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Brain Research Bulletin|December 17, 2025
Neural damage and inflammation in myotonic dystrophy type 1: Longitudinal analysis of serum NFL, GFAP, and IL-6Joana Garmendia, Garazi Labayru, Ainhoa Alberro, et al.Developmental Neuropsychology|June 29, 2021
Small for Gestational Age Moderate to Late Preterm Children: A Neuropsychological Follow-upGarazi Labayru, Jone Aliri, Andrea Santos, et al.Neuroimage. Clinical|December 5, 2019
Regional brain atrophy in gray and white matter is associated with cognitive impairment in Myotonic Dystrophy type 1Garazi Labayru, Ibai Diez, Jorge Sepulcre, et al.Journal of Neuromuscular Diseases|March 22, 2024
Patient-Reported Outcome Measures in Neuromuscular Diseases: A Scoping ReviewNicoline Voet, Ronne Pater, Joana Garmendia, et al.Scientific Reports|March 8, 2022
White matter integrity changes and neurocognitive functioning in adult-late onset DM1: a follow-up DTI studyGarazi Labayru, Borja Camino, Antonio Jimenez-Marin, et al.Annals of Clinical and Translational Neurology|September 4, 2020
Neurodegeneration trajectory in pediatric and adult/late DM1: A follow-up MRI study across a decadeGarazi Labayru, Antonio Jimenez-Marin, Esther Fernández, et al.Neuropathology and Applied Neurobiology|May 6, 2021
Transcriptional signatures of synaptic vesicle genes define myotonic dystrophy type I neurodegenerationAntonio Jimenez-Marin, Ibai Diez, Garazi Labayru, 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.Pageof 2