Extending the clinicopathological spectrum of neurofilament inclusion disease

Acta Neuropathologica

Volumn 109, Issue 4, 2005, Pages 427-432

  Josephs, Keith A ^a   Uchikado, Hirotake ^b   McComb, Rodney D ^c   Bashir, Rifaat ^c   Wszolek, Zbigniew ^b   Swanson, Jerry ^a   Matsumoto, Joseph ^a   Shaw, Gerry ^d   Dickson, Dennis W ^b  

^a MAYO CLINIC ROCHESTER   (United States)

^b MAYO CLINIC   (United States)

^c UNIVERSITY OF NEBRASKA MEDICAL CENTER   (United States)

^d UNIVERSITY OF FLORIDA COLLEGE OF MEDICINE   (United States)

Author keywords

Internexin; Motor neuron disease; Multiple system atrophy; Neurofilament inclusion disease; Striatonigral degeneration

Indexed keywords

ALPHA INTERNEXIN;

ADULT; ARTICLE; BRAIN DISEASE; CASE REPORT; CELL INCLUSION; CELL LOSS; CLINICAL FEATURE; DEGENERATIVE DISEASE; GLIOSIS; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; MALE; MOTOR NEURON DISEASE; NEUROFILAMENT; NEUROFILAMENT INCLUSION DISEASE; NEUROPATHOLOGY; PRIORITY JOURNAL; PUTAMEN; PYRAMIDAL SIGN; PYRAMIDAL TRACT; SHY DRAGER SYNDROME; SUBSTANTIA NIGRA;

CARRIER PROTEINS; HUMANS; IMMUNOHISTOCHEMISTRY; INCLUSION BODIES; INTERMEDIATE FILAMENT PROTEINS; INTERMEDIATE FILAMENTS; MALE; MIDDLE AGED; NEURODEGENERATIVE DISEASES; NEUROFILAMENT PROTEINS; STAINING AND LABELING;

EID: 18344376568     PISSN: 00016322     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00401-004-0974-4     Document Type: Article

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