ADOLFO JOSE
LOPEZ DE MUNAIN ARREGUI
IRAKASLE ELKARTUA
Myriam
Barandiaran Amillano
Myriam Barandiaran Amillano-rekin lankidetzan egindako argitalpenak (12)
2024
2019
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Longitudinal neuropsychological study of presymptomatic c.709-1G>A progranulin mutation carriers
Journal of the International Neuropsychological Society, Vol. 25, Núm. 1, pp. 39-47
2018
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Blood Markers in Healthy-Aged Nonagenarians: A Combination of High Telomere Length and Low Amyloidβ Are Strongly Associated With Healthy Aging in the Oldest Old
Frontiers in Aging Neuroscience, Vol. 10
2017
2015
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MAPT H1 haplotype is associated with late-onset Alzheimer's disease risk in APOE ε 4 noncarriers: Results from the dementia genetics Spanish consortium
Journal of Alzheimer's Disease, Vol. 49, Núm. 2, pp. 343-352
2014
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Cognitive dysfunction in Parkinson's disease related to the R1441G mutation in LRRK2
Parkinsonism and Related Disorders, Vol. 20, Núm. 10, pp. 1097-1100
2013
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Distinctive age-related temporal cortical thinning in asymptomatic granulin gene mutation carriers
Neurobiology of Aging, Vol. 34, Núm. 5, pp. 1462-1468
2012
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Neuropsychological features of asymptomatic c.709-1G>A progranulin mutation carriers
Journal of the International Neuropsychological Society, Vol. 18, Núm. 6, pp. 1086-1090
2011
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Prion protein codon 129 polymorphism modifies age at onset of frontotemporal dementia with the C.709-1G>a progranulin mutation
Alzheimer Disease and Associated Disorders, Vol. 25, Núm. 1, pp. 93-95
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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Frontotemporoparietal dementia: Clinical phenotype associated with the c.709-1G>A PGRN mutation
Neurology, Vol. 73, Núm. 17, pp. 1367-1374
2008
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Mutations in Progranulin Gene: Clinical, Pathological, and Ribonucleic Acid Expression Findings
Biological Psychiatry, Vol. 63, Núm. 10, pp. 946-952