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Annals of Clinical and Translational Neurology|December 7, 2019
Leukocyte telomere length in patients with myotonic dystrophy type I: a pilot studyYoujin Wang, Ana Best, Roberto Fernández-Torrón, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|April 7, 2022
A Ca2+-Dependent Mechanism Boosting Glycolysis and OXPHOS by Activating Aralar-Malate-Aspartate Shuttle, upon Neuronal StimulationIrene Pérez-Liébana, Inés Juaristi, Paloma González-Sánchez, et al.
Human Molecular Genetics|November 10, 2012
Expanded CTG repeats trigger miRNA alterations in Drosophila that are conserved in myotonic dystrophy type 1 patientsJuan M Fernandez-Costa, Amparo Garcia-Lopez, Sheila Zuñiga, et al.
Journal of Neuroimmunology|October 25, 2003
A genomic screen of Spanish multiple sclerosis patients reveals multiple loci associated with the diseaseRobert Goertsches, Pablo Villoslada, Manuel Comabella, et al.
Frontiers in Cell and Developmental Biology|April 14, 2022
Defects of Nutrient Signaling and Autophagy in NeurodegenerationJon Ondaro, Haizea Hernandez-Eguiazu, Maddi Garciandia-Arcelus, et al.
European Journal of Neurology|January 31, 2025
Small fiber neuropathy in the post-COVID condition and Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: Clinical significance and diagnostic challengesNaiara Azcue, Sara Teijeira-Portas, Beatriz Tijero-Merino, et al.
Aging Cell|October 16, 2024
Altered tubulin detyrosination due to SVBP malfunction induces cytokinesis failure and senescence, underlying a complex hereditary spastic paraplegiaNathalie Launay, Maria Espinosa-Alcantud, Edgard Verdura, et al.
European Journal of Human Genetics : EJHG|March 19, 2015
Double SMCHD1 variants in FSHD2: the synergistic effect of two SMCHD1 variants on D4Z4 hypomethylation and disease penetrance in FSHD2Marlinde L van den Boogaard, Richard J F L Lemmers, Pilar Camaño, et al.
Annals of Neurology|April 12, 2006
CAPN3 mutations in patients with idiopathic eosinophilic myositisMartin Krahn, Adolfo Lopez de Munain, Nathalie Streichenberger, et al.
Plos One|November 10, 2011
Genetic and epigenetic modifications of Sox2 contribute to the invasive phenotype of malignant gliomasMarta M Alonso, Ricardo Diez-Valle, Lorea Manterola, et al.
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