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Sharon I de Vries

Showing results (1-10 of 12) with videos related to

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Cell Reports|January 4, 2019
High-Frequency Microdomain Ca<sup>2+</sup> Transients and Waves during Early Myelin Internode RemodelingArne Battefeld, Marko A Popovic, Sharon I de Vries, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 9, 2016
Covariation of axon initial segment location and dendritic tree normalizes the somatic action potentialMustafa S Hamada, Sarah Goethals, Sharon I de Vries, et al.
Cell Transplantation|September 28, 2011
Stem cells in burn escharVincent C van der Veen, Marcel Vlig, Florine J van Milligen, et al.
Medrxiv : the Preprint Server for Health Sciences|August 20, 2025
Creatine/creatinine ratio and myostatin as biomarkers to monitor muscle function in Duchenne Muscular Dystrophy patientsChiara Degan, Roula Tsonaka, Sharon I de Vries, et al.
Journal of Cachexia, Sarcopenia and Muscle|June 16, 2026
Creatine/Creatinine Ratio and Myostatin as Biomarkers to Monitor Muscle Function in Duchenne Muscular Dystrophy PatientsChiara Degan, Roula Tsonaka, Sharon I de Vries, et al.
Human Molecular Genetics|September 22, 2018
Loss of CRB2 in Müller glial cells modifies a CRB1-associated retinitis pigmentosa phenotype into a Leber congenital amaurosis phenotypePeter M Quinn, Aat A Mulder, C Henrique Alves, et al.
Annals of Clinical and Translational Neurology|April 25, 2018
Axonal abnormalities in vanishing white matterMelanie D Klok, Marianna Bugiani, Sharon I de Vries, et al.
Acta Neuropathologica|June 25, 2021
Complement-associated loss of CA2 inhibitory synapses in the demyelinated hippocampus impairs memoryValeria Ramaglia, Mohit Dubey, M Alfonso Malpede, et al.
Medrxiv : the Preprint Server for Health Sciences|January 8, 2026
Evaluation of a serum protein signature as monitoring biomarker for Duchenne Muscular Dystrophy in a long-term clinical trial with corticosteroidsChiara Degan, Rebecca A Tobin, Sharon I de Vries, et al.
Scientific Reports|November 14, 2025
Circulating protein biomarkers identified in two independent clinical trial cohorts of glucocorticoid-naive Duchenne muscular dystrophy patientsFatemeh Ahmadiharchegani, Rebecca A Tobin, Chiara Degan, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Cell Reports|January 4, 2019
High-Frequency Microdomain Ca<sup>2+</sup> Transients and Waves during Early Myelin Internode RemodelingArne Battefeld, Marko A Popovic, Sharon I de Vries, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 9, 2016
Covariation of axon initial segment location and dendritic tree normalizes the somatic action potentialMustafa S Hamada, Sarah Goethals, Sharon I de Vries, et al.
Cell Transplantation|September 28, 2011
Stem cells in burn escharVincent C van der Veen, Marcel Vlig, Florine J van Milligen, et al.
Medrxiv : the Preprint Server for Health Sciences|August 20, 2025
Creatine/creatinine ratio and myostatin as biomarkers to monitor muscle function in Duchenne Muscular Dystrophy patientsChiara Degan, Roula Tsonaka, Sharon I de Vries, et al.
Journal of Cachexia, Sarcopenia and Muscle|June 16, 2026
Creatine/Creatinine Ratio and Myostatin as Biomarkers to Monitor Muscle Function in Duchenne Muscular Dystrophy PatientsChiara Degan, Roula Tsonaka, Sharon I de Vries, et al.
Human Molecular Genetics|September 22, 2018
Loss of CRB2 in Müller glial cells modifies a CRB1-associated retinitis pigmentosa phenotype into a Leber congenital amaurosis phenotypePeter M Quinn, Aat A Mulder, C Henrique Alves, et al.
Annals of Clinical and Translational Neurology|April 25, 2018
Axonal abnormalities in vanishing white matterMelanie D Klok, Marianna Bugiani, Sharon I de Vries, et al.
Acta Neuropathologica|June 25, 2021
Complement-associated loss of CA2 inhibitory synapses in the demyelinated hippocampus impairs memoryValeria Ramaglia, Mohit Dubey, M Alfonso Malpede, et al.
Medrxiv : the Preprint Server for Health Sciences|January 8, 2026
Evaluation of a serum protein signature as monitoring biomarker for Duchenne Muscular Dystrophy in a long-term clinical trial with corticosteroidsChiara Degan, Rebecca A Tobin, Sharon I de Vries, et al.
Scientific Reports|November 14, 2025
Circulating protein biomarkers identified in two independent clinical trial cohorts of glucocorticoid-naive Duchenne muscular dystrophy patientsFatemeh Ahmadiharchegani, Rebecca A Tobin, Chiara Degan, et al.
Pageof 2