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Showing results (291-300 of 300) with videos related to

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Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|September 11, 2020
The NEALS primary lateral sclerosis registrySabrina Paganoni, Fabiola De Marchi, James Chan, et al.
The Lancet. Neurology|March 13, 2012
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional studyElisa Majounie, Alan E Renton, Kin Mok, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|February 19, 2021
Preface: promoting research in PLS: current knowledge and future challengesHiroshi Mitsumoto, Martin R Turner, , et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|May 4, 2013
ALS Untangled No. 20: the Deanna protocol, Christina Fournier, Bedlack Bedlack, et al.
Science Translational Medicine|February 23, 2022
Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALSPaul J Hop, Ramona A J Zwamborn, Eilis Hannon, et al.
Nature Genetics|March 31, 2026
Large-scale exome analyses reveal new rare variant contributions in amyotrophic lateral sclerosisPaul J Hop, Maarten Kooyman, Brendan J Kenna, et al.
Nature Genetics|February 1, 2022
Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biologyWouter van Rheenen, Rick A A van der Spek, Mark K Bakker, et al.
Nature Genetics|December 7, 2021
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biologyWouter van Rheenen, Rick A A van der Spek, Mark K Bakker, et al.
Neuron|March 24, 2018
Genome-wide Analyses Identify KIF5A as a Novel ALS GeneAude Nicolas, Kevin P Kenna, Alan E Renton, et al.
JAMA Neurology|August 30, 2021
Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral SclerosisJanel O Johnson, Ruth Chia, Danny E Miller, et al.
Pageof 30

Showing results (291-300 of 300) with videos related to

Sort By:
Pageof 30
You have reached the last page of results.This site can display upto 300 results.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|September 11, 2020
The NEALS primary lateral sclerosis registrySabrina Paganoni, Fabiola De Marchi, James Chan, et al.
The Lancet. Neurology|March 13, 2012
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional studyElisa Majounie, Alan E Renton, Kin Mok, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|February 19, 2021
Preface: promoting research in PLS: current knowledge and future challengesHiroshi Mitsumoto, Martin R Turner, , et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|May 4, 2013
ALS Untangled No. 20: the Deanna protocol, Christina Fournier, Bedlack Bedlack, et al.
Science Translational Medicine|February 23, 2022
Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALSPaul J Hop, Ramona A J Zwamborn, Eilis Hannon, et al.
Nature Genetics|March 31, 2026
Large-scale exome analyses reveal new rare variant contributions in amyotrophic lateral sclerosisPaul J Hop, Maarten Kooyman, Brendan J Kenna, et al.
Nature Genetics|February 1, 2022
Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biologyWouter van Rheenen, Rick A A van der Spek, Mark K Bakker, et al.
Nature Genetics|December 7, 2021
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biologyWouter van Rheenen, Rick A A van der Spek, Mark K Bakker, et al.
Neuron|March 24, 2018
Genome-wide Analyses Identify KIF5A as a Novel ALS GeneAude Nicolas, Kevin P Kenna, Alan E Renton, et al.
JAMA Neurology|August 30, 2021
Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral SclerosisJanel O Johnson, Ruth Chia, Danny E Miller, et al.
Pageof 30