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Results: 1-17 |
Results: 17
Creutzfeldt-Jakob disease after receipt of a previously unimplicated brandof dura mater graft
Authors: Hannah, EL Belay, ED Gambetti, P Krause, G Parchi, P Capellari, S Hoffman, RE Schonberger, LB
Citation: El. Hannah et al., Creutzfeldt-Jakob disease after receipt of a previously unimplicated brandof dura mater graft, NEUROLOGY, 56(8), 2001, pp. 1080-1083
Creutzfeldt-Jakob disease in unusually young patients who consumed venison
Authors: Belay, ED Gambetti, P Schonberger, LB Parchi, P Lyon, DR Capellari, S McQuiston, JH Bradley, K Dowdle, G Crutcher, JM Nichols, CR
Citation: Ed. Belay et al., Creutzfeldt-Jakob disease in unusually young patients who consumed venison, ARCH NEUROL, 58(10), 2001, pp. 1673-1678
Intracerebral distribution of the abnormal isoform of the prion protein insporadic Creutzfeldt-Jakob disease and fatal insomnia
Authors: Parchi, P Capellari, S Gambetti, P
Citation: P. Parchi et al., Intracerebral distribution of the abnormal isoform of the prion protein insporadic Creutzfeldt-Jakob disease and fatal insomnia, MICROSC RES, 50(1), 2000, pp. 16-25
PrPSc typing by N-terminal sequencing and mass spectrometry
Authors: Chen, SG Zou, W Parchi, P Gambetti, P
Citation: Sg. Chen et al., PrPSc typing by N-terminal sequencing and mass spectrometry, ARCH VIROL, 2000, pp. 209-216
Genetic influence on the structural variations of the abnormal prion protein
Authors: Parchi, P Zou, WQ Wang, W Brown, P Capellari, S Ghetti, B Kopp, N Schulz-Schaeffer, WJ Kretzschmar, HA Head, MW Ironside, JW Gambetti, P Chen, SG
Citation: P. Parchi et al., Genetic influence on the structural variations of the abnormal prion protein, P NAS US, 97(18), 2000, pp. 10168-10172
Effect of the E200K mutation on prion protein metabolism - Comparative study of a cell model and human brain
Authors: Capellari, S Parchi, P Russo, CM Sanford, J Sy, MS Gambetti, P Petersen, RB
Citation: S. Capellari et al., Effect of the E200K mutation on prion protein metabolism - Comparative study of a cell model and human brain, AM J PATH, 157(2), 2000, pp. 613-622
Tau gene mutation in familial progressive subcortical gliosis
Authors: Goedert, M Spillantini, MG Crowther, RA Chen, SG Parchi, P Tabaton, M Lanska, DJ Markesbery, WR Wilhelmsen, KC Dickson, DW Petersen, RB Gambetti, P
Citation: M. Goedert et al., Tau gene mutation in familial progressive subcortical gliosis, NAT MED, 5(4), 1999, pp. 454-457
Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects
Authors: Parchi, P Giese, A Capellari, S Brown, P Schulz-Schaeffer, W Windl, O Zerr, I Budka, H Kopp, N Piccardo, P Poser, S Rojiani, A Streichemberger, N Julien, J Vital, C Ghetti, B Gambetti, P Kretzschmar, H
Citation: P. Parchi et al., Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects, ANN NEUROL, 46(2), 1999, pp. 224-233
A novel phenotype in familial Creutzfeldt-Jakob disease: Prion protein gene E200K mutation coupled with valine at codon 129 and type 2 protease-resistant prion protein
Authors: Hainfellner, JA Parchi, P Kitamoto, T Jarius, C Gambetti, P Budka, H
Citation: Ja. Hainfellner et al., A novel phenotype in familial Creutzfeldt-Jakob disease: Prion protein gene E200K mutation coupled with valine at codon 129 and type 2 protease-resistant prion protein, ANN NEUROL, 45(6), 1999, pp. 812-816
Inherited prion diseases
Authors: Gambetti, P Petersen, RB Parchi, P Chen, SG Capellari, S Goldfarb, L Gabizon, R Montagna, P Lugaresi, E Piccardo, P Ghetti, B
Citation: P. Gambetti et al., Inherited prion diseases, COLD S H MG, 38, 1999, pp. 509-583
Insomnia in prion diseases: Sporadic and familial
Authors: Gambetti, P Parchi, P
Citation: P. Gambetti et P. Parchi, Insomnia in prion diseases: Sporadic and familial, N ENG J MED, 340(21), 1999, pp. 1675-1677
A subtype of sporadic prion disease mimicking fatal familial insomnia
Authors: Parchi, P Capellari, S Chin, S Schwarz, HB Schecter, NP Butts, JD Hudkins, P Burns, DK Powers, JM Gambetti, P
Citation: P. Parchi et al., A subtype of sporadic prion disease mimicking fatal familial insomnia, NEUROLOGY, 52(9), 1999, pp. 1757-1763
Type 1 protease resistant prion protein and valine homozygosity at codon 129 of PRNP identify a subtype of sporadic Creutzfeldt-Jakob disease
Authors: Worrall, BB Herman, ST Capellari, S Lynch, T Chin, S Gambetti, P Parchi, P
Citation: Bb. Worrall et al., Type 1 protease resistant prion protein and valine homozygosity at codon 129 of PRNP identify a subtype of sporadic Creutzfeldt-Jakob disease, J NE NE PSY, 67(5), 1999, pp. 671-674
Protease resistant prion proteins are not present in sporadic "poor outcome" schizophrenia
Authors: Arnold, SE Trojanowski, JQ Parchi, P
Citation: Se. Arnold et al., Protease resistant prion proteins are not present in sporadic "poor outcome" schizophrenia, J NE NE PSY, 66(1), 1999, pp. 90-92
Abnormal diffusion-weighted magnetic resonance images in Creutzfeldt-Jakobdisease
Authors: Bahn, MM Parchi, P
Citation: Mm. Bahn et P. Parchi, Abnormal diffusion-weighted magnetic resonance images in Creutzfeldt-Jakobdisease, ARCH NEUROL, 56(5), 1999, pp. 577-583
Agent strain variation in human prion diseases: Insight from transmission to primates
Authors: Parchi, P Brown, P Capellari, S Gibbs, CJ Gambetti, P
Citation: P. Parchi et al., Agent strain variation in human prion diseases: Insight from transmission to primates, ALZHEIMER'S DISEASE AND RELATED DISORDERS, 1999, pp. 561-567
Inherited prion disease: Molecular pathology and cell models
Authors: Parchi, P Capellari, S Zanusso, G Singh, N Gambetti, P Petersen, RB
Citation: P. Parchi et al., Inherited prion disease: Molecular pathology and cell models, PRIONS: MOLECULAR AND CELLULAR BIOLOGY, 1997, pp. 67-85
Risultati: 1-17 |