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C Voermans

Showing results (241-250 of 344) with videos related to

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Neurology|December 17, 2024
Longitudinal Insights Into Childhood Onset Facioscapulohumeral Dystrophy: A 5-Year Natural History StudyJildou N Dijkstra, Helena T M Boon, Anne Koekkoek, et al.
Neuromuscular Disorders : NMD|December 31, 2023
Bone quality in LAMA2-related muscular dystrophy and SELENON-related congenital myopathy, a one-year prospective natural history studyKarlijn Bouman, Anne T M Dittrich, Jan T Groothuis, et al.
Neurology|October 15, 2017
Adding quantitative muscle MRI to the FSHD clinical trial toolboxKarlien Mul, Sanne C C Vincenten, Nicol C Voermans, et al.
Journal of Neuromuscular Diseases|April 25, 2025
Liver function in X-linked myotubular myopathy and autosomal dominant centronuclear myopathy: Data of the unite-CNM studyS Colombo, B S Cowling, L Eyler, et al.
Neuromuscular Disorders : NMD|November 6, 2017
Early onset facioscapulohumeral dystrophy - a systematic review using individual patient dataRianne J M Goselink, Nicol C Voermans, Kees Okkersen, et al.
British Journal of Anaesthesia|January 31, 2025
Pathogenicity assessment of seven RYR1 variants in patients with confirmed susceptibility to malignant hyperthermia in the NetherlandsLuuk R van den Bersselaar, Anja H Schiemann, Chu-Ya Yang, et al.
Disability and Rehabilitation|September 27, 2023
Psychosocial functioning in patients with altered facial expression: a scoping review in five neurological diseasesNathaniël B Rasing, Willianne van de Geest-Buit, On Ying A Chan, et al.
Genes|September 27, 2025
Rhabdomyolysis in the Era of Next-Generation Sequencing: Selecting Patients with a High Likelihood of a Genetic Susceptibility Using 'RHABDO' FeaturesNick Kruijt, Sanne A J H van de Camp, Jasper J Kramer, et al.
Acta Neurologica Scandinavica|April 11, 2018
Phenotype and genotype of muscle ryanodine receptor rhabdomyolysis-myalgia syndromeN Witting, P Laforêt, N C Voermans, et al.
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.
Pageof 35

Showing results (241-250 of 344) with videos related to

Sort By:
Pageof 35
Neurology|December 17, 2024
Longitudinal Insights Into Childhood Onset Facioscapulohumeral Dystrophy: A 5-Year Natural History StudyJildou N Dijkstra, Helena T M Boon, Anne Koekkoek, et al.
Neuromuscular Disorders : NMD|December 31, 2023
Bone quality in LAMA2-related muscular dystrophy and SELENON-related congenital myopathy, a one-year prospective natural history studyKarlijn Bouman, Anne T M Dittrich, Jan T Groothuis, et al.
Neurology|October 15, 2017
Adding quantitative muscle MRI to the FSHD clinical trial toolboxKarlien Mul, Sanne C C Vincenten, Nicol C Voermans, et al.
Journal of Neuromuscular Diseases|April 25, 2025
Liver function in X-linked myotubular myopathy and autosomal dominant centronuclear myopathy: Data of the unite-CNM studyS Colombo, B S Cowling, L Eyler, et al.
Neuromuscular Disorders : NMD|November 6, 2017
Early onset facioscapulohumeral dystrophy - a systematic review using individual patient dataRianne J M Goselink, Nicol C Voermans, Kees Okkersen, et al.
British Journal of Anaesthesia|January 31, 2025
Pathogenicity assessment of seven RYR1 variants in patients with confirmed susceptibility to malignant hyperthermia in the NetherlandsLuuk R van den Bersselaar, Anja H Schiemann, Chu-Ya Yang, et al.
Disability and Rehabilitation|September 27, 2023
Psychosocial functioning in patients with altered facial expression: a scoping review in five neurological diseasesNathaniël B Rasing, Willianne van de Geest-Buit, On Ying A Chan, et al.
Genes|September 27, 2025
Rhabdomyolysis in the Era of Next-Generation Sequencing: Selecting Patients with a High Likelihood of a Genetic Susceptibility Using 'RHABDO' FeaturesNick Kruijt, Sanne A J H van de Camp, Jasper J Kramer, et al.
Acta Neurologica Scandinavica|April 11, 2018
Phenotype and genotype of muscle ryanodine receptor rhabdomyolysis-myalgia syndromeN Witting, P Laforêt, N C Voermans, et al.
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.
Pageof 35