Begona Indakoetxea

San Sebastian, PV, Spain

Last Updated: 09/26/2026

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Found 10 publications

Correction to: A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity.

Correction to: A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity.

Journal: Acta neuropathologica

Published: January 20, 2020

Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study.

Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study.

Journal: The Lancet. Neurology

Published: May 21, 2019

A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity.

A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity.

Journal: Acta neuropathologica

Published: March 23, 2019

Longitudinal Neuropsychological Study of Presymptomatic c.709-1G>A Progranulin Mutation Carriers.

Longitudinal Neuropsychological Study of Presymptomatic c.709-1G>A Progranulin Mutation Carriers.

Journal: Journal of the International Neuropsychological Society : JINS

Published: October 30, 2018

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.

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.

Journal: Frontiers in aging neuroscience

Published: July 30, 2018

The unexpected co-occurrence of GRN and MAPT p.A152T in Basque families: Clinical and pathological characteristics.

The unexpected co-occurrence of GRN and MAPT p.A152T in Basque families: Clinical and pathological characteristics.

Journal: PloS one

Published: October 31, 2016

MAPT H1 Haplotype is Associated with Late-Onset Alzheimer's Disease Risk in APOEɛ4 Noncarriers: Results from the Dementia Genetics Spanish Consortium.

MAPT H1 Haplotype is Associated with Late-Onset Alzheimer's Disease Risk in APOEɛ4 Noncarriers: Results from the Dementia Genetics Spanish Consortium.

Journal: Journal of Alzheimer's disease : JAD

Published: October 08, 2015

Investigation of the role of rare TREM2 variants in frontotemporal dementia subtypes.

Investigation of the role of rare TREM2 variants in frontotemporal dementia subtypes.

Journal: Neurobiology of aging

Published: April 28, 2014

Neuropsychological features of asymptomatic c.709-1G>A progranulin mutation carriers.

Neuropsychological features of asymptomatic c.709-1G>A progranulin mutation carriers.

Journal: Journal of the International Neuropsychological Society : JINS

Published: November 20, 2012

Distinctive age-related temporal cortical thinning in asymptomatic granulin gene mutation carriers.

Distinctive age-related temporal cortical thinning in asymptomatic granulin gene mutation carriers.

Journal: Neurobiology of aging

Published: March 20, 2012

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Last Updated: 09/26/2026