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John Ravits

Showing results (31-40 of 102) with videos related to

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The Lancet. Neurology|February 22, 2025
Amyotrophic lateral sclerosis caused by hexanucleotide repeat expansions in C9orf72: from genetics to therapeuticsSarah Mizielinska, Guillaume M Hautbergue, Tania F Gendron, et al.
European Journal of Neurology|January 25, 2024
Misfolded alpha-synuclein in amyotrophic lateral sclerosis: Implications for diagnosis and treatmentRichard Smith, Hanna Hovren, Robert Bowser, et al.
Acta Neuropathologica|January 23, 2019
Antisense RNA foci are associated with nucleoli and TDP-43 mislocalization in C9orf72-ALS/FTD: a quantitative studyOlubankole Aladesuyi Arogundade, Jennifer E Stauffer, Shahram Saberi, et al.
Acta Neuropathologica Communications|February 20, 2016
Neuregulin 1 confers neuroprotection in SOD1-linked amyotrophic lateral sclerosis mice via restoration of C-boutons of spinal motor neuronsJurate Lasiene, Okiru Komine, Noriko Fujimori-Tonou, et al.
Acta Neuropathologica|October 7, 2021
Nuclear depletion of RNA-binding protein ELAVL3 (HuC) in sporadic and familial amyotrophic lateral sclerosisSandra Diaz-Garcia, Vivian I Ko, Sonia Vazquez-Sanchez, et al.
Annals of Neurology|November 11, 2014
Amyotrophic lateral sclerosis onset is influenced by the burden of rare variants in known amyotrophic lateral sclerosis genesJanet Cady, Peggy Allred, Taha Bali, et al.
ERJ Open Research|September 27, 2023
Effectiveness of long-term noninvasive ventilation measured by remote monitoring in neuromuscular diseaseJeremy E Orr, Kenneth Chen, Florin Vaida, et al.
Neuron|December 7, 2023
Challenges of profiling motor neuron transcriptomes from human spinal cordOlivia Gautier, Jacob A Blum, James Maksymetz, et al.
Human Molecular Genetics|October 30, 2009
Sporadic ALS has compartment-specific aberrant exon splicing and altered cell-matrix adhesion biologyStuart J Rabin, Jae Mun Hugo Kim, Michael Baughn, et al.
Acta Neuropathologica|March 31, 2017
Mutant TDP-43 within motor neurons drives disease onset but not progression in amyotrophic lateral sclerosisDara Ditsworth, Marcus Maldonado, Melissa McAlonis-Downes, et al.
Pageof 11

Showing results (31-40 of 102) with videos related to

Sort By:
Pageof 11
The Lancet. Neurology|February 22, 2025
Amyotrophic lateral sclerosis caused by hexanucleotide repeat expansions in C9orf72: from genetics to therapeuticsSarah Mizielinska, Guillaume M Hautbergue, Tania F Gendron, et al.
European Journal of Neurology|January 25, 2024
Misfolded alpha-synuclein in amyotrophic lateral sclerosis: Implications for diagnosis and treatmentRichard Smith, Hanna Hovren, Robert Bowser, et al.
Acta Neuropathologica|January 23, 2019
Antisense RNA foci are associated with nucleoli and TDP-43 mislocalization in C9orf72-ALS/FTD: a quantitative studyOlubankole Aladesuyi Arogundade, Jennifer E Stauffer, Shahram Saberi, et al.
Acta Neuropathologica Communications|February 20, 2016
Neuregulin 1 confers neuroprotection in SOD1-linked amyotrophic lateral sclerosis mice via restoration of C-boutons of spinal motor neuronsJurate Lasiene, Okiru Komine, Noriko Fujimori-Tonou, et al.
Acta Neuropathologica|October 7, 2021
Nuclear depletion of RNA-binding protein ELAVL3 (HuC) in sporadic and familial amyotrophic lateral sclerosisSandra Diaz-Garcia, Vivian I Ko, Sonia Vazquez-Sanchez, et al.
Annals of Neurology|November 11, 2014
Amyotrophic lateral sclerosis onset is influenced by the burden of rare variants in known amyotrophic lateral sclerosis genesJanet Cady, Peggy Allred, Taha Bali, et al.
ERJ Open Research|September 27, 2023
Effectiveness of long-term noninvasive ventilation measured by remote monitoring in neuromuscular diseaseJeremy E Orr, Kenneth Chen, Florin Vaida, et al.
Neuron|December 7, 2023
Challenges of profiling motor neuron transcriptomes from human spinal cordOlivia Gautier, Jacob A Blum, James Maksymetz, et al.
Human Molecular Genetics|October 30, 2009
Sporadic ALS has compartment-specific aberrant exon splicing and altered cell-matrix adhesion biologyStuart J Rabin, Jae Mun Hugo Kim, Michael Baughn, et al.
Acta Neuropathologica|March 31, 2017
Mutant TDP-43 within motor neurons drives disease onset but not progression in amyotrophic lateral sclerosisDara Ditsworth, Marcus Maldonado, Melissa McAlonis-Downes, et al.
Pageof 11