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Matthew B Harms

Showing results (21-30 of 68) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|December 14, 2021
High-impact rare genetic variants in severe schizophreniaAnthony W Zoghbi, Ryan S Dhindsa, Terry E Goldberg, et al.
Neurobiology of Aging|April 20, 2013
Lack of C9ORF72 coding mutations supports a gain of function for repeat expansions in amyotrophic lateral sclerosisMatthew B Harms, Janet Cady, Craig Zaidman, et al.
Medrxiv : the Preprint Server for Health Sciences|October 24, 2023
Rare variant analyses validate known ALS genes in a multi-ethnic population and identifies <i>ANTXR2</i> as a candidate in PLSTess D Pottinger, Joshua E Motelow, Gundula Povysil, et al.
Neuromuscular Disorders : NMD|December 24, 2019
Congenital fiber type disproportion caused by TPM3 mutation: A report of two atypical casesCristiane Araújo Martins Moreno, Eduardo de Paula Estephan, Alan Fappi, et al.
Research Square|January 10, 2024
Rare variant analyses validate known ALS genes in a multi-ethnic population and identifies <i>ANTXR2</i> as a candidate in PLSTess D Pottinger, Joshua E Motelow, Gundula Povysil, et al.
BMC Genomics|July 2, 2024
Rare variant analyses validate known ALS genes in a multi-ethnic population and identifies ANTXR2 as a candidate in PLSTess D Pottinger, Joshua E Motelow, Gundula Povysil, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 8, 2020
Primary lateral sclerosis: consensus diagnostic criteriaMartin R Turner, Richard J Barohn, Philippe Corcia, et al.
Annals of Neurology|December 15, 2015
MORC2 mutations cause axonal Charcot-Marie-Tooth disease with pyramidal signsObaid M Albulym, Marina L Kennerson, Matthew B Harms, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|September 4, 2025
A <i>VAPB</i> (P56S) mutation in a Dutch patient with familial motor neuron disease: a case reportSean W Willemse, Koen C Demaegd, Ruben P A Van Eijk, et al.
JAMA Neurology|February 19, 2014
TREM2 variant p.R47H as a risk factor for sporadic amyotrophic lateral sclerosisJanet Cady, Erica D Koval, Bruno A Benitez, et al.
Pageof 7

Showing results (21-30 of 68) with videos related to

Sort By:
Pageof 7
Proceedings of the National Academy of Sciences of the United States of America|December 14, 2021
High-impact rare genetic variants in severe schizophreniaAnthony W Zoghbi, Ryan S Dhindsa, Terry E Goldberg, et al.
Neurobiology of Aging|April 20, 2013
Lack of C9ORF72 coding mutations supports a gain of function for repeat expansions in amyotrophic lateral sclerosisMatthew B Harms, Janet Cady, Craig Zaidman, et al.
Medrxiv : the Preprint Server for Health Sciences|October 24, 2023
Rare variant analyses validate known ALS genes in a multi-ethnic population and identifies <i>ANTXR2</i> as a candidate in PLSTess D Pottinger, Joshua E Motelow, Gundula Povysil, et al.
Neuromuscular Disorders : NMD|December 24, 2019
Congenital fiber type disproportion caused by TPM3 mutation: A report of two atypical casesCristiane Araújo Martins Moreno, Eduardo de Paula Estephan, Alan Fappi, et al.
Research Square|January 10, 2024
Rare variant analyses validate known ALS genes in a multi-ethnic population and identifies <i>ANTXR2</i> as a candidate in PLSTess D Pottinger, Joshua E Motelow, Gundula Povysil, et al.
BMC Genomics|July 2, 2024
Rare variant analyses validate known ALS genes in a multi-ethnic population and identifies ANTXR2 as a candidate in PLSTess D Pottinger, Joshua E Motelow, Gundula Povysil, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 8, 2020
Primary lateral sclerosis: consensus diagnostic criteriaMartin R Turner, Richard J Barohn, Philippe Corcia, et al.
Annals of Neurology|December 15, 2015
MORC2 mutations cause axonal Charcot-Marie-Tooth disease with pyramidal signsObaid M Albulym, Marina L Kennerson, Matthew B Harms, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|September 4, 2025
A <i>VAPB</i> (P56S) mutation in a Dutch patient with familial motor neuron disease: a case reportSean W Willemse, Koen C Demaegd, Ruben P A Van Eijk, et al.
JAMA Neurology|February 19, 2014
TREM2 variant p.R47H as a risk factor for sporadic amyotrophic lateral sclerosisJanet Cady, Erica D Koval, Bruno A Benitez, et al.
Pageof 7