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Emna Hentati

Showing results (1-10 of 8) with videos related to

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Handbook of Clinical Neurology|August 13, 2013
Giant axonal neuropathyFayçal Hentati, Emna Hentati, Rim Amouri
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 studyEmna Hentati, Samia Ben Sassi, Fatma Nabli, et al.
Parkinsonism & Related Disorders|October 26, 2010
Genetic variation of the mitochondrial complex I subunit NDUFV2 and Parkinson's diseaseKenya Nishioka, Carles Vilariño-Güell, Stephanie A Cobb, et al.
Parkinsonism & Related Disorders|November 8, 2011
Cognitive dysfunction in Tunisian LRRK2 associated Parkinson's diseaseSamia Ben Sassi, Fatma Nabli, Emna Hentati, et al.
Neurobiology of Aging|December 21, 2013
Comparative study of Parkinson's disease and leucine-rich repeat kinase 2 p.G2019S parkinsonismJoanne Trinh, Rim Amouri, John E Duda, et al.
The Lancet. Neurology|October 4, 2016
DNM3 and genetic modifiers of age of onset in LRRK2 Gly2019Ser parkinsonism: a genome-wide linkage and association studyJoanne Trinh, Emil K Gustavsson, Carles Vilariño-Güell, et al.
American Journal of Human Genetics|July 19, 2011
VPS35 mutations in Parkinson diseaseCarles Vilariño-Güell, Christian Wider, Owen A Ross, et al.
American Journal of Human Genetics|September 13, 2011
Translation initiator EIF4G1 mutations in familial Parkinson diseaseMarie-Christine Chartier-Harlin, Justus C Dachsel, Carles Vilariño-Güell, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Handbook of Clinical Neurology|August 13, 2013
Giant axonal neuropathyFayçal Hentati, Emna Hentati, Rim Amouri
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 studyEmna Hentati, Samia Ben Sassi, Fatma Nabli, et al.
Parkinsonism & Related Disorders|October 26, 2010
Genetic variation of the mitochondrial complex I subunit NDUFV2 and Parkinson's diseaseKenya Nishioka, Carles Vilariño-Güell, Stephanie A Cobb, et al.
Parkinsonism & Related Disorders|November 8, 2011
Cognitive dysfunction in Tunisian LRRK2 associated Parkinson's diseaseSamia Ben Sassi, Fatma Nabli, Emna Hentati, et al.
Neurobiology of Aging|December 21, 2013
Comparative study of Parkinson's disease and leucine-rich repeat kinase 2 p.G2019S parkinsonismJoanne Trinh, Rim Amouri, John E Duda, et al.
The Lancet. Neurology|October 4, 2016
DNM3 and genetic modifiers of age of onset in LRRK2 Gly2019Ser parkinsonism: a genome-wide linkage and association studyJoanne Trinh, Emil K Gustavsson, Carles Vilariño-Güell, et al.
American Journal of Human Genetics|July 19, 2011
VPS35 mutations in Parkinson diseaseCarles Vilariño-Güell, Christian Wider, Owen A Ross, et al.
American Journal of Human Genetics|September 13, 2011
Translation initiator EIF4G1 mutations in familial Parkinson diseaseMarie-Christine Chartier-Harlin, Justus C Dachsel, Carles Vilariño-Güell, et al.
Pageof 1