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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
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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
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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
Authors:
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
Authors:
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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
Authors:
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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
Authors:
PICCARDO P
TAGLIAVINI F
DLOUHY SR
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BUGIANI M
BUGIANI O
LANGEVELD JPM
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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
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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
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