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Shree Pandya

Showing results (41-50 of 55) with videos related to

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Journal of Child Neurology|December 14, 2011
Use of complementary and alternative medicine by males with Duchenne or Becker muscular dystrophySarah K Nabukera, Paul A Romitti, Kimberly A Campbell, et al.
The Lancet. Neurology|February 4, 2018
Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and neuromuscular, rehabilitation, endocrine, and gastrointestinal and nutritional managementDavid J Birnkrant, Katharine Bushby, Carla M Bann, et al.
Muscle & Nerve|June 6, 2015
Myotonic dystrophy health index: Correlations with clinical tests and patient functionChad Heatwole, Rita Bode, Nicholas E Johnson, et al.
Neurology|August 28, 2016
Efficacy and safety of deflazacort vs prednisone and placebo for Duchenne muscular dystrophyRobert C Griggs, J Phillip Miller, Cheryl R Greenberg, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|October 13, 2006
The muscular Dystrophy Surveillance Tracking and Research Network (MD STARnet): surveillance methodologyLisa A Miller, Paul A Romitti, Christopher Cunniff, et al.
Annals of Neurology|August 10, 2013
Splicing biomarkers of disease severity in myotonic dystrophyMasayuki Nakamori, Krzysztof Sobczak, Araya Puwanant, et al.
Muscle & Nerve|April 8, 2015
Spinal muscular atrophy functional composite score: A functional measure in spinal muscular atrophyJacqueline Montes, Allan M Glanzman, Elena S Mazzone, et al.
Muscle & Nerve|September 19, 2012
A quantitative measure of handgrip myotonia in non-dystrophic myotoniaJeffrey M Statland, Brian N Bundy, Yunxia Wang, et al.
Neurology|February 12, 2016
Randomized, placebo-controlled trials of dichlorphenamide in periodic paralysisValeria A Sansone, James Burge, Michael P McDermott, et al.
Muscle & Nerve|November 5, 2020
Association of genetic mutations and loss of ambulation in childhood-onset dystrophinopathyGregory Haber, Kristin M Conway, Pangaja Paramsothy, et al.
Pageof 6

Showing results (41-50 of 55) with videos related to

Sort By:
Pageof 6
Journal of Child Neurology|December 14, 2011
Use of complementary and alternative medicine by males with Duchenne or Becker muscular dystrophySarah K Nabukera, Paul A Romitti, Kimberly A Campbell, et al.
The Lancet. Neurology|February 4, 2018
Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and neuromuscular, rehabilitation, endocrine, and gastrointestinal and nutritional managementDavid J Birnkrant, Katharine Bushby, Carla M Bann, et al.
Muscle & Nerve|June 6, 2015
Myotonic dystrophy health index: Correlations with clinical tests and patient functionChad Heatwole, Rita Bode, Nicholas E Johnson, et al.
Neurology|August 28, 2016
Efficacy and safety of deflazacort vs prednisone and placebo for Duchenne muscular dystrophyRobert C Griggs, J Phillip Miller, Cheryl R Greenberg, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|October 13, 2006
The muscular Dystrophy Surveillance Tracking and Research Network (MD STARnet): surveillance methodologyLisa A Miller, Paul A Romitti, Christopher Cunniff, et al.
Annals of Neurology|August 10, 2013
Splicing biomarkers of disease severity in myotonic dystrophyMasayuki Nakamori, Krzysztof Sobczak, Araya Puwanant, et al.
Muscle & Nerve|April 8, 2015
Spinal muscular atrophy functional composite score: A functional measure in spinal muscular atrophyJacqueline Montes, Allan M Glanzman, Elena S Mazzone, et al.
Muscle & Nerve|September 19, 2012
A quantitative measure of handgrip myotonia in non-dystrophic myotoniaJeffrey M Statland, Brian N Bundy, Yunxia Wang, et al.
Neurology|February 12, 2016
Randomized, placebo-controlled trials of dichlorphenamide in periodic paralysisValeria A Sansone, James Burge, Michael P McDermott, et al.
Muscle & Nerve|November 5, 2020
Association of genetic mutations and loss of ambulation in childhood-onset dystrophinopathyGregory Haber, Kristin M Conway, Pangaja Paramsothy, et al.
Pageof 6