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WINTHROP BE
BIVALACQUA TJ
CHAMPION HC
LAMBERT DG
ILGENFRITZ CT
JONES CK
KADOWITZ PJ
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YOUNG K
JONES CK
PICCARDO P
LAZZARINI A
GOLBE LI
ZIMMERMAN TR
DICKSON DW
MCLACHLAN DC
STGEORGEHYSLOP P
LENNOX A
PERLMAN S
VINTERS HV
HODES ME
DLOUHY S
GHETTI B
Citation: K. Young et al., GERSTMANN-STRAUSSLER-SCHEINKER DISEASE WITH MUTATION AT CODON-102 ANDMETHIONINE AT CODON-129 OF PRNP IN PREVIOUSLY UNREPORTED PATIENTS, Neurology, 45(6), 1995, pp. 1127-1134
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PICCARDO P
GHETTI B
DICKSON DW
VINTERS HV
GIACCONE G
BUGIANI O
TAGLIAVINI F
YOUNG K
DLOUHY SR
SEILER C
JONES CK
LAZZARINI A
GOLBE LI
ZIMMERMAN TR
PERLMAN SL
MCLACHLAN DC
STGEORGEHYSLOP PH
LENNOX A
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Authors:
PICCARDO P
YOUNG K
JONES CK
SEILER C
LAZZARINI A
GOLBE LI
ZIMMERMAN TR
DICKSON DW
VINTERS HV
LENNOX A
PERLMAN SL
MCLACHLAN DC
GEORGEHYSLOP PS
GIACCONE G
BUGIANI O
TAGLIAVINI F
DLOUHY SR
GHETTI B
Citation: P. Piccardo et al., GERSTMANN-STRAUSSLER-SCHEINKER (GSS) DISEASE (P102L) - PRION PROTEIN (PRP) CORE DEPOSITS ARE BEST RECOGNIZED BY ANTIBODIES DIRECTED TO EPITOPES SPANNING PRP RESIDUES 90-165, Journal of neuropathology and experimental neurology, 54(3), 1995, pp. 448-448
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YOUNG K
JONES CK
LAZZARINI A
GOLBE LI
ZIMMERMAN TR
DICKSON DW
VINTERS HV
HODES ME
DLOUHY S
GHETTI B
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