Related references
Note: Only part of the references are listed.TDP-43-immunoreactive neuronal and glial inclusions in the neostriatum in amyotrophic lateral sclerosis with and without dementia
Haixin Zhang et al.
ACTA NEUROPATHOLOGICA (2008)
Concurrence of TDP-43, tau and α-synuclein pathology in brains of Alzheimer's disease and dementia with Lewy bodies
Shinji Higashi et al.
BRAIN RESEARCH (2007)
TDP-43 proteinopathy in frontotemporal lobar degeneration and amyotrophic lateral sclerosis - Protein misfolding diseases without amyloidosis
Manuela Neumann et al.
ARCHIVES OF NEUROLOGY (2007)
A reassessment of the neuropathology of frontotemporal dementia linked to chromosome 3
Ida Elisabeth Holm et al.
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY (2007)
TDP-43: a novel neurodegenerative proteinopathy
Mark S. Forman et al.
CURRENT OPINION IN NEUROBIOLOGY (2007)
Linking SIRT2 to Parkinson's disease
Adam L. Garske et al.
ACS CHEMICAL BIOLOGY (2007)
TDP-43 proteinopathy: the neuropathology underlying major forms of sporadic and familial frontotemporal lobar degeneration and motor neuron disease
Linda K. Kwong et al.
ACTA NEUROPATHOLOGICA (2007)
TDP-43 in differential diagnosis of motor neuron disorders
Dennis W. Dickson et al.
ACTA NEUROPATHOLOGICA (2007)
Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: consensus of the Consortium for Frontotemporal Lobar Degeneration
Nigel J. Cairns et al.
ACTA NEUROPATHOLOGICA (2007)
TDP-43 in familial and sporadic frontotemporal lobar degeneration with ubiquitin inclusions
Nigel J. Cairns et al.
AMERICAN JOURNAL OF PATHOLOGY (2007)
Amyloid deposition begins in the striatum of presenilin-1 mutation carriers from two unrelated pedigrees
William E. Klunk et al.
JOURNAL OF NEUROSCIENCE (2007)
TDP-43 pathology in familial frontotemporal dementia and motor neuron disease without Progranulin mutations
Harro Seelaar et al.
BRAIN (2007)
TDP-43 immunoreactivity in hippocampal sclerosis and Alzheimer's disease
Catalina Amador-Ortiz et al.
ANNALS OF NEUROLOGY (2007)
Ubiquitinated pathological lesions in frontotemporal lobar degeneration contain the TAR DNA-binding protein, TDP-43
Yvonne Davidson et al.
ACTA NEUROPATHOLOGICA (2007)
The ubiquitin-binding protein p62 identifies argyrophilic grain pathology with greater sensitivity than conventional silver stains
Ian S. Scott et al.
ACTA NEUROPATHOLOGICA (2007)
TDP-43-positive white matter pathology in frontotemporal lobar degeneration with ubiquitin-positive inclusions
Manuela Neumann et al.
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY (2007)
TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
Tetsuaki Arai et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2006)
Immunoreactivities of p62, an ubiqutin-binding protein, in the spinal anterior horn cells of patients with amyotrophic lateral sclerosis
Yuji Mizuno et al.
JOURNAL OF THE NEUROLOGICAL SCIENCES (2006)
Heterogeneity of ubiquitin pathology in frontotemporal lobar degeneration: classification and relation to clinical phenotype
Ian R. A. Mackenzie et al.
ACTA NEUROPATHOLOGICA (2006)
Dementia lacking distinctive histology (DLDH) revisited
Ian R. A. Mackenzie et al.
ACTA NEUROPATHOLOGICA (2006)
Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
Manuela Neumann et al.
SCIENCE (2006)
Staging of Alzheimer disease-associated neurofibrillary pathology using paraffin sections and immunocytochemistry
Heiko Braak et al.
ACTA NEUROPATHOLOGICA (2006)
Heterogeneous inclusions in neurofilament inclusion disease
Hirotake Uchikado et al.
NEUROPATHOLOGY (2006)
Pathological heterogeneity of frontotemporal lobar degeneration with ubiquitin-positive inclusions delineated by ubiquitin immunohistochemistry and novel monoclonal antibodies
Deepak M. Sampathu et al.
AMERICAN JOURNAL OF PATHOLOGY (2006)
An autopsy case of frontotemporal dementia with severe dysarthria and motor neuron disease showing numerous basophilic inclusions
Kenji Ishihara et al.
NEUROPATHOLOGY (2006)
ALS phenotypes with mutations in CHMP2B (charged multivesicular body protein 2B)
N. Parkinson et al.
NEUROLOGY (2006)
Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17
Matt Baker et al.
NATURE (2006)
Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21
Marc Cruts et al.
NATURE (2006)
Interlaboratory comparison of assessments of Alzheimer disease-related lesions:: a study of the BrainNet Europe consortium
Irina Alafuzoff et al.
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY (2006)
Comparative study of commercially available anti-α-synuclein antibodies
E Croisier et al.
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY (2006)
Frontotemporal dementia: Clinicopathological correlations
Mark S. Forman et al.
ANNALS OF NEUROLOGY (2006)
A family with tau-negative frontotemporal dementia and neuronal intranuclear inclusions linked to chromosome 17
IR Mackenzie et al.
BRAIN (2006)
Characterization of ubiquitinated intraneuronal inclusions in a novel Belgian frontotemporal lobar degeneration family
Daniel Pirici et al.
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY (2006)
Ubiquitin-positive inclusions and progression of pathology in frontotemporal dementia and motor neurone disease identifies a group with mainly early pathology
C Kersaitis et al.
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY (2006)
Signaling, polyubiquitination, trafficking, and inclusions: Sequestosome 1/p62's role in neurodegenerative disease
Marie W. Wooten et al.
JOURNAL OF BIOMEDICINE AND BIOTECHNOLOGY (2006)
Histopathological changes underlying frontotemporal lobar degeneration with clinicopathological correlation
J Shi et al.
ACTA NEUROPATHOLOGICA (2005)
Ubiquitin immunohistochemistry of frontotemporal lobar degeneration differentiates cases with and without motor neuron disease
O Katsuse et al.
ALZHEIMER DISEASE & ASSOCIATED DISORDERS (2005)
Ubiquitin immunohistochemistry suggests classic motor neuron disease, motor neuron disease with dementia, and frontotemporal dementia of the motor neuron disease type represent a clinicopathologic spectrum
IRA Mackenzie et al.
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY (2005)
Frontotemporal lobar degeneration - Demographic characteristics of 353 patients
JK Johnson et al.
ARCHIVES OF NEUROLOGY (2005)
The neuropathology of frontotemporal lobar degeneration with respect to the cytological and biochemical characteristics of tau protein
S Taniguchi et al.
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY (2004)
Cortical ubiquitin-positive inclusions in frontotemporal dementia without motor neuron disease:: a quantitative immunocytochemical study
E Kövari et al.
ACTA NEUROPATHOLOGICA (2004)
Clinicopathological correlates in frontotemporal dementia
JR Hodges et al.
ANNALS OF NEUROLOGY (2004)
Frontotemporal lobar degeneration and ubiquitin immunohistochemistry
KA Josephs et al.
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY (2004)
Amyotrophic lateral sclerosis with neuronal intranuclear protein inclusions
D Seilhean et al.
ACTA NEUROPATHOLOGICA (2004)
Ubiquitin and ubiquitin-related proteins in the brains of patients with atypical Pick's disease without Pick bodies and dementia with motor neuron disease
Y Furukawa et al.
NEUROPATHOLOGY (2004)
Frontotemporal lobar degeneration with ubiquitin-only-immunoreactive neuronal changes: broadening the clinical picture to include progressive supranuclear palsy
DC Paviour et al.
BRAIN (2004)
Frontotemporal lobar degeneration with motor neuron disease-type inclusions predominates in 76 cases of frontotemporal degeneration
AM Lipton et al.
ACTA NEUROPATHOLOGICA (2004)
α-internexin is present in the pathological inclusions of neuronal intermediate filament inclusion disease
NJ Cairns et al.
AMERICAN JOURNAL OF PATHOLOGY (2004)
Increased expression of p62 in expanded polyglutamine-expressing cells and its association with polyglutamine inclusions
U Nagaoka et al.
JOURNAL OF NEUROCHEMISTRY (2004)
Neurofilament inclusion body disease: a new proteinopathy?
KA Josephs et al.
BRAIN (2003)
The prevalence and causes of dementia in people under the age of 65 years
RJ Harvey et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2003)
Ubiquitin-mediated sequestration of normal cellular proteins into polyglutamine aggregates
KM Donaldson et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2003)
Neuronal and glial inclusions in frontotemporal dementia with or without motor neuron disease are immunopositive for p62
T Arai et al.
NEUROSCIENCE LETTERS (2003)
Staging of brain pathology related to sporadic Parkinson's disease
H Braak et al.
NEUROBIOLOGY OF AGING (2003)
Inter-laboratory and inter-observer reproducibility of immunohistochemical assessment of the Ki-67 labelling index in a large multi-centre trial
M Mengel et al.
JOURNAL OF PATHOLOGY (2002)
The prevalence of frontotemporal dementia
E Ratnavalli et al.
NEUROLOGY (2002)
Early accumulation of p62 in neurofibrillary tangles in Alzheimer's disease: possible role in tangle formation
E Kuusisto et al.
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY (2002)
Tau negative frontal lobe dementia at 17q21: significant finemapping of the candidate region to a 4.8 cM interval
R Rademakers et al.
MOLECULAR PSYCHIATRY (2002)
Clinical and pathological diagnosis of Frontotemporal Dementia - Report of the work group on Frontotemporal Dementia and Pick's disease
GM McKhann et al.
ARCHIVES OF NEUROLOGY (2001)
Familial frontotemporal dementia with ubiquitin-positive inclusions is linked to chromosome 17q2l-22
SM Rosso et al.
BRAIN (2001)
Characterization and functional implications of the RNA binding properties of nuclear factor TDP-43, a novel splicing regulator of CFTR exon 9
E Buratti et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2001)
Ubiquitin-binding protein p62 is present in neuronal and glial inclusions in human tauopathies and synucleinopathies
E Kuusisto et al.
NEUROREPORT (2001)
Nuclear factor TDP-43 and SR proteins promote in vitro and in vivo CFTR exon 9 skipping
E Buratti et al.
EMBO JOURNAL (2001)
Familial frontotemporal dementia with ubiquitin inclusion bodies and without motor neuron disease
E Kövari et al.
ACTA NEUROPATHOLOGICA (2000)