati, Samia Ben Sassi, Fatma Nabli, et al.
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Search research articles
Search
Showing results (1-10 of 30) with videos related to
Sort By:
Page
of 3
Handbook of Clinical Neurology
|
August 13, 2013
Giant axonal neuropathy
Fayçal Hentati, Emna Hentati, Rim Amouri
La Tunisie Medicale
|
August 29, 2007
[Acute polyradiculoneuropathy. Guillain-Barre syndrome]
Ilhem Turki, Salwa Djaïet, S Boukhris, et al.
Journal of Molecular Neuroscience : MN
|
June 17, 2009
A novel SACS gene mutation in a Tunisian family
Yosr Bouhlal, Ghada El Euch-Fayeche, Fayçal Hentati, et al.
Parkinsonism & Related Disorders
|
April 1, 2011
Autosomal recessive spastic ataxia of Charlevoix-Saguenay: an overview
Yosr Bouhlal, Rim Amouri, Ghada El Euch-Fayeche, et al.
Brain : a Journal of Neurology
|
December 27, 2013
Molecular, clinical and peripheral neuropathy study of Tunisian patients with ataxia with vitamin E deficiency
Ghada 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 scoliosis
Rim Amouri, Houda Nehdi, Yosr Bouhlal, et al.
Journal of Stroke and Cerebrovascular Diseases : the Official Journal of National Stroke Association
|
June 12, 2010
Cerebral venous thrombosis presenting with cerebellar ataxia and cortical blindness
Samia Ben Sassi, Habiba Mizouni, Fatma Nabli, et al.
Biological Research for Nursing
|
December 10, 2020
Association of <i>Bgl</i>II Polymorphism in <i>ITGA2</i> and (894G/T and -786T/C) Polymorphisms in eNOS Gene With Stroke Susceptibility in Tunisian Patients α2 Gene Polymorphism in α2β1 Integrin and eNOS Gene Variants and Stroke
Akrem Jalel, Fatma Midani, Sondess Hadj Fredj, et al.
Journal of Neurogenetics
|
June 24, 2008
Autosomal recessive ataxia caused by three distinct gene defects in a single consanguineous family
Yosr Bouhlal, Mourad Zouari, Mounir Kefi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
February 25, 2018
Disability progression in multiple sclerosis: a Tunisian prospective cohort study
Emna Hentati, Samia Ben Sassi, Fatma Nabli, et al.
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of 3