ADOLFO JOSÉ LÓPEZ DE MUNAIN ARREGUI-rekin lankidetzan egindako argitalpenak (21)
2023
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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
2022
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Senescence plays a role in myotonic dystrophy type 1
JCI insight, Vol. 7, Núm. 19
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Targeting Myotonic Dystrophy Type 1 with Metformin
International Journal of Molecular Sciences, Vol. 23, Núm. 5
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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
2020
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Leukocyte telomere length in patients with myotonic dystrophy type I: a pilot study
Annals of Clinical and Translational Neurology, Vol. 7, Núm. 1, pp. 126-131
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Myotonic Dystrophy type 1 cells display impaired metabolism and mitochondrial dysfunction that are reversed by metformin
Aging, Vol. 12, Núm. 7, pp. 6260-6275
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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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Encefalomielitis extensa por borrelia: Una forma atípica de neuroborreliosis
Revista de Neurologia, Vol. 68, Núm. 4, pp. 169-170
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T cells and immune functions of plasma extracellular vesicles are differentially modulated from adults to centenarians
Aging, Vol. 11, Núm. 22, pp. 10723-10741
2018
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Cancer phenotype in myotonic dystrophy patients: Results from a meta-analysis
Muscle and Nerve, Vol. 58, Núm. 4, pp. 517-522
2016
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Cancer risk in DM1 is sex-related and linked to miRNA-200/141 downregulation
Neurology, Vol. 87, Núm. 12, pp. 1250-1257
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Identification and Characterization of the Dermal Panniculus Carnosus Muscle Stem Cells
Stem Cell Reports, Vol. 7, Núm. 3, pp. 411-424
2015
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Muscle wasting in myotonic dystrophies: A model of premature aging
Frontiers in Aging Neuroscience, Vol. 7, Núm. JUN
2014
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A small noncoding RNA signature found in exosomes of GBM patient serum as a diagnostic tool
Neuro-Oncology, Vol. 16, Núm. 4, pp. 520-527
2012
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Oncogenicity of the developmental transcription factor Sox9
Cancer Research, Vol. 72, Núm. 5, pp. 1301-1315
2011
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Neurocognitive disorder detection based on feature vectors extracted from VBM analysis of structural MRI
Computers in Biology and Medicine, Vol. 41, Núm. 8, pp. 600-610
2010
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A Novel PRNP Y218N mutation in gerstmann-sträussler-scheinker disease with neurofibrillary degeneration
Journal of Neuropathology and Experimental Neurology, Vol. 69, Núm. 8, pp. 789-800
2009
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Neuropathology of Parkinson's disease with the R1441G mutation in LRRK2
Movement Disorders, Vol. 24, Núm. 13, pp. 1998-2001
2008
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Cerebrotendinous xanthomatosis: Neuropathological findings
Journal of Neurology, Vol. 255, Núm. 6, pp. 839-842
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Mutations in Progranulin Gene: Clinical, Pathological, and Ribonucleic Acid Expression Findings
Biological Psychiatry, Vol. 63, Núm. 10, pp. 946-952