Immunohistochemistry distinguishes between Pick's disease and corticobasal degeneration [4]

Journal of Neurology Neurosurgery and Psychiatry

Volumn 69, Issue 6, 2000, Pages 835-836

  Bell, K ^a   Cairns, N J ^a   Lantos, P L ^a   Rossor, M N ^a  

^a KING'S COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ISOPROTEIN; TAU PROTEIN;

CHROMOSOME 17; CLINICAL ARTICLE; CONTROLLED STUDY; CORTICOBASAL DEGENERATION; DIAGNOSTIC PROCEDURE; DIFFERENTIAL DIAGNOSIS; ELECTROPHORETIC MOBILITY; HUMAN; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; LETTER; NIEMANN PICK DISEASE; PHENOTYPE; PRIORITY JOURNAL;

BASAL GANGLIA DISEASES; BRAIN; HUMANS; IMMUNOHISTOCHEMISTRY; PICK DISEASE OF THE BRAIN;

EID: 0033653144     PISSN: 00223050     EISSN: None     Source Type: Journal    
DOI: 10.1136/jnnp.69.6.835     Document Type: Letter

References (4)

1. Cracking an enigma: The puzzle of unusual dementias
2. Tau mutations in familial frontotemporal dementia
3. Regulation of expression, phosphorylation and biological activity of tau during differentiation in SY5Y cells
4. Vulnerable neuronal subsets in Alzheimer's and Pick's disease are distinguished by their tau isoform distribution and phosphorylation