MIREN
ZULAICA IJURCO
Investigadora hasta 2022
Pierre and Marie Curie University
París, FranciaPublicaciones en colaboración con investigadores/as de Pierre and Marie Curie University (14)
2023
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Cerebellar and subcortical atrophy contribute to psychiatric symptoms in frontotemporal dementia
Human Brain Mapping, Vol. 44, Núm. 7, pp. 2684-2700
2022
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Cognitive composites for genetic frontotemporal dementia: GENFI-Cog
Alzheimer's Research and Therapy, Vol. 14, Núm. 1
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Conceptual framework for the definition of preclinical and prodromal frontotemporal dementia
Alzheimer's and Dementia, Vol. 18, Núm. 7, pp. 1408-1423
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Differential impairment of cerebrospinal fluid synaptic biomarkers in the genetic forms of frontotemporal dementia
Alzheimer's Research and Therapy, Vol. 14, Núm. 1
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Examining empathy deficits across familial forms of frontotemporal dementia within the GENFI cohort
Cortex, Vol. 150, pp. 12-28
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New insights into the genetic etiology of Alzheimer's disease and related dementias
Nature genetics, Vol. 54, Núm. 4, pp. 412-436
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Structural brain splitting is a hallmark of Granulin-related frontotemporal dementia
Neurobiology of Aging, Vol. 114, pp. 94-104
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The CBI-R detects early behavioural impairment in genetic frontotemporal dementia
Annals of Clinical and Translational Neurology, Vol. 9, Núm. 5, pp. 644-658
2021
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Common variants in Alzheimer's disease and risk stratification by polygenic risk scores
Nature communications, Vol. 12, Núm. 1, pp. 3417
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Differential early subcortical involvement in genetic FTD within the GENFI cohort
NeuroImage: Clinical, Vol. 30
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Impairment of episodic memory in genetic frontotemporal dementia: A genfi study
Alzheimer's and Dementia: Diagnosis, Assessment and Disease Monitoring, Vol. 13, Núm. 1
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Progression of Behavioral Disturbances and Neuropsychiatric Symptoms in Patients with Genetic Frontotemporal Dementia
JAMA Network Open, Vol. 4, Núm. 1
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The Revised Self-Monitoring Scale detects early impairment of social cognition in genetic frontotemporal dementia within the GENFI cohort
Alzheimer's Research and Therapy, Vol. 13, Núm. 1
2018
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Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study
The Lancet Neurology, Vol. 17, Núm. 6, pp. 548-558