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Results: 1-25/110
CLINICAL-FEATURES OF FATAL FAMILIAL INSOMNIA - PHENOTYPIC VARIABILITYIN RELATION TO A POLYMORPHISM AT CODON-129 OF THE PRION PROTEIN GENE
Authors: MONTAGNA P CORTELLI P AVONI P TINUPER P PLAZZI G GALLASSI R PORTALUPPI F JULIEN J VITAL C DELISLE MB GAMBETTI P LUGARESI E
Citation: P. Montagna et al., CLINICAL-FEATURES OF FATAL FAMILIAL INSOMNIA - PHENOTYPIC VARIABILITYIN RELATION TO A POLYMORPHISM AT CODON-129 OF THE PRION PROTEIN GENE, Brain pathology, 8(3), 1998, pp. 515-520
THE PATHOPHYSIOLOGY OF FATAL FAMILIAL INSOMNIA
Authors: LUGARESI E TOBLER I GAMBETTI P MONTAGNA P
Citation: E. Lugaresi et al., THE PATHOPHYSIOLOGY OF FATAL FAMILIAL INSOMNIA, Brain pathology, 8(3), 1998, pp. 521-526
NEURONAL APOPTOSIS IN FATAL FAMILIAL INSOMNIA
Authors: DORANDEU A WINGERTSMANN L CHRETIEN F DELISLE MB VITAL C PARCHI P MONTAGNA P LUGARESI E IRONSIDE JW BUDKA H GAMBETTI P GRAY F
Citation: A. Dorandeu et al., NEURONAL APOPTOSIS IN FATAL FAMILIAL INSOMNIA, Brain pathology, 8(3), 1998, pp. 531-537
MOLECULAR PATHOLOGY OF FATAL FAMILIAL INSOMNIA
Authors: PARCHI P PETERSEN RB CHEN SG AUTILIOGAMBETTI L CAPELLARI S MONARI L CORTELLI P MONTAGNA P LUGARESI E GAMBETTI P
Citation: P. Parchi et al., MOLECULAR PATHOLOGY OF FATAL FAMILIAL INSOMNIA, Brain pathology, 8(3), 1998, pp. 539-548
CONCLUSIONS OF THE SYMPOSIUM
Authors: GAMBETTI P LUGARESI E
Citation: P. Gambetti et E. Lugaresi, CONCLUSIONS OF THE SYMPOSIUM, Brain pathology, 8(3), 1998, pp. 571-575
NEURONAL APOPTOSIS IN HUMAN PRION DISEASES
Authors: GRAY F DORANDEU A WINGERTSMANN L DELISLE MB MONTAGUA P LUGARESI E GAMBETTI P VITAL C
Citation: F. Gray et al., NEURONAL APOPTOSIS IN HUMAN PRION DISEASES, Modern pathology, 11(1), 1998, pp. 159-159
PRION ENCEPHALOPATHY WITH INSERTION OF OCTAPEPTIDE REPEATS - THE NUMBER OF REPEATS DETERMINES THE TYPE OF CEREBELLAR DEPOSITS
Authors: VITAL C GRAY F VITAL A PARCHI P CAPELLARI S PETERSEN RB FERRER X JARNIER D JULIEN J GAMBETTI P
Citation: C. Vital et al., PRION ENCEPHALOPATHY WITH INSERTION OF OCTAPEPTIDE REPEATS - THE NUMBER OF REPEATS DETERMINES THE TYPE OF CEREBELLAR DEPOSITS, Neuropathology and applied neurobiology, 24(2), 1998, pp. 125-130
FATAL FAMILIAL INSOMNIA IN A NEW ITALIAN KINDRED
Authors: PADOVANI A DALESSANDRO M PARCHI P CORTELLI P ANZOLA GP MONTAGNA P VIGNOLO LA PETRAROLI R POCCHIARI M LUGARESI E GAMBETTI P
Citation: A. Padovani et al., FATAL FAMILIAL INSOMNIA IN A NEW ITALIAN KINDRED, Neurology, 51(5), 1998, pp. 1491-1494
CREUTZFELDT-JAKOB-DISEASE WITH LONG-DURATION AND PANENCEPHALOPATHIC LESIONS - MOLECULAR ANALYSIS OF ONE CASE
Authors: GHORAYEB I SERIES C PARCHI P SAWAN B GUEZ S LAPLANCHE JL CAPELLARI S GAMBETTI P VITAL C
Citation: I. Ghorayeb et al., CREUTZFELDT-JAKOB-DISEASE WITH LONG-DURATION AND PANENCEPHALOPATHIC LESIONS - MOLECULAR ANALYSIS OF ONE CASE, Neurology, 51(1), 1998, pp. 271-274
A NOVEL MOLECULAR AND CLINICOPATHOLOGICAL PHENOTYPE OF PRION DISEASE IN AN AMERICAN
Authors: CAPELLARI S POWERS JM PETERSEN RB GAMBETTI P PARCHI P
Citation: S. Capellari et al., A NOVEL MOLECULAR AND CLINICOPATHOLOGICAL PHENOTYPE OF PRION DISEASE IN AN AMERICAN, Neurology, 50(4), 1998, pp. 4114-4114
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
NEURODEGENERATION - CHAPERONING BRAIN DISEASES
Authors: WELCH WJ GAMBETTI P
Citation: Wj. Welch et P. Gambetti, NEURODEGENERATION - CHAPERONING BRAIN DISEASES, Nature, 392(6671), 1998, pp. 23-24
PRION PROTEIN EXPRESSION IN DIFFERENT SPECIES - ANALYSIS WITH A PANELOF NEW MABS
Authors: ZANUSSO G LIU DC FERRARI S HEGYI I YIN XH AGUZZI A HORNEMANN S LIEMANN S GLOCKSHUBER R MANSON JC BROWN P PETERSEN RB GAMBETTI P SY MS
Citation: G. Zanusso et al., PRION PROTEIN EXPRESSION IN DIFFERENT SPECIES - ANALYSIS WITH A PANELOF NEW MABS, Proceedings of the National Academy of Sciences of the United Statesof America, 95(15), 1998, pp. 8812-8816
DIFFERENT PATTERNS OF TRUNCATED PRION PROTEIN-FRAGMENTS CORRELATE WITH DISTINCT PHENOTYPES IN P102L GERSTMANN-STRAUSSLER-SCHEINKER-DISEASE
Authors: PARCHI P CHEN SG BROWN P ZOU WQ CAPELLARI S BUDKA H HAINFELLNER J REYES PF GOLDEN GT HAUW JJ GAJDUSEK DC GAMBETTI P
Citation: P. Parchi et al., DIFFERENT PATTERNS OF TRUNCATED PRION PROTEIN-FRAGMENTS CORRELATE WITH DISTINCT PHENOTYPES IN P102L GERSTMANN-STRAUSSLER-SCHEINKER-DISEASE, Proceedings of the National Academy of Sciences of the United Statesof America, 95(14), 1998, pp. 8322-8327
NEURONAL APOPTOSIS IN HUMAN PRION DISEASES
Authors: GRAY F DORANDEU A WINGERTSMANN L DELISLE MB BUDKA H GAMBETTI P IRONSIDE JW VITAL C
Citation: F. Gray et al., NEURONAL APOPTOSIS IN HUMAN PRION DISEASES, Journal of neuropathology and experimental neurology, 57(5), 1998, pp. 95-95
FATAL SPORADIC INSOMNIA (THALAMIC FORM OF SPORADIC CREUTZFELDT-JAKOB-DISEASE)
Authors: PARCHI P CAPELLARI S CHIN S POWERS JM SCHWARZ HB BURNS DK GAMBETTI P
Citation: P. Parchi et al., FATAL SPORADIC INSOMNIA (THALAMIC FORM OF SPORADIC CREUTZFELDT-JAKOB-DISEASE), Journal of neuropathology and experimental neurology, 57(5), 1998, pp. 198-198
FAMILIAL MUTATIONS AND THE THERMODYNAMIC STABILITY OF THE RECOMBINANTHUMAN PRION PROTEIN
Authors: SWIETNICKI W PETERSEN RB GAMBETTI P SUREWICZ WK
Citation: W. Swietnicki et al., FAMILIAL MUTATIONS AND THE THERMODYNAMIC STABILITY OF THE RECOMBINANTHUMAN PRION PROTEIN, The Journal of biological chemistry, 273(47), 1998, pp. 31048-31052
REGULATION OF BRAIN G-PROTEIN G(O) BY ALZHEIMERS-DISEASE GENE PRESENILIN-1
Authors: SMINE A XU XM NISHIYAMA K KATADA T GAMBETTI P YADAV SP WU X SHI YC YASUHARA S HOMBURGER V OKAMOTO T
Citation: A. Smine et al., REGULATION OF BRAIN G-PROTEIN G(O) BY ALZHEIMERS-DISEASE GENE PRESENILIN-1, The Journal of biological chemistry, 273(26), 1998, pp. 16281-16288
FAMILIAL PARKINSONISM AND DEMENTIA WITH BALLOONED NEURONS, ARGYROPHILIC NEURONAL INCLUSIONS, ATYPICAL NEUROFIBRILLARY TANGLES, TAU-NEGATIVEASTROCYTIC FIBRILLARY TANGLES, AND LEWY BODIES
Authors: MIZUTANI T INOSE T NAKAJIMA S KAKIMI S UCHIGATA M IKEDA K GAMBETTI P TAKASU T
Citation: T. Mizutani et al., FAMILIAL PARKINSONISM AND DEMENTIA WITH BALLOONED NEURONS, ARGYROPHILIC NEURONAL INCLUSIONS, ATYPICAL NEUROFIBRILLARY TANGLES, TAU-NEGATIVEASTROCYTIC FIBRILLARY TANGLES, AND LEWY BODIES, Acta Neuropathologica, 95(1), 1998, pp. 15-27
ALLELIC ORIGIN OF THE ABNORMAL PRION PROTEIN ISOFORM IN FAMILIAL PRION DISEASES
Authors: CHEN SG PARCHI P BROWN P CAPELLARI S ZOU WQ COCHRAN EJ VNENCAKJONES CL JULIEN J VITAL C MIKOL J LUGARESI E AUTILIOGAMBETTI L GAMBETTI P
Citation: Sg. Chen et al., ALLELIC ORIGIN OF THE ABNORMAL PRION PROTEIN ISOFORM IN FAMILIAL PRION DISEASES, Nature medicine, 3(9), 1997, pp. 1009-1015
MUTANT PRION PROTEIN IN GERSTMANN-STAUSSLER-SCHEINKER-DISEASE Y145AMBER IS DEGRADED BY THE PROTEASOMAL PATHWAY
Authors: ZANUSSO G PETERSEN RB KANOUSH R GAMBETTI P SINGH N
Citation: G. Zanusso et al., MUTANT PRION PROTEIN IN GERSTMANN-STAUSSLER-SCHEINKER-DISEASE Y145AMBER IS DEGRADED BY THE PROTEASOMAL PATHWAY, Molecular biology of the cell, 8, 1997, pp. 493-493
INTERRELATIONSHIP OF THE POSTTRANSLATIONAL MODIFICATIONS TO THE PRIONPROTEIN
Authors: CAPELLARI S GAMBETTI P PETERSEN RB
Citation: S. Capellari et al., INTERRELATIONSHIP OF THE POSTTRANSLATIONAL MODIFICATIONS TO THE PRIONPROTEIN, Molecular biology of the cell, 8, 1997, pp. 1803-1803
N-TERMINALLY-MODIFIED WATER-SOLUBLE AMYLOID BETA-PEPTIDES ARE AGGREGATED IN THE BRAIN BUT NOT IN THE CEREBROSPINAL-FLUID
Authors: RUSSO C GAMBETTI P TELLER JK
Citation: C. Russo et al., N-TERMINALLY-MODIFIED WATER-SOLUBLE AMYLOID BETA-PEPTIDES ARE AGGREGATED IN THE BRAIN BUT NOT IN THE CEREBROSPINAL-FLUID, The FASEB journal, 11(9), 1997, pp. 689-689
TYPE-1 PRION PROTEIN IN A PATIENT WITH VALINE VALINE AT CODON-129 OF THE PRION PROTEIN GENE/
Authors: WORRALL BB HERMAN ST LYNCH T GAMBETTI P PARCHI P
Citation: Bb. Worrall et al., TYPE-1 PRION PROTEIN IN A PATIENT WITH VALINE VALINE AT CODON-129 OF THE PRION PROTEIN GENE/, Annals of neurology, 42(3), 1997, pp. 40-40
TRANSTHYRETIN AMYLOIDOSIS - A NEW MUTATION ASSOCIATED WITH DEMENTIA
Authors: PETERSEN RB GOREN H COHEN M RICHARDSON SL TRESSER N LYNN A GALI M ESTES M GAMBETTI P
Citation: Rb. Petersen et al., TRANSTHYRETIN AMYLOIDOSIS - A NEW MUTATION ASSOCIATED WITH DEMENTIA, Annals of neurology, 41(3), 1997, pp. 307-313
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