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C Voermans

Showing results (281-290 of 344) with videos related to

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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.
Brain Communications|October 5, 2022
Targeted transcript analysis in muscles from patients with genetically diverse congenital myopathiesChristoph Bachmann, Martina Franchini, Luuk R Van den Bersselaar, et al.
BMC Neurology|August 18, 2016
Facioscapulohumeral dystrophy in children: design of a prospective, observational study on natural history, predictors and clinical impact (iFocus FSHD)Rianne J M Goselink, Tim H A Schreuder, Karlien Mul, et al.
American Journal of Medical Genetics. Part A|July 3, 2024
Nerve enlargement in patients with Noonan syndrome: A retrospective cohort studyFieke Draaisma, Erika K S M Leenders, Corrie E Erasmus, et al.
Clinical Genetics|August 31, 2021
Clinical, genetic, and histological features of centronuclear myopathy in the NetherlandsStacha F I Reumers, Corrie E Erasmus, Karlijn Bouman, et al.
Viruses|September 5, 2020
Inter-Laboratory Reproducibility of Inducible HIV-1 Reservoir Quantification by TILDACynthia Lungu, Francesco A Procopio, Ronald J Overmars, et al.
Journal of Neuromuscular Diseases|May 8, 2023
Muscle Ultrasound Abnormalities in Individuals with RYR1-Related Malignant Hyperthermia SusceptibilityLuuk R van den Bersselaar, Nens van Alfen, Nick Kruijt, et al.
Medicine|August 20, 2021
The neuromuscular and multisystem features of RYR1-related malignant hyperthermia and rhabdomyolysis: A study protocolLuuk R van den Bersselaar, Nick Kruijt, Gert-Jan Scheffer, 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.
Human Mutation|April 2, 2019
Aberrant regulation of epigenetic modifiers contributes to the pathogenesis in patients with selenoprotein N-related myopathiesChristoph Bachmann, Faiza Noreen, Nicol C Voermans, et al.
Pageof 35

Showing results (281-290 of 344) with videos related to

Sort By:
Pageof 35
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.
Brain Communications|October 5, 2022
Targeted transcript analysis in muscles from patients with genetically diverse congenital myopathiesChristoph Bachmann, Martina Franchini, Luuk R Van den Bersselaar, et al.
BMC Neurology|August 18, 2016
Facioscapulohumeral dystrophy in children: design of a prospective, observational study on natural history, predictors and clinical impact (iFocus FSHD)Rianne J M Goselink, Tim H A Schreuder, Karlien Mul, et al.
American Journal of Medical Genetics. Part A|July 3, 2024
Nerve enlargement in patients with Noonan syndrome: A retrospective cohort studyFieke Draaisma, Erika K S M Leenders, Corrie E Erasmus, et al.
Clinical Genetics|August 31, 2021
Clinical, genetic, and histological features of centronuclear myopathy in the NetherlandsStacha F I Reumers, Corrie E Erasmus, Karlijn Bouman, et al.
Viruses|September 5, 2020
Inter-Laboratory Reproducibility of Inducible HIV-1 Reservoir Quantification by TILDACynthia Lungu, Francesco A Procopio, Ronald J Overmars, et al.
Journal of Neuromuscular Diseases|May 8, 2023
Muscle Ultrasound Abnormalities in Individuals with RYR1-Related Malignant Hyperthermia SusceptibilityLuuk R van den Bersselaar, Nens van Alfen, Nick Kruijt, et al.
Medicine|August 20, 2021
The neuromuscular and multisystem features of RYR1-related malignant hyperthermia and rhabdomyolysis: A study protocolLuuk R van den Bersselaar, Nick Kruijt, Gert-Jan Scheffer, 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.
Human Mutation|April 2, 2019
Aberrant regulation of epigenetic modifiers contributes to the pathogenesis in patients with selenoprotein N-related myopathiesChristoph Bachmann, Faiza Noreen, Nicol C Voermans, et al.
Pageof 35