Search research articles
Contact Us
Filters
Showing results (21-30 of 40) with videos related to
Page
of 4
Sort By:
Frontiers in Chemistry
|
January 23, 2023
Chemically diverse activity-based probes with unexpected inhibitory mechanisms targeting trypsin-like serine proteases
Alba 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 phenotype
Alfonsina 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 1
Alfonsina 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 Sites
Andrés 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 Thrombectomy
Alicia 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 Dysregulation
Emma 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 statins
Judit 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 statins
Judit 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 phenotype
Alfonsina 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 outcome
Elena Cortés-Vicente, Rodrigo Álvarez-Velasco, Francesc Pla-Junca, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 40) with videos related to
Sort By:
Page
of 4
Frontiers in Chemistry
|
January 23, 2023
Chemically diverse activity-based probes with unexpected inhibitory mechanisms targeting trypsin-like serine proteases
Alba 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 phenotype
Alfonsina 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 1
Alfonsina 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 Sites
Andrés 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 Thrombectomy
Alicia 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 Dysregulation
Emma 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 statins
Judit 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 statins
Judit 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 phenotype
Alfonsina 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 outcome
Elena Cortés-Vicente, Rodrigo Álvarez-Velasco, Francesc Pla-Junca, et al.
Page
of 4