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Nicol C Voermans

Showing results (1-10 of 218) with videos related to

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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|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
Muscle & Nerve|July 23, 2024
Diagnostic workup of rhabdomyolysis: Genetic testing should precede neurophysiological testingNicol C Voermans, Salman Bhai, Pascal Laforet, et al.
Journal of Pain and Symptom Management|April 5, 2011
High frequency of neuropathic pain in Ehlers-Danlos syndrome: an association with axonal polyneuropathy and compression neuropathy?Nicol C Voermans, Hans Knoop, Baziel G van Engelen
The Lancet. Neurology|November 17, 2023
Gene therapy for X-linked myotubular myopathy: the challengesNicol C Voermans, Ana Ferreiro, Annemieke Aartsema-Rus, et al.
Pageof 22

Showing results (1-10 of 218) with videos related to

Sort By:
Pageof 22
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|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
Muscle & Nerve|July 23, 2024
Diagnostic workup of rhabdomyolysis: Genetic testing should precede neurophysiological testingNicol C Voermans, Salman Bhai, Pascal Laforet, et al.
Journal of Pain and Symptom Management|April 5, 2011
High frequency of neuropathic pain in Ehlers-Danlos syndrome: an association with axonal polyneuropathy and compression neuropathy?Nicol C Voermans, Hans Knoop, Baziel G van Engelen
The Lancet. Neurology|November 17, 2023
Gene therapy for X-linked myotubular myopathy: the challengesNicol C Voermans, Ana Ferreiro, Annemieke Aartsema-Rus, et al.
Pageof 22