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Results: 1-25/127
FRONTOTEMPORAL DEMENTIA AND PARKINSONISM LINKED TO CHROMOSOME-17 - A NEW GROUP OF TAUOPATHIES
Authors: SPILLANTINI MG BIRD TD GHETTI B
Citation: Mg. Spillantini et al., FRONTOTEMPORAL DEMENTIA AND PARKINSONISM LINKED TO CHROMOSOME-17 - A NEW GROUP OF TAUOPATHIES, Brain pathology, 8(2), 1998, pp. 387-402
CHARACTERIZATION OF MURINE GIRK2 TRANSCRIPT ISOFORMS - STRUCTURE AND DIFFERENTIAL EXPRESSION
Authors: WEI JJ HODES ME PIVA R FENG Y WANG Y GHETTI B DLOUHY SR
Citation: Jj. Wei et al., CHARACTERIZATION OF MURINE GIRK2 TRANSCRIPT ISOFORMS - STRUCTURE AND DIFFERENTIAL EXPRESSION, Genomics (San Diego, Calif.), 51(3), 1998, pp. 379-390
ABNORMAL CEREBROSPINAL-FLUID BETA-AMYLOID AND TAU-PROTEIN IN CREUTZFELDT-JAKOB-DISEASE
Authors: SHORT RA FARLOW M PICCARDO P GHETTI B
Citation: Ra. Short et al., ABNORMAL CEREBROSPINAL-FLUID BETA-AMYLOID AND TAU-PROTEIN IN CREUTZFELDT-JAKOB-DISEASE, Annals of neurology, 44(3), 1998, pp. 218-218
APO E-EPSILON-4 HOMOZYGOSITY ASSOCIATED WITH AP ANGIOPATHY AND PERIVASCULAR TAU-PATHOLOGY WITHOUT NEURITIC PLAQUES IN SENILE DEMENTIA
Authors: VIDAL RG CALERO M PICCARDO P FARLOW MR UNVERZAGT FW MENDEZ E JIMENEZHUETE A BEAVIS R GALLO B GHISO J FRANGIONE B GHETTI B
Citation: Rg. Vidal et al., APO E-EPSILON-4 HOMOZYGOSITY ASSOCIATED WITH AP ANGIOPATHY AND PERIVASCULAR TAU-PATHOLOGY WITHOUT NEURITIC PLAQUES IN SENILE DEMENTIA, Neurology, 50(4), 1998, pp. 6105-6105
THE MOLECULAR AND CLINICOPATHOLOGICAL SPECTRUM OF PHENOTYPES OF SPORADIC CREUTZFELDT-JAKOB-DISEASE (SCJD)
Authors: PARCHI P GIESE A CAPILLARI S BROWN P SCHULZSCHAEFFER WJ WINDL O BUDKA H JULIEN J KOPP N POSER S ROJIANI AM STREICHENBERGER N VITAL C ZERR I GHETTI B KRETZSCHMAR HA GAMBETTI P
Citation: P. Parchi et al., THE MOLECULAR AND CLINICOPATHOLOGICAL SPECTRUM OF PHENOTYPES OF SPORADIC CREUTZFELDT-JAKOB-DISEASE (SCJD), Neurology, 50(4), 1998, pp. 44001-44001
CREUTZFELDT-JAKOB-DISEASE IN A HUSBAND-AND-WIFE
Authors: BROWN P CERVENAKOVA L MCSHANE L GOLDFARB LG BISHOP K BASTIAN F KIRKPATRICK J PICCARDO P GHETTI B GAJDUSEK DC
Citation: P. Brown et al., CREUTZFELDT-JAKOB-DISEASE IN A HUSBAND-AND-WIFE, Neurology, 50(3), 1998, pp. 684-688
MUTATION IN THE TAU-GENE IN FAMILIAL MULTIPLE SYSTEM TAUOPATHY WITH PRESENILE-DEMENTIA
Authors: SPILLANTINI MG MURRELL JR GOEDERT M FARLOW MR KLUG A GHETTI B
Citation: Mg. Spillantini et al., MUTATION IN THE TAU-GENE IN FAMILIAL MULTIPLE SYSTEM TAUOPATHY WITH PRESENILE-DEMENTIA, Proceedings of the National Academy of Sciences of the United Statesof America, 95(13), 1998, pp. 7737-7741
GENOMIC ORGANIZATION OF GIRK2, A POTASSIUM CHANNEL GENE IN MICE
Authors: WEI JJ HODES ME FENG Y GHETTI B DLOUHY SR
Citation: Jj. Wei et al., GENOMIC ORGANIZATION OF GIRK2, A POTASSIUM CHANNEL GENE IN MICE, Journal of neuropathology and experimental neurology, 57(5), 1998, pp. 68-68
TAU-CYTOPATHOLOGY IN A PATIENT WITH FAMILIAL EARLY-ONSET DEMENTIA
Authors: GEARING M LEVEY AI JONES R WALTON W SHOFFNER JM SCHMIDT ML TROJANOWSKI JO GHETTI B MIRRA SS
Citation: M. Gearing et al., TAU-CYTOPATHOLOGY IN A PATIENT WITH FAMILIAL EARLY-ONSET DEMENTIA, Journal of neuropathology and experimental neurology, 57(5), 1998, pp. 160-160
LACK OF APOE GENE REDUCES AMYLOID FORMATION IN TRANSGENIC MICE OVEREXPRESSING APP(V717F)
Authors: VERINA T BALES K DODEL RC DU Y ALTSTIEL L BENDER M HYSLOP P JOHNSTONE EM LITTLE SP CUMMINS DJ PICCARDO P PAUL S GHETTI B
Citation: T. Verina et al., LACK OF APOE GENE REDUCES AMYLOID FORMATION IN TRANSGENIC MICE OVEREXPRESSING APP(V717F), Journal of neuropathology and experimental neurology, 57(5), 1998, pp. 173-173
DISTINCTIVE PRP ISOFORMS IN GERSTMANN-STRAUSSLER-SCHEINKER-DISEASE WITH TANGLES
Authors: LIEVENS PMJ QUAGLIO E PICCARDO P TRANCHANT C WARTER JM BIRD T BUGIANI O GHETTI B TAGLIAVINI F
Citation: Pmj. Lievens et al., DISTINCTIVE PRP ISOFORMS IN GERSTMANN-STRAUSSLER-SCHEINKER-DISEASE WITH TANGLES, Journal of neuropathology and experimental neurology, 57(5), 1998, pp. 194-194
GERSTMANN-STRAUSSLER-SCHEINKER-DISEASE (GSS) WITH A MUTATION AT PRIONPROTEIN (PRP) RESIDUE-212
Authors: YOUNG K PICCARDO P KISH SJ ANG LC DLOUHY S GHETTI B
Citation: K. Young et al., GERSTMANN-STRAUSSLER-SCHEINKER-DISEASE (GSS) WITH A MUTATION AT PRIONPROTEIN (PRP) RESIDUE-212, Journal of neuropathology and experimental neurology, 57(5), 1998, pp. 195-195
PRION PROTEIN ISOFORMS IN THE NEW VARIANT OF GERSTMANN-STRAUSSLER-SCHEINKER-DISEASE Q212P
Authors: PICCARDO P KISH SJ ANG LC YOUNG K BUGIANI O TAGLIAVINI F DLOUHY SR GHETTI B
Citation: P. Piccardo et al., PRION PROTEIN ISOFORMS IN THE NEW VARIANT OF GERSTMANN-STRAUSSLER-SCHEINKER-DISEASE Q212P, Journal of neuropathology and experimental neurology, 57(5), 1998, pp. 196-196
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
ALTERED RESPONSES TO POTASSIUM IN CEREBELLAR NEURONS FROM WEAVER HETEROZYGOTE MICE
Authors: FOX AP DLOUHY S GHETTI B HURLEY JH NUCIFORA PGP NELSON DJ WON L HELLER A
Citation: Ap. Fox et al., ALTERED RESPONSES TO POTASSIUM IN CEREBELLAR NEURONS FROM WEAVER HETEROZYGOTE MICE, Experimental Brain Research, 123(3), 1998, pp. 298-306
APOLIPOPROTEIN-E, AMYLOID DEPOSITION AND MEMORY IN THE V717F (HUAPP) TRANSGENIC MOUSE - FROM NEUROPATHOLOGY TO BEHAVIOR
Authors: PAUL SM BALES KR VERINA T GHETTI B DODART JC MATHIS C
Citation: Sm. Paul et al., APOLIPOPROTEIN-E, AMYLOID DEPOSITION AND MEMORY IN THE V717F (HUAPP) TRANSGENIC MOUSE - FROM NEUROPATHOLOGY TO BEHAVIOR, Brain research, 809(1), 1998, pp. 41-41
LEWY BODIES CONTAIN ALTERED ALPHA-SYNUCLEIN IN BRAINS OF MANY FAMILIAR ALZHEIMERS-DISEASE PATIENTS WITH MUTATIONS IN PRESENILIN AND AMYLOIDPRECURSOR PROTEIN GENES
Authors: LIPPA CF FUJIWARA H MANN DMA GIASSON B BABA M SCHMIDT ML NEE LE OCONNELL B POLLEN DA GEORGEHYSLOP PS GHETTI B NOCHLIN D BIRD TD CAIRNS NJ LEE VMY IWATSUBO T TROJANOWSKI JQ
Citation: Cf. Lippa et al., LEWY BODIES CONTAIN ALTERED ALPHA-SYNUCLEIN IN BRAINS OF MANY FAMILIAR ALZHEIMERS-DISEASE PATIENTS WITH MUTATIONS IN PRESENILIN AND AMYLOIDPRECURSOR PROTEIN GENES, The American journal of pathology, 153(5), 1998, pp. 1365-1370
ENDOGENOUS PROTEOLYTIC CLEAVAGE OF NORMAL AND DISEASE-ASSOCIATED ISOFORMS OF THE HUMAN PRION PROTEIN IN NEURAL AND NONNEURAL TISSUES
Authors: JIMENEZHUETE A LIEVENS PMJ VIDAL R PICCARDO P GHETTI B TAGLIAVINI F FRANGIONE B PRELLI F
Citation: A. Jimenezhuete et al., ENDOGENOUS PROTEOLYTIC CLEAVAGE OF NORMAL AND DISEASE-ASSOCIATED ISOFORMS OF THE HUMAN PRION PROTEIN IN NEURAL AND NONNEURAL TISSUES, The American journal of pathology, 153(5), 1998, pp. 1561-1572
AN ANTIBODY RAISED AGAINST A CONSERVED SEQUENCE OF THE PRION PROTEIN RECOGNIZES PATHOLOGICAL ISOFORMS IN HUMAN AND ANIMAL PRION DISEASES, INCLUDING CREUTZFELDT-JAKOB-DISEASE AND BOVINE SPONGIFORM ENCEPHALOPATHY
Authors: PICCARDO P LANGEVELD JPM HILL AF DLOUHY SR YOUNG K GIACCONE G ROSSI G BUGIANI M BUGIANI O MELOEN RH COLLINGE J TAGLIAVINI F GHETTI B
Citation: P. Piccardo et al., AN ANTIBODY RAISED AGAINST A CONSERVED SEQUENCE OF THE PRION PROTEIN RECOGNIZES PATHOLOGICAL ISOFORMS IN HUMAN AND ANIMAL PRION DISEASES, INCLUDING CREUTZFELDT-JAKOB-DISEASE AND BOVINE SPONGIFORM ENCEPHALOPATHY, The American journal of pathology, 152(6), 1998, pp. 1415-1420
FDG-PET AND MRI IN TEMPORAL-LOBE EPILEPSY - RELATIONSHIP TO FEBRILE SEIZURES, HIPPOCAMPAL SCLEROSIS AND OUTCOME
Authors: SALANOVA V MARKAND O WORTH R SMITH R WELLMAN H HUTCHINS G PARK H GHETTI B AZZARELLI B
Citation: V. Salanova et al., FDG-PET AND MRI IN TEMPORAL-LOBE EPILEPSY - RELATIONSHIP TO FEBRILE SEIZURES, HIPPOCAMPAL SCLEROSIS AND OUTCOME, Acta neurologica Scandinavica, 97(3), 1998, pp. 146-153
LACK OF APOLIPOPROTEIN-E DRAMATICALLY REDUCES AMYLOID BETA-PEPTIDE DEPOSITION
Authors: BALES KR VERINA T DODEL RC DU YS ALTSTIEL L BENDER M HYSLOP P JOHNSTONE EM LITTLE SP CUMMINS DJ PICCARDO P GHETTI B PAUL SM
Citation: Kr. Bales et al., LACK OF APOLIPOPROTEIN-E DRAMATICALLY REDUCES AMYLOID BETA-PEPTIDE DEPOSITION, Nature genetics, 17(3), 1997, pp. 263-264
MOLECULAR PATHOLOGY OF CHROMOSOME-17 LINKED MULTIPLE SYSTEM TAUOPATHYWITH PRESENILE-DEMENTIA (MSTD)
Authors: GHETTI B MURRELL J FARLOW MR CROWTHER RA GOEDERT M SPILLANTINI MG
Citation: B. Ghetti et al., MOLECULAR PATHOLOGY OF CHROMOSOME-17 LINKED MULTIPLE SYSTEM TAUOPATHYWITH PRESENILE-DEMENTIA (MSTD), Brain pathology, 7(4), 1997, pp. 1175-1175
SPECIES AND DISEASE-SPECIFIC PRION PROTEIN (PRP) ISOFORMS ARE DETECTED BY ANTIBODIES (ABS) RAISED AGAINST A HIGHLY CONSERVED MID-REGION SEQUENCE
Authors: PICCARDO P TAGLIAVINI F DLOUHY SR YOUNG K SEILER C ROSSI G HILL AF BUGIANI M BUGIANI O LANGEVELD JPM COLLINGE J GHETTI B
Citation: P. Piccardo et al., SPECIES AND DISEASE-SPECIFIC PRION PROTEIN (PRP) ISOFORMS ARE DETECTED BY ANTIBODIES (ABS) RAISED AGAINST A HIGHLY CONSERVED MID-REGION SEQUENCE, Brain pathology, 7(4), 1997, pp. 1248-1248
COEXISTENCE OF PRION PROTEIN (PRP) AMYLOID, NEUROFIBRILLARY TANGLES, AND LEWY BODIES IN GERSTMANN-STRAUSSLER-SCHEINKER-DISEASE WITH PRION GENE (PRNP) MUTATION F198S
Authors: MIRRA SS YOUNG K GEARING M JONES R EVATT ML PICCARDO P GHETTI B
Citation: Ss. Mirra et al., COEXISTENCE OF PRION PROTEIN (PRP) AMYLOID, NEUROFIBRILLARY TANGLES, AND LEWY BODIES IN GERSTMANN-STRAUSSLER-SCHEINKER-DISEASE WITH PRION GENE (PRNP) MUTATION F198S, Brain pathology, 7(4), 1997, pp. 1379-1379
A POSSIBLE ROLE FOR TYROSINE KINASES IN THE REGULATION OF THE NEURONAL DOPAMINE TRANSPORTER IN MOUSE STRIATUM
Authors: SIMON JR BARE DJ GHETTI B RICHTER JA
Citation: Jr. Simon et al., A POSSIBLE ROLE FOR TYROSINE KINASES IN THE REGULATION OF THE NEURONAL DOPAMINE TRANSPORTER IN MOUSE STRIATUM, Neuroscience letters, 224(3), 1997, pp. 201-205
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