Current clinical diagnosis in Creutzfeldt-Jakob disease: Identification of uncommon variants

Annals of Neurology

Volumn 48, Issue 3, 2000, Pages 323-329

  Zerr, Inga ^a   Schulz Schaeffer, Walter J ^a   Giese, Armin ^a   Bodemer, Monika ^a   Schröter, Andreas ^a   Henkel, Karsten ^a   Tschampa, Henriette J ^a   Windl, Otto ^a   Pfahlberg, Annette ^b   Steinhoff, Bernhard J ^a   Gefeller, Olaf ^b   Kretzschmar, Hans A ^a   Poser, Sigrid ^a  

^a UNIVERSITY OF GÖTTINGEN   (Germany)

^b UNIVERSITY OF ERLANGEN NUREMBERG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

METHIONINE; PRION PROTEIN; VALINE;

AMINO ACID ANALYSIS; ARTICLE; BASAL GANGLION; CEREBROSPINAL FLUID ANALYSIS; CREUTZFELDT JAKOB DISEASE; DIAGNOSTIC ACCURACY; ELECTROENCEPHALOGRAM; ELECTROPHORETIC MOBILITY; ENZYME ACTIVITY; GENETIC HETEROGENEITY; HUMAN; MAJOR CLINICAL STUDY; NUCLEAR MAGNETIC RESONANCE IMAGING; PHENOTYPE; PRIORITY JOURNAL; RELIABILITY;

14-3-3 PROTEINS; ADULT; AGE OF ONSET; AGED; AGED, 80 AND OVER; CREUTZFELDT-JAKOB SYNDROME; ELECTROENCEPHALOGRAPHY; FEMALE; GENOTYPE; HUMANS; MAGNETIC RESONANCE IMAGING; MALE; MIDDLE AGED; PROTEINS; TYROSINE 3-MONOOXYGENASE;

EID: 0033844156     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/1531-8249(200009)48:3<323::AID-ANA6>3.0.CO;2-5     Document Type: Article

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