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Kate Bushby

Showing results (71-80 of 151) with videos related to

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The American Journal of Pathology|January 27, 2004
Abnormalities in alpha-dystroglycan expression in MDC1C and LGMD2I muscular dystrophiesSusan C Brown, Silvia Torelli, Martin Brockington, et al.
Neuromuscular Disorders : NMD|November 13, 2017
MEGF10 related myopathies: A new case with adult onset disease with prominent respiratory failure and review of reported phenotypesElizabeth Harris, Chiara Marini-Bettolo, Ana Töpf, et al.
Muscle & Nerve|November 25, 2015
Prophylactic oral bisphosphonate therapy in duchenne muscular dystrophyRamesh Srinivasan, David Rawlings, Claire L Wood, et al.
Neuromuscular Disorders : NMD|September 5, 2002
Mutations in the nebulin gene can cause severe congenital nemaline myopathyCarina Wallgren-Pettersson, Kati Donner, Caroline Sewry, et al.
Neuromuscular Disorders : NMD|April 17, 2010
Revertant fibres and dystrophin traces in Duchenne muscular dystrophy: implication for clinical trialsVirginia Arechavala-Gomeza, Maria Kinali, Lucy Feng, et al.
Neurology|December 3, 2021
Clinical and Genetic Characteristics in Young, Glucocorticoid-Naive Boys With Duchenne Muscular DystrophyMarianela Schiava, Rachel Amos, Henriette VanRuiten, et al.
Human Molecular Genetics|December 17, 2013
Mutations in the collagen XII gene define a new form of extracellular matrix-related myopathyDebbie Hicks, Golara Torabi Farsani, Steven Laval, et al.
The American Journal of Pathology|January 13, 2011
Long-term blocking of calcium channels in mdx mice results in differential effects on heart and skeletal muscleLouise H Jørgensen, Alison Blain, Elizabeth Greally, et al.
Plos One|November 28, 2013
Dystromirs as serum biomarkers for monitoring the disease severity in Duchenne muscular DystrophyIrina T Zaharieva, Mattia Calissano, Mariacristina Scoto, et al.
Neuromuscular Disorders : NMD|August 16, 2017
A comparative study of care practices for young boys with Duchenne muscular dystrophy between Japan and European countries: Implications of early diagnosisFumi Takeuchi, Hirofumi Komaki, Zentaro Yamagata, et al.
Pageof 16

Showing results (71-80 of 151) with videos related to

Sort By:
Pageof 16
The American Journal of Pathology|January 27, 2004
Abnormalities in alpha-dystroglycan expression in MDC1C and LGMD2I muscular dystrophiesSusan C Brown, Silvia Torelli, Martin Brockington, et al.
Neuromuscular Disorders : NMD|November 13, 2017
MEGF10 related myopathies: A new case with adult onset disease with prominent respiratory failure and review of reported phenotypesElizabeth Harris, Chiara Marini-Bettolo, Ana Töpf, et al.
Muscle & Nerve|November 25, 2015
Prophylactic oral bisphosphonate therapy in duchenne muscular dystrophyRamesh Srinivasan, David Rawlings, Claire L Wood, et al.
Neuromuscular Disorders : NMD|September 5, 2002
Mutations in the nebulin gene can cause severe congenital nemaline myopathyCarina Wallgren-Pettersson, Kati Donner, Caroline Sewry, et al.
Neuromuscular Disorders : NMD|April 17, 2010
Revertant fibres and dystrophin traces in Duchenne muscular dystrophy: implication for clinical trialsVirginia Arechavala-Gomeza, Maria Kinali, Lucy Feng, et al.
Neurology|December 3, 2021
Clinical and Genetic Characteristics in Young, Glucocorticoid-Naive Boys With Duchenne Muscular DystrophyMarianela Schiava, Rachel Amos, Henriette VanRuiten, et al.
Human Molecular Genetics|December 17, 2013
Mutations in the collagen XII gene define a new form of extracellular matrix-related myopathyDebbie Hicks, Golara Torabi Farsani, Steven Laval, et al.
The American Journal of Pathology|January 13, 2011
Long-term blocking of calcium channels in mdx mice results in differential effects on heart and skeletal muscleLouise H Jørgensen, Alison Blain, Elizabeth Greally, et al.
Plos One|November 28, 2013
Dystromirs as serum biomarkers for monitoring the disease severity in Duchenne muscular DystrophyIrina T Zaharieva, Mattia Calissano, Mariacristina Scoto, et al.
Neuromuscular Disorders : NMD|August 16, 2017
A comparative study of care practices for young boys with Duchenne muscular dystrophy between Japan and European countries: Implications of early diagnosisFumi Takeuchi, Hirofumi Komaki, Zentaro Yamagata, et al.
Pageof 16