Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Matthew B Harms

Showing results (1-10 of 68) with videos related to

Pageof 7
Sort By:
Seminars in Neurology|November 24, 2015
Neuromuscular EmergenciesRobert Bucelli, Matthew B Harms
Neurologic Clinics|November 2, 2013
Clinical neurogenetics: amyotrophic lateral sclerosisMatthew B Harms, Robert H Baloh
Journal of Neurology|October 9, 2013
Ultrasound of inherited vs. acquired demyelinating polyneuropathiesCraig M Zaidman, Matthew B Harms, Alan Pestronk
Neuromuscular Disorders : NMD|June 24, 2018
Homozygous recessive MYH2 mutation mimicking dominant MYH2 associated myopathyAndrew R Findlay, Matthew B Harms, Alan Pestronk, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|February 19, 2021
Genetics of primary lateral sclerosisVincenzo Silani, Philippe Corcia, Matthew B Harms, et al.
Annals of Clinical and Translational Neurology|September 11, 2023
Evidence-based consensus guidelines for ALS genetic testing and counselingJennifer Roggenbuck, Breda H F Eubank, Joshua Wright, et al.
The Journal of Biological Chemistry|June 13, 2014
Myopathy-causing mutations in an HSP40 chaperone disrupt processing of specific client conformersKevin C Stein, Rocio Bengoechea, Matthew B Harms, et al.
Journal of Genetic Counseling|March 13, 2024
Individuals' experiences in genetic counseling and predictive testing for familial amyotrophic lateral sclerosisConnolly G Steigerwald, Carina Bertolini, Martin McElhiney, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|August 2, 2024
The Answer ALS return of results study: Answering the duty to discloseJennifer Roggenbuck, Mackenzie Kaschalk, Rory Eustace, et al.
Human Molecular Genetics|March 3, 2016
Poly-dipeptides encoded by the C9ORF72 repeats block global protein translationKohsuke Kanekura, Takuya Yagi, Alexander J Cammack, et al.
Pageof 7

Showing results (1-10 of 68) with videos related to

Sort By:
Pageof 7
Seminars in Neurology|November 24, 2015
Neuromuscular EmergenciesRobert Bucelli, Matthew B Harms
Neurologic Clinics|November 2, 2013
Clinical neurogenetics: amyotrophic lateral sclerosisMatthew B Harms, Robert H Baloh
Journal of Neurology|October 9, 2013
Ultrasound of inherited vs. acquired demyelinating polyneuropathiesCraig M Zaidman, Matthew B Harms, Alan Pestronk
Neuromuscular Disorders : NMD|June 24, 2018
Homozygous recessive MYH2 mutation mimicking dominant MYH2 associated myopathyAndrew R Findlay, Matthew B Harms, Alan Pestronk, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|February 19, 2021
Genetics of primary lateral sclerosisVincenzo Silani, Philippe Corcia, Matthew B Harms, et al.
Annals of Clinical and Translational Neurology|September 11, 2023
Evidence-based consensus guidelines for ALS genetic testing and counselingJennifer Roggenbuck, Breda H F Eubank, Joshua Wright, et al.
The Journal of Biological Chemistry|June 13, 2014
Myopathy-causing mutations in an HSP40 chaperone disrupt processing of specific client conformersKevin C Stein, Rocio Bengoechea, Matthew B Harms, et al.
Journal of Genetic Counseling|March 13, 2024
Individuals' experiences in genetic counseling and predictive testing for familial amyotrophic lateral sclerosisConnolly G Steigerwald, Carina Bertolini, Martin McElhiney, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|August 2, 2024
The Answer ALS return of results study: Answering the duty to discloseJennifer Roggenbuck, Mackenzie Kaschalk, Rory Eustace, et al.
Human Molecular Genetics|March 3, 2016
Poly-dipeptides encoded by the C9ORF72 repeats block global protein translationKohsuke Kanekura, Takuya Yagi, Alexander J Cammack, et al.
Pageof 7