Search research articles
Contact Us
Filters
Showing results (21-30 of 203) with videos related to
Page
of 21
Sort By:
Seminars in Pediatric Neurology
|
December 17, 2011
Nemaline myopathies
Carina 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 challenges
Gianina 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 production
Julien Ochala, Hiroyuki Iwamoto, Gianina Ravenscroft, et al.
F1000Research
|
January 12, 2019
Recent advances in understanding congenital myopathies
Gianina 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 gene
Ebtesam 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 therapies
Nigel 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 noncompaction
Josef Finsterer, Claudia Stöllberger, Oliver Brandau, et al.
Muscle & Nerve
|
November 13, 2015
Health care utilization and costs for children and adults with duchenne muscular dystrophy
Lucinda 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 anticipation
Josef 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 kindred
David O Hutchinson, Amanda Charlton, Nigel G Laing, et al.
Page
of 21
Search research articles
Search
Showing results (21-30 of 203) with videos related to
Sort By:
Page
of 21
Seminars in Pediatric Neurology
|
December 17, 2011
Nemaline myopathies
Carina 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 challenges
Gianina 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 production
Julien Ochala, Hiroyuki Iwamoto, Gianina Ravenscroft, et al.
F1000Research
|
January 12, 2019
Recent advances in understanding congenital myopathies
Gianina 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 gene
Ebtesam 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 therapies
Nigel 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 noncompaction
Josef Finsterer, Claudia Stöllberger, Oliver Brandau, et al.
Muscle & Nerve
|
November 13, 2015
Health care utilization and costs for children and adults with duchenne muscular dystrophy
Lucinda 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 anticipation
Josef 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 kindred
David O Hutchinson, Amanda Charlton, Nigel G Laing, et al.
Page
of 21