Neuronal intranuclear inclusions distinguish familial FTD-MND type from sporadic cases

Acta Neuropathologica

Volumn 105, Issue 6, 2003, Pages 543-548

  Mackenzie, Ian R A ^a   Feldman, Howard ^b  

^a VANCOUVER GENERAL HOSPITAL   (Canada)

^b UNIVERSITY OF BRITISH COLUMBIA   (Canada)

Author keywords

Frontotemporal dementia; Intranuclear inclusions; Motor neuron disease; Ubiquitin

Indexed keywords

UBIQUITIN;

ARTICLE; AUTOPSY; CELL NUCLEUS INCLUSION BODY; CLINICAL ARTICLE; CLINICAL FEATURE; COGNITIVE DEFECT; CONTROLLED STUDY; DENTATE NUCLEUS; FAMILIAL DISEASE; FAMILY; FRONTOTEMPORAL DEMENTIA; GRANULE CELL; HIPPOCAMPUS; HISTOLOGY; HUMAN; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; IMMUNOREACTIVITY; MOTOR CORTEX; MOTOR NEURON DISEASE; NEUROPATHOLOGY; PATHOGENESIS; PRIORITY JOURNAL; SENSITIVITY AND SPECIFICITY; CELL INCLUSION; CLASSIFICATION; COMPARATIVE STUDY; CYTOPLASM; DEMENTIA; FEMALE; MALE; METABOLISM; METHODOLOGY; PATHOLOGY;

CYTOPLASM; DEMENTIA; FEMALE; HUMANS; IMMUNOHISTOCHEMISTRY; INCLUSION BODIES; MALE; MOTOR NEURON DISEASE; UBIQUITIN;

EID: 0038452351     PISSN: 00016322     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00401-003-0678-1     Document Type: Article

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