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Disability and Rehabilitation
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July 11, 2022
Facing facial weakness: psychosocial outcomes of facial weakness and reduced facial function in facioscapulohumeral muscular dystrophy
W 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 galactose
N 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 cataract
I 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 dystrophy
T 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 syndrome
N C Voermans, K Verrijp, L Eshuis, et al.
JIMD Reports
|
May 13, 2024
Oral ribose supplementation in dystroglycanopathy: A single case study
R 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 investigations
N 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 mutations
G J Knuiman, B Küsters, L Eshuis, et al.
European Journal of Neurology
|
May 12, 2015
RYR1-related myopathies: a wide spectrum of phenotypes throughout life
M 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 rhabdomyolysis
N Dlamini, N C Voermans, S Lillis, et al.
Page
of 9
Search research articles
Search
Showing results (71-80 of 81) with videos related to
Sort By:
Page
of 9
Disability and Rehabilitation
|
July 11, 2022
Facing facial weakness: psychosocial outcomes of facial weakness and reduced facial function in facioscapulohumeral muscular dystrophy
W 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 galactose
N 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 cataract
I 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 dystrophy
T 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 syndrome
N C Voermans, K Verrijp, L Eshuis, et al.
JIMD Reports
|
May 13, 2024
Oral ribose supplementation in dystroglycanopathy: A single case study
R 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 investigations
N 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 mutations
G J Knuiman, B Küsters, L Eshuis, et al.
European Journal of Neurology
|
May 12, 2015
RYR1-related myopathies: a wide spectrum of phenotypes throughout life
M 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 rhabdomyolysis
N Dlamini, N C Voermans, S Lillis, et al.
Page
of 9