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

Bryan Lecky

Showing results (1-10 of 9) with videos related to

Pageof 1
Sort By:
BMJ (Clinical Research Ed.)|November 8, 2008
Statin induced myopathySivakumar Sathasivam, Bryan Lecky
Plastic and Reconstructive Surgery|July 27, 2011
Silhouette thread lift as an ancillary procedure in an unusual case of necrotizing myopathy of the faceAnuj Mishra, Belkys Husein, Bryan Lecky, et al.
Journal of the American College of Cardiology|April 22, 2014
Elevation of cardiac troponin T, but not cardiac troponin I, in patients with neuromuscular diseases: implications for the diagnosis of myocardial infarctionDylmitr Rittoo, Alan Jones, Bryan Lecky, et al.
Archives of Neurology|June 19, 2010
Giant Virchow-Robin spaces: functional magnetic resonance imaging and tractographySui Hsien Wong, Kumar Das, Mani Puthuran, et al.
The Cochrane Database of Systematic Reviews|October 13, 2009
WITHDRAWN: Immunosuppressant and immunomodulatory treatment for dermatomyositis and polymyositisErnest Hs Choy, Jessica E Hoogendijk, Bryan Lecky, et al.
Neuromuscular Disorders : NMD|May 6, 2014
Distal weakness with respiratory insufficiency caused by the m.8344A > G "MERRF" mutationEmma L Blakely, Charlotte L Alston, Bryan Lecky, et al.
European Journal of Human Genetics : EJHG|June 2, 2011
Phenotypic heterogeneity in British patients with a founder mutation in the FHL1 geneAnna Sarkozy, Christian Windpassinger, Judith Hudson, et al.
Rheumatology (Oxford, England)|November 30, 2014
Second-line agents in myositis: 1-year factorial trial of additional immunosuppression in patients who have partially responded to steroidsFowzia Ibrahim, Ernest Choy, Patrick Gordon, et al.
Clinical Science (London, England : 1979)|January 29, 2015
Novel MTND1 mutations cause isolated exercise intolerance, complex I deficiency and increased assembly factor expressionGrainne S Gorman, Emma L Blakely, Hue-Tran Hornig-Do, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
BMJ (Clinical Research Ed.)|November 8, 2008
Statin induced myopathySivakumar Sathasivam, Bryan Lecky
Plastic and Reconstructive Surgery|July 27, 2011
Silhouette thread lift as an ancillary procedure in an unusual case of necrotizing myopathy of the faceAnuj Mishra, Belkys Husein, Bryan Lecky, et al.
Journal of the American College of Cardiology|April 22, 2014
Elevation of cardiac troponin T, but not cardiac troponin I, in patients with neuromuscular diseases: implications for the diagnosis of myocardial infarctionDylmitr Rittoo, Alan Jones, Bryan Lecky, et al.
Archives of Neurology|June 19, 2010
Giant Virchow-Robin spaces: functional magnetic resonance imaging and tractographySui Hsien Wong, Kumar Das, Mani Puthuran, et al.
The Cochrane Database of Systematic Reviews|October 13, 2009
WITHDRAWN: Immunosuppressant and immunomodulatory treatment for dermatomyositis and polymyositisErnest Hs Choy, Jessica E Hoogendijk, Bryan Lecky, et al.
Neuromuscular Disorders : NMD|May 6, 2014
Distal weakness with respiratory insufficiency caused by the m.8344A > G "MERRF" mutationEmma L Blakely, Charlotte L Alston, Bryan Lecky, et al.
European Journal of Human Genetics : EJHG|June 2, 2011
Phenotypic heterogeneity in British patients with a founder mutation in the FHL1 geneAnna Sarkozy, Christian Windpassinger, Judith Hudson, et al.
Rheumatology (Oxford, England)|November 30, 2014
Second-line agents in myositis: 1-year factorial trial of additional immunosuppression in patients who have partially responded to steroidsFowzia Ibrahim, Ernest Choy, Patrick Gordon, et al.
Clinical Science (London, England : 1979)|January 29, 2015
Novel MTND1 mutations cause isolated exercise intolerance, complex I deficiency and increased assembly factor expressionGrainne S Gorman, Emma L Blakely, Hue-Tran Hornig-Do, et al.
Pageof 1