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

Heather M Johnston

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

Pageof 1
Sort By:
Brain & Development|April 12, 2003
The floppy weak infant revisitedHeather M Johnston
Archives of Neurology|April 12, 2012
Corticomotoneuronal integrity and adaptation in spinal muscular atrophyMichelle A Farrar, Steve Vucic, Heather M Johnston, et al.
Frontiers in Psychology|December 7, 2016
Replication Rate, Framing, and Format Affect Attitudes and Decisions about Science ClaimsRalph M Barnes, Stephanie J Tobin, Heather M Johnston, et al.
The Journal of Pediatrics|July 20, 2012
Pathophysiological insights derived by natural history and motor function of spinal muscular atrophyMichelle A Farrar, Steve Vucic, Heather M Johnston, et al.
Journal of Experimental Psychology. General|July 19, 2006
The time of our lives: life span development of timing and event trackingJ Devin McAuley, Mari Riess Jones, Shayla Holub, et al.
Plos One|January 31, 2018
The effect of ad hominem attacks on the evaluation of claims promoted by scientistsRalph M Barnes, Heather M Johnston, Noah MacKenzie, et al.
Journal of Paediatrics and Child Health|May 27, 2010
Bilateral subdural hygromas and cephalhaematomas in male twins with severe myotubular myopathy caused by a Novel c.431delT (p.Leu144fs) mutation in MTM1 geneTejasvi Chaudhari, David A Todd, Alison L Kent, et al.
Plos One|January 26, 2010
Dystrophin gene mutation location and the risk of cognitive impairment in Duchenne muscular dystrophyPeter J Taylor, Grant A Betts, Sarah Maroulis, et al.
Brain : a Journal of Neurology|September 20, 2011
Dysfunction of axonal membrane conductances in adolescents and young adults with spinal muscular atrophyMichelle A Farrar, Steve Vucic, Cindy S-Y Lin, et al.
Journal of Medical Genetics|January 30, 2007
Measurement of the clinical utility of a combined mutation detection protocol in carriers of Duchenne and Becker muscular dystrophyPeter J Taylor, Sarah Maroulis, Glenda L Mullan, et al.
Pageof 1

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

Sort By:
Pageof 1
Brain & Development|April 12, 2003
The floppy weak infant revisitedHeather M Johnston
Archives of Neurology|April 12, 2012
Corticomotoneuronal integrity and adaptation in spinal muscular atrophyMichelle A Farrar, Steve Vucic, Heather M Johnston, et al.
Frontiers in Psychology|December 7, 2016
Replication Rate, Framing, and Format Affect Attitudes and Decisions about Science ClaimsRalph M Barnes, Stephanie J Tobin, Heather M Johnston, et al.
The Journal of Pediatrics|July 20, 2012
Pathophysiological insights derived by natural history and motor function of spinal muscular atrophyMichelle A Farrar, Steve Vucic, Heather M Johnston, et al.
Journal of Experimental Psychology. General|July 19, 2006
The time of our lives: life span development of timing and event trackingJ Devin McAuley, Mari Riess Jones, Shayla Holub, et al.
Plos One|January 31, 2018
The effect of ad hominem attacks on the evaluation of claims promoted by scientistsRalph M Barnes, Heather M Johnston, Noah MacKenzie, et al.
Journal of Paediatrics and Child Health|May 27, 2010
Bilateral subdural hygromas and cephalhaematomas in male twins with severe myotubular myopathy caused by a Novel c.431delT (p.Leu144fs) mutation in MTM1 geneTejasvi Chaudhari, David A Todd, Alison L Kent, et al.
Plos One|January 26, 2010
Dystrophin gene mutation location and the risk of cognitive impairment in Duchenne muscular dystrophyPeter J Taylor, Grant A Betts, Sarah Maroulis, et al.
Brain : a Journal of Neurology|September 20, 2011
Dysfunction of axonal membrane conductances in adolescents and young adults with spinal muscular atrophyMichelle A Farrar, Steve Vucic, Cindy S-Y Lin, et al.
Journal of Medical Genetics|January 30, 2007
Measurement of the clinical utility of a combined mutation detection protocol in carriers of Duchenne and Becker muscular dystrophyPeter J Taylor, Sarah Maroulis, Glenda L Mullan, et al.
Pageof 1