Diagnosis of human prion disease

Proceedings of the National Academy of Sciences of the United States of America

Volumn 102, Issue 9, 2005, Pages 3501-3506

  Safar, Jiri G ^a,b   Geschwind, Michael D ^a,b   Deering, Camille ^a   Didorenko, Svetlana ^a   Sattavat, Mamta ^a   Sanchez, Henry ^a   Serban, Ana ^a   Vey, Martin ^c   Baron, Henry ^d   Giles, Kurt ^a,b   Miller, Bruce L ^a,b   DeArmond, Stephen J ^a   Prusiner, Stanley B ^a,b  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c ZLB Behring   (Germany)

^d ZLB Behring   (France)

Author keywords

Creutzfeldt Jakob disease; Detection; Endpoint titration; Immunoassay; Neurodegeneration

Indexed keywords

CELL PROTEIN; PRION PROTEIN; PROTEINASE;

ARTICLE; BRAIN BIOPSY; BRAIN TISSUE; CONTROLLED STUDY; CREUTZFELDT JAKOB DISEASE; GRAY MATTER; HUMAN; HUMAN TISSUE; IMMUNOASSAY; IMMUNOHISTOCHEMISTRY; PRION DISEASE; PRIORITY JOURNAL; PROTEIN CONFORMATION; PROTEIN DEGRADATION; SERODIAGNOSIS; WHITE MATTER;

BIOPSY; BRAIN; CODON; CREUTZFELDT-JAKOB SYNDROME; FEMALE; HUMANS; MIDDLE AGED; POLYMORPHISM, GENETIC; PRPSC PROTEINS; SENSITIVITY AND SPECIFICITY;

EID: 20044383009     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.0409651102     Document Type: Article

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