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Morten Duno

Showing results (11-20 of 108) with videos related to

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JAMA Neurology|November 13, 2013
Severe axial myopathy in McArdle diseaseNanna Witting, Morten Duno, Monique Piraud, et al.
Neurology. Genetics|March 31, 2017
Phenotypes, genotypes, and prevalence of congenital myopathies older than 5 years in DenmarkNanna Witting, Ulla Werlauff, Morten Duno, et al.
Muscle & Nerve|July 15, 2015
Prevalence and phenotypes of congenital myopathy due to α-actin 1 gene mutationsNanna Witting, Ulla Werlauff, Morten Duno, et al.
Clinical Neurology and Neurosurgery|January 28, 2015
Clinical and neurophysiological response to pharmacological treatment of DOK7 congenital myasthenia in an older patientNanna Witting, Clarissa Crone, Morten Duno, et al.
Ophthalmic Genetics|September 25, 2012
Blue cone monochromatism in a female due to skewed X-inactivationAnja L Frederiksen, Morten Duno, Lotte G Welinder
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.
Ophthalmic Genetics|January 11, 2012
Phenotypic and genetic spectrum of Danish patients with ABCA4-related retinopathyMorten Duno, Marianne Schwartz, Pernille L Larsen, 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.
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 11

Showing results (11-20 of 108) with videos related to

Sort By:
Pageof 11
JAMA Neurology|November 13, 2013
Severe axial myopathy in McArdle diseaseNanna Witting, Morten Duno, Monique Piraud, et al.
Neurology. Genetics|March 31, 2017
Phenotypes, genotypes, and prevalence of congenital myopathies older than 5 years in DenmarkNanna Witting, Ulla Werlauff, Morten Duno, et al.
Muscle & Nerve|July 15, 2015
Prevalence and phenotypes of congenital myopathy due to α-actin 1 gene mutationsNanna Witting, Ulla Werlauff, Morten Duno, et al.
Clinical Neurology and Neurosurgery|January 28, 2015
Clinical and neurophysiological response to pharmacological treatment of DOK7 congenital myasthenia in an older patientNanna Witting, Clarissa Crone, Morten Duno, et al.
Ophthalmic Genetics|September 25, 2012
Blue cone monochromatism in a female due to skewed X-inactivationAnja L Frederiksen, Morten Duno, Lotte G Welinder
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.
Ophthalmic Genetics|January 11, 2012
Phenotypic and genetic spectrum of Danish patients with ABCA4-related retinopathyMorten Duno, Marianne Schwartz, Pernille L Larsen, 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.
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 11