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Neurology, ISSN 0028-3878, 10/2004, Volume 63, Issue 8, pp. 1376 - 1384
Journal Article
Journal Article
Brain, ISSN 0006-8950, 10/2003, Volume 126, Issue 10, pp. 2291 - 2303
We describe four cases of a new clinicopathological entity presenting with either a frontotemporal dementia or corticobasal degeneration syndrome with a mean... 
Ubiquitin | Neurofilament inclusion body disease | Neurofilament | Frontotemporal dementia | Corticobasal degeneration | corticobasal degeneration | neurofilament inclusion body disease | PICKS-DISEASE | frontotemporal dementia | AMYOTROPHIC-LATERAL-SCLEROSIS | ALPHA-SYNUCLEIN | NEUROSCIENCES | ubiquitin | NEURODEGENERATIVE DISEASES | CLINICAL NEUROLOGY | PATHOLOGICAL DIAGNOSIS | NEURONAL INTRANUCLEAR INCLUSIONS | neurofilament | CREUTZFELDT-JAKOB-DISEASE | LEWY BODIES | Ubiquitin - analysis | Basal Ganglia - diagnostic imaging | Frontal Lobe - metabolism | Inclusion Bodies - chemistry | Humans | Middle Aged | Basal Ganglia - metabolism | Brain Stem - metabolism | Tomography, Emission-Computed, Single-Photon | Ubiquitin - metabolism | Neurodegenerative Diseases - diagnosis | Dementia - diagnosis | Male | Temporal Lobe - diagnostic imaging | Dementia - metabolism | Brain Stem - pathology | Neurofilament Proteins - analysis | Fatal Outcome | Adult | Female | Temporal Lobe - pathology | Neurons - chemistry | Brain Stem - diagnostic imaging | Basal Ganglia - pathology | Neurodegenerative Diseases - metabolism | Microscopy, Electron | Temporal Lobe - metabolism | Immunohistochemistry - methods | Radiography | Frontal Lobe - diagnostic imaging | Magnetic Resonance Imaging | Tomography, Emission-Computed | Neurofilament Proteins - metabolism | Frontal Lobe - pathology | Index Medicus | Abridged Index Medicus
Journal Article
Journal of Neuropathology and Experimental Neurology, ISSN 0022-3069, 2005, Volume 64, Issue 6, pp. 545 - 552
Neuronal intranuclear inclusion disease (NIID) is a rare and heterogeneous group of slowly progressive neurodegenerative disorders characterized by the... 
Intranuclear inclusions | Neurodegeneration | SUMO | intranuclear inclusions | ATROPHY | neurodegeneration | BODIES | PATHOLOGY | PROTEINS | CELL | NEUROSCIENCES | CLINICAL NEUROLOGY | DEGENERATION | Crystallins - metabolism | Neurons - pathology | Microscopy, Electron, Transmission - methods | Humans | Ubiquitin - metabolism | tau Proteins - metabolism | Male | Peptides - deficiency | Receptors, Glucocorticoid - metabolism | Glial Fibrillary Acidic Protein - metabolism | Neoplasm Proteins - metabolism | Antigens, CD - metabolism | Brain - metabolism | Neurons - ultrastructure | Peptides - metabolism | Brain - ultrastructure | Neurons - metabolism | Neurodegenerative Diseases - classification | Tumor Suppressor Proteins - metabolism | Neurodegenerative Diseases - pathology | Nuclear Proteins - metabolism | Neurodegenerative Diseases - metabolism | Synucleins | Intranuclear Inclusion Bodies - pathology | Immunohistochemistry - methods | Nerve Tissue Proteins - metabolism | Transcription Factors - metabolism | Antigens, Differentiation, Myelomonocytic - metabolism | Adolescent | Brain - pathology | HSP90 Heat-Shock Proteins - metabolism | Neurofilament Proteins - metabolism | Intranuclear Inclusion Bodies - metabolism | Intranuclear Inclusion Bodies - ultrastructure | Promyelocytic Leukemia Protein | alpha-Synuclein | Index Medicus
Journal Article
Acta Neuropathologica, ISSN 0001-6322, 2/2011, Volume 121, Issue 2, pp. 219 - 228
Neuronal intermediate filament inclusion disease (NIFID), a rare form of frontotemporal lobar degeneration (FTLD), is characterized neuropathologically by... 
Pathology | Neurosciences | Neurofilament intermediate filament inclusion disease (NIFID) | Medicine & Public Health | Neuronal cytoplasmic inclusions (NCI) | ‘Fused in sarcoma’ (FUS) | Density | Neuronal intranuclear inclusions (NII) | 'Fused in sarcoma' (FUS) | ALPHA-INTERNEXIN | GLIAL INCLUSIONS | AMYOTROPHIC-LATERAL-SCLEROSIS | PATHOLOGY | FRONTOTEMPORAL LOBAR DEGENERATION | NEUROSCIENCES | CLINICAL NEUROLOGY | PATHOLOGICAL LESIONS | PRINCIPAL-COMPONENTS-ANALYSIS | NEUROFILAMENT INCLUSIONS | CREUTZFELDT-JAKOB-DISEASE | PROGRESSIVE SUPRANUCLEAR PALSY | CORTICOBASAL DEGENERATION | Severity of Illness Index | Neurons - pathology | Neurodegenerative Diseases - pathology | Frontal Lobe - metabolism | Neuroglia - pathology | Humans | Middle Aged | Male | RNA-Binding Protein FUS - metabolism | Temporal Lobe - metabolism | Intranuclear Inclusion Bodies - pathology | Young Adult | Neurons - classification | Analysis of Variance | Inclusion Bodies - pathology | Adult | Female | Neuroglia - metabolism | Neurons - metabolism | Inclusion Bodies - metabolism | Temporal Lobe - pathology | Frontal Lobe - pathology | Immunohistochemistry | Ubiquitin | Viral antibodies | Medical colleges | Sarcoma | Neurons | Antibodies | Amyotrophic lateral sclerosis | Intermediate filament proteins | Alzheimer's disease | Antigenic determinants | Index Medicus
Journal Article
Journal of Molecular Neuroscience, ISSN 0895-8696, 11/2011, Volume 45, Issue 3, pp. 409 - 421
Fused in sarcoma (FUS)-immunoreactive neuronal and glial inclusions define a novel molecular pathology called FUS proteinopathy. FUS has been shown to be a... 
Neurochemistry | Neurology | Neurosciences | Neurofilament | Biomedicine | FUS | α-Internexin | Proteomics | Frontotemporal lobar degeneration | Immunoelectron microscopy | Neuronal intermediate filament inclusion disease | Cell Biology | alpha-Internexin | PRO-ONCOPROTEIN TLS/FUS | BODY DISEASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | AMYOTROPHIC-LATERAL-SCLEROSIS | NEUROSCIENCES | NEURODEGENERATIVE DISEASES | NUCLEAR FACTOR TDP-43 | IN-VIVO | TARDBP MUTATIONS | CFTR EXON-9 | INTRANUCLEAR INCLUSIONS | Immunohistochemistry | Frontotemporal Lobar Degeneration - pathology | Neurons - pathology | Intermediate Filaments - pathology | Microscopy, Electron, Transmission - methods | Humans | Middle Aged | Male | RNA-Binding Protein FUS - metabolism | Intermediate Filaments - metabolism | Frontotemporal Lobar Degeneration - metabolism | Brain - pathology | Inclusion Bodies - pathology | Adult | Female | Aged | Microscopy, Immunoelectron - methods | Neurofilament Proteins - metabolism | Immunopathology | Usage | Care and treatment | Sarcoma | Transmission electron microscopes | Diagnosis | Research | Index Medicus | RNA | Intermediate filaments | FUS gene | Amyotrophic lateral sclerosis | Nervous system | Neuronal-glial interactions | Cytomegalic inclusion disease | FUS protein | Inclusion bodies | Euchromatin | Neurofilament protein | Immunoreactivity | Mutation | Frontotemporal dementia | Cytoplasm | Esclerosi lateral amiotròfica | Neurodegenerative diseases | Malalties neurodegeneratives | immunoelectron microscopy | neurofilament | frontotemporal lobar degeneration | α-internexin
Journal Article
Acta Neuropathologica, ISSN 0001-6322, 9/2004, Volume 108, Issue 3, pp. 213 - 223
Journal Article
Journal of Neural Transmission, ISSN 0300-9564, 11/2011, Volume 118, Issue 11, pp. 1651 - 1657
Neuronal intermediate filament inclusion disease (NIFID), a rare form of frontotemporal lobar degeneration (FTLD), is characterized neuropathologically by... 
Neurology | Neurosciences | Neurofilament intermediate filament inclusion disease (NIFID) | Medicine & Public Health | Neuronal cytoplasmic inclusions (NCI) | Spatial pattern | Pharmacology/Toxicology | Psychiatry | ‘Fused in sarcoma’ (FUS) | Cortico-cortical projections | 'Fused in sarcoma' (FUS) | Corticocortical projections | ALPHA-INTERNEXIN | NEUROFIBRILLARY TANGLES | NEURODEGENERATIVE DISORDERS | ALZHEIMERS-DISEASE | AMYOTROPHIC-LATERAL-SCLEROSIS | FRONTOTEMPORAL LOBAR DEGENERATION | NEUROSCIENCES | CLINICAL NEUROLOGY | BRAIN-TISSUE | HISTOLOGICAL SECTIONS | PRINCIPAL-COMPONENTS-ANALYSIS | NEUROFILAMENT INCLUSIONS | Frontotemporal Lobar Degeneration - pathology | Neurons - pathology | Humans | Middle Aged | Cerebral Cortex - pathology | Male | RNA-Binding Protein FUS - metabolism | Frontotemporal Lobar Degeneration - physiopathology | Cerebral Cortex - metabolism | Young Adult | Frontotemporal Lobar Degeneration - metabolism | Inclusion Bodies - pathology | Adult | Female | Neurons - metabolism | Inclusion Bodies - metabolism | Intermediate Filament Proteins - metabolism | Immunohistochemistry | Ubiquitin | Medical colleges | Nervous system diseases | Sarcoma | Neurons | Genes | Intermediate filament proteins | Alzheimer's disease | Antigenic determinants | Index Medicus | Temporal lobe | Neurodegenerative diseases | Intermediate filaments | Cortex | Boundaries | Epitopes | Atrophy | Cytomegalic inclusion disease | Dentate gyrus | FUS protein | Gliosis | Tau protein | Inclusion bodies | Neurofilaments | Degeneration | Frontotemporal dementia | Cortex (temporal)
Journal Article
Journal Article