Frontotemporal dementia or frontotemporal lobar degeneration--overview of a group of proteinopathies.

C Haberland - Ideggyógyászati szemle, 2010 - europepmc.org
Frontotemporal dementia is the second most common early onset dementia after Alzheimer
disease. Frontotemporal dementias are a complex group of dementias. The clinical …

Frontotemporal lobar degeneration (FTLD): review and update for clinical neurologists

I Hernandez, MV Fernandez, L Tarraga… - Current Alzheimer …, 2018 - ingentaconnect.com
Background: Frontotemporal Dementia (FTD) is a heterogeneous group of disorders and the
second most frequent cause of early onset dementia making it the highest number of …

[HTML][HTML] Clinic, neuropathology and molecular genetics of frontotemporal dementia: a mini-review

X Pan, X Chen - Translational neurodegeneration, 2013 - Springer
Frontotemporal lobar degeneration (FTLD) represents a group of clinically,
neuropathologically and genetically heterogeneous disorders with plenty of overlaps …

Clinical, genetic and neuroimaging features of frontotemporal dementia

R Convery, S Mead, JD Rohrer - Neuropathology and Applied …, 2019 - Wiley Online Library
Frontotemporal dementia (FTD) is a heterogeneous group of disorders causing
neurodegeneration within a network of areas centred on the frontal and temporal lobes …

Biological basis and psychiatric symptoms in frontotemporal dementia

K Mori, M Ikeda - Psychiatry and Clinical Neurosciences, 2022 - Wiley Online Library
Frontotemporal dementia is a neurodegenerative disease characterized by focal
degeneration of the frontal and temporal lobes, clinically presenting with disinhibited …

Tau rather than TDP-43 proteins are potential cerebrospinal fluid biomarkers for frontotemporal lobar degeneration subtypes: a pilot study

HB Kuiperij, AAM Versleijen, M Beenes… - Journal of …, 2017 - content.iospress.com
Background: Frontotemporal dementia (FTD) is a heterogeneous disease both at the
clinical, genetic, and pathobiological level. The underlying pathological spectrum (termed …

Frontotemporal lobar degeneration: genetics and clinical phenotypes

M Serpente, D Galimberti - Neurodegenerative Diseases: Clinical Aspects …, 2014 - Springer
Frontotemporal lobar degeneration (FTLD) is the most frequent dementia in the presenile
population. It presents with different syndromes, including behavioral variant frontotemporal …

[图书][B] Biomarkers in Frontotemporal Dementia: Findings from the Genfi Study

L Öijerstedt - 2021 - search.proquest.com
Frontotemporal dementia (FTD) is a group of neurodegenerative diseases including a wide
range of clinical phenotypes, neuropathological hallmarks, and genetic causes. People with …

Clinical phenotypes and genetic biomarkers of FTLD

D Galimberti, E Scarpini - Journal of Neural Transmission, 2012 - Springer
Frontotemporal lobar degeneration (FTLD) is the most frequent neurodegenerative disorder
with a presenile onset. It presents with a spectrum of clinical manifestations, ranging from …

Frontotemporal dementia spectrum: first genetic screen in a Greek cohort

EM Ramos, C Koros, DR Dokuru, V Van Berlo… - Neurobiology of …, 2019 - Elsevier
Frontotemporal dementia (FTD) is a heterogeneous group of neurodegenerative syndromes
associated with several causative and susceptibility genes. Herein, we aimed to determine …