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Showing results (261-270 of 300) with videos related to

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Neurobiology of Aging|January 21, 2018
High frequency of C9orf72 hexanucleotide repeat expansion in amyotrophic lateral sclerosis patients from two founder populations sharing the same risk haplotypeOrly Goldstein, Mali Gana-Weisz, Beatrice Nefussy, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|April 3, 2018
"ALS reversals": demographics, disease characteristics, treatments, and co-morbiditiesDaniel Harrison, Paul Mehta, Michael A van Es, et al.
Analytical Chemistry|July 4, 2012
Array-based disease diagnostics using lipid/polydiacetylene vesicles encapsulated in a sol-gel matrixS Kolusheva, R Yossef, A Kugel, et al.
The American Journal of Cardiology|December 15, 1996
Exercise echocardiography in postmenopausal hormone users with mild systemic hypertensionA Pines, E Z Fisman, I Shapira, et al.
Journal of Neurology|April 16, 2024
Genetic diagnosis and detection rates using C9orf72 repeat expansion and a multi-gene panel in amyotrophic lateral sclerosisDalit Barel, Daphna Marom, Penina Ponger, et al.
Brain : a Journal of Neurology|February 27, 2008
Thrombin receptor PAR-1 on myelin at the node of Ranvier: a new anatomy and physiology of conduction blockEfrat Shavit, Orit Beilin, Amos D Korczyn, et al.
Annals of the Rheumatic Diseases|August 19, 2005
Evoked potential studies in the antiphospholipid syndrome: differential diagnosis from multiple sclerosisD Paran, J Chapman, A D Korczyn, et al.
Journal of the Neurological Sciences|May 21, 2019
Rare homozygosity in amyotrophic lateral sclerosis suggests the contribution of recessive variants to disease geneticsOrly Goldstein, Merav Kedmi, Mali Gana-Weisz, et al.
Brain : a Journal of Neurology|September 29, 2014
Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosisJanel O Johnson, Shannon M Glynn, J Raphael Gibbs, et al.
The Israel Medical Association Journal : IMAJ|January 24, 2014
Oculopharyngeal muscular dystrophy among Bulgarian Jews: a new cluster?Sergiu C Blumen, Anat Kesler, Ron Dabby, et al.
Pageof 30

Showing results (261-270 of 300) with videos related to

Sort By:
Pageof 30
Neurobiology of Aging|January 21, 2018
High frequency of C9orf72 hexanucleotide repeat expansion in amyotrophic lateral sclerosis patients from two founder populations sharing the same risk haplotypeOrly Goldstein, Mali Gana-Weisz, Beatrice Nefussy, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|April 3, 2018
"ALS reversals": demographics, disease characteristics, treatments, and co-morbiditiesDaniel Harrison, Paul Mehta, Michael A van Es, et al.
Analytical Chemistry|July 4, 2012
Array-based disease diagnostics using lipid/polydiacetylene vesicles encapsulated in a sol-gel matrixS Kolusheva, R Yossef, A Kugel, et al.
The American Journal of Cardiology|December 15, 1996
Exercise echocardiography in postmenopausal hormone users with mild systemic hypertensionA Pines, E Z Fisman, I Shapira, et al.
Journal of Neurology|April 16, 2024
Genetic diagnosis and detection rates using C9orf72 repeat expansion and a multi-gene panel in amyotrophic lateral sclerosisDalit Barel, Daphna Marom, Penina Ponger, et al.
Brain : a Journal of Neurology|February 27, 2008
Thrombin receptor PAR-1 on myelin at the node of Ranvier: a new anatomy and physiology of conduction blockEfrat Shavit, Orit Beilin, Amos D Korczyn, et al.
Annals of the Rheumatic Diseases|August 19, 2005
Evoked potential studies in the antiphospholipid syndrome: differential diagnosis from multiple sclerosisD Paran, J Chapman, A D Korczyn, et al.
Journal of the Neurological Sciences|May 21, 2019
Rare homozygosity in amyotrophic lateral sclerosis suggests the contribution of recessive variants to disease geneticsOrly Goldstein, Merav Kedmi, Mali Gana-Weisz, et al.
Brain : a Journal of Neurology|September 29, 2014
Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosisJanel O Johnson, Shannon M Glynn, J Raphael Gibbs, et al.
The Israel Medical Association Journal : IMAJ|January 24, 2014
Oculopharyngeal muscular dystrophy among Bulgarian Jews: a new cluster?Sergiu C Blumen, Anat Kesler, Ron Dabby, et al.
Pageof 30