Office of Rare Diseases neuropathologic criteria for corticobasal degeneration. - Test2 - elhamkhani - TriplyDB

Office of Rare Diseases neuropathologic criteria for corticobasal degeneration.

Office of Rare Diseases neuropathologic criteria for corticobasal degeneration.

http://www.wikidata.org/entity/Q48447237

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Predicting amyloid status in corticobasal syndrome using modified clinical criteria, magnetic resonance imaging and fluorodeoxyglucose positron emission tomography Interface between tauopathies and synucleinopathies: A tale of two proteins Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease Clinical, cognitive and anatomical evolution from nonfluent progressive aphasia to corticobasal syndrome: a case report Argyrophilic grains: a distinct disease or an additive pathology?Neuropathology of non-Alzheimer degenerative disorders TSPO imaging in parkinsonian disorders Characteristics of Tau and Its Ligands in PET Imaging Genetics Underlying Atypical Parkinsonism and Related Neurodegenerative Disorders Therapeutic and diagnostic challenges for frontotemporal dementia Clinicopathologic assessment and imaging of tauopathies in neurodegenerative dementias The first NINDS/NIBIB consensus meeting to define neuropathological criteria for the diagnosis of chronic traumatic encephalopathy The corticobasal syndrome-Alzheimer's disease conundrum Neurofibrillary tangle-predominant dementia: comparison with classical Alzheimer disease Validation of the new consensus criteria for the diagnosis of corticobasal degeneration Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.Frontotemporal Dementia.Signal alterations of the basal ganglia in the differential diagnosis of Parkinson's disease: a retrospective case-controlled MRI data bank analysis.Iron metabolism in Parkinsonian syndromes.Pedigree with frontotemporal lobar degeneration--motor neuron disease and Tar DNA binding protein-43 positive neuropathology: genetic linkage to chromosome 9.Multiprotein deposits in neurodegenerative disorders: our experience in the tissue brain bank of Navarra.Translocator Protein-18 kDa (TSPO) Positron Emission Tomography (PET) Imaging and Its Clinical Impact in Neurodegenerative Diseases Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: consensus of the Consortium for Frontotemporal Lobar Degeneration Seizures in corticobasal degeneration: a case report.Sporadic corticobasal syndrome due to FTLD-TDP.Quantitative neuropathology: an update on automated methodologies and implications for large scale cohorts.Disentangling the neural correlates of corticobasal syndrome and corticobasal degeneration with systematic and quantitative ALE meta-analyses Abnormal Resting-State Functional Connectivity in Progressive Supranuclear Palsy and Corticobasal Syndrome.Assessment of amyloid β in pathologically confirmed frontotemporal dementia syndromes.A mutation affecting the sodium/proton exchanger, SLC9A6, causes mental retardation with tau deposition.Biomarkers in frontotemporal lobar degenerations--progress and challenges.Dopamine Transporter SPECT Imaging in Corticobasal Syndrome.Frontal white matter tracts sustaining speech production in primary progressive aphasia Temporoparietal atrophy: a marker of AD pathology independent of clinical diagnosis.An unusual cause of dementia: essential diagnostic elements of corticobasal degeneration-a case report and review of the literature Frontotemporal lobar degeneration: epidemiology, pathophysiology, diagnosis and management.Anatomical differences between CBS-corticobasal degeneration and CBS-Alzheimer's disease.Visuoperception test predicts pathologic diagnosis of Alzheimer disease in corticobasal syndrome Multimodal predictors for Alzheimer disease in nonfluent primary progressive aphasia.Symmetric corticobasal degeneration (S-CBD).

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P2860

Office of Rare Diseases neuropathologic criteria for corticobasal degeneration.

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P2860

Neuropathological stageing of Alzheimer-related changes

Comparative biochemistry of tau in progressive supranuclear palsy, corticobasal degeneration, FTDP-17 and Pick's disease

Accumulation of abnormally phosphorylated tau precedes the formation of neurofibrillary tangles in Alzheimer's disease

Dementia with grains (argyrophilic grain disease)

The corticobasal degeneration syndrome overlaps progressive aphasia and frontotemporal dementia.

Neuropathologic substrates of ischemic vascular dementia.

Update on the neuropathological diagnosis of frontotemporal dementias.

Astrocytic plaques and tufts of abnormal fibers do not coexist in corticobasal degeneration and progressive supranuclear palsy.

Familial dementia lacking specific pathological features presenting with clinical features of corticobasal degeneration.

Preliminary NINDS neuropathologic criteria for Steele-Richardson-Olszewski syndrome (progressive supranuclear palsy).

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