Lista de obras - Isabel Santana - Dominio Público Uruguay

A pan-European study of the C9orf72 repeat associated with FTLD: geographic prevalence, genomic instability, and intermediate repeats

artículo científico publicado en 2013

Adaptive visual memory reorganization in right medial temporal lobe epilepsy

artículo científico publicado en 2008

Addition of the Aβ42/40 ratio to the cerebrospinal fluid biomarker profile increases the predictive value for underlying Alzheimer's disease dementia in mild cognitive impairment

artículo científico publicado en 2018

Adiponectin and sporadic Alzheimer's disease: Clinical and molecular links.

artículo científico publicado en 2017

Advanced MRI study of migrainous infarction presenting as cortical laminar necrosis - Case report and literature review

artículo científico publicado en 2018

Alzheimer's Disease Assessment Scale - Cognitive Subscale (ADAS-Cog): Normative Data for the Portuguese Population.

artículo científico publicado en 2018

Amyloid β-induced ER stress is enhanced under mitochondrial dysfunction conditions.

artículo científico publicado en 2011

Analysis of neurodegenerative disease-causing genes in dementia with Lewy bodies

scientific article published on 29 January 2020

Apolipoprotein E epsilon4 allele is a risk factor for Alzheimer's disease: the central region of portugal (Coimbra) as a case study.

artículo científico publicado en 1999

Association between butyrylcholinesterase and cerebrospinal fluid biomarkers in Alzheimer's disease patients.

artículo científico publicado en 2017

Association of Cerebral Amyloid-β Aggregation With Cognitive Functioning in Persons Without Dementia

artículo científico publicado en 2017

Association of HFE common mutations with Parkinson's disease, Alzheimer's disease and mild cognitive impairment in a Portuguese cohort

artículo científico publicado en 2006

Biparietal variant of Alzheimer's disease: a rare presentation of a common disease

artículo científico publicado en 2015

CSF Tau proteins reduce misdiagnosis of sporadic Creutzfeldt-Jakob disease suspected cases with inconclusive 14-3-3 result.

artículo científico publicado en 2016

Cerebrospinal Fluid Total Prion Protein in the Spectrum of Prion Diseases

artículo científico publicado en 2018

Cerebrospinal fluid Aβ40 is similarly reduced in patients with Frontotemporal Lobar Degeneration and Alzheimer's Disease.

artículo científico publicado en 2015

Cerebrospinal fluid biomarkers in trials for Alzheimer and Parkinson diseases

artículo científico publicado en 2014

Cerebrospinal fluid lipocalin 2 as a novel biomarker for the differential diagnosis of vascular dementia

artículo científico publicado en 2020

Characterization of an FTLD-PDB family with the coexistence of SQSTM1 mutation and hexanucleotide (G₄C₂) repeat expansion in C9orf72 gene

artículo científico publicado en 2015

Clinical Reasoning: A 55-year-old man with rapidly progressive dementia and parkinsonism.

artículo científico publicado en 2017

Clock drawing test in mild cognitive impairment: Correlation with cerebral perfusion in single-photon emission computed tomography

artículo científico publicado en 2019

Cognitive deficits in middle-aged and older adults with bipolar disorder and cognitive complaints: comparison with mild cognitive impairment

artículo científico publicado en 2009

Cognitive effects of therapy with topiramate in patients with refractory partial epilepsy

artículo científico publicado en 2002

Comparison of four verbal memory tests for the diagnosis and predictive value of mild cognitive impairment

artículo científico publicado en 2012

Construct Validity of the Montreal Cognitive Assessment (MoCA).

artículo científico publicado en 2011

Construct and diagnostic validities of the Free and Cued Selective Reminding Test in the Alzheimer's disease spectrum.

artículo científico publicado en 2016

Cytochrome c oxidase is decreased in Alzheimer's disease platelets

artículo científico publicado en 2004

Data mining methods in the prediction of Dementia: A real-data comparison of the accuracy, sensitivity and specificity of linear discriminant analysis, logistic regression, neural networks, support vector machines, classification trees and random fo

artículo científico publicado en 2011

Deleterious ABCA7 mutations and transcript rescue mechanisms in early onset Alzheimer's disease

artículo científico publicado en 2017

Diagnostic value of CSF protein profile in a Portuguese population of sCJD patients

artículo científico publicado en 2009

Differences between Early and Late-Onset Alzheimer's Disease in Neuropsychological Tests

artículo científico publicado en 2012

Do MCI patients with vitamin B12 deficiency have distinctive cognitive deficits?

artículo científico publicado en 2013

Does Caffeine Consumption Modify Cerebrospinal Fluid Amyloid-β Levels in Patients with Alzheimer's Disease?

artículo científico publicado en 2015

Effects of apolipoprotein E genotype on blood lipid composition and membrane platelet fluidity in Alzheimer’s disease

article

Epigenetic regulation of BACE1 in Alzheimer's disease patients and in transgenic mice.

artículo científico publicado en 2012

Exome sequencing reveals an unexpected genetic cause of disease: NOTCH3 mutation in a Turkish family with Alzheimer's disease

artículo científico publicado en 2012

Free and Cued Selective Reminding Test is superior to the Wechsler Memory Scale in discriminating mild cognitive impairment from Alzheimer's disease

artículo científico publicado en 2014

Frontotemporal dementia and mitochondrial DNA transitions

artículo científico publicado en 2004

Frontotemporal dementia: neuroanatomical correlates of an atypical presentation

artículo científico

Genetic Variation of MT-ND Genes in Frontotemporal Lobar Degeneration: Biochemical Phenotype-Genotype Correlation

artículo científico publicado en 2015

Genetic basis of Alzheimer's dementia: role of mtDNA mutations.

artículo científico publicado en 2006

Genetic screening of Alzheimer's disease genes in Iberian and African samples yields novel mutations in presenilins and APP

artículo científico publicado en 2008

Genetic variability in CLU and its association with Alzheimer's disease

artículo científico publicado en 2010

Genetic variability in SQSTM1 and risk of early-onset Alzheimer dementia: a European early-onset dementia consortium study

artículo científico publicado en 2015

Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture

artículo científico publicado en 2021

Heritability and genetic variance of dementia with Lewy bodies

scientific article published on 03 April 2019

Impaired processing of 3D motion-defined faces in mild cognitive impairment and healthy aging: an fMRI study

artículo científico publicado en 2012

Impairment of social cognition in multiple sclerosis: Amygdala atrophy is the main predictor.

artículo científico publicado en 2016

Increased CSF tau is associated with a higher risk of seizures in patients with Alzheimer's disease

scientific article published on 02 August 2019

Influence of apolipoprotein E genotype on blood redox status of Alzheimer's disease patients.

artículo científico publicado en 1999

Lower CSF Amyloid-Beta1-42 Predicts a Higher Mortality Rate in Frontotemporal Dementia

artículo científico publicado en 2019

MicroRNA deregulation and chemotaxis and phagocytosis impairment in Alzheimer's disease

artículo científico publicado en 2015

Mitochondria dysfunction of Alzheimer's disease cybrids enhances Abeta toxicity

artículo científico publicado en 2004

Mitochondrial DNA variants in a portuguese population of patients with Alzheimer's disease

artículo científico publicado en 2005

Montreal Cognitive Assessment (MoCA): Normative study for the Portuguese population ⬇️

artículo científico publicado el 4 de julio de 2011

Montreal Cognitive Assessment (MoCA): validation study for frontotemporal dementia

artículo científico publicado en 2012

Montreal Cognitive Assessment (MoCA): validation study for vascular dementia

artículo científico publicado en 2012

Montreal Cognitive Assessment: Influence of Sociodemographic and Health Variables ⬇️

artículo científico publicado el 24 de enero de 2012

Montreal cognitive assessment: validation study for mild cognitive impairment and Alzheimer disease.

artículo científico publicado en 2013

Multiple dural arteriovenous fistulas presenting as rapidly progressive dementia

artículo científico publicado en 2012

Novel progranulin mutation: Screening for PGRN mutations in a Portuguese series of FTD/CBS cases

article

Obesity as a risk factor for Alzheimer's disease: the role of adipocytokines

artículo científico publicado en 2014

Oxidative damage and progression to Alzheimer's disease in patients with mild cognitive impairment.

artículo científico publicado en 2010

Oxidative stress involving changes in Nrf2 and ER stress in early stages of Alzheimer's disease

artículo científico publicado en 2015

Peripheral inflammatory cytokines as biomarkers in Alzheimer's disease and mild cognitive impairment

artículo científico publicado en 2007

Peripheral oxidative damage in mild cognitive impairment and mild Alzheimer's disease.

artículo científico publicado en 2008

Predicting progression of mild cognitive impairment to dementia using neuropsychological data: a supervised learning approach using time windows.

artículo científico publicado en 2017

Prediction of long-term (5 years) conversion to dementia using neuropsychological tests in a memory clinic setting

artículo científico

Premorbid IQ influence on screening tests' scores in healthy patients and patients with cognitive impairment

artículo científico publicado en 2013

Prevalence and prognosis of Alzheimer's disease at the mild cognitive impairment stage

artículo científico publicado en 2015

Prevalence of cerebral amyloid pathology in persons without dementia: a meta-analysis

artículo científico publicado en 2015

Primary bilateral thalamic astrocytoma presenting with head tremor, ataxia, and dementia

artículo científico publicado en 2010

Prodromal metabolic phenotype in MCI cybrids: implications for Alzheimer's disease.

artículo científico publicado en 2013

Progranulin peripheral levels as a screening tool for the identification of subjects with progranulin mutations in a Portuguese cohort

artículo científico publicado en 2013

Prosopagnosia as the Presenting Symptom of Whipple Disease

artículo científico publicado en 2016

Pseudohypoparathyroidism type I-b with neurological involvement is associated with a homozygous PTH1R mutation.

artículo científico publicado en 2016

Psychometric properties of the Montreal Cognitive Assessment (MoCA): an analysis using the Rasch model.

artículo científico publicado en 2014

Rare Variants in PLD3 Do Not Affect Risk for Early-Onset Alzheimer Disease in a European Consortium Cohort

artículo científico publicado en 2015

Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration

artículo científico publicado en 2014

Retinal texture biomarkers may help to discriminate between Alzheimer's, Parkinson's, and healthy controls

artículo científico publicado en 2019

Scaling Cognitive Domains of the Montreal Cognitive Assessment: An Analysis Using the Partial Credit Model

artículo científico publicado en 2015

Selective Reminding and Free and Cued Selective Reminding in Mild Cognitive Impairment and Alzheimer Disease

artículo científico

Serial position effects in Alzheimer's disease, mild cognitive impairment, and normal aging: predictive value for conversion to dementia

artículo científico publicado en 2012

Severe post-influenza (H1N1) encephalitis involving pulvinar nuclei in an adult patient

artículo científico publicado en 2015

Single Word Repetition Predicts Long-Term Outcome of Aphasia Caused by an Ischemic Stroke

scientific article published on 11 December 2019

Sporadic Creutzfeldt-Jakob disease causing a 2-years slowly progressive isolated dementia

artículo científico publicado en 2009

Sporadic Creutzfeldt–Jakob disease diagnostic accuracy is improved by a new CSF ELISA 14-3-3γ assay

artículo científico publicado en 2016

TBK1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis

scientific article published on 23 December 2016

TeLPI performance in subjects with mild cognitive impairment and Alzheimer disease: a validation study.

artículo científico publicado en 2013

Temporal Integration of 3D Coherent Motion Cues Defining Visual Objects of Unknown Orientation is Impaired in Amnestic Mild Cognitive Impairment and Alzheimer's Disease ⬇️

artículo científico publicado el 1 de enero de 2012

The Clock Drawing Test: Portuguese norms, by age and education, for three different scoring systems

artículo científico publicado en 2013

The Epidemiology of Dementia and Alzheimer Disease in Portugal: Estimations of Prevalence and Treatment-Costs

artículo científico publicado en 2015

The Head Turning Sign in Dementia and Mild Cognitive Impairment: Its Relationship to Cognition, Behavior, and Cerebrospinal Fluid Biomarkers

artículo científico publicado en 2018

The Influence of Adipose Tissue on Brain Development, Cognition, and Risk of Neurodegenerative Disorders.

artículo científico publicado en 2017

The Portuguese version of Addenbrooke's Cognitive Examination-Revised (ACE-R) in the diagnosis of subcortical vascular dementia and Alzheimer's disease

artículo científico publicado en 2014

The Portuguese who could no longer speak French: primary progressive aphasia in a bilingual man.

artículo científico publicado en 2010

The Quadruple Helix-Based Innovation Model of Reference Sites for Active and Healthy Ageing in Europe: The Ageing@Coimbra Case Study.

artículo científico publicado en 2018

The Relevance of Sociodemographic and Health Variables on MMSE Normative Data

artículo científico publicado en 2014

The free and cued selective reminding test distinguishes frontotemporal dementia from Alzheimer's disease

artículo científico publicado en 2014

The free and cued selective reminding test for predicting progression to Alzheimer's disease in patients with mild cognitive impairment: A prospective longitudinal study

artículo científico publicado en 2015

The free and cued selective reminding test: Validation for mild cognitive impairment and Alzheimer's disease

artículo científico

The impact of automated hippocampal volumetry on diagnostic confidence in patients with suspected Alzheimer's disease: A European Alzheimer's Disease Consortium study

artículo científico publicado en 2017

The inner fluctuations of the brain in presymptomatic Frontotemporal Dementia: The chronnectome fingerprint

artículo científico publicado en 2019

The neural basis of fatigue in multiple sclerosis: A multimodal MRI approach

scientific article published on 01 December 2018

The use of biomarkers for the etiologic diagnosis of MCI in Europe: an EADC survey

artículo científico publicado en 2014

Theory of Mind and Executive Functions are Dissociated in Multiple Sclerosis

artículo científico publicado en 2017

Three-Dimensional Face Recognition in Mild Cognitive Impairment: A Psychophysical and Structural MR Study

artículo científico publicado en 2016

Transthyretin decrease in plasma of MCI and AD patients: investigation of mechanisms for disease modulation.

artículo científico publicado en 2012

Transthyretin stability is critical in assisting beta amyloid clearance- Relevance of transthyretin stabilization in Alzheimer's disease.

artículo científico publicado en 2017

Validation studies of the Portuguese experimental version of the Montreal Cognitive Assessment (MoCA): confirmatory factor analysis.

artículo científico publicado en 2009

Validity and Clinical Utility of Different Clock Drawing Test Scoring Systems in Multiple Forms of Dementia

artículo científico publicado en 2018

Variant Creutzfeldt-Jakob [corrected] disease: the second case in Portugal and in the same geographical region.

artículo científico publicado en 2007

Whole-exome sequencing reveals PSEN1 and ATP7B combined variants as a possible cause of early-onset Lewy body dementia: a case study of genotype–phenotype correlation

artículo científico publicado en 2022

[Malformations in cortical development in patients with epilepsy. Neuroimaging of 17 cases]

artículo científico publicado en 2001

Lista de obras de Isabel Santana

A pan-European study of the C9orf72 repeat associated with FTLD: geographic prevalence, genomic instability, and intermediate repeats

Adaptive visual memory reorganization in right medial temporal lobe epilepsy

Addition of the Aβ42/40 ratio to the cerebrospinal fluid biomarker profile increases the predictive value for underlying Alzheimer's disease dementia in mild cognitive impairment

Adiponectin and sporadic Alzheimer's disease: Clinical and molecular links.

Advanced MRI study of migrainous infarction presenting as cortical laminar necrosis - Case report and literature review

Alzheimer's Disease Assessment Scale - Cognitive Subscale (ADAS-Cog): Normative Data for the Portuguese Population.

Amyloid β-induced ER stress is enhanced under mitochondrial dysfunction conditions.

Analysis of neurodegenerative disease-causing genes in dementia with Lewy bodies

Apolipoprotein E epsilon4 allele is a risk factor for Alzheimer's disease: the central region of portugal (Coimbra) as a case study.

Association between butyrylcholinesterase and cerebrospinal fluid biomarkers in Alzheimer's disease patients.

Association of Cerebral Amyloid-β Aggregation With Cognitive Functioning in Persons Without Dementia

Association of HFE common mutations with Parkinson's disease, Alzheimer's disease and mild cognitive impairment in a Portuguese cohort

Biparietal variant of Alzheimer's disease: a rare presentation of a common disease

CSF Tau proteins reduce misdiagnosis of sporadic Creutzfeldt-Jakob disease suspected cases with inconclusive 14-3-3 result.

Cerebrospinal Fluid Total Prion Protein in the Spectrum of Prion Diseases

Cerebrospinal fluid Aβ40 is similarly reduced in patients with Frontotemporal Lobar Degeneration and Alzheimer's Disease.

Cerebrospinal fluid biomarkers in trials for Alzheimer and Parkinson diseases

Cerebrospinal fluid lipocalin 2 as a novel biomarker for the differential diagnosis of vascular dementia

Characterization of an FTLD-PDB family with the coexistence of SQSTM1 mutation and hexanucleotide (G₄C₂) repeat expansion in C9orf72 gene

Clinical Reasoning: A 55-year-old man with rapidly progressive dementia and parkinsonism.

Clock drawing test in mild cognitive impairment: Correlation with cerebral perfusion in single-photon emission computed tomography

Cognitive deficits in middle-aged and older adults with bipolar disorder and cognitive complaints: comparison with mild cognitive impairment

Cognitive effects of therapy with topiramate in patients with refractory partial epilepsy

Comparison of four verbal memory tests for the diagnosis and predictive value of mild cognitive impairment

Construct Validity of the Montreal Cognitive Assessment (MoCA).

Construct and diagnostic validities of the Free and Cued Selective Reminding Test in the Alzheimer's disease spectrum.

Cytochrome c oxidase is decreased in Alzheimer's disease platelets

Data mining methods in the prediction of Dementia: A real-data comparison of the accuracy, sensitivity and specificity of linear discriminant analysis, logistic regression, neural networks, support vector machines, classification trees and random fo

Deleterious ABCA7 mutations and transcript rescue mechanisms in early onset Alzheimer's disease

Diagnostic value of CSF protein profile in a Portuguese population of sCJD patients

Differences between Early and Late-Onset Alzheimer's Disease in Neuropsychological Tests

Do MCI patients with vitamin B12 deficiency have distinctive cognitive deficits?

Does Caffeine Consumption Modify Cerebrospinal Fluid Amyloid-β Levels in Patients with Alzheimer's Disease?

Effects of apolipoprotein E genotype on blood lipid composition and membrane platelet fluidity in Alzheimer’s disease

Epigenetic regulation of BACE1 in Alzheimer's disease patients and in transgenic mice.

Exome sequencing reveals an unexpected genetic cause of disease: NOTCH3 mutation in a Turkish family with Alzheimer's disease

Free and Cued Selective Reminding Test is superior to the Wechsler Memory Scale in discriminating mild cognitive impairment from Alzheimer's disease

Frontotemporal dementia and mitochondrial DNA transitions

Frontotemporal dementia: neuroanatomical correlates of an atypical presentation

Genetic Variation of MT-ND Genes in Frontotemporal Lobar Degeneration: Biochemical Phenotype-Genotype Correlation

Genetic basis of Alzheimer's dementia: role of mtDNA mutations.

Genetic screening of Alzheimer's disease genes in Iberian and African samples yields novel mutations in presenilins and APP

Genetic variability in CLU and its association with Alzheimer's disease

Genetic variability in SQSTM1 and risk of early-onset Alzheimer dementia: a European early-onset dementia consortium study

Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture

Heritability and genetic variance of dementia with Lewy bodies

Impaired processing of 3D motion-defined faces in mild cognitive impairment and healthy aging: an fMRI study

Impairment of social cognition in multiple sclerosis: Amygdala atrophy is the main predictor.

Increased CSF tau is associated with a higher risk of seizures in patients with Alzheimer's disease

Influence of apolipoprotein E genotype on blood redox status of Alzheimer's disease patients.

Lower CSF Amyloid-Beta1-42 Predicts a Higher Mortality Rate in Frontotemporal Dementia

MicroRNA deregulation and chemotaxis and phagocytosis impairment in Alzheimer's disease

Mitochondria dysfunction of Alzheimer's disease cybrids enhances Abeta toxicity

Mitochondrial DNA variants in a portuguese population of patients with Alzheimer's disease

Montreal Cognitive Assessment (MoCA): Normative study for the Portuguese population ⬇️

Montreal Cognitive Assessment (MoCA): validation study for frontotemporal dementia

Montreal Cognitive Assessment (MoCA): validation study for vascular dementia

Montreal Cognitive Assessment: Influence of Sociodemographic and Health Variables ⬇️

Montreal cognitive assessment: validation study for mild cognitive impairment and Alzheimer disease.

Multiple dural arteriovenous fistulas presenting as rapidly progressive dementia

Novel progranulin mutation: Screening for PGRN mutations in a Portuguese series of FTD/CBS cases

Obesity as a risk factor for Alzheimer's disease: the role of adipocytokines

Oxidative damage and progression to Alzheimer's disease in patients with mild cognitive impairment.

Oxidative stress involving changes in Nrf2 and ER stress in early stages of Alzheimer's disease

Peripheral inflammatory cytokines as biomarkers in Alzheimer's disease and mild cognitive impairment

Peripheral oxidative damage in mild cognitive impairment and mild Alzheimer's disease.

Predicting progression of mild cognitive impairment to dementia using neuropsychological data: a supervised learning approach using time windows.

Prediction of long-term (5 years) conversion to dementia using neuropsychological tests in a memory clinic setting

Premorbid IQ influence on screening tests' scores in healthy patients and patients with cognitive impairment

Prevalence and prognosis of Alzheimer's disease at the mild cognitive impairment stage

Prevalence of cerebral amyloid pathology in persons without dementia: a meta-analysis

Primary bilateral thalamic astrocytoma presenting with head tremor, ataxia, and dementia

Prodromal metabolic phenotype in MCI cybrids: implications for Alzheimer's disease.

Progranulin peripheral levels as a screening tool for the identification of subjects with progranulin mutations in a Portuguese cohort

Prosopagnosia as the Presenting Symptom of Whipple Disease

Pseudohypoparathyroidism type I-b with neurological involvement is associated with a homozygous PTH1R mutation.

Psychometric properties of the Montreal Cognitive Assessment (MoCA): an analysis using the Rasch model.

Rare Variants in PLD3 Do Not Affect Risk for Early-Onset Alzheimer Disease in a European Consortium Cohort

Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration