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Results: 1-8 |
Results: 8
PHENOTYPIC VARIABILITY OF GERSTMANN-STRAUSSLER-SCHEINKER-DISEASE IS ASSOCIATED WITH PRION PROTEIN HETEROGENEITY
Authors: PICCARDO P DLOUHY SR LIEVENS PMJ YOUNG K THOMAS DP NOCHLIN D DICKSON DW VINTERS HV ZIMMERMAN TR MACKENZIE IRA KISH SJ ANG LC DECARLI C POCCHIARI M BROWN P GIBBS CJ GAJDUSEK DC BUGIANI O IRONSIDE J TAGLIAVINI F GHETTI B
Citation: P. Piccardo et al., PHENOTYPIC VARIABILITY OF GERSTMANN-STRAUSSLER-SCHEINKER-DISEASE IS ASSOCIATED WITH PRION PROTEIN HETEROGENEITY, Journal of neuropathology and experimental neurology, 57(10), 1998, pp. 979-988
FOLLOW-UP-STUDY OF RISK-FACTORS IN PROGRESSIVE SUPRANUCLEAR PALSY
Authors: GOLBE LI RUBIN RS CODY RP BELSH JM DUVOISIN RC GROSMANN C LEPORE FE MARK MH SACHDEO RC SAGE JI ZIMMERMAN TR
Citation: Li. Golbe et al., FOLLOW-UP-STUDY OF RISK-FACTORS IN PROGRESSIVE SUPRANUCLEAR PALSY, Neurology, 47(1), 1996, pp. 148-154
GERSTMANN-STRAUSSLER-SCHEINKER DISEASE WITH MUTATION AT CODON-102 ANDMETHIONINE AT CODON-129 OF PRNP IN PREVIOUSLY UNREPORTED PATIENTS
Authors: 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
GERSTMANN-STRAUSSLER-SCHEINKER DISEASE (PRNP P102L) - AMYLOID DEPOSITS ARE BEST RECOGNIZED BY ANTIBODIES DIRECTED TO EPITOPES IN PRP REGION90-165
Authors: 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
Citation: P. Piccardo et al., GERSTMANN-STRAUSSLER-SCHEINKER DISEASE (PRNP P102L) - AMYLOID DEPOSITS ARE BEST RECOGNIZED BY ANTIBODIES DIRECTED TO EPITOPES IN PRP REGION90-165, Journal of neuropathology and experimental neurology, 54(6), 1995, pp. 790-801
GERSTMANN-STRAUSSLER-SCHEINKER (GSS) DISEASE (P102L) - PRION PROTEIN (PRP) CORE DEPOSITS ARE BEST RECOGNIZED BY ANTIBODIES DIRECTED TO EPITOPES SPANNING PRP RESIDUES 90-165
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
SEVERE EVENING DYSKINESIAS IN ADVANCED PARKINSONS-DISEASE - CLINICAL DESCRIPTION, RELATION TO PLASMA LEVODOPA, AND TREATMENT
Authors: ZIMMERMAN TR SAGE JI LANG AE MARK MH
Citation: Tr. Zimmerman et al., SEVERE EVENING DYSKINESIAS IN ADVANCED PARKINSONS-DISEASE - CLINICAL DESCRIPTION, RELATION TO PLASMA LEVODOPA, AND TREATMENT, Movement disorders, 9(2), 1994, pp. 173-177
A CLINICAL GENETIC-STUDY OF PARKINSONS-DISEASE - EVIDENCE FOR DOMINANT TRANSMISSION
Authors: LAZZARINI AM MYERS RH ZIMMERMAN TR MARK MH GOLBE LI SAGE JI JOHNSON WG DUVOISIN RC
Citation: Am. Lazzarini et al., A CLINICAL GENETIC-STUDY OF PARKINSONS-DISEASE - EVIDENCE FOR DOMINANT TRANSMISSION, Neurology, 44(3), 1994, pp. 499-506
PRNP CODON-129 POLYMORPHISM AND GERSTMANN-STRAUSSLER-SCHEINKER (GSS)WITH MUTATION AT CODON-102
Authors: YOUNG K JONES CK LAZZARINI A GOLBE LI ZIMMERMAN TR DICKSON DW VINTERS HV HODES ME DLOUHY S GHETTI B
Citation: K. Young et al., PRNP CODON-129 POLYMORPHISM AND GERSTMANN-STRAUSSLER-SCHEINKER (GSS)WITH MUTATION AT CODON-102, American journal of human genetics, 53(3), 1993, pp. 1258-1258
Risultati: 1-8 |