Clinical and neuroanatomical signatures of tissue pathology in frontotemporal lobar degeneration

Atrophy, hypometabolism and white matter abnormalities in semantic dementia tell a coherent story

(2011) J. Acosta-Cabronero et al.   BRAIN

Clinical phenotypes in autopsy-confirmed Pick disease

(2011) O. Piguet et al.   NEUROLOGY

Progression of language decline and cortical atrophy in subtypes of primary progressive aphasia

(2011) E. Rogalski et al.   NEUROLOGY

Classification of primary progressive aphasia and its variants

(2011) M. L. Gorno-Tempini et al.   NEUROLOGY

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

(2010) Hazel Urwin et al.   ACTA NEUROPATHOLOGICA

Alzheimer Disease–like Phenotype Associated With the c.154delA Mutation in Progranulin

(2010) Brendan J. Kelley et al.   ARCHIVES OF NEUROLOGY

Does corticobasal degeneration exist? A clinicopathological re-evaluation

(2010) H. Ling et al.   BRAIN

Divergent network connectivity changes in behavioural variant frontotemporal dementia and Alzheimer’s disease

(2010) Juan Zhou et al.   BRAIN

Caudate atrophy on MRI is a characteristic feature of FTLD-FUS

(2010) K. A. Josephs et al.   EUROPEAN JOURNAL OF NEUROLOGY

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

(2010) H. Seelaar et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

Distinct profiles of brain atrophy in frontotemporal lobar degeneration caused by progranulin and tau mutations

(2010) Jonathan D. Rohrer et al.   NEUROIMAGE

Asymmetric TDP-43 distribution in primary progressive aphasia with progranulin mutation

(2010) G. Gliebus et al.   NEUROLOGY

TDP-43 subtypes are associated with distinct atrophy patterns in frontotemporal dementia

(2010) J. D. Rohrer et al.   NEUROLOGY

Abundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion disease

(2009) Manuela Neumann et al.   ACTA NEUROPATHOLOGICA

FUS pathology in basophilic inclusion body disease

(2009) David G. Munoz et al.   ACTA NEUROPATHOLOGICA

Clinicopathological characterization of Pick’s disease versus frontotemporal lobar degeneration with ubiquitin/TDP-43-positive inclusions

(2009) Osamu Yokota et al.   ACTA NEUROPATHOLOGICA

Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update

(2009) Ian R. A. Mackenzie et al.   ACTA NEUROPATHOLOGICA

Clinical and Pathological Continuum of Multisystem TDP-43 Proteinopathies

(2009) Felix Geser et al.   ARCHIVES OF NEUROLOGY

With or without FUS, it is the anatomy that dictates the dementia phenotype

(2009) S. Weintraub et al.   BRAIN

A new subtype of frontotemporal lobar degeneration with FUS pathology

(2009) M. Neumann et al.   BRAIN

Distinct anatomical subtypes of the behavioural variant of frontotemporal dementia: a cluster analysis study

(2009) J. L. Whitwell et al.   BRAIN

Delusions in frontotemporal lobar degeneration

(2009) Rohani Omar et al.   JOURNAL OF NEUROLOGY

No association of PGRN 3′UTR rs5848 in frontotemporal lobar degeneration

(2009) Sara Rollinson et al.   NEUROBIOLOGY OF AGING

MRI Correlates of Protein Deposition and Disease Severity in Postmortem Frontotemporal Lobar Degeneration

(2009) Jennifer L. Whitwell et al.   Neurodegenerative Diseases

Progressive logopenic/phonological aphasia: Erosion of the language network

(2009) Jonathan D. Rohrer et al.   NEUROIMAGE

The heritability and genetics of frontotemporal lobar degeneration

(2009) J. D. Rohrer et al.   NEUROLOGY

Atrophy patterns in histologic vs clinical groupings of frontotemporal lobar degeneration

(2009) J.M.S. Pereira et al.   NEUROLOGY

Atrophy patterns in IVS10+16, IVS10+3, N279K, S305N, P301L, and V337M MAPT mutations

(2009) J. L. Whitwell et al.   NEUROLOGY

Neurodegenerative Diseases Target Large-Scale Human Brain Networks

(2009) William W. Seeley et al.   NEURON

Progranulin-associated primary progressive aphasia: A distinct phenotype?

(2009) Jonathan D. Rohrer et al.   NEUROPSYCHOLOGIA

Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendations

(2008) Ian R. A. Mackenzie et al.   ACTA NEUROPATHOLOGICA

Cortical α-synuclein load is associated with amyloid-β plaque burden in a subset of Parkinson’s disease patients

(2008) Tammaryn Lashley et al.   ACTA NEUROPATHOLOGICA

Alzheimer and frontotemporal pathology in subsets of primary progressive aphasia

(2008) Marsel Mesulam et al.   ANNALS OF NEUROLOGY

Frontal Paralimbic Network Atrophy in Very Mild Behavioral Variant Frontotemporal Dementia

(2008) William W. Seeley et al.   ARCHIVES OF NEUROLOGY

Selective functional, regional, and neuronal vulnerability in frontotemporal dementia

(2008) William W Seeley   CURRENT OPINION IN NEUROLOGY

Apraxia of speech and nonfluent aphasia: a new clinical marker for corticobasal degeneration and progressive supranuclear palsy

(2008) Keith A Josephs et al.   CURRENT OPINION IN NEUROLOGY

The two faces of protein misfolding: gain- and loss-of-function in neurodegenerative diseases

(2008) Konstanze F Winklhofer et al.   EMBO JOURNAL

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

(2008) Rosa Rademakers et al.   HUMAN MOLECULAR GENETICS

Clinicopathological and genetic correlates of frontotemporal lobar degeneration and corticobasal degeneration

(2008) Albert Lladó et al.   JOURNAL OF NEUROLOGY

Ventral and dorsal pathways for language

(2008) D. Saur et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Prominent phenotypic variability associated with mutations in Progranulin

(2007) Brendan J. Kelley et al.   NEUROBIOLOGY OF AGING

Neuropsychological findings in clinically atypical autopsy confirmed corticobasal degeneration and progressive supranuclear palsy

(2007) Wendy A. VanVoorst et al.   PARKINSONISM & RELATED DISORDERS

Voxel-based morphometry in autopsy proven PSP and CBD

(2006) Keith A. Josephs et al.   NEUROBIOLOGY OF AGING