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Nigel F Clarke

Showing results (1-10 of 67) with videos related to

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Seminars in Pediatric Neurology|December 17, 2011
Congenital fiber-type disproportionNigel F Clarke
Neuromuscular Disorders : NMD|March 23, 2011
Congenital fibre type disproportion--a syndrome at the crossroads of the congenital myopathiesNigel F Clarke
Advances in Experimental Medicine and Biology|February 3, 2009
Skeletal muscle disease due to mutations in tropomyosin, troponin and cofilinNigel F Clarke
Journal of Neuropathology and Experimental Neurology|October 25, 2003
Congenital fiber type disproportion--30 years onNigel F Clarke, Kathryn N North
Handbook of Clinical Neurology|April 30, 2013
Congenital myopathiesNorma Beatriz Romero, Nigel F Clarke
Current Opinion in Neurology|September 3, 2013
Recent advances in nemaline myopathyNorma B Romero, Sarah A Sandaradura, Nigel F Clarke
Trends in Molecular Medicine|October 17, 2012
Mapping domains and mutations on the skeletal muscle ryanodine receptor channelJean H Hwang, Francesco Zorzato, Nigel F Clarke, et al.
American Journal of Medical Genetics. Part A|August 25, 2004
Fragile X syndrome phenotype with normal FMR1 gene studiesNigel F Clarke, David Mowat, R Frank Kooy, et al.
Annals of Neurology|September 21, 2005
A novel X-linked form of congenital fiber-type disproportionNigel F Clarke, Robert L L Smith, Melanie Bahlo, et al.
Neuromuscular Disorders : NMD|April 7, 2009
Cap disease due to mutation of the beta-tropomyosin gene (TPM2)Nigel F Clarke, Ana Domazetovska, Leigh Waddell, et al.
Pageof 7

Showing results (1-10 of 67) with videos related to

Sort By:
Pageof 7
Seminars in Pediatric Neurology|December 17, 2011
Congenital fiber-type disproportionNigel F Clarke
Neuromuscular Disorders : NMD|March 23, 2011
Congenital fibre type disproportion--a syndrome at the crossroads of the congenital myopathiesNigel F Clarke
Advances in Experimental Medicine and Biology|February 3, 2009
Skeletal muscle disease due to mutations in tropomyosin, troponin and cofilinNigel F Clarke
Journal of Neuropathology and Experimental Neurology|October 25, 2003
Congenital fiber type disproportion--30 years onNigel F Clarke, Kathryn N North
Handbook of Clinical Neurology|April 30, 2013
Congenital myopathiesNorma Beatriz Romero, Nigel F Clarke
Current Opinion in Neurology|September 3, 2013
Recent advances in nemaline myopathyNorma B Romero, Sarah A Sandaradura, Nigel F Clarke
Trends in Molecular Medicine|October 17, 2012
Mapping domains and mutations on the skeletal muscle ryanodine receptor channelJean H Hwang, Francesco Zorzato, Nigel F Clarke, et al.
American Journal of Medical Genetics. Part A|August 25, 2004
Fragile X syndrome phenotype with normal FMR1 gene studiesNigel F Clarke, David Mowat, R Frank Kooy, et al.
Annals of Neurology|September 21, 2005
A novel X-linked form of congenital fiber-type disproportionNigel F Clarke, Robert L L Smith, Melanie Bahlo, et al.
Neuromuscular Disorders : NMD|April 7, 2009
Cap disease due to mutation of the beta-tropomyosin gene (TPM2)Nigel F Clarke, Ana Domazetovska, Leigh Waddell, et al.
Pageof 7