The neurovascular unit coming of age: a journey through neurovascular coupling in health and disease

C Iadecola - Neuron, 2017 - cell.com
The concept of the neurovascular unit (NVU), formalized at the 2001 Stroke Progress
Review Group meeting of the National Institute of Neurological Disorders and Stroke …

An update on genetic frontotemporal dementia

CV Greaves, JD Rohrer - Journal of neurology, 2019 - Springer
Frontotemporal dementia (FTD) is a highly heritable group of neurodegenerative disorders,
with around 30% of patients having a strong family history. The majority of that heritability is …

Fibrinogen in neurological diseases: mechanisms, imaging and therapeutics

MA Petersen, JK Ryu, K Akassoglou - Nature Reviews Neuroscience, 2018 - nature.com
The blood coagulation protein fibrinogen is deposited in the brain in a wide range of
neurological diseases and traumatic injuries with blood–brain barrier (BBB) disruption …

Frontotemporal dementia: latest evidence and clinical implications

JJ Young, M Lavakumar, D Tampi… - Therapeutic …, 2018 - journals.sagepub.com
Background: Frontotemporal dementia (FTD) describes a cluster of neurocognitive
syndromes that present with impairment of executive functioning, changes in behavior, and …

Plasma glial fibrillary acidic protein is raised in progranulin-associated frontotemporal dementia

C Heller, MS Foiani, K Moore, R Convery… - Journal of Neurology …, 2020 - jnnp.bmj.com
Background There are few validated fluid biomarkers in frontotemporal dementia (FTD).
Glial fibrillary acidic protein (GFAP) is a measure of astrogliosis, a known pathological …

Network structure and transcriptomic vulnerability shape atrophy in frontotemporal dementia

G Shafiei, V Bazinet, M Dadar, AL Manera, DL Collins… - Brain, 2023 - academic.oup.com
Connections among brain regions allow pathological perturbations to spread from a single
source region to multiple regions. Patterns of neurodegeneration in multiple diseases …

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

EL van der Ende, LH Meeter, JM Poos… - The Lancet …, 2019 - thelancet.com
Summary Background Neurofilament light chain (NfL) is a promising blood biomarker in
genetic frontotemporal dementia, with elevated concentrations in symptomatic carriers of …

Microglial lysosome dysfunction contributes to white matter pathology and TDP-43 proteinopathy in GRN-associated FTD

Y Wu, W Shao, TW Todd, J Tong, M Yue, S Koga… - Cell reports, 2021 - cell.com
Loss-of-function mutations in the progranulin gene (GRN), which encodes progranulin
(PGRN), are a major cause of frontotemporal dementia (FTD). GRN-associated FTD is …

Genotype–phenotype links in frontotemporal lobar degeneration

S Van Mossevelde, S Engelborghs… - Nature Reviews …, 2018 - nature.com
Frontotemporal lobar degeneration (FTLD) represents a group of neurodegenerative brain
diseases with highly heterogeneous clinical, neuropathological and genetic characteristics …

Microglial burden, activation and dystrophy patterns in frontotemporal lobar degeneration

IOC Woollacott, CE Toomey, C Strand… - Journal of …, 2020 - Springer
Background Microglial dysfunction is implicated in frontotemporal lobar degeneration
(FTLD). Although studies have reported excessive microglial activation or senescence …