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18F-florbetapir Positron Emission Tomography-determined Cerebral β-Amyloid Deposition and Neurocognitive Performance after Cardiac Surgery

artículo científico publicado en 2018

A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers

A blood-based screening tool for Alzheimer's disease that spans serum and plasma: findings from TARC and ADNI

artículo científico publicado en 2011

A brief report on WAIS-R normative data collection in Mayo's Older African Americans Normative Studies

artículo científico publicado en 2005

A candidate regulatory variant at the TREM gene cluster associates with decreased Alzheimer's disease risk and increased TREML1 and TREM2 brain gene expression

artículo científico publicado en 2016

A comprehensive screening of copy number variability in dementia with Lewy bodies

scientific article published on 24 October 2018

A computerized technique to assess language use patterns in patients with frontotemporal dementia

artículo científico publicado en 2010

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

article by Sven J. van der Lee et al published 27 May 2019 in Acta Neuropathologica

A novel de novo pathogenic mutation in the CACNA1A gene

artículo científico publicado en 2012

A soluble phosphorylated tau signature links tau, amyloid and the evolution of stages of dominantly inherited Alzheimer's disease

artículo científico publicado en 2020

A yeast functional screen predicts new candidate ALS disease genes

artículo científico publicado en 2011

ABCA7 loss-of-function variants, expression, and neurologic disease risk

artículo científico publicado en 2017

ABI3 and PLCG2 missense variants as risk factors for neurodegenerative diseases in Caucasians and African Americans

artículo científico publicado en 2018

APOE ε4 is associated with severity of Lewy body pathology independent of Alzheimer pathology

scientific article published on 24 August 2018

Abnormal daytime sleepiness in dementia with Lewy bodies compared to Alzheimer's disease using the Multiple Sleep Latency Test

artículo científico publicado en 2014

Abnormal expression of homeobox genes and transthyretin in C9ORF72 expansion carriers

artículo científico publicado en 2017

African American exome sequencing identifies potential risk variants at Alzheimer disease loci

artículo científico publicado en 2017

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

Age- and disease-dependent increase of the mitophagy marker phospho-ubiquitin in normal aging and Lewy body disease

artículo científico publicado en 2018

Amyloid-β and tau biomarkers and clinical phenotype in dementia with Lewy bodies

artículo científico publicado en 2020

An atlas of cortical circular RNA expression in Alzheimer disease brains demonstrates clinical and pathological associations

artículo científico publicado en 2019

An autoradiographic evaluation of AV-1451 Tau PET in dementia

artículo científico publicado en 2016

An evaluation of the impact of MAPT, SNCA and APOE on the burden of Alzheimer's and Lewy body pathology

artículo científico publicado en 2012

Analysis of C9orf72 repeat expansions in a large international cohort of dementia with Lewy bodies.

artículo científico publicado en 2016

Analysis of COQ2 gene in multiple system atrophy

artículo científico publicado en 2014

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

scientific article published on 29 January 2020

Analysis of the C9orf72 repeat in Parkinson's disease, essential tremor and restless legs syndrome

artículo científico publicado en 2012

ApoE variant p.V236E is associated with markedly reduced risk of Alzheimer's disease

artículo científico publicado en 2014

Assessment of executive function declines in presymptomatic and mildly symptomatic familial frontotemporal dementia: NIH-EXAMINER as a potential clinical trial endpoint

scientific article published on 01 January 2020

Association and heterogeneity at the GAPDH locus in Alzheimer's disease

artículo científico publicado en 2012

Association between apolipoprotein E genotype and Alzheimer disease in African American subjects

artículo científico publicado en 2002

Association between repeat sizes and clinical and pathological characteristics in carriers of C9ORF72 repeat expansions (Xpansize-72): a cross-sectional cohort study

artículo científico publicado en 2013

Association of ABI3 and PLCG2 missense variants with disease risk and neuropathology in Lewy body disease and progressive supranuclear palsy

artículo científico publicado en 2020

Association of Long Runs of Homozygosity With Alzheimer Disease Among African American Individuals

artículo científico publicado en 2015

Association of MAPT haplotypes with Alzheimer's disease risk and MAPT brain gene expression levels

artículo científico publicado en 2014

Association of common KIBRA variants with episodic memory and AD risk

artículo científico publicado en 2010

Association of common genetic variants in GPCPD1 with scaling of visual cortical surface area in humans

artículo científico publicado en 2012

Association of low plasma Abeta42/Abeta40 ratios with increased imminent risk for mild cognitive impairment and Alzheimer disease

artículo científico publicado en 2007

Ataxin-2 as potential disease modifier in C9ORF72 expansion carriers

artículo científico publicado en 2014

Ataxin-2 repeat-length variation and neurodegeneration

artículo científico publicado en 2011

Author Correction: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

scientific article published on 01 September 2019

Automated detection of imaging features of disproportionately enlarged subarachnoid space hydrocephalus using machine learning methods

artículo científico publicado en 2018

Awareness of genetic risk in the Dominantly Inherited Alzheimer Network (DIAN)

scientific article published on 01 January 2020

BDNF Val66Met moderates memory impairment, hippocampal function and tau in preclinical autosomal dominant Alzheimer's disease

artículo científico publicado en 2016

BRI2 (ITM2b) inhibits Abeta deposition in vivo

artículo científico publicado en 2008

Biphasic cortical macro- and microstructural changes in autosomal dominant Alzheimer's disease

artículo científico publicado en 2020

Brain MR Spectroscopy Changes Precede Frontotemporal Lobar Degeneration Phenoconversion in Mapt Mutation Carriers

artículo científico publicado en 2019

Brain expression genome-wide association study (eGWAS) identifies human disease-associated variants

artículo científico publicado en 2012

Brain volumetric deficits in MAPT mutation carriers: a multisite study

artículo científico publicado en 2020

C9ORF72 repeat expansions in cases with previously identified pathogenic mutations

artículo científico publicado en 2013

C9orf72 hexanucleotide repeat expansions in clinical Alzheimer disease

artículo científico publicado en 2013

CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia

artículo científico publicado en 2016

Cerebellar ataxia in progressive supranuclear palsy: An autopsy study of PSP-C.

artículo científico publicado en 2016

Cerebellar c9RAN proteins associate with clinical and neuropathological characteristics of C9ORF72 repeat expansion carriers

artículo científico publicado en 2015

Cerebral amyloidosis associated with cognitive decline in autosomal dominant Alzheimer disease

artículo científico publicado en 2015

Cerebrospinal fluid dynamics disorders: Relationship to Alzheimer biomarkers and cognition

artículo científico publicado en 2019

Characterization of frontotemporal dementia and/or amyotrophic lateral sclerosis associated with the GGGGCC repeat expansion in C9ORF72

artículo científico publicado en 2012

Chronic traumatic encephalopathy pathology in a neurodegenerative disorders brain bank

artículo científico publicado en 2015

Clinical and volumetric changes with increasing functional impairment in familial frontotemporal lobar degeneration

artículo científico publicado en 2020

Clinical, pathophysiological and genetic features of motor symptoms in autosomal dominant Alzheimer's disease

artículo científico publicado en 2019

Clinicopathologic and 11C-Pittsburgh compound B implications of Thal amyloid phase across the Alzheimer's disease spectrum

artículo científico publicado en 2015

Clinicopathologic variability of the GRN A9D mutation, including amyotrophic lateral sclerosis

artículo científico publicado en 2013

Cognitive and behavioral features of c9FTD/ALS ⬇️

artículo científico publicado el 20 de julio de 2012

Cognitive impairment in progressive supranuclear palsy is associated with tau burden

artículo científico publicado en 2017

Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions

artículo científico publicado en 2010

Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease

artículo científico publicado en 2011

Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease

artículo científico publicado en 2011

Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementia

artículo científico publicado en 2008

Comparing biological markers of Alzheimer's disease across blood fraction and platforms: Comparing apples to oranges

artículo científico publicado en 2016

Computerized Analysis of Speech and Language to Identify Psycholinguistic Correlates of Frontotemporal Lobar Degeneration ⬇️

artículo científico publicado el 1 de septiembre de 2010

Concordant association of insulin degrading enzyme gene (IDE) variants with IDE mRNA, Abeta, and Alzheimer's disease

artículo científico publicado en 2010

Consensus classification of posterior cortical atrophy

artículo científico publicado en 2017

Conserved brain myelination networks are altered in Alzheimer's and other neurodegenerative diseases

artículo científico publicado en 2017

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

scientific article published on 18 January 2020

Correction: Rare Variants in APP, PSEN1 and PSEN2 Increase Risk for AD in Late-Onset Alzheimer's Disease Families

artículo científico publicado en 2012

Corrigendum to "Genome-wide association interaction analysis for Alzheimer's disease." [Neurobiol. Aging 35 (2014) 2436-2443].

artículo científico publicado en 2015

Corticospinal tract degeneration associated with TDP-43 type C pathology and semantic dementia

artículo científico publicado en 2013

Decreased body mass index in the preclinical stage of autosomal dominant Alzheimer's disease

artículo científico publicado en 2017

Dementia with Lewy bodies may present as dementia and REM sleep behavior disorder without parkinsonism or hallucinations

artículo científico publicado en 2002

Development of methodology for conducting clinical trials in frontotemporal lobar degeneration

artículo científico publicado en 2008

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

artículo científico publicado en 2017

Differential item functioning of the Boston Naming Test in cognitively normal African American and Caucasian older adults

artículo científico publicado en 2009

Diffuse Lewy body disease manifesting as corticobasal syndrome: A rare form of Lewy body disease

Discrepancies between self-reported years of education and estimated reading level among elderly community-dwelling African-Americans: Analysis of the MOAANS data.

artículo científico publicado en 2007

Distribution and characteristics of transactive response DNA binding protein 43 kDa pathology in progressive supranuclear palsy

artículo científico publicado en 2016

Effect of BDNFVal66Met on disease markers in dominantly inherited Alzheimer's disease

scientific article published on 25 August 2018

Effects of multiple genetic loci on age at onset in late-onset Alzheimer disease: a genome-wide association study

artículo científico publicado en 2014

Elevated amyloid beta protein (Abeta42) and late onset Alzheimer's disease are associated with single nucleotide polymorphisms in the urokinase-type plasminogen activator gene

artículo científico publicado en 2004

Emerging cerebrospinal fluid biomarkers in autosomal dominant Alzheimer's disease

artículo científico publicado en 2019

Erratum to: Genetically-controlled Vesicle-Associated Membrane Protein 1 expression may contribute to Alzheimer's pathophysiology and susceptibility

artículo científico publicado en 2015

Erratum to: Network-driven plasma proteomics expose molecular changes in the Alzheimer's brain

artículo científico publicado en 2016

Evaluation of memory endophenotypes for association with CLU, CR1, and PICALM variants in black and white subjects

artículo científico publicado en 2013

Evaluation of the role of SNCA variants in survival without neurological disease

artículo científico publicado en 2012

Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases

artículo científico publicado en 2012

Excessive Daytime Sleepiness in Major Dementia Syndromes

scientific article published on 10 February 2019

Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS

artículo científico publicado en 2011

Extensive transcriptomic study emphasizes importance of vesicular transport in C9orf72 expansion carriers

scientific article published on 08 October 2019

FTDP-17 with Pick body-like inclusions associated with a novel tau mutation, p.E372G.

artículo científico publicado en 2016

FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degeneration

artículo científico publicado en 2010

Factors associated with the onset and persistence of post-lumbar puncture headache

artículo científico publicado en 2015

Fine mapping of the -T catenin gene to a quantitative trait locus on chromosome 10 in late-onset Alzheimer's disease pedigrees ⬇️

artículo científico publicado el 14 de octubre de 2003

Frontal lobe 1H MR spectroscopy in asymptomatic and symptomatic MAPT mutation carriers

artículo científico publicado en 2019

Frontotemporal dementia and its subtypes: a genome-wide association study

artículo científico publicado en 2014

Functional and genetic analysis of haplotypic sequence variation at the nicastrin genomic locus

artículo científico publicado en 2012

Fus gene mutations in familial and sporadic amyotrophic lateral sclerosis

artículo científico publicado en 2010

Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies.

artículo científico publicado en 2014

Genetic and clinical features of progranulin-associated frontotemporal lobar degeneration

artículo científico publicado en 2011

Genetic association of progressive supranuclear palsy (PSP) risk loci variants with brain gene expression and neuropathology endophenotypes

article

Genetic heterogeneity in Alzheimer disease and implications for treatment strategies

artículo científico publicado en 2014

Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

artículo científico publicado en 2019

Genetic modifiers in carriers of repeat expansions in the C9ORF72 gene

artículo científico publicado en 2014

Genetic risk factors for the posterior cortical atrophy variant of Alzheimer's disease

artículo científico publicado en 2016

Genetic screening of a large series of North American sporadic and familial frontotemporal dementia cases

artículo científico publicado en 2020

Genetic variants in a haplotype block spanning IDE are significantly associated with plasma Abeta42 levels and risk for Alzheimer disease

artículo científico publicado en 2004

Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's disease

artículo científico publicado en 2009

Genetically-controlled Vesicle-Associated Membrane Protein 1 expression may contribute to Alzheimer's pathophysiology and susceptibility

artículo científico publicado en 2015

Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD

scientific article published on 09 February 2019

Genome-wide analysis of genetic correlation in dementia with Lewy bodies, Parkinson's and Alzheimer's diseases

artículo científico publicado en 2015

Genome-wide analysis of genetic loci associated with Alzheimer disease

artículo científico publicado en 2010

Genome-wide association interaction analysis for Alzheimer's disease

artículo científico publicado en 2014

Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy

artículo científico publicado en 2015

Genome-wide screen identifies rs646776 near sortilin as a regulator of progranulin levels in human plasma

artículo científico publicado en 2010

Global and local ancestry in African-Americans: Implications for Alzheimer's disease risk

artículo científico publicado en 2015

Glutathione S-transferase omega genes in Alzheimer and Parkinson disease risk, age-at-diagnosis and brain gene expression: an association study with mechanistic implications

artículo científico publicado en 2012

Guidelines for the standardization of preanalytic variables for blood-based biomarker studies in Alzheimer's disease research

artículo científico publicado en 2015

Habitual exercise levels are associated with cerebral amyloid load in presymptomatic autosomal dominant Alzheimer's disease

artículo científico publicado en 2017

Handedness and language learning disability differentially distribute in progressive aphasia variants

artículo científico publicado en 2013

Heritability of different forms of memory in the Late Onset Alzheimer's Disease Family Study

artículo científico publicado en 2011

Human whole genome genotype and transcriptome data for Alzheimer's and other neurodegenerative diseases

artículo científico publicado en 2016

Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms

artículo científico publicado en 2007

In-depth clinico-pathological examination of RNA foci in a large cohort of C9ORF72 expansion carriers

artículo científico publicado en 2017

Increased prevalence of autoimmune disease within C9 and FTD/MND cohorts: Completing the picture

scientific article published on 28 October 2016

Individualized atrophy scores predict dementia onset in familial frontotemporal lobar degeneration

artículo científico publicado en 2020

Investigation of 15 of the top candidate genes for late-onset Alzheimer's disease

artículo científico publicado en 2011

LRRK2 variation and dementia with Lewy bodies

artículo científico publicado en 2016

LRRTM3 interacts with APP and BACE1 and has variants associating with late-onset Alzheimer's disease (LOAD).

artículo científico publicado en 2013

Late-onset Alzheimer disease genetic variants in posterior cortical atrophy and posterior AD.

artículo científico publicado en 2014

Late-onset Alzheimer disease risk variants mark brain regulatory loci

artículo científico publicado en 2015

Late-onset Alzheimer's risk variants in memory decline, incident mild cognitive impairment, and Alzheimer's disease

artículo científico publicado en 2014

Length of normal alleles of C9ORF72 GGGGCC repeat do not influence disease phenotype

artículo científico publicado en 2012

Linear vs volume measures of ventricle size: Relation to present and future gait and cognition

artículo científico publicado en 2019

Linking protective GAB2 variants, increased cortical GAB2 expression and decreased Alzheimer's disease pathology

artículo científico publicado en 2013

Longitudinal cognitive and biomarker changes in dominantly inherited Alzheimer disease

artículo científico publicado en 2018

MAPT haplotype H1G is associated with increased risk of dementia with Lewy bodies

artículo científico publicado en 2016

MAPT haplotype diversity in multiple system atrophy

artículo científico publicado en 2016

MRI and pathology of REM sleep behavior disorder in dementia with Lewy bodies

artículo científico publicado en 2013

Mayo's Older African Americans Normative Studies: normative data for commonly used clinical neuropsychological measures

artículo científico publicado en 2005

Mild Cognitive Impairment at Risk for Lewy Body Dementia

scientific article published on 06 January 2021

Mild cognitive impairment associated with limbic and neocortical Lewy body disease: a clinicopathological study

artículo científico publicado en 2009

Mitochondrial targeting sequence variants of the CHCHD2 gene are a risk for Lewy body disorders

artículo científico publicado en 2015

Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration

artículo científico publicado en 2006

Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids

artículo científico publicado en 2011

Network-driven plasma proteomics expose molecular changes in the Alzheimer's brain

artículo científico publicado en 2016

Neurological manifestations of autosomal dominant familial Alzheimer's disease: a comparison of the published literature with the Dominantly Inherited Alzheimer Network observational study (DIAN-OBS).

artículo científico publicado en 2016

Neuropathologic features of frontotemporal lobar degeneration with ubiquitin-positive inclusions with progranulin gene (PGRN) mutations

artículo científico publicado en 2007

Neuropathological features of corticobasal degeneration presenting as corticobasal syndrome or Richardson syndrome

artículo científico publicado en 2011

Neuropsychiatric features in 36 pathologically confirmed cases of corticobasal degeneration

artículo científico publicado en 2007

Neuropsychological differentiation of dementia with Lewy bodies from normal aging and Alzheimer's disease

artículo científico publicado en 2006

Nonamnestic mild cognitive impairment progresses to dementia with Lewy bodies

artículo científico publicado en 2013

Novel Alzheimer Disease Risk Loci and Pathways in African American Individuals Using the African Genome Resources Panel: A Meta-analysis ⬇️

artículo científico publicado en 2020

Novel clinical associations with specific C9ORF72 transcripts in patients with repeat expansions in C9ORF72.

artículo científico publicado en 2015

Novel late-onset Alzheimer disease loci variants associate with brain gene expression

artículo científico publicado en 2012

Novel mutation in MAPT exon 13 (p.N410H) causes corticobasal degeneration

scientific article published on February 2014

Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosis

artículo científico publicado en 2008

Off-label medication use in frontotemporal dementia

artículo científico publicado en 2010

P4-095 Analysis of Alzheimer's disease candidate genes on chromosome 10

article

Pathogenicity of exonic indels in fused in sarcoma in amyotrophic lateral sclerosis ⬇️

artículo científico publicado el 12 de noviembre de 2010

Patterns of brain atrophy in clinical variants of frontotemporal lobar degeneration

artículo científico publicado en 2013

Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative

artículo científico publicado en 2007

Pick's disease: clinicopathologic characterization of 21 cases

artículo científico publicado en 2020

Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family members

scientific article published on 21 January 2009

Polygenic risk scores in familial Alzheimer disease

artículo científico publicado en 2017

Polysomnographic findings in dementia with Lewy bodies

artículo científico publicado en 2013

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

Profilin-1 mutations are rare in patients with amyotrophic lateral sclerosis and frontotemporal dementia

artículo científico publicado en 2013

Prominent phenotypic variability associated with mutations in Progranulin

artículo científico publicado en 2007

Quality of life and caregiver burden in familial frontotemporal lobar degeneration: Analyses of symptomatic and asymptomatic individuals within the LEFFTDS cohort

artículo científico publicado en 2020

RAB39B gene mutations are not a common cause of Parkinson's disease or dementia with Lewy bodies

artículo científico publicado en 2016

Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease

artículo científico publicado en 2017

Rare variants in APP, PSEN1 and PSEN2 increase risk for AD in late-onset Alzheimer's disease families

artículo científico publicado en 2012

Rarity of the Alzheimer disease-protective APP A673T variant in the United States

artículo científico publicado en 2015

Rates of Brain Atrophy Across Disease Stages in Familial Frontotemporal Dementia Associated With MAPT, GRN, and C9orf72 Pathogenic Variants

artículo científico publicado en 2020

Rates of lobar atrophy in asymptomatic MAPT mutation carriers

artículo científico publicado en 2019

Relationship between physical activity, cognition, and Alzheimer pathology in autosomal dominant Alzheimer's disease

artículo científico publicado en 2018

Relationships between big-five personality factors and Alzheimer's disease pathology in autosomal dominant Alzheimer's disease

scientific article published on 23 June 2020

Replication of BIN1 association with Alzheimer's disease and evaluation of genetic interactions

artículo científico publicado en 2011

Replication of CLU, CR1, and PICALM associations with alzheimer disease.

artículo científico publicado en 2010

Replication of EPHA1 and CD33 associations with late-onset Alzheimer's disease: a multi-centre case-control study

artículo científico publicado en 2011

Replication of progressive supranuclear palsy genome-wide association study identifies SLCO1A2 and DUSP10 as new susceptibility loci

scholarly article by Monica Y Sanchez-Contreras published in July 2018

Role for the microtubule-associated protein tau variant p.A152T in risk of α-synucleinopathies

artículo científico publicado en 2015

Sequence of Alzheimer disease biomarker changes in cognitively normal adults: A cross-sectional study

artículo científico publicado en 2020

Serum neurofilament dynamics predicts neurodegeneration and clinical progression in presymptomatic Alzheimer’s disease

artículo científico publicado en 2019

Serum neurofilament light chain levels are associated with white matter integrity in autosomal dominant Alzheimer's disease

scientific article published on 06 June 2020

Shining a light on posterior cortical atrophy

artículo científico publicado en 2012

Single-subject grey matter network trajectories over the disease course of autosomal dominant Alzheimer's disease

scientific article published on 15 July 2020

Spatial patterns of neuroimaging biomarker change in individuals from families with autosomal dominant Alzheimer's disease: a longitudinal study

artículo científico publicado en 2018

Spt4 selectively regulates the expression of C9orf72 sense and antisense mutant transcripts

artículo científico publicado en 2016

Subtypes of dementia with Lewy bodies are associated with α-synuclein and tau distribution

scientific article published on 19 June 2020

TARDBP mutations in Parkinson's disease

artículo científico publicado en 2012

TDP-43 frontotemporal lobar degeneration and autoimmune disease

artículo científico publicado en 2013

THAL AMYLOID PHASE: CLINICOPATHOLOGIC AND PIB-PET IMPLICATIONS OF AD PATHOPHYSIOLOGY

TMEM106B p.T185S regulates TMEM106B protein levels: implications for frontotemporal dementia

scientific article published on July 2013

TMEM106B protects C9ORF72 expansion carriers against frontotemporal dementia

scientific article published on 03 January 2014

TREM2 in neurodegeneration: evidence for association of the p.R47H variant with frontotemporal dementia and Parkinson's disease

artículo científico publicado en 2013

TREM2 is associated with increased risk for Alzheimer's disease in African Americans

artículo científico publicado en 2015

TREM2 p.R47H substitution is not associated with dementia with Lewy bodies

artículo científico publicado en 2016

TYROBP genetic variants in early-onset Alzheimer's disease

artículo científico publicado en 2016

Telephone assessment of cognitive function in the late-onset Alzheimer's disease family study

artículo científico publicado en 2010

The Alzheimer's Disease Centers' Uniform Data Set (UDS): the neuropsychologic test battery

artículo científico publicado en 2009

The Role of Cardiovascular Risk Factors and Stroke in Familial Alzheimer Disease

artículo científico publicado en 2016

The Uniform Data Set (UDS): clinical and cognitive variables and descriptive data from Alzheimer Disease Centers

artículo científico publicado en 2006

The limbic and neocortical contribution of α-synuclein, tau, and amyloid β to disease duration in dementia with Lewy bodies

artículo científico publicado en 2017

The longitudinal evaluation of familial frontotemporal dementia subjects protocol: Framework and methodology

scientific article published on 06 January 2020

The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease

artículo científico publicado en 2007

Tracking white matter degeneration in asymptomatic and symptomatic MAPT mutation carriers

artículo científico publicado en 2019

Trajectory of lobar atrophy in asymptomatic and symptomatic GRN mutation carriers: a longitudinal MRI study

scientific article published on 12 December 2019

Transethnic genome-wide scan identifies novel Alzheimer's disease loci

artículo científico publicado en 2017

Truncated stathmin-2 is a marker of TDP-43 pathology in frontotemporal dementia

artículo científico publicado en 2020

Two novel loci, COBL and SLC10A2, for Alzheimer's disease in African Americans

artículo científico publicado en 2016

Utility of the global CDR® plus NACC FTLD rating and development of scoring rules: Data from the ARTFL/LEFFTDS Consortium

scientific article published on 01 January 2020

Validation of the Mayo Sleep Questionnaire to screen for REM sleep behavior disorder in an aging and dementia cohort.

artículo científico publicado en 2011

Validation of the neuropathologic criteria of the third consortium for dementia with Lewy bodies for prospectively diagnosed cases

artículo científico publicado en 2008

Variants in the ATP-binding cassette transporter (ABCA7), apolipoprotein E ϵ4,and the risk of late-onset Alzheimer disease in African Americans

artículo científico publicado en 2013

Whole-genome sequencing reveals important role for TBK1 and OPTN mutations in frontotemporal lobar degeneration without motor neuron disease

artículo científico publicado en 2015

β-Amyloid PET and neuropathology in dementia with Lewy bodies

artículo científico publicado en 2019

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