Area of research
Neurology · Physiology
Research interest
Research interests include Amyotrophic Lateral Sclerosis Research, Parkinson's Disease Mechanisms and Treatments, Alzheimer's disease research and treatments, and Dementia and Cognitive Impairment Research.
Genetic forms of primary progressive aphasia within the GENetic Frontotemporal dementia Initiative (GENFI) cohort: comparison with sporadic primary progressive aphasia
Elevated CSF and plasma complement proteins in genetic frontotemporal dementia: results from the GENFI study
Cognitive composites for genetic frontotemporal dementia: GENFI-Cog
Progression of Behavioral Disturbances and Neuropsychiatric Symptoms in Patients With Genetic Frontotemporal Dementia
Characterizing the Clinical Features and Atrophy Patterns of <i>MAPT</i> -Related Frontotemporal Dementia With Disease Progression Modeling
Differential early subcortical involvement in genetic FTD within the GENFI cohort
A data-driven disease progression model of fluid biomarkers in genetic frontotemporal dementia
A panel of CSF proteins separates genetic frontotemporal dementia from presymptomatic mutation carriers: a GENFI study
The Revised Self-Monitoring Scale detects early impairment of social cognition in genetic frontotemporal dementia within the GENFI cohort
Plasma glial fibrillary acidic protein is raised in progranulin-associated frontotemporal dementia.
Neuronal pentraxin 2: a synapse-derived CSF biomarker in genetic frontotemporal dementia.
Social cognition impairment in genetic frontotemporal dementia within the GENFI cohort
Social cognition impairment in genetic frontotemporal dementia within the GENFI cohort.
Faster Cortical Thinning and Surface Area Loss in Presymptomatic and Symptomatic C9orf72 Repeat Expansion Adult Carriers.
Abnormal pain perception is associated with thalamo-cortico-striatal atrophy in <i>C9orf72</i> expansion carriers in the GENFI cohort.
Serum neurofilament light chain in genetic frontotemporal dementia: a longitudinal, multicentre cohort study
Serum neurofilament light chain in genetic frontotemporal dementia: a longitudinal, multicentre cohort study.
Functional network resilience to pathology in presymptomatic genetic frontotemporal dementia
The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population-Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight.
Functional network resilience to pathology in presymptomatic genetic frontotemporal dementia.
White matter hyperintensities in progranulin-associated frontotemporal dementia: A longitudinal GENFI study
The inner fluctuations of the brain in presymptomatic Frontotemporal Dementia: The chronnectome fingerprint
The inner fluctuations of the brain in presymptomatic Frontotemporal Dementia: The chronnectome fingerprint.
White matter hyperintensities in progranulin-associated frontotemporal dementia: A longitudinal GENFI study.
Education modulates brain maintenance in presymptomatic frontotemporal dementia.
Using global team science to identify genetic parkinson's disease worldwide.
The genetic architecture of Parkinson disease in Spain: characterizing population-specific risk, differential haplotype structures, and providing etiologic insight
Alzheimer’s disease cerebrospinal fluid biomarker in cognitively normal subjects
<i>SCN4A</i>pore mutation pathogenetically contributes to autosomal dominant essential tremor and may increase susceptibility to epilepsy
The ACMSD gene, involved in tryptophan metabolism, is mutated in a family with cortical myoclonus, epilepsy, and parkinsonism