| human | Q5 |
| P496 | ORCID iD | 0000-0003-2511-0911 |
| P1053 | ResearcherID | L-4933-2014 |
| P108 | employer | University of the Basque Country | Q1232428 |
| P106 | occupation | researcher | Q1650915 |
| Q92588948 | Age-related cognitive decline in myotonic dystrophy type 1: An 11-year longitudinal follow-up study |
| Q48904473 | Cognitive function in facioscapulohumeral dystrophy correlates with the molecular defect. |
| Q47176340 | Cognitive/personality pattern and triplet expansion size in adult myotonic dystrophy type 1 (DM1): CTG repeats, cognition and personality in DM1. |
| Q48263880 | Distinctive age-related temporal cortical thinning in asymptomatic granulin gene mutation carriers. |
| Q79164457 | Genes related to iron metabolism and susceptibility to Alzheimer's disease in Basque population |
| Q38336368 | Mis-splicing of Tau exon 10 in myotonic dystrophy type 1 is reproduced by overexpression of CELF2 but not by MBNL1 silencing. |
| Q51563888 | Neurocognitive disorder detection based on feature vectors extracted from VBM analysis of structural MRI. |
| Q91642284 | Regional brain atrophy in gray and white matter is associated with cognitive impairment in Myotonic Dystrophy type 1 |
| Q58701414 | Social cognition in myotonic dystrophy type 1: Specific or secondary impairment? |
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