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Nanna Witting

Showing results (11-20 of 78) with videos related to

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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.
JAMA Neurology|November 13, 2013
Severe axial myopathy in McArdle diseaseNanna Witting, Morten Duno, Monique Piraud, 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.
Frontiers in Neurology|January 20, 2021
Quantitative Muscle MRI as Outcome Measure in Patients With Becker Muscular Dystrophy-A 1-Year Follow-Up StudyAisha M Sheikh, Karen Rudolf, Nanna Witting, et al.
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.
Acta Neuropathologica Communications|June 14, 2021
Autophagy is affected in patients with hypokalemic periodic paralysis: an involvement in vacuolar myopathy?Thomas O Krag, Sonja Holm-Yildiz, Nanna Witting, et al.
International Journal of Cardiology|September 16, 2011
Cardiac manifestations of myotonic dystrophy type 1Helle Petri, John Vissing, Nanna Witting, et al.
Neurology|January 8, 2016
Two- and 6-minute walk tests assess walking capability equally in neuromuscular diseasesLinda Kahr Andersen, Kirsten Lykke Knak, Nanna Witting, et al.
Acta Ophthalmologica|July 16, 2013
Delayed diagnosis of oculopharyngeal muscular dystrophy in Denmark: from initial ptosis to genetic testingAurore Mensah, Nanna Witting, Morten Duno, et al.
Pageof 8

Showing results (11-20 of 78) with videos related to

Sort By:
Pageof 8
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.
JAMA Neurology|November 13, 2013
Severe axial myopathy in McArdle diseaseNanna Witting, Morten Duno, Monique Piraud, 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.
Frontiers in Neurology|January 20, 2021
Quantitative Muscle MRI as Outcome Measure in Patients With Becker Muscular Dystrophy-A 1-Year Follow-Up StudyAisha M Sheikh, Karen Rudolf, Nanna Witting, et al.
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.
Acta Neuropathologica Communications|June 14, 2021
Autophagy is affected in patients with hypokalemic periodic paralysis: an involvement in vacuolar myopathy?Thomas O Krag, Sonja Holm-Yildiz, Nanna Witting, et al.
International Journal of Cardiology|September 16, 2011
Cardiac manifestations of myotonic dystrophy type 1Helle Petri, John Vissing, Nanna Witting, et al.
Neurology|January 8, 2016
Two- and 6-minute walk tests assess walking capability equally in neuromuscular diseasesLinda Kahr Andersen, Kirsten Lykke Knak, Nanna Witting, et al.
Acta Ophthalmologica|July 16, 2013
Delayed diagnosis of oculopharyngeal muscular dystrophy in Denmark: from initial ptosis to genetic testingAurore Mensah, Nanna Witting, Morten Duno, et al.
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