Clinicopathologic characteristics of sporadic Japanese Creutzfeldt-Jakob disease classified according to prion protein gene polymorphism and prion protein type

Acta Neuropathologica

Volumn 112, Issue 5, 2006, Pages 561-571

  Iwasaki, Yasushi ^a   Yoshida, Mari ^b   Hashizume, Yoshio ^b   Kitamoto, Tetsuyuki ^c   Sobue, Gen ^a  

^a NAGOYA UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

^b AICHI MEDICAL UNIVERSITY   (Japan)

^c TOHOKU UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

Author keywords

Panencephalopathic type; Polymorphic codon 129; Prion protein deposition; Sporadic Creutzfeldt Jakob disease; Western blot analysis

Indexed keywords

PRION PROTEIN;

ADULT; AGED; ANTIBODY LABELING; ARTICLE; BRAIN SPONGIOSIS; CAUCASIAN; CLINICAL ARTICLE; CLINICAL FEATURE; CODON; CONTROLLED STUDY; CREUTZFELDT JAKOB DISEASE; DIFFERENTIAL DIAGNOSIS; DISEASE CLASSIFICATION; DISEASE DURATION; FEMALE; GENETIC POLYMORPHISM; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; JAPAN; MALE; MYOCLONUS; ONSET AGE; PHENOTYPE; PRIORITY JOURNAL; WESTERN BLOTTING;

ADULT; AGED; AGED, 80 AND OVER; ASIAN CONTINENTAL ANCESTRY GROUP; BLOTTING, WESTERN; CREUTZFELDT-JAKOB SYNDROME; EUROPEAN CONTINENTAL ANCESTRY GROUP; FEMALE; HUMANS; MALE; MIDDLE AGED; NEOCORTEX; PHENOTYPE; POLYMORPHISM, GENETIC; PRIONS; RETROSPECTIVE STUDIES;

EID: 33749663648     PISSN: 00016322     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00401-006-0111-7     Document Type: Article

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