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JAMA Neurology
|
November 13, 2013
Severe axial myopathy in McArdle disease
Nanna Witting, Morten Duno, Monique Piraud, et al.
Neurology. Genetics
|
March 31, 2017
Phenotypes, genotypes, and prevalence of congenital myopathies older than 5 years in Denmark
Nanna Witting, Ulla Werlauff, Morten Duno, et al.
Muscle & Nerve
|
July 15, 2015
Prevalence and phenotypes of congenital myopathy due to α-actin 1 gene mutations
Nanna 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 patient
Nanna Witting, Clarissa Crone, Morten Duno, et al.
Ophthalmic Genetics
|
September 25, 2012
Blue cone monochromatism in a female due to skewed X-inactivation
Anja 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 disease
John Vissing, Morten Duno, Marianne Schwartz, et al.
Ophthalmic Genetics
|
January 11, 2012
Phenotypic and genetic spectrum of Danish patients with ABCA4-related retinopathy
Morten 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 Denmark
Morten 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 disease
Nanna Witting, Morten Duno, Alfred Peter Born, et al.
Muscle & Nerve
|
February 10, 2015
LAMA2-related myopathy: Frequency among congenital and limb-girdle muscular dystrophies
Nicoline Løkken, Alfred Peter Born, Morten Duno, et al.
Page
of 11
Search research articles
Search
Showing results (11-20 of 108) with videos related to
Sort By:
Page
of 11
JAMA Neurology
|
November 13, 2013
Severe axial myopathy in McArdle disease
Nanna Witting, Morten Duno, Monique Piraud, et al.
Neurology. Genetics
|
March 31, 2017
Phenotypes, genotypes, and prevalence of congenital myopathies older than 5 years in Denmark
Nanna Witting, Ulla Werlauff, Morten Duno, et al.
Muscle & Nerve
|
July 15, 2015
Prevalence and phenotypes of congenital myopathy due to α-actin 1 gene mutations
Nanna 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 patient
Nanna Witting, Clarissa Crone, Morten Duno, et al.
Ophthalmic Genetics
|
September 25, 2012
Blue cone monochromatism in a female due to skewed X-inactivation
Anja 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 disease
John Vissing, Morten Duno, Marianne Schwartz, et al.
Ophthalmic Genetics
|
January 11, 2012
Phenotypic and genetic spectrum of Danish patients with ABCA4-related retinopathy
Morten 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 Denmark
Morten 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 disease
Nanna Witting, Morten Duno, Alfred Peter Born, et al.
Muscle & Nerve
|
February 10, 2015
LAMA2-related myopathy: Frequency among congenital and limb-girdle muscular dystrophies
Nicoline Løkken, Alfred Peter Born, Morten Duno, et al.
Page
of 11