CSF detection of the 14-3-3 protein in unselected patients with dementia

Neurology

Volumn 56, Issue 11, 2001, Pages 1528-1533

  Burkhard, Pierre R ^a   Sanchez, Jean Charles ^a   Landis, Theodor ^a   Hochstrasser, Denis F ^a  

^a UNIVERSITY HOSPITAL   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

PROTEIN 14 3 3;

ADOLESCENT; ADULT; AGED; ARTICLE; CEREBROSPINAL FLUID ANALYSIS; CORRELATION FUNCTION; CREUTZFELDT JAKOB DISEASE; DEMENTIA; DIAGNOSTIC ACCURACY; FEMALE; HUMAN; IMMUNOASSAY; IMMUNOBLOTTING; MAJOR CLINICAL STUDY; MALE; PATIENT SELECTION; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN CEREBROSPINAL FLUID LEVEL; PROTEIN EXPRESSION;

EID: 0035849483     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.56.11.1528     Document Type: Article

References (26)

1. Human spongiform encephalopathy: The National Institutes of Health series of 300 cases of experimentally transmitted disease
2. The 14-3-3 brain protein in cerebrospinal fluid as a marker for transmissible spongiform encephalopathies
3. Abnormal proteins in the cerebrospinal fluid of patients with Creutzfeldt-Jakob disease
4. Diagnosis of Creutzfeldt-Jakob disease by two-dimensional gel electrophoresis of cerebrospinal fluid
5. Detection of 14-3-3 protein in the cerebrospinal fluid supports the diagnosis of Creutzfeldt-Jakob disease
6. Detection of 14-3-3 protein in the CSF of genetic Creutzfeldt-Jakob disease
7. 14-3-3 Protein, neuronspecific enolase, and S-100 protein in cerebrospinal fluid of patients with Creutzfeldt-Jakob disease
8. 14-3-3 Testing in diagnosing Creutzfeldt-Jakob disease. A prospective study in 112 patients
9. Analysis of EEG and CSF 14-3-3 proteins as aids to the diagnosis of Creutzfeldt-Jakob disease
10. Creutzfeldt-Jakob disease: Diagnostic value of protein 14-3-3 and neuronal specific enolase assay in cerebrospinal fluid
11. Creutzfeldt-Jakob disease and related transmissible spongiform encephalopathies
12. New diagnostic tests for prion diseases
13. The 14-3-3 brain protein and transmissible spongiform encephalopathy
14. Creutzfeldt-Jakob disease: Clinical features, epidemiology and tests
15. The 14-3-3 brain protein and transmissible spongiform encephalopathy
16. Diagnostic usefulness of the determination of protein 14-3-3 in cerebrospinal fluid in Creutzfeldt-Jakob disease
17. A new variant of Creutzfeldt-Jakob disease in the UK
18. Cerebrospinal-fluid test for new-variant Creutzfeldt-Jakob disease
19. The 14-3-3 protein detectable in the cerebrospinal fluid of patients with prion-unrelated neurological diseases is expressed constitutively in neurons and glial cells in culture
20. Cerebrospinal fluid diagnosis of Creutzfeldt-Jakob disease
21. Detection of 14-3-3 brain protein in the cerebrospinal fluid of patients with paraneoplastic disorders
22. Detection of 14-3-3 protein in the CSF of a patient with Hashimoto's encephalopathy
23. 14-3-3 Protein in the cerebrospinal fluid of patients with acute transverse myelitis
24. Creutzfeldt-Jakob disease: Patterns of worldwide occurrence and the significance of familial and sporadic clustering
25. Premortem diagnosis of Creutzfeldt-Jakob disease by cerebrospinal fluid analysis
26. An enzyme-linked immunosorbent assay to quantify 14-3-3 proteins in the cerebrospinal fluid of suspected Creutzfeldt-Jakob disease patients