Variably protease-sensitive prionopathy: A new sporadic disease of the prion protein

Annals of Neurology

Volumn 68, Issue 2, 2010, Pages 162-172

  Zou, Wen Quan ^a   Puoti, Gianfranco ^a   Xiao, Xiangzhu ^a   Yuan, Jue ^a   Qing, Liuting ^a   Cali, Ignazio ^a   Shimoji, Miyuki ^a   Langeveld, Jan P M ^b   Castellani, Rudy ^c   Notari, Silvio ^a   Crain, Barbara ^d   Schmidt, Robert E ^e   Geschwind, Michael ^f   DeArmond, Stephen J ^f   Cairns, Nigel J ^e   Dickson, Dennis ^g   Honig, Lawrence ^h   Torres, Juan Maria ⁱ   Mastrianni, James ^j   Capellari, Sabina ^k   Giaccone, Giorgio ^l   Belay, Ermias D ^m   Schonberger, Lawrence B ^m   Cohen, Mark ^a   Perry, George ⁿ   Kong, Qingzhong ^a   Parchi, Piero ^k   Tagliavini, Fabrizio ^l   Gambetti, Pierluigi ^a   more..

^a CASE WESTERN RESERVE UNIVERSITY   (United States)

^b WAGENINGEN UNIVERSITY   (Netherlands)

^c UNIVERSITY OF MARYLAND MEDICAL CENTER   (United States)

^d JOHNS HOPKINS UNIVERSITY   (United States)

^e WASHINGTON UNIVERSITY   (United States)

^f UNIVERSITY OF CALIFORNIA   (United States)

^g MAYO CLINIC   (United States)

^h Och Spine at New York Presbyterian Hospitals   (United States)

ⁱ Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria   (Spain)

^j UNIVERSITY OF CHICAGO   (United States)

^k UNIVERSITY OF BOLOGNA   (Italy)

^l DEPARTMENT OF NEUROSURGERY   (Italy)

^m CENTERS FOR DISEASE CONTROL AND PREVENTION   (United States)

ⁿ University of San Antonio   (United States)

more..

Author keywords

[No Author keywords available]

Indexed keywords

METHIONINE; PRION PROTEIN; VALINE; PEPTIDE HYDROLASE; PRION;

ADULT; AGED; ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; CREUTZFELDT JAKOB DISEASE; DISEASE DURATION; ELECTROPHORESIS; GENE MUTATION; GENOTYPE; GERSTMANN STRAUSSLER SCHEINKER SYNDROME; HETEROZYGOSITY; HISTOPATHOLOGY; HOMOZYGOSITY; HUMAN; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; PHENOTYPE; PRION DISEASE; PRIORITY JOURNAL; VARIABLY PROTEASE SENSITIVE PRIONOPATHY; BRAIN; CHEMISTRY; DEMENTIA; ENZYMOLOGY; FEMALE; GENETIC SCREENING; GENETIC VARIABILITY; GENETICS; MALE; METABOLISM; MIDDLE AGED; NUCLEOTIDE SEQUENCE; PATHOLOGY; PHYSIOLOGY; PRION; TOXICITY; VERY ELDERLY; YOUNG ADULT;

ADULT; AGED; AGED, 80 AND OVER; BRAIN; DEMENTIA; DNA MUTATIONAL ANALYSIS; FEMALE; GENETIC TESTING; GENETIC VARIATION; HUMANS; MALE; MIDDLE AGED; PEPTIDE HYDROLASES; PHENOTYPE; PRION DISEASES; PRIONS; YOUNG ADULT;

EID: 77955302607     PISSN: 03645134     EISSN: 15318249     Source Type: Journal    
DOI: 10.1002/ana.22094     Document Type: Article

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