[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 …

[HTML][HTML] Frontotemporal dementias: Recent advances and current controversies

CE Leyton, JR Hodges - Annals of Indian Academy of Neurology, 2010 - journals.lww.com
Frontotemporal dementia (FTD) syndromes comprise a heterogeneous group of
neurodegenerative conditions characterized by atrophy in the frontal and temporal lobes …

Frontotemporal lobar degeneration: epidemiology, pathology, diagnosis and management

RE Seltman, BR Matthews - CNS drugs, 2012 - Springer
Frontotemporal lobar degeneration (FTLD) describes a spectrum of clinically, pathologically
and genetically heterogeneous neurodegenerative disorders of unknown aetiology. FTLD …

[HTML][HTML] Progress and challenges in frontotemporal dementia research: a 20-year review

JR Hodges, O Piguet - Journal of Alzheimer's disease, 2018 - content.iospress.com
The landscape of frontotemporal dementia (FTD) has evolved remarkably in recent years
and is barely recognizable from two decades ago. Knowledge of the clinical …

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

H Seelaar, JD Rohrer, YAL Pijnenburg… - Journal of Neurology …, 2011 - jnnp.bmj.com
Frontotemporal dementia (FTD) is the second most common young-onset dementia and is
clinically characterised by progressive behavioural change, executive dysfunction and …

Frontotemporal dementia

EM Devenney, RM Ahmed, JR Hodges - Handbook of clinical neurology, 2019 - Elsevier
Frontotemporal dementia (FTD) is the second commonest cause of young onset dementia.
Our understanding of FTD and its related syndromes has advanced significantly in recent …

Phenotypic signatures of genetic frontotemporal dementia

JD Rohrer, JD Warren - Current opinion in neurology, 2011 - journals.lww.com
Phenotypic signatures of genetic frontotemporal dementia : Current Opinion in Neurology
Phenotypic signatures of genetic frontotemporal dementia : Current Opinion in Neurology Log in …

The clinical spectrum of sporadic and familial forms of frontotemporal dementia

IOC Woollacott, JD Rohrer - Journal of neurochemistry, 2016 - Wiley Online Library
The term frontotemporal dementia (FTD) describes a clinically, genetically and
pathologically diverse group of neurodegenerative disorders. Symptoms of FTD can present …

An update on clinical, genetic and pathological aspects of frontotemporal lobar degenerations

T Lashley, JD Rohrer, S Mead… - Neuropathology and …, 2015 - Wiley Online Library
The development of our understanding of frontotemporal dementia (FTD) has gathered pace
over the last 10 years. After taking a back seat to A lzheimer's disease for many years FTD …