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Showing results (61-70 of 83) with videos related to

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Muscle & Nerve|February 18, 2022
Cardiac and pulmonary findings in dysferlinopathy: A 3-year, longitudinal studyUrsula Moore, Roberto Fernandez-Torron, Marni Jacobs, et al.
Brain : a Journal of Neurology|July 24, 2024
Decoding the muscle transcriptome of patients with late-onset Pompe disease reveals markers of disease progressionAlexandra Monceau, Rasya Gokul Nath, Xavier Suárez-Calvet, et al.
Neurology|February 20, 2020
Clinical and therapeutic features of myasthenia gravis in adults based on age at onsetElena Cortés-Vicente, Rodrigo Álvarez-Velasco, Sonia Segovia, et al.
European Journal of Neurology|March 15, 2021
Clinical characteristics and outcomes of thymoma-associated myasthenia gravisRodrigo Álvarez-Velasco, Gerardo Gutiérrez-Gutiérrez, Juan Carlos Trujillo, et al.
Brain : a Journal of Neurology|March 13, 2023
Anoctamin-5 related muscle disease: clinical and genetic findings in a large European cohortAlexander de Bruyn, Federica Montagnese, Sonja Holm-Yildiz, et al.
Neurology. Genetics|September 8, 2016
The Clinical Outcome Study for dysferlinopathy: An international multicenter studyElizabeth Harris, Catherine L Bladen, Anna Mayhew, et al.
Orphanet Journal of Rare Diseases|February 14, 2024
EURO-NMD registry: federated FAIR infrastructure, innovative technologies and concepts of a patient-centred registry for rare neuromuscular disordersAntonio Atalaia, Dagmar Wandrei, Nawel Lalout, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 31, 2018
Teenage exercise is associated with earlier symptom onset in dysferlinopathy: a retrospective cohort studyUrsula R Moore, Marni Jacobs, Roberto Fernandez-Torron, et al.
Brain : a Journal of Neurology|November 12, 2024
HMGCS1 variants cause rigid spine syndrome amenable to mevalonic acid treatment in an animal modelLein N H Dofash, Lee B Miles, Yoshihiko Saito, et al.
Journal of Neuromuscular Diseases|July 29, 2025
Real-world data on spinal muscular atrophy in Spain: Insights from over 500 individuals in the CuidAME projectCristina Puig-Ram, Sonia Segovia, Rocio Garcia-Uzquiano, et al.
Pageof 9

Showing results (61-70 of 83) with videos related to

Sort By:
Pageof 9
Muscle & Nerve|February 18, 2022
Cardiac and pulmonary findings in dysferlinopathy: A 3-year, longitudinal studyUrsula Moore, Roberto Fernandez-Torron, Marni Jacobs, et al.
Brain : a Journal of Neurology|July 24, 2024
Decoding the muscle transcriptome of patients with late-onset Pompe disease reveals markers of disease progressionAlexandra Monceau, Rasya Gokul Nath, Xavier Suárez-Calvet, et al.
Neurology|February 20, 2020
Clinical and therapeutic features of myasthenia gravis in adults based on age at onsetElena Cortés-Vicente, Rodrigo Álvarez-Velasco, Sonia Segovia, et al.
European Journal of Neurology|March 15, 2021
Clinical characteristics and outcomes of thymoma-associated myasthenia gravisRodrigo Álvarez-Velasco, Gerardo Gutiérrez-Gutiérrez, Juan Carlos Trujillo, et al.
Brain : a Journal of Neurology|March 13, 2023
Anoctamin-5 related muscle disease: clinical and genetic findings in a large European cohortAlexander de Bruyn, Federica Montagnese, Sonja Holm-Yildiz, et al.
Neurology. Genetics|September 8, 2016
The Clinical Outcome Study for dysferlinopathy: An international multicenter studyElizabeth Harris, Catherine L Bladen, Anna Mayhew, et al.
Orphanet Journal of Rare Diseases|February 14, 2024
EURO-NMD registry: federated FAIR infrastructure, innovative technologies and concepts of a patient-centred registry for rare neuromuscular disordersAntonio Atalaia, Dagmar Wandrei, Nawel Lalout, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 31, 2018
Teenage exercise is associated with earlier symptom onset in dysferlinopathy: a retrospective cohort studyUrsula R Moore, Marni Jacobs, Roberto Fernandez-Torron, et al.
Brain : a Journal of Neurology|November 12, 2024
HMGCS1 variants cause rigid spine syndrome amenable to mevalonic acid treatment in an animal modelLein N H Dofash, Lee B Miles, Yoshihiko Saito, et al.
Journal of Neuromuscular Diseases|July 29, 2025
Real-world data on spinal muscular atrophy in Spain: Insights from over 500 individuals in the CuidAME projectCristina Puig-Ram, Sonia Segovia, Rocio Garcia-Uzquiano, et al.
Pageof 9