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Frontotemporal Dementia: Correlations Between Psychiatric Symptoms and Pathology

Annals of neurology, 2020-06, Vol.87 (6), p.950-961

2020

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Psychiatric symptoms of frontotemporal dementia and subcortical (co-)pathology burden: new insights

Brain (London, England : 1878), 2023-01, Vol.146 (1), p.307-320

2023

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FTD-tau S320F mutation stabilizes local structure and allosterically promotes amyloid motif-dependent aggregation

Nature communications, 2023-03, Vol.14 (1), p.1625-1625, Article 1625

2023

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The clinical and pathological phenotype of C9ORF72 hexanucleotide repeat expansions

Brain (London, England : 1878), 2012-03, Vol.135 (Pt 3), p.723-735

2012

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Refining the Spectrum of Neuronal Intranuclear Inclusion Disease: A Case Report

Journal of neuropathology and experimental neurology, 2019-07, Vol.78 (7), p.665-670

2019

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Apolipoprotein L1 is increased in frontotemporal lobar degeneration post-mortem brain but not in ante-mortem cerebrospinal fluid

Neurobiology of disease, 2022-10, Vol.172, p.105813-105813, Article 105813

2022

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Underlying genetic variation in familial frontotemporal dementia: sequencing of 198 patients

Neurobiology of aging, 2021-01, Vol.97, p.148.e9-148.e16

2021

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Structural and functional brain connectivity in presymptomatic familial frontotemporal dementia

Neurology, 2013-02, Vol.80 (9), p.814

2013

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Frequency of ubiquitin and FUS-positive, TDP-43-negative frontotemporal lobar degeneration

Journal of neurology, 2010-05, Vol.257 (5), p.747-753

2010

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Optineurin inclusions occur in a minority of TDP-43 positive ALS and FTLD-TDP cases and are rarely observed in other neurodegenerative disorders

Acta neuropathologica, 2011-04, Vol.121 (4), p.519-527

2011

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Mapping the genetic landscape of early-onset Alzheimer's disease in a cohort of 36 families

Alzheimer's research & therapy, 2022-06, Vol.14 (1), p.77-77, Article 77

2022

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Mindfulness-Based Stress Reduction in Pre-symptomatic Genetic Frontotemporal Dementia: A Pilot Study

Frontiers in psychiatry, 2022-04, Vol.13, p.864391-864391

2022

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Presymptomatic and early pathological features of MAPT-associated frontotemporal lobar degeneration

Acta neuropathologica communications, 2023-08, Vol.11 (1), p.126-126, Article 126

2023

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Proteomics of the dentate gyrus reveals semantic dementia specific molecular pathology

Acta neuropathologica communications, 2022-12, Vol.10 (1), p.190-190, Article 190

2022

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Letter to the editor on a paper by Kaivola et al. (2020): carriership of two copies of C9orf72 hexanucleotide repeat intermediate-length alleles is not associated with amyotrophic lateral sclerosis or frontotemporal dementia

Acta neuropathologica communications, 2022-09, Vol.10 (1), p.141-3, Article 141

2022

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Cerebral blood flow in presymptomatic MAPT and GRN mutation carriers: A longitudinal arterial spin labeling study

NeuroImage clinical, 2016-01, Vol.12 (C), p.460-465

2016

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Distinctive cell‐free DNA methylation characterizes presymptomatic genetic frontotemporal dementia

Annals of clinical and translational neurology, 2024-03, Vol.11 (3), p.744-756

2024

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In vivo PET imaging of neuroinflammation in familial frontotemporal dementia

Journal of neurology, neurosurgery and psychiatry, 2021-03, Vol.92 (3), p.231

2021

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HR23B pathology preferentially co-localizes with p62, pTDP-43 and poly-GA in C9ORF72-linked frontotemporal dementia and amyotrophic lateral sclerosis

Acta neuropathologica communications, 2019-03, Vol.7 (1), p.39-39, Article 39

2019

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Symmetrical Corticobasal Syndrome Caused by a Novel c.314dup Progranulin Mutation

Journal of molecular neuroscience, 2011-11, Vol.45 (3), p.354-358

2011

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Variation at GRN 3'-UTR rs5848 is not associated with a risk of frontotemporal lobar degeneration in Dutch population

PloS one, 2009-10, Vol.4 (10), p.e7494-e7494

2009

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Clinical, genetic and pathological heterogeneity of frontotemporal dementia: a review

Journal of Neurology, Neurosurgery and Psychiatry, 2011-05, Vol.82 (5), p.476-486

2011

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Recommendations to distinguish behavioural variant frontotemporal dementia from psychiatric disorders

Brain (London, England : 1878), 2020-06, Vol.143 (6), p.1632-1650

2020

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The influence of vascular pathology on the generalizability of machine learning models for cognitive performance estimation

Alzheimer's & dementia, 2023-12, Vol.19 (S17), p.n/a

2023

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

Lancet neurology, 2020-02, Vol.19 (2), p.145-156

2020

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Frontotemporal Dementia: Correlations Between Psychiatric Symptoms and Pathology

Psychiatric symptoms of frontotemporal dementia and subcortical (co-)pathology burden: new insights

FTD-tau S320F mutation stabilizes local structure and allosterically promotes amyloid motif-dependent aggregation

The clinical and pathological phenotype of C9ORF72 hexanucleotide repeat expansions

Refining the Spectrum of Neuronal Intranuclear Inclusion Disease: A Case Report

Apolipoprotein L1 is increased in frontotemporal lobar degeneration post-mortem brain but not in ante-mortem cerebrospinal fluid

Underlying genetic variation in familial frontotemporal dementia: sequencing of 198 patients

Structural and functional brain connectivity in presymptomatic familial frontotemporal dementia

Frequency of ubiquitin and FUS-positive, TDP-43-negative frontotemporal lobar degeneration

Optineurin inclusions occur in a minority of TDP-43 positive ALS and FTLD-TDP cases and are rarely observed in other neurodegenerative disorders

Mapping the genetic landscape of early-onset Alzheimer's disease in a cohort of 36 families

Mindfulness-Based Stress Reduction in Pre-symptomatic Genetic Frontotemporal Dementia: A Pilot Study

Presymptomatic and early pathological features of MAPT-associated frontotemporal lobar degeneration

Proteomics of the dentate gyrus reveals semantic dementia specific molecular pathology

Letter to the editor on a paper by Kaivola et al. (2020): carriership of two copies of C9orf72 hexanucleotide repeat intermediate-length alleles is not associated with amyotrophic lateral sclerosis or frontotemporal dementia

Cerebral blood flow in presymptomatic MAPT and GRN mutation carriers: A longitudinal arterial spin labeling study

Distinctive cell‐free DNA methylation characterizes presymptomatic genetic frontotemporal dementia

In vivo PET imaging of neuroinflammation in familial frontotemporal dementia

HR23B pathology preferentially co-localizes with p62, pTDP-43 and poly-GA in C9ORF72-linked frontotemporal dementia and amyotrophic lateral sclerosis

Symmetrical Corticobasal Syndrome Caused by a Novel c.314dup Progranulin Mutation

Variation at GRN 3'-UTR rs5848 is not associated with a risk of frontotemporal lobar degeneration in Dutch population

Clinical, genetic and pathological heterogeneity of frontotemporal dementia: a review

Recommendations to distinguish behavioural variant frontotemporal dementia from psychiatric disorders

The influence of vascular pathology on the generalizability of machine learning models for cognitive performance estimation

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

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