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Neurology, ISSN 0028-3878, 04/2007, Volume 68, Issue 16, pp. 1274 - 1283
Objective: To investigate the clinical features of autopsy-proven corticobasal degeneration (CBD). Methods: We evaluated symptoms, signs, and... 
HETEROGENEITY | BASAL GANGLIONIC DEGENERATION | NEUROPSYCHOLOGICAL MEASURES | ALZHEIMERS-DISEASE | FRONTOTEMPORAL DEMENTIA | POSITRON EMISSION TOMOGRAPHY | PICKS-DISEASE | APHASIA | CLINICAL NEUROLOGY | PROGRESSIVE SUPRANUCLEAR PALSY | NEURONAL ACHROMASIA | Predictive Value of Tests | Language Disorders - diagnosis | Neurodegenerative Diseases - psychology | Humans | Middle Aged | Movement Disorders - diagnosis | Neurodegenerative Diseases - diagnosis | tau Proteins - metabolism | Male | Apraxias - etiology | Apraxias - physiopathology | Language Disorders - physiopathology | Neural Pathways - pathology | Neurofibrillary Tangles - metabolism | Cognition Disorders - etiology | Apraxias - diagnosis | Basal Ganglia Diseases - diagnosis | Basal Ganglia Diseases - etiology | Female | Registries | Neural Pathways - physiopathology | Tauopathies - psychology | Tauopathies - physiopathology | Neurofibrillary Tangles - pathology | Cognition Disorders - physiopathology | Brain - physiopathology | Disease Progression | Neuropsychological Tests | Cognition Disorders - diagnosis | Language Disorders - etiology | Movement Disorders - physiopathology | Neurodegenerative Diseases - physiopathology | Neurologic Examination | Basal Ganglia Diseases - physiopathology | Tauopathies - diagnosis | Movement Disorders - etiology | Age of Onset | Brain - pathology | Aged | Longitudinal Studies
Journal Article
Journal Article
Ageing Research Reviews, ISSN 1568-1637, 2017, Volume 36, pp. 50 - 63
Highlights • We reviewed the emerging tau PET literature across various neurodegenerative conditions and non-AD tauopathies. • Focal tau pathology has been... 
Neurology | Internal Medicine | Tauopathies | MRI | Neurodegeneration | Tau | PET | Dementia | Cognitive impairment | TAUOPATHY MOUSE MODEL | ALZHEIMERS-DISEASE | FRONTOTEMPORAL DEMENTIA | NEUROFIBRILLARY PATHOLOGY | MILD COGNITIVE IMPAIRMENT | LATE-LIFE DEPRESSION | CELL BIOLOGY | GERIATRICS & GERONTOLOGY | POSITRON-EMISSION-TOMOGRAPHY | MEDIAL TEMPORAL-LOBE | PROGRESSIVE SUPRANUCLEAR PALSY | LEWY BODY DEMENTIA | Humans | tau Proteins - metabolism | Dementia - physiopathology | Temporal Lobe - diagnostic imaging | Dementia - metabolism | Neurofibrillary Tangles - metabolism | Tauopathies - diagnostic imaging | Cognitive Dysfunction - diagnostic imaging | Tauopathies - physiopathology | Neurodegenerative Diseases - diagnostic imaging | Biomarkers - metabolism | Dementia - diagnostic imaging | Neurofibrillary Tangles - pathology | Alzheimer Disease - physiopathology | Plaque, Amyloid - pathology | Cognitive Dysfunction - metabolism | Neurodegenerative Diseases - metabolism | Positron-Emission Tomography - methods | Cognitive Dysfunction - physiopathology | Temporal Lobe - metabolism | Tauopathies - metabolism | Temporal Lobe - physiopathology | Animals | Neurodegenerative Diseases - physiopathology | Plaque, Amyloid - physiopathology | Alzheimer Disease - metabolism | Fluorine Radioisotopes - metabolism | Plaque, Amyloid - metabolism | Alzheimer Disease - diagnostic imaging | Medicine, Experimental | Medical research | Nervous system diseases | PET imaging | Alzheimer's disease
Journal Article
Journal Article
Annals of Neurology, ISSN 0364-5134, 06/2006, Volume 59, Issue 6, pp. 952 - 962
Journal Article
European Journal of Neurology, ISSN 1351-5101, 2009, Volume 16, Issue 3, pp. 297 - 309
Tauopathies with parkinsonism represent a spectrum of disease entities unified by the pathologic accumulation of hyperphosphorylated tau protein fragments... 
microtubule‐associated protein tau | corticobasal degeneration | parkinsonism | frontotemporal dementia with parkinsonism linked to chromosome 17 | Parkinson disease | tauopathies | multiple system atrophy | progressive supranuclear palsy | Parkinsonism | Tauopathies | Progressive supranuclear palsy | Multiple system atrophy | Frontotemporal dementia with parkinsonism linked to chromosome 17 | Corticobasal degeneration | Microtubule-associated protein tau | TAU-PROTEIN | NEUROFIBRILLARY TANGLES | ATYPICAL PARKINSONISM | ALZHEIMERS-DISEASE | GLYCOGEN-SYNTHASE KINASE-3 | FRONTOTEMPORAL DEMENTIA | NEUROSCIENCES | CLINICAL NEUROLOGY | microtubule-associated protein tau | MITOCHONDRIAL COMPLEX-I | MOUSE MODEL | TRANSGENIC MICE | Geography | Supranuclear Palsy, Progressive - physiopathology | Parkinsonian Disorders - complications | Humans | Tauopathies - pathology | Dementia - physiopathology | Dementia - genetics | Niemann-Pick Disease, Type C - physiopathology | Supranuclear Palsy, Progressive - complications | Pick Disease of the Brain - pathology | tau Proteins - genetics | Drug Design | Tauopathies - complications | Tauopathies - therapy | Niemann-Pick Disease, Type C - diagnosis | Tauopathies - physiopathology | Parkinsonian Disorders - physiopathology | Pick Disease of the Brain - complications | Parkinson Disease, Postencephalitic - physiopathology | Protein-Serine-Threonine Kinases - genetics | Parkinson Disease, Postencephalitic - complications | Leucine-Rich Repeat Serine-Threonine Protein Kinase-2 | Animals | Dementia - complications | Parkinsonian Disorders - pathology | Parkinsonian Disorders - therapy | Models, Biological | Biomarkers | Mutation | Niemann-Pick Disease, Type C - complications | Supranuclear Palsy, Progressive - diagnosis | Medical colleges | Care and treatment | Orphan drugs | Neurosciences | Parkinson's disease | Amyotrophic lateral sclerosis | Biological markers | Banks (Finance) | Natural history | microtubule-associated protein tau, multiple system atrophy | Review
Journal Article
JNEN: Journal of Neuropathology & Experimental Neurology, ISSN 0022-3069, 09/2004, Volume 63, Issue 9, pp. 911 - 918
Journal Article
Journal Article
Neurology, ISSN 0028-3878, 2005, Volume 65, Issue 10, pp. 1636 - 1638
Neurofibrillary degeneration (NFD) occurs in the brains of patients with myotonic dystrophy (DM) type 1. The authors report a similar tau pathology in the CNS... 
RNA | MYOTONIC-DYSTROPHY TYPE-1 | CLINICAL NEUROLOGY | Immunohistochemistry | Neurons - pathology | RNA-Binding Proteins - genetics | Neurofibrillary Tangles - genetics | Myotonic Dystrophy - diagnosis | tau Proteins - immunology | Humans | Middle Aged | tau Proteins - metabolism | Male | Antibody Specificity - genetics | Brain - metabolism | Epitopes - immunology | tau Proteins - genetics | DNA Mutational Analysis | Female | Neurons - metabolism | Tauopathies - physiopathology | Neurofibrillary Tangles - immunology | Neurofibrillary Tangles - pathology | Genetic Predisposition to Disease - genetics | Myotonic Dystrophy - classification | Myotonin-Protein Kinase | Brain - physiopathology | Protein-Serine-Threonine Kinases - genetics | Exons - genetics | Hippocampus - pathology | Epitopes - genetics | Mutation - genetics | Tauopathies - classification | Hippocampus - metabolism | Myotonic Dystrophy - physiopathology | Tauopathies - diagnosis | Brain - pathology | Inclusion Bodies - pathology | Aged | Hippocampus - physiopathology | Antibody Specificity/genetics | Comparative Study | Neurofibrillary Tangles/genetics/immunology/pathology | Neurons/metabolism/pathology | Mutation/genetics | Genetic Predisposition to Disease/genetics | RNA-Binding Proteins/genetics | Myotonic Dystrophy/classification/diagnosis/physiopathology | Protein-Serine-Threonine Kinases/genetics | Epitopes/genetics/immunology | Tauopathies/classification/diagnosis/physiopathology | Hippocampus/metabolism/pathology/physiopathology | tau Proteins/genetics/immunology/metabolism | Research Support; Non-U.S. Gov't | Brain/metabolism/pathology/physiopathology | Exons/genetics | Inclusion Bodies/pathology
Journal Article