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Results: 1-12 |
Results: 12
MOLECULAR ANALYSIS OF CLN3 TO CLARIFY AN ATYPICAL, PROTRACTED JUVENILE NEURONAL CEROID-LIPOFUSCINOSIS
Authors: WISNIEWSKI KE ZHONG N KIDA E KACZMARSKI W KACZMARSKI A BROWN WT SCHWARTZ KO STENROOS S LAZZARINI A RUBIN AJ JOHNSON WG
Citation: Ke. Wisniewski et al., MOLECULAR ANALYSIS OF CLN3 TO CLARIFY AN ATYPICAL, PROTRACTED JUVENILE NEURONAL CEROID-LIPOFUSCINOSIS, Annals of neurology, 42(3), 1997, pp. 49-49
PELIZAEUS-MERZBACHER-LIKE-DISEASE - EXCLUSION OF THE PROTEOLIPID PROTEIN LOCUS AND DOCUMENTATION OF A NEW LOCUS ON XQ
Authors: LAZZARINI A SCHWARZ KO JIANG S STENROOS ES LEHNER T JOHNSON WG
Citation: A. Lazzarini et al., PELIZAEUS-MERZBACHER-LIKE-DISEASE - EXCLUSION OF THE PROTEOLIPID PROTEIN LOCUS AND DOCUMENTATION OF A NEW LOCUS ON XQ, Neurology, 49(3), 1997, pp. 824-832
NOVEL TEICOPLANINS BY DIRECTED BIOSYNTHESIS
Authors: LAZZARINI A BORGHI A ZERILLI LF FERRARI P COLOMBO L LANCINI GC
Citation: A. Lazzarini et al., NOVEL TEICOPLANINS BY DIRECTED BIOSYNTHESIS, Journal of antibiotics, 50(2), 1997, pp. 180-183
REDUCED FECUNDITY IN MALE ALS GENE-CARRIERS
Authors: JOHNSON WG LUCEK PR CHATKUPT S FURMAN Y LUSTERBERGER A LAZZARINI A
Citation: Wg. Johnson et al., REDUCED FECUNDITY IN MALE ALS GENE-CARRIERS, American journal of medical genetics, 59(2), 1995, pp. 149-153
SHORT TANDEM REPEAT POLYMORPHISM LINKAGE STUDIES IN A NEW FAMILY WITHX-LINKED MENTAL-RETARDATION (MRX20)
Authors: LAZZARINI A STENROOS ES LEHNER T MCKOY V GOLD B MCCORMACK MK REID CS OTT J JOHNSON WG
Citation: A. Lazzarini et al., SHORT TANDEM REPEAT POLYMORPHISM LINKAGE STUDIES IN A NEW FAMILY WITHX-LINKED MENTAL-RETARDATION (MRX20), American journal of medical genetics, 57(4), 1995, pp. 552-557
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
FAMILIAL LEWY BODY DISEASE
Authors: MARK MH DICKSON DW SAGE JI SCHWARZ KO WALTERS AS LAZZARINI A DUVOISIN RC MILLER DC GORDON MF FRIEDMAN JH GOLDMAN JE
Citation: Mh. Mark et al., FAMILIAL LEWY BODY DISEASE, Neurology, 44(4), 1994, pp. 10000248-10000248
TRINUCLEOTIDE REPEAT LENGTH INSTABILITY AND AGE-OF-ONSET IN HUNTINGTONS-DISEASE
Authors: DUYAO M AMBROSE C MYERS R NOVELLETTO A PERSICHETTI F FRONTALI M FOLSTEIN S ROSS C FRANZ M ABBOTT M GRAY J CONNEALLY P YOUNG A PENNEY J HOLLINGSWORTH Z SHOULSON I LAZZARINI A FALEK A KOROSHETZ W SAX D BIRD E VONSATTEL J BONILLA E ALVIR J CONDE JB CHA JH DURE L GOMEZ F RAMOS M SANCHEZRAMOS J SNODGRASS S DEYOUNG M WEXLER N MOSCOWITZ C PENCHASZADEH G MACFARLANE H ANDERSON M JENKINS B SRINIDHI J BARNES G GUSELLA J MACDONALD M
Citation: M. Duyao et al., TRINUCLEOTIDE REPEAT LENGTH INSTABILITY AND AGE-OF-ONSET IN HUNTINGTONS-DISEASE, Nature genetics, 4(4), 1993, pp. 387-392
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
IS REDUCED FERTILITY AN EXPRESSION OF THE ALS GENE
Authors: JOHNSON WG LUCEK P CHATKUPT S FURMAN Y LUSTENBERGER A LAZZARINI A
Citation: Wg. Johnson et al., IS REDUCED FERTILITY AN EXPRESSION OF THE ALS GENE, American journal of human genetics, 53(3), 1993, pp. 1424-1424
Risultati: 1-12 |