Lista de obras -

'Under pressure': is there a link between orthostatic hypotension and cognitive impairment in α-synucleinopathies?

artículo científico publicado en 2016

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

scientific article published on 03 December 2019

Characterizing familial corticobasal syndrome due to Alzheimer's disease pathology and PSEN1 mutations

artículo científico publicado en 2016

Cognitive and psychiatric symptoms in genetically determined Parkinson's disease: a systematic review

artículo científico publicado en 2019

Comparison of Pittsburgh compound B and florbetapir in cross-sectional and longitudinal studies

article

Computer-Based Driving in Dementia Decision Tool With Mail Support: Cluster Randomized Controlled Trial.

artículo científico publicado en 2018

DRD2 and SLC6A3 moderate impact of maternal depressive symptoms on infant cortisol.

artículo científico publicado en 2015

Deconstructing normal pressure hydrocephalus: Ventriculomegaly as early sign of neurodegeneration.

artículo científico publicado en 2017

Diagnosis and management of dementia with Lewy bodies: Fourth consensus report of the DLB Consortium

artículo científico publicado en 2017

Distinct patterns of brain atrophy in Genetic Frontotemporal Dementia Initiative (GENFI) cohort revealed by visual rating scales.

artículo científico publicado en 2018

Editorial: CPPM 2013 Onward: Building a Socio-Technical GPS for Global Personalized Medicine – A Welcome to Editors-In-Chief Adrian LLerena (Spain) and Ross A. McKinnon (Australia)

article

Educational Needs and Considerations for a Visual Educational Tool to Discuss Parkinson's Disease

scholarly article by Sean J Udow et al published 27 November 2017 in Movement disorders clinical practice

End of the Beginning and Public Health Pharmacogenomics: Knowledge in 'Mode 2' and P5 Medicine

artículo científico publicado en 2012

Forward Look: Tenth Anniversary of the Human Genome Sequence and 21 Century Postgenomics Global Health - A Close Up on Africa and Women's Health

artículo científico publicado en 2011

Intra-familial clinical heterogeneity due to FTLD-U with TDP-43 proteinopathy caused by a novel deletion in progranulin gene (PGRN).

artículo científico publicado en 2010

Investigation of c9orf72 in 4 neurodegenerative disorders

artículo científico publicado en 2012

MATERNAL SELF-REPORTED DEPRESSIVE SYMPTOMS AND MATERNAL CORTISOL LEVELS INTERACT TO PREDICT INFANT CORTISOL LEVELS.

artículo científico publicado en 2016

Maternal sensitivity and infant and mother adrenocortical function across challenges

artículo científico publicado en 2013

Neurofilament light chain: a biomarker for genetic frontotemporal dementia

scientific article published on July 2016

Neuroimaging and clinical features in adults with a 22q11.2 deletion at risk of Parkinson's disease

artículo científico publicado en 2017

Novel splicing mutation in the progranulin gene causing familial corticobasal syndrome

artículo científico publicado en 2006

Orthostatic hypotension and dementia incidence: links and implications

artículo científico publicado en 2019

Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study.

artículo científico publicado en 2018

Presymptomatic cognitive and neuroanatomical changes in genetic frontotemporal dementia in the Genetic Frontotemporal dementia Initiative (GENFI) study: a cross-sectional analysis.

artículo científico publicado en 2015

Prevalence of amyloid-β pathology in distinct variants of primary progressive aphasia

artículo científico publicado en 2018

Progranulin plasma levels predict the presence of GRN mutations in asymptomatic subjects and do not correlate with brain atrophy: results from the GENFI study

artículo científico publicado en 2017

Public Health Pharmacogenomics and the Design Principles for Global Public Goods - Moving Genomics to Responsible Innovation

artículo científico publicado en 2013

Recommendations to distinguish behavioural variant frontotemporal dementia from psychiatric disorders

artículo científico publicado en 2020

Research criteria for the diagnosis of prodromal dementia with Lewy bodies

scientific article published on 02 April 2020

Serum neurofilament light chain in genetic frontotemporal dementia: a longitudinal, multicentre cohort study

artículo científico publicado en 2019

Summary cortisol reactivity indicators: Interrelations and meaning

artículo científico publicado en 2015

Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease

artículo científico publicado en 2018

Tau PET in autosomal dominant Alzheimer's disease: relationship with cognition, dementia and other biomarkers

scientific article published on 01 April 2019

Typical features of Parkinson disease and diagnostic challenges with microdeletion 22q11.2.

artículo científico publicado en 2018

Uncovering the heterogeneity and temporal complexity of neurodegenerative diseases with Subtype and Stage Inference

artículo científico publicado en 2018

White matter hyperintensities are seen only in GRN mutation carriers in the GENFI cohort

artículo científico publicado en 2017

White matter hyperintensities in progranulin-associated frontotemporal dementia: A longitudinal GENFI study

scientific article published on 06 November 2019

Lista de obras de

'Under pressure': is there a link between orthostatic hypotension and cognitive impairment in α-synucleinopathies?

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

Characterizing familial corticobasal syndrome due to Alzheimer's disease pathology and PSEN1 mutations

Cognitive and psychiatric symptoms in genetically determined Parkinson's disease: a systematic review

Comparison of Pittsburgh compound B and florbetapir in cross-sectional and longitudinal studies

Computer-Based Driving in Dementia Decision Tool With Mail Support: Cluster Randomized Controlled Trial.

DRD2 and SLC6A3 moderate impact of maternal depressive symptoms on infant cortisol.

Deconstructing normal pressure hydrocephalus: Ventriculomegaly as early sign of neurodegeneration.

Diagnosis and management of dementia with Lewy bodies: Fourth consensus report of the DLB Consortium

Distinct patterns of brain atrophy in Genetic Frontotemporal Dementia Initiative (GENFI) cohort revealed by visual rating scales.

Editorial: CPPM 2013 Onward: Building a Socio-Technical GPS for Global Personalized Medicine – A Welcome to Editors-In-Chief Adrian LLerena (Spain) and Ross A. McKinnon (Australia)

Educational Needs and Considerations for a Visual Educational Tool to Discuss Parkinson's Disease

End of the Beginning and Public Health Pharmacogenomics: Knowledge in 'Mode 2' and P5 Medicine

Forward Look: Tenth Anniversary of the Human Genome Sequence and 21 Century Postgenomics Global Health - A Close Up on Africa and Women's Health

Intra-familial clinical heterogeneity due to FTLD-U with TDP-43 proteinopathy caused by a novel deletion in progranulin gene (PGRN).

Investigation of c9orf72 in 4 neurodegenerative disorders

MATERNAL SELF-REPORTED DEPRESSIVE SYMPTOMS AND MATERNAL CORTISOL LEVELS INTERACT TO PREDICT INFANT CORTISOL LEVELS.

Maternal sensitivity and infant and mother adrenocortical function across challenges

Neurofilament light chain: a biomarker for genetic frontotemporal dementia

Neuroimaging and clinical features in adults with a 22q11.2 deletion at risk of Parkinson's disease

Novel splicing mutation in the progranulin gene causing familial corticobasal syndrome

Orthostatic hypotension and dementia incidence: links and implications

Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study.

Presymptomatic cognitive and neuroanatomical changes in genetic frontotemporal dementia in the Genetic Frontotemporal dementia Initiative (GENFI) study: a cross-sectional analysis.

Prevalence of amyloid-β pathology in distinct variants of primary progressive aphasia

Progranulin plasma levels predict the presence of GRN mutations in asymptomatic subjects and do not correlate with brain atrophy: results from the GENFI study

Public Health Pharmacogenomics and the Design Principles for Global Public Goods - Moving Genomics to Responsible Innovation

Recommendations to distinguish behavioural variant frontotemporal dementia from psychiatric disorders

Research criteria for the diagnosis of prodromal dementia with Lewy bodies

Serum neurofilament light chain in genetic frontotemporal dementia: a longitudinal, multicentre cohort study

Summary cortisol reactivity indicators: Interrelations and meaning

Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease

Tau PET in autosomal dominant Alzheimer's disease: relationship with cognition, dementia and other biomarkers

Typical features of Parkinson disease and diagnostic challenges with microdeletion 22q11.2.

Uncovering the heterogeneity and temporal complexity of neurodegenerative diseases with Subtype and Stage Inference

White matter hyperintensities are seen only in GRN mutation carriers in the GENFI cohort

White matter hyperintensities in progranulin-associated frontotemporal dementia: A longitudinal GENFI study