Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects

Annals of Neurology

Volumn 46, Issue 2, 1999, Pages 224-233

  Parchi, Piero ^a   Giese, Armin ^b   Capellari, Sabina ^a   Brown, Paul ^c   Schulz Schaeffer, Walter ^b   Windl, Otto ^b   Zerr, Inga ^b   Budka, Herbert ^d   Kopp, Nicolas ^e   Piccardo, Pedro ^g   Poser, Sigrid ^b   Rojiani, Amyn ^h   Streichemberger, Nathalie ^e   Julien, Jean ^f   Vital, Claude ^f   Ghetti, Bernardino ^a   Gambetti, Pierluigi ^a   Kretzschmar, Hans ^b  

^a CASE WESTERN RESERVE UNIVERSITY   (United States)

^b UNIVERSITY OF GÖTTINGEN   (Germany)

^c NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE   (United States)

^d MEDICAL UNIVERSITY OF VIENNA   (Austria)

^e HÔPITAL NEUROLOGIQUE   (France)

^f BORDEAUX UNIVERSITY HOSPITAL   (France)

^g INDIANA UNIVERSITY SCHOOL OF MEDICINE   (United States)

^h UNIVERSITY OF SOUTH FLORIDA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

METHIONINE; PRION PROTEIN; VALINE;

ARTICLE; ATAXIA; CREUTZFELDT JAKOB DISEASE; DISEASE CLASSIFICATION; GENOTYPE; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; KURU; MAJOR CLINICAL STUDY; NEUROPATHOLOGY; PHENOTYPE; PRIORITY JOURNAL;

ADULT; AGE OF ONSET; AGED; AGED, 80 AND OVER; BRAIN; CREUTZFELDT-JAKOB SYNDROME; ELECTROENCEPHALOGRAPHY; HUMANS; IMMUNOHISTOCHEMISTRY; MIDDLE AGED; PHENOTYPE;

EID: 0032816292     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/1531-8249(199908)46:2<224::AID-ANA12>3.0.CO;2-W     Document Type: Article

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