Publicaciones en las que colabora con Garazi Labayru Isuzquiza (17)
2024
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Altered tubulin detyrosination due to SVBP malfunction induces cytokinesis failure and senescence, underlying a complex hereditary spastic paraplegia
Aging Cell
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CNS involvement in myotonic dystrophy type 1: does sex play a role?
Frontiers in Neurology , Vol. 15
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Patient-Reported Outcome Measures in Neuromuscular Diseases: A Scoping Review
Journal of neuromuscular diseases, Vol. 11, Núm. 3, pp. 567-577
2023
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267th ENMC International workshop: psychological interventions for improving quality of life in slowly progressive neuromuscular disorders
Neuromuscular Disorders
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Executive functions and daily functioning in myotonic dystrophy type 1 ecological assessment with virtual reality
Neuromuscular Disorders, Vol. 33, Núm. 12, pp. 917-922
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Shedding light on motor premanifest myotonic dystrophy type 1: A molecular, muscular and central nervous system follow-up study
European Journal of Neurology, Vol. 30, Núm. 1, pp. 215-223
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Visuoconstructional impairment in DM1: exploring underlying cognitive processes through the Rey complex figure
Journal of Clinical and Experimental Neuropsychology, Vol. 45, Núm. 6, pp. 597-605
2022
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A validated WAIS-IV short-form to estimate intellectual functioning in myotonic dystrophy type 1
Neuromuscular Disorders, Vol. 32, Núm. 9, pp. 749-753
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Muturreko goiztiarren profil neuropsikologikoaren luzetarako azterketa
Uztaro: giza eta gizarte-zientzien aldizkaria, Núm. 121, pp. 137-152
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White matter integrity changes and neurocognitive functioning in adult-late onset DM1: a follow-up DTI study
Scientific reports, Vol. 12, Núm. 1, pp. 3988
2021
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A Validated WISC-V Short-Form to Estimate Intellectual Functioning in Very Preterm Children at Early School Age
Frontiers in Psychology, Vol. 12
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Small for Gestational Age Moderate to Late Preterm Children: A Neuropsychological Follow-up
Developmental Neuropsychology, Vol. 46, Núm. 4, pp. 277-287
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Transcriptional signatures of synaptic vesicle genes define myotonic dystrophy type I neurodegeneration
Neuropathology and Applied Neurobiology, Vol. 47, Núm. 7, pp. 1092-1108
2020
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Age-related cognitive decline in myotonic dystrophy type 1: An 11-year longitudinal follow-up study
Journal of Neuropsychology, Vol. 14, Núm. 1, pp. 121-134
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Neurodegeneration trajectory in pediatric and adult/late DM1: A follow-up MRI study across a decade
Annals of Clinical and Translational Neurology, Vol. 7, Núm. 10, pp. 1802-1815
2019
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Regional brain atrophy in gray and white matter is associated with cognitive impairment in Myotonic Dystrophy type 1
NeuroImage: Clinical, Vol. 24
2018
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Social cognition in myotonic dystrophy type 1: Specific or secondary impairment?
PLoS ONE, Vol. 13, Núm. 9