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C Voermans

Showing results (221-230 of 344) with videos related to

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Neuromuscular Disorders : NMD|December 23, 2018
Functional impairments, fatigue and quality of life in RYR1-related myopathies: A questionnaire studyE van Ruitenbeek, J A E Custers, C Verhaak, et al.
International Journal of Microbiology|February 27, 2023
Standardization of SARS-CoV-2 Nucleic Acid Amplification Techniques by Calibration and Quantification to the First WHO International Standard for SARS-CoV-2 RNAJolanda J C Voermans, Daphne G J C Mulders, Rob J J Beerkens, et al.
Journal of Neuromuscular Diseases|November 21, 2022
RYR-1-Related Diseases International Research Workshop: From Mechanisms to Treatments Pittsburgh, PA, U.S.A., 21-22 July 2022Thomas N O'Connor, Luuk R van den Bersselaar, Yu Seby Chen, et al.
Scientific Reports|January 27, 2022
Facioscapulohumeral dystrophy transcriptome signatures correlate with different stages of disease and are marked by different MRI biomarkersAnita van den Heuvel, Saskia Lassche, Karlien Mul, et al.
Neurology|October 22, 2021
Natural History of Facioscapulohumeral Dystrophy in Children: A 2-Year Follow-upJildou N Dijkstra, Rianne J M Goselink, Nens van Alfen, et al.
European Journal of Neurology|September 26, 2020
The etiology of rhabdomyolysis: an interaction between genetic susceptibility and external triggersN Kruijt, L R van den Bersselaar, E J Kamsteeg, et al.
Neurology|January 23, 2020
Preserved single muscle fiber specific force in facioscapulohumeral muscular dystrophySaskia Lassche, Nicol C Voermans, Robbert van der Pijl, et al.
Neuromuscular Disorders : NMD|January 14, 2017
The yield of diagnostic work-up of patients presenting with myalgia, exercise intolerance, or fatigue: A prospective observational studyM G E Te Riele, T H A Schreuder, N van Alfen, et al.
Disability and Rehabilitation|May 18, 2026
Congenital myopathies in adult patients: lived experiences and coping mechanismsLizan Stinissen, Erin Peet, Sanne A J H van de Camp, et al.
Journal of Neuromuscular Diseases|August 23, 2024
Cardiac Involvement in LAMA2-Related Muscular Dystrophy and SELENON-Related Congenital Myopathy: A Case SeriesKarlijn Bouman, Frederik M A van den Heuvel, Reinder Evertz, et al.
Pageof 35

Showing results (221-230 of 344) with videos related to

Sort By:
Pageof 35
Neuromuscular Disorders : NMD|December 23, 2018
Functional impairments, fatigue and quality of life in RYR1-related myopathies: A questionnaire studyE van Ruitenbeek, J A E Custers, C Verhaak, et al.
International Journal of Microbiology|February 27, 2023
Standardization of SARS-CoV-2 Nucleic Acid Amplification Techniques by Calibration and Quantification to the First WHO International Standard for SARS-CoV-2 RNAJolanda J C Voermans, Daphne G J C Mulders, Rob J J Beerkens, et al.
Journal of Neuromuscular Diseases|November 21, 2022
RYR-1-Related Diseases International Research Workshop: From Mechanisms to Treatments Pittsburgh, PA, U.S.A., 21-22 July 2022Thomas N O'Connor, Luuk R van den Bersselaar, Yu Seby Chen, et al.
Scientific Reports|January 27, 2022
Facioscapulohumeral dystrophy transcriptome signatures correlate with different stages of disease and are marked by different MRI biomarkersAnita van den Heuvel, Saskia Lassche, Karlien Mul, et al.
Neurology|October 22, 2021
Natural History of Facioscapulohumeral Dystrophy in Children: A 2-Year Follow-upJildou N Dijkstra, Rianne J M Goselink, Nens van Alfen, et al.
European Journal of Neurology|September 26, 2020
The etiology of rhabdomyolysis: an interaction between genetic susceptibility and external triggersN Kruijt, L R van den Bersselaar, E J Kamsteeg, et al.
Neurology|January 23, 2020
Preserved single muscle fiber specific force in facioscapulohumeral muscular dystrophySaskia Lassche, Nicol C Voermans, Robbert van der Pijl, et al.
Neuromuscular Disorders : NMD|January 14, 2017
The yield of diagnostic work-up of patients presenting with myalgia, exercise intolerance, or fatigue: A prospective observational studyM G E Te Riele, T H A Schreuder, N van Alfen, et al.
Disability and Rehabilitation|May 18, 2026
Congenital myopathies in adult patients: lived experiences and coping mechanismsLizan Stinissen, Erin Peet, Sanne A J H van de Camp, et al.
Journal of Neuromuscular Diseases|August 23, 2024
Cardiac Involvement in LAMA2-Related Muscular Dystrophy and SELENON-Related Congenital Myopathy: A Case SeriesKarlijn Bouman, Frederik M A van den Heuvel, Reinder Evertz, et al.
Pageof 35