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John Vissing

Showing results (81-90 of 416) with videos related to

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Journal of Neuromuscular Diseases|March 1, 2021
Progression or Not - A Small Natural History Study of Genetical Confirmed Congenital MyopathiesUlla Werlauff, Pernille Diemer Hansen, Nanna Witting, et al.
Journal of Neurology|February 6, 2007
31P-MRS of skeletal muscle is not a sensitive diagnostic test for mitochondrial myopathyTina Dysgaard Jeppesen, Bjørn Quistorff, Flemming Wibrand, et al.
Annals of Neurology|May 24, 2006
Aerobic conditioning: an effective therapy in McArdle's diseaseRonald G Haller, Phil Wyrick, Tanja Taivassalo, et al.
Brain : a Journal of Neurology|May 13, 2009
Splice mutations preserve myophosphorylase activity that ameliorates the phenotype in McArdle diseaseJohn Vissing, Morten Duno, Marianne Schwartz, et al.
Neuromuscular Disorders : NMD|September 19, 2016
216th ENMC international workshop: Clinical readiness in FKRP related myopathies January 15-17, 2016 Naarden, The NetherlandsIsabelle Richard, Jean-Pierre Laurent, Sebahattin Cirak, et al.
Muscle & Nerve|March 28, 2003
Decrement of compound muscle action potential is related to mutation type in myotonia congenitaEskild Colding-Jørgensen, Morten DunØ, Marianne Schwartz, et al.
European Journal of Human Genetics : EJHG|March 14, 2008
cDNA analyses of CAPN3 enhance mutation detection and reveal a low prevalence of LGMD2A patients in DenmarkMorten Duno, Marie-Louise Sveen, Marianne Schwartz, et al.
Muscle & Nerve|October 12, 2012
LGMD2L with bone affection: overlapping phenotype of dominant and recessive ANO5-induced diseaseNanna Witting, Morten Duno, Alfred Peter Born, et al.
Neurology|August 23, 2006
Do carriers of PYGM mutations have symptoms of McArdle disease?Susanne Tvede Andersen, Morten Dunø, Marianne Schwartz, et al.
Muscle & Nerve|February 10, 2015
LAMA2-related myopathy: Frequency among congenital and limb-girdle muscular dystrophiesNicoline Løkken, Alfred Peter Born, Morten Duno, et al.
Pageof 42

Showing results (81-90 of 416) with videos related to

Sort By:
Pageof 42
Journal of Neuromuscular Diseases|March 1, 2021
Progression or Not - A Small Natural History Study of Genetical Confirmed Congenital MyopathiesUlla Werlauff, Pernille Diemer Hansen, Nanna Witting, et al.
Journal of Neurology|February 6, 2007
31P-MRS of skeletal muscle is not a sensitive diagnostic test for mitochondrial myopathyTina Dysgaard Jeppesen, Bjørn Quistorff, Flemming Wibrand, et al.
Annals of Neurology|May 24, 2006
Aerobic conditioning: an effective therapy in McArdle's diseaseRonald G Haller, Phil Wyrick, Tanja Taivassalo, et al.
Brain : a Journal of Neurology|May 13, 2009
Splice mutations preserve myophosphorylase activity that ameliorates the phenotype in McArdle diseaseJohn Vissing, Morten Duno, Marianne Schwartz, et al.
Neuromuscular Disorders : NMD|September 19, 2016
216th ENMC international workshop: Clinical readiness in FKRP related myopathies January 15-17, 2016 Naarden, The NetherlandsIsabelle Richard, Jean-Pierre Laurent, Sebahattin Cirak, et al.
Muscle & Nerve|March 28, 2003
Decrement of compound muscle action potential is related to mutation type in myotonia congenitaEskild Colding-Jørgensen, Morten DunØ, Marianne Schwartz, et al.
European Journal of Human Genetics : EJHG|March 14, 2008
cDNA analyses of CAPN3 enhance mutation detection and reveal a low prevalence of LGMD2A patients in DenmarkMorten Duno, Marie-Louise Sveen, Marianne Schwartz, et al.
Muscle & Nerve|October 12, 2012
LGMD2L with bone affection: overlapping phenotype of dominant and recessive ANO5-induced diseaseNanna Witting, Morten Duno, Alfred Peter Born, et al.
Neurology|August 23, 2006
Do carriers of PYGM mutations have symptoms of McArdle disease?Susanne Tvede Andersen, Morten Dunø, Marianne Schwartz, et al.
Muscle & Nerve|February 10, 2015
LAMA2-related myopathy: Frequency among congenital and limb-girdle muscular dystrophiesNicoline Løkken, Alfred Peter Born, Morten Duno, et al.
Pageof 42