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C Voermans

Showing results (1-10 of 344) with videos related to

Pageof 35
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Neuromuscular Disorders : NMD|April 2, 2026
The importance of patient engagement in scientific research on facioscapulohumeral muscular dystrophyNicol C Voermans
Current Opinion in Neurology|August 19, 2016
Congenital myopathies: not only a paediatric topicHeinz Jungbluth, Nicol C Voermans
Disability and Rehabilitation|November 17, 2010
Both pain and fatigue are important possible determinants of disability in patients with the Ehlers-Danlos syndrome hypermobility typeNicol C Voermans, Hans Knoop
Iranian Journal of Neurology|January 30, 2015
Neurological manifestations of Ehlers-Danlos syndrome(s): A reviewMarco Castori, Nicol C Voermans
Neurology|March 27, 2019
Author response: A family-based study into penetrance in facioscapulohumeral muscular dystrophy type 1Nicol C Voermans, Rianne J Goselink
Neuromuscular Disorders : NMD|September 26, 2008
Differential diagnosis of muscular hypotonia in infants: the kyphoscoliotic type of Ehlers-Danlos syndrome (EDS VI)N C Voermans, B G van Engelen
Revue Neurologique|September 25, 2016
RYR1-related rhabdomyolysis: A common but probably underdiagnosed manifestation of skeletal muscle ryanodine receptor dysfunctionN C Voermans, M Snoeck, H Jungbluth
Neuromuscular Disorders : NMD|August 9, 2011
Coffee and muscle crampsN C Voermans, B G van Engelen
Neuromuscular Disorders : NMD|November 26, 2025
Meeting report: The FSHD society 2025 international research congressLucienne Ronco, Stephen Tapscott, Nicol C Voermans, et al.
European Journal of Medical Genetics|March 1, 2015
Facioscapulohumeral muscular dystrophy as a genetic cause of pectus excavatumKarlien Mul, George W Padberg, Nicol C Voermans
Pageof 35

Showing results (1-10 of 344) with videos related to

Sort By:
Pageof 35
Neuromuscular Disorders : NMD|April 2, 2026
The importance of patient engagement in scientific research on facioscapulohumeral muscular dystrophyNicol C Voermans
Current Opinion in Neurology|August 19, 2016
Congenital myopathies: not only a paediatric topicHeinz Jungbluth, Nicol C Voermans
Disability and Rehabilitation|November 17, 2010
Both pain and fatigue are important possible determinants of disability in patients with the Ehlers-Danlos syndrome hypermobility typeNicol C Voermans, Hans Knoop
Iranian Journal of Neurology|January 30, 2015
Neurological manifestations of Ehlers-Danlos syndrome(s): A reviewMarco Castori, Nicol C Voermans
Neurology|March 27, 2019
Author response: A family-based study into penetrance in facioscapulohumeral muscular dystrophy type 1Nicol C Voermans, Rianne J Goselink
Neuromuscular Disorders : NMD|September 26, 2008
Differential diagnosis of muscular hypotonia in infants: the kyphoscoliotic type of Ehlers-Danlos syndrome (EDS VI)N C Voermans, B G van Engelen
Revue Neurologique|September 25, 2016
RYR1-related rhabdomyolysis: A common but probably underdiagnosed manifestation of skeletal muscle ryanodine receptor dysfunctionN C Voermans, M Snoeck, H Jungbluth
Neuromuscular Disorders : NMD|August 9, 2011
Coffee and muscle crampsN C Voermans, B G van Engelen
Neuromuscular Disorders : NMD|November 26, 2025
Meeting report: The FSHD society 2025 international research congressLucienne Ronco, Stephen Tapscott, Nicol C Voermans, et al.
European Journal of Medical Genetics|March 1, 2015
Facioscapulohumeral muscular dystrophy as a genetic cause of pectus excavatumKarlien Mul, George W Padberg, Nicol C Voermans
Pageof 35