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Nigel F Clarke

Showing results (11-20 of 67) with videos related to

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Muscle & Nerve|July 15, 2011
Using complementary DNA from MyoD-transduced fibroblasts to sequence large muscle genesLeigh B Waddell, Nicole Monnier, Sandra T Cooper, et al.
American Journal of Medical Genetics. Part A|February 22, 2013
Young Australian adults with NF1 have poor access to health care, high complication rates, and limited disease knowledgeEmily C Oates, Jonathan M Payne, Sheryl L Foster, et al.
Neuromuscular Disorders : NMD|December 17, 2008
Germinal mosaicism for LMNA mimics autosomal recessive congenital muscular dystrophySamira Makri, Nigel F Clarke, Pascale Richard, et al.
American Journal of Medical Genetics. Part A|July 29, 2003
D-2-hydroxyglutaric aciduria: a case with an intermediate phenotype and prenatal diagnosis of two affected fetusesNigel F Clarke, Ian Andrews, Kevin Carpenter, et al.
Neuromuscular Disorders : NMD|June 1, 2014
Whole exome sequencing identifies three recessive FIG4 mutations in an apparently dominant pedigree with Charcot-Marie-Tooth diseaseManoj P Menezes, Leigh Waddell, Guy M Lenk, et al.
Journal of Molecular Medicine (Berlin, Germany)|January 23, 2013
Neuromuscular junction abnormalities in DNM2-related centronuclear myopathyElizabeth M Gibbs, Nigel F Clarke, Kristy Rose, et al.
Neuromuscular Disorders : NMD|January 25, 2015
ResponseManoj P Menezes, Leigh Waddell, Guy M Lenk, et al.
Practical Neurology|April 24, 2017
A 'limb-girdle muscular dystrophy' responsive to asthma therapyEoin Mulroy, Roula Ghaoui, David Hutchinson, et al.
Muscle & Nerve|July 19, 2012
Novel FLNC mutation in a patient with myofibrillar myopathy in combination with late-onset cerebellar ataxiaGiorgio Tasca, Zagaa Odgerel, Mauro Monforte, et al.
Annals of Neurology|March 28, 2007
The pathogenesis of ACTA1-related congenital fiber type disproportionNigel F Clarke, Biljana Ilkovski, Sandra Cooper, et al.
Pageof 7

Showing results (11-20 of 67) with videos related to

Sort By:
Pageof 7
Muscle & Nerve|July 15, 2011
Using complementary DNA from MyoD-transduced fibroblasts to sequence large muscle genesLeigh B Waddell, Nicole Monnier, Sandra T Cooper, et al.
American Journal of Medical Genetics. Part A|February 22, 2013
Young Australian adults with NF1 have poor access to health care, high complication rates, and limited disease knowledgeEmily C Oates, Jonathan M Payne, Sheryl L Foster, et al.
Neuromuscular Disorders : NMD|December 17, 2008
Germinal mosaicism for LMNA mimics autosomal recessive congenital muscular dystrophySamira Makri, Nigel F Clarke, Pascale Richard, et al.
American Journal of Medical Genetics. Part A|July 29, 2003
D-2-hydroxyglutaric aciduria: a case with an intermediate phenotype and prenatal diagnosis of two affected fetusesNigel F Clarke, Ian Andrews, Kevin Carpenter, et al.
Neuromuscular Disorders : NMD|June 1, 2014
Whole exome sequencing identifies three recessive FIG4 mutations in an apparently dominant pedigree with Charcot-Marie-Tooth diseaseManoj P Menezes, Leigh Waddell, Guy M Lenk, et al.
Journal of Molecular Medicine (Berlin, Germany)|January 23, 2013
Neuromuscular junction abnormalities in DNM2-related centronuclear myopathyElizabeth M Gibbs, Nigel F Clarke, Kristy Rose, et al.
Neuromuscular Disorders : NMD|January 25, 2015
ResponseManoj P Menezes, Leigh Waddell, Guy M Lenk, et al.
Practical Neurology|April 24, 2017
A 'limb-girdle muscular dystrophy' responsive to asthma therapyEoin Mulroy, Roula Ghaoui, David Hutchinson, et al.
Muscle & Nerve|July 19, 2012
Novel FLNC mutation in a patient with myofibrillar myopathy in combination with late-onset cerebellar ataxiaGiorgio Tasca, Zagaa Odgerel, Mauro Monforte, et al.
Annals of Neurology|March 28, 2007
The pathogenesis of ACTA1-related congenital fiber type disproportionNigel F Clarke, Biljana Ilkovski, Sandra Cooper, et al.
Pageof 7