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Alba Ramos

Showing results (21-30 of 40) with videos related to

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Frontiers in Chemistry|January 23, 2023
Chemically diverse activity-based probes with unexpected inhibitory mechanisms targeting trypsin-like serine proteasesAlba Ramos-Llorca, Lisse Decraecker, Valérie M Y Cacheux, et al.
Neurology. Genetics|August 18, 2020
Three-dimensional imaging in myotonic dystrophy type 1: Linking molecular alterations with disease phenotypeAlfonsina Ballester-Lopez, Judit Núñez-Manchón, Emma Koehorst, et al.
Genes|July 11, 2020
The Need for Establishing a Universal CTG Sizing Method in Myotonic Dystrophy Type 1Alfonsina Ballester-Lopez, Ian Linares-Pardo, Emma Koehorst, et al.
Journal of the American Heart Association|November 22, 2024
Dispersion of Activation in Single-Beat Global Maps During Programmed Ventricular Stimulation Identifies Infarct-Related Ventricular Tachycardia Isthmus SitesAndrés Redondo-Rodríguez, Alba Ramos-Prada, Jorge G Quintanilla, et al.
Stroke (Hoboken, N.J.)|January 26, 2026
Prognostic Accuracy of N20 Somatosensory Potential in Patients With Acute Ischemic Stroke and Endovascular ThrombectomyAlicia Martinez-Piñeiro, Giuseppe Lucente, María Hernandez-Perez, et al.
Biomedicines|June 24, 2022
An Integrative Analysis of DNA Methylation Pattern in Myotonic Dystrophy Type 1 Samples Reveals a Distinct DNA Methylation Profile between Tissues and a Novel Muscle-Associated Epigenetic DysregulationEmma Koehorst, Renato Odria, Júlia Capó, et al.
Journal of Inherited Metabolic Disease|June 22, 2018
Manifesting heterozygotes in McArdle disease: a myth or a reality-role of statinsJudit Núñez-Manchón, Alfonsina Ballester-Lopez, Emma Koehorst, et al.
Journal of Inherited Metabolic Disease|July 22, 2018
Correction to: Manifesting heterozygotes in McArdle disease: a myth or a reality-role of statinsJudit Núñez-Manchón, Alfonsina Ballester-Lopez, Emma Koehorst, et al.
Human Mutation|October 15, 2019
A DM1 family with interruptions associated with atypical symptoms and late onset but not with a milder phenotypeAlfonsina Ballester-Lopez, Emma Koehorst, Miriam Almendrote, et al.
Annals of Clinical and Translational Neurology|January 26, 2022
Drug-refractory myasthenia gravis: Clinical characteristics, treatments, and outcomeElena Cortés-Vicente, Rodrigo Álvarez-Velasco, Francesc Pla-Junca, et al.
Pageof 4

Showing results (21-30 of 40) with videos related to

Sort By:
Pageof 4
Frontiers in Chemistry|January 23, 2023
Chemically diverse activity-based probes with unexpected inhibitory mechanisms targeting trypsin-like serine proteasesAlba Ramos-Llorca, Lisse Decraecker, Valérie M Y Cacheux, et al.
Neurology. Genetics|August 18, 2020
Three-dimensional imaging in myotonic dystrophy type 1: Linking molecular alterations with disease phenotypeAlfonsina Ballester-Lopez, Judit Núñez-Manchón, Emma Koehorst, et al.
Genes|July 11, 2020
The Need for Establishing a Universal CTG Sizing Method in Myotonic Dystrophy Type 1Alfonsina Ballester-Lopez, Ian Linares-Pardo, Emma Koehorst, et al.
Journal of the American Heart Association|November 22, 2024
Dispersion of Activation in Single-Beat Global Maps During Programmed Ventricular Stimulation Identifies Infarct-Related Ventricular Tachycardia Isthmus SitesAndrés Redondo-Rodríguez, Alba Ramos-Prada, Jorge G Quintanilla, et al.
Stroke (Hoboken, N.J.)|January 26, 2026
Prognostic Accuracy of N20 Somatosensory Potential in Patients With Acute Ischemic Stroke and Endovascular ThrombectomyAlicia Martinez-Piñeiro, Giuseppe Lucente, María Hernandez-Perez, et al.
Biomedicines|June 24, 2022
An Integrative Analysis of DNA Methylation Pattern in Myotonic Dystrophy Type 1 Samples Reveals a Distinct DNA Methylation Profile between Tissues and a Novel Muscle-Associated Epigenetic DysregulationEmma Koehorst, Renato Odria, Júlia Capó, et al.
Journal of Inherited Metabolic Disease|June 22, 2018
Manifesting heterozygotes in McArdle disease: a myth or a reality-role of statinsJudit Núñez-Manchón, Alfonsina Ballester-Lopez, Emma Koehorst, et al.
Journal of Inherited Metabolic Disease|July 22, 2018
Correction to: Manifesting heterozygotes in McArdle disease: a myth or a reality-role of statinsJudit Núñez-Manchón, Alfonsina Ballester-Lopez, Emma Koehorst, et al.
Human Mutation|October 15, 2019
A DM1 family with interruptions associated with atypical symptoms and late onset but not with a milder phenotypeAlfonsina Ballester-Lopez, Emma Koehorst, Miriam Almendrote, et al.
Annals of Clinical and Translational Neurology|January 26, 2022
Drug-refractory myasthenia gravis: Clinical characteristics, treatments, and outcomeElena Cortés-Vicente, Rodrigo Álvarez-Velasco, Francesc Pla-Junca, et al.
Pageof 4