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N C Voermans

Showing results (71-80 of 81) with videos related to

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Disability and Rehabilitation|July 11, 2022
Facing facial weakness: psychosocial outcomes of facial weakness and reduced facial function in facioscapulohumeral muscular dystrophyW A van de Geest-Buit, N B Rasing, K Mul, et al.
Neuromuscular Disorders : NMD|February 14, 2017
PGM1 deficiency: Substrate use during exercise and effect of treatment with galactoseN C Voermans, N Preisler, K L Madsen, et al.
Neuromuscular Disorders : NMD|October 3, 2022
Having an eye for myotonic dystrophy: A qualitative study on experiences and support needs in myotonic dystrophy type 1 patients with a diagnostic delay after early-onset cataractI E A Karnebeek, H T M Boon, A M P Huis, et al.
Journal of Neurology|October 28, 2020
Characterizing the face in facioscapulohumeral muscular dystrophyT G J Loonen, C G C Horlings, S C C Vincenten, et al.
Connective Tissue Research|March 17, 2011
Mild muscular features in tenascin-X knockout mice, a model of Ehlers-danlos syndromeN C Voermans, K Verrijp, L Eshuis, et al.
JIMD Reports|May 13, 2024
Oral ribose supplementation in dystroglycanopathy: A single case studyR M J Thewissen, M A Post, D M Maas, et al.
Journal of Neurology|September 1, 2019
Scapular dyskinesis in myotonic dystrophy type 1: clinical characteristics and genetic investigationsN C Voermans, R C van der Bilt, J IJspeert, et al.
Journal of Neurology|February 22, 2019
The histopathological spectrum of malignant hyperthermia and rhabdomyolysis due to RYR1 mutationsG J Knuiman, B Küsters, L Eshuis, et al.
European Journal of Neurology|May 12, 2015
RYR1-related myopathies: a wide spectrum of phenotypes throughout lifeM Snoeck, B G M van Engelen, B Küsters, et al.
Neuromuscular Disorders : NMD|May 1, 2013
Mutations in RYR1 are a common cause of exertional myalgia and rhabdomyolysisN Dlamini, N C Voermans, S Lillis, et al.
Pageof 9

Showing results (71-80 of 81) with videos related to

Sort By:
Pageof 9
Disability and Rehabilitation|July 11, 2022
Facing facial weakness: psychosocial outcomes of facial weakness and reduced facial function in facioscapulohumeral muscular dystrophyW A van de Geest-Buit, N B Rasing, K Mul, et al.
Neuromuscular Disorders : NMD|February 14, 2017
PGM1 deficiency: Substrate use during exercise and effect of treatment with galactoseN C Voermans, N Preisler, K L Madsen, et al.
Neuromuscular Disorders : NMD|October 3, 2022
Having an eye for myotonic dystrophy: A qualitative study on experiences and support needs in myotonic dystrophy type 1 patients with a diagnostic delay after early-onset cataractI E A Karnebeek, H T M Boon, A M P Huis, et al.
Journal of Neurology|October 28, 2020
Characterizing the face in facioscapulohumeral muscular dystrophyT G J Loonen, C G C Horlings, S C C Vincenten, et al.
Connective Tissue Research|March 17, 2011
Mild muscular features in tenascin-X knockout mice, a model of Ehlers-danlos syndromeN C Voermans, K Verrijp, L Eshuis, et al.
JIMD Reports|May 13, 2024
Oral ribose supplementation in dystroglycanopathy: A single case studyR M J Thewissen, M A Post, D M Maas, et al.
Journal of Neurology|September 1, 2019
Scapular dyskinesis in myotonic dystrophy type 1: clinical characteristics and genetic investigationsN C Voermans, R C van der Bilt, J IJspeert, et al.
Journal of Neurology|February 22, 2019
The histopathological spectrum of malignant hyperthermia and rhabdomyolysis due to RYR1 mutationsG J Knuiman, B Küsters, L Eshuis, et al.
European Journal of Neurology|May 12, 2015
RYR1-related myopathies: a wide spectrum of phenotypes throughout lifeM Snoeck, B G M van Engelen, B Küsters, et al.
Neuromuscular Disorders : NMD|May 1, 2013
Mutations in RYR1 are a common cause of exertional myalgia and rhabdomyolysisN Dlamini, N C Voermans, S Lillis, et al.
Pageof 9