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Dominic B Rowe

Showing results (41-50 of 56) with videos related to

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Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|July 10, 2019
Safety and tolerability of Triumeq in amyotrophic lateral sclerosis: the Lighthouse trialJulian Gold, Dominic B Rowe, Matthew C Kiernan, et al.
Science Advances|May 5, 2023
Short tandem repeat expansions in sporadic amyotrophic lateral sclerosis and frontotemporal dementiaLyndal Henden, Liam G Fearnley, Natalie Grima, et al.
Parkinsonism & Related Disorders|November 16, 2019
Whole genome sequencing for the genetic diagnosis of heterogenous dystonia phenotypesKishore R Kumar, Ryan L Davis, Michel C Tchan, et al.
European Journal of Human Genetics : EJHG|April 28, 2021
Polygenic risk score analysis for amyotrophic lateral sclerosis leveraging cognitive performance, educational attainment and schizophreniaRestuadi Restuadi, Fleur C Garton, Beben Benyamin, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 7, 2019
Genetic and immunopathological analysis of CHCHD10 in Australian amyotrophic lateral sclerosis and frontotemporal dementia and transgenic TDP-43 miceEmily P McCann, Jennifer A Fifita, Natalie Grima, et al.
Acta Neuropathologica Communications|January 3, 2024
Letter to the editor on: Hornerin deposits in neuronal intranuclear inclusion disease: direct identification of proteins with compositionally biased regions in inclusions by Park et al. (2022)Huihui Luo, Emil K Gustavsson, Hannah Macpherson, et al.
Annals of Clinical and Translational Neurology|August 11, 2020
Neuronal intranuclear inclusion disease is genetically heterogeneousZhongbo Chen, Wai Yan Yau, Zane Jaunmuktane, et al.
Cell Reports|October 28, 2020
Genome-wide Meta-analysis Finds the ACSL5-ZDHHC6 Locus Is Associated with ALS and Links Weight Loss to the Disease GeneticsAlfredo Iacoangeli, Tian Lin, Ahmad Al Khleifat, et al.
NPJ Genomic Medicine|March 7, 2020
Significant out-of-sample classification from methylation profile scoring for amyotrophic lateral sclerosisMarta F Nabais, Tian Lin, Beben Benyamin, et al.
Nature Communications|September 22, 2017
Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosisBeben Benyamin, Ji He, Qiongyi Zhao, et al.
Pageof 6

Showing results (41-50 of 56) with videos related to

Sort By:
Pageof 6
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|July 10, 2019
Safety and tolerability of Triumeq in amyotrophic lateral sclerosis: the Lighthouse trialJulian Gold, Dominic B Rowe, Matthew C Kiernan, et al.
Science Advances|May 5, 2023
Short tandem repeat expansions in sporadic amyotrophic lateral sclerosis and frontotemporal dementiaLyndal Henden, Liam G Fearnley, Natalie Grima, et al.
Parkinsonism & Related Disorders|November 16, 2019
Whole genome sequencing for the genetic diagnosis of heterogenous dystonia phenotypesKishore R Kumar, Ryan L Davis, Michel C Tchan, et al.
European Journal of Human Genetics : EJHG|April 28, 2021
Polygenic risk score analysis for amyotrophic lateral sclerosis leveraging cognitive performance, educational attainment and schizophreniaRestuadi Restuadi, Fleur C Garton, Beben Benyamin, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 7, 2019
Genetic and immunopathological analysis of CHCHD10 in Australian amyotrophic lateral sclerosis and frontotemporal dementia and transgenic TDP-43 miceEmily P McCann, Jennifer A Fifita, Natalie Grima, et al.
Acta Neuropathologica Communications|January 3, 2024
Letter to the editor on: Hornerin deposits in neuronal intranuclear inclusion disease: direct identification of proteins with compositionally biased regions in inclusions by Park et al. (2022)Huihui Luo, Emil K Gustavsson, Hannah Macpherson, et al.
Annals of Clinical and Translational Neurology|August 11, 2020
Neuronal intranuclear inclusion disease is genetically heterogeneousZhongbo Chen, Wai Yan Yau, Zane Jaunmuktane, et al.
Cell Reports|October 28, 2020
Genome-wide Meta-analysis Finds the ACSL5-ZDHHC6 Locus Is Associated with ALS and Links Weight Loss to the Disease GeneticsAlfredo Iacoangeli, Tian Lin, Ahmad Al Khleifat, et al.
NPJ Genomic Medicine|March 7, 2020
Significant out-of-sample classification from methylation profile scoring for amyotrophic lateral sclerosisMarta F Nabais, Tian Lin, Beben Benyamin, et al.
Nature Communications|September 22, 2017
Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosisBeben Benyamin, Ji He, Qiongyi Zhao, et al.
Pageof 6