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Nigel G Laing

Showing results (21-30 of 203) with videos related to

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Seminars in Pediatric Neurology|December 17, 2011
Nemaline myopathiesCarina Wallgren-Pettersson, Caroline A Sewry, Kristen J Nowak, et al.
Seminars in Cell & Developmental Biology|August 14, 2016
New era in genetics of early-onset muscle disease: Breakthroughs and challengesGianina Ravenscroft, Mark R Davis, Phillipa Lamont, et al.
Human Molecular Genetics|June 21, 2013
Skeletal and cardiac α-actin isoforms differently modulate myosin cross-bridge formation and myofibre force productionJulien Ochala, Hiroyuki Iwamoto, Gianina Ravenscroft, et al.
F1000Research|January 12, 2019
Recent advances in understanding congenital myopathiesGianina Ravenscroft, Robert J Bryson-Richardson, Kristen J Nowak, et al.
Neuromuscular Disorders : NMD|March 25, 2017
Lethal multiple pterygium syndrome: A severe phenotype associated with a novel mutation in the nebulin geneEbtesam Abdalla, Gianina Ravenscroft, Louay Zayed, et al.
The Clinical Biochemist. Reviews|September 14, 2011
Molecular diagnosis of duchenne muscular dystrophy: past, present and future in relation to implementing therapiesNigel G Laing, Mark R Davis, Klair Bayley, et al.
International Journal of Cardiology|April 15, 2014
Novel MYH7 mutation associated with mild myopathy but life-threatening ventricular arrhythmias and noncompactionJosef Finsterer, Claudia Stöllberger, Oliver Brandau, et al.
Muscle & Nerve|November 13, 2015
Health care utilization and costs for children and adults with duchenne muscular dystrophyLucinda J Teoh, Elizabeth A Geelhoed, Klair Bayley, et al.
Neuromuscular Disorders : NMD|June 24, 2014
Distal myosin heavy chain-7 myopathy due to the novel transition c.5566G>A (p.E1856K) with high interfamilial cardiac variability and putative anticipationJosef Finsterer, Oliver Brandau, Claudia Stöllberger, et al.
Neuromuscular Disorders : NMD|January 24, 2006
Autosomal dominant nemaline myopathy with intranuclear rods due to mutation of the skeletal muscle ACTA1 gene: clinical and pathological variability within a kindredDavid O Hutchinson, Amanda Charlton, Nigel G Laing, et al.
Pageof 21

Showing results (21-30 of 203) with videos related to

Sort By:
Pageof 21
Seminars in Pediatric Neurology|December 17, 2011
Nemaline myopathiesCarina Wallgren-Pettersson, Caroline A Sewry, Kristen J Nowak, et al.
Seminars in Cell & Developmental Biology|August 14, 2016
New era in genetics of early-onset muscle disease: Breakthroughs and challengesGianina Ravenscroft, Mark R Davis, Phillipa Lamont, et al.
Human Molecular Genetics|June 21, 2013
Skeletal and cardiac α-actin isoforms differently modulate myosin cross-bridge formation and myofibre force productionJulien Ochala, Hiroyuki Iwamoto, Gianina Ravenscroft, et al.
F1000Research|January 12, 2019
Recent advances in understanding congenital myopathiesGianina Ravenscroft, Robert J Bryson-Richardson, Kristen J Nowak, et al.
Neuromuscular Disorders : NMD|March 25, 2017
Lethal multiple pterygium syndrome: A severe phenotype associated with a novel mutation in the nebulin geneEbtesam Abdalla, Gianina Ravenscroft, Louay Zayed, et al.
The Clinical Biochemist. Reviews|September 14, 2011
Molecular diagnosis of duchenne muscular dystrophy: past, present and future in relation to implementing therapiesNigel G Laing, Mark R Davis, Klair Bayley, et al.
International Journal of Cardiology|April 15, 2014
Novel MYH7 mutation associated with mild myopathy but life-threatening ventricular arrhythmias and noncompactionJosef Finsterer, Claudia Stöllberger, Oliver Brandau, et al.
Muscle & Nerve|November 13, 2015
Health care utilization and costs for children and adults with duchenne muscular dystrophyLucinda J Teoh, Elizabeth A Geelhoed, Klair Bayley, et al.
Neuromuscular Disorders : NMD|June 24, 2014
Distal myosin heavy chain-7 myopathy due to the novel transition c.5566G>A (p.E1856K) with high interfamilial cardiac variability and putative anticipationJosef Finsterer, Oliver Brandau, Claudia Stöllberger, et al.
Neuromuscular Disorders : NMD|January 24, 2006
Autosomal dominant nemaline myopathy with intranuclear rods due to mutation of the skeletal muscle ACTA1 gene: clinical and pathological variability within a kindredDavid O Hutchinson, Amanda Charlton, Nigel G Laing, et al.
Pageof 21