AAAAAA

   
Results: 1-14 |
Results: 14
A TRANSMEMBRANE FORM OF THE PRION PROTEIN IN NEURODEGENERATIVE DISEASE
Authors: HEGDE RS MASTRIANNI JA SCOTT MR DEFEA KA TREMBLAY P TORCHIA M DEARMOND SJ PRUSINER SB LINGAPPA VR
Citation: Rs. Hegde et al., A TRANSMEMBRANE FORM OF THE PRION PROTEIN IN NEURODEGENERATIVE DISEASE, Science, 279(5352), 1998, pp. 827-834
CREUTZFELDT-JAKOB-DISEASE (CJD) AFTER BLOOD PRODUCT TRANSFUSION FROM A DONOR WITH CJD
Authors: PATRY D CURRY B EASTON D MASTRIANNI JA HOGAN DB
Citation: D. Patry et al., CREUTZFELDT-JAKOB-DISEASE (CJD) AFTER BLOOD PRODUCT TRANSFUSION FROM A DONOR WITH CJD, Neurology, 50(6), 1998, pp. 1872-1873
CHANGES OF HIPPOCAMPAL N-ACETYL ASPARTATE AND VOLUME IN ALZHEIMERS-DISEASE - A PROTON MR SPECTROSCOPIC IMAGING AND MRI STUDY
Authors: SCHUFF N AMEND D EZEKIEL F STEINMAN SK TANABE J NORMAN D JAGUST W KRAMER JH MASTRIANNI JA FEIN G WEINER MW
Citation: N. Schuff et al., CHANGES OF HIPPOCAMPAL N-ACETYL ASPARTATE AND VOLUME IN ALZHEIMERS-DISEASE - A PROTON MR SPECTROSCOPIC IMAGING AND MRI STUDY, Neurology, 49(6), 1997, pp. 1513-1521
FATAL SPORADIC INSOMNIA (FSI) - FATAL FAMILIAL INSOMNIA (FFI) PHENOTYPE WITHOUT A MUTATION OF THE PRION PROTEIN (PRP) GENE
Authors: MASTRIANNI JA NIXON R LAYZER R DEARMOND SJ PRUSINER SB
Citation: Ja. Mastrianni et al., FATAL SPORADIC INSOMNIA (FSI) - FATAL FAMILIAL INSOMNIA (FFI) PHENOTYPE WITHOUT A MUTATION OF THE PRION PROTEIN (PRP) GENE, Neurology, 48(3), 1997, pp. 5036-5036
MUTATION OF THE PRION PROTEIN GENE AT CODON-208 IN FAMILIAL CREUTZFELDT-JAKOB-DISEASE
Authors: MASTRIANNI JA IANNICOLA C MYERS RM DEARMOND S PRUSINER SB
Citation: Ja. Mastrianni et al., MUTATION OF THE PRION PROTEIN GENE AT CODON-208 IN FAMILIAL CREUTZFELDT-JAKOB-DISEASE, Neurology, 47(5), 1996, pp. 1305-1312
EXPLORING MECHANISMS OF PRION PROPAGATION USING MICE EXPRESSING HUMANAND CHIMERIC MOUSE-HUMAN PRION PROTEIN TRANSGENES
Authors: TELLING GC MASTRIANNI JA DEARMOND SJ PRUSINER SB
Citation: Gc. Telling et al., EXPLORING MECHANISMS OF PRION PROPAGATION USING MICE EXPRESSING HUMANAND CHIMERIC MOUSE-HUMAN PRION PROTEIN TRANSGENES, Neurology, 46(2), 1996, pp. 3085-3085
THE PREVALENCE OF HERITABLE PRION DISEASE IS UNDERESTIMATED BY CLINICAL-ASSESSMENT
Authors: MASTRIANNI JA PRUSINER SB
Citation: Ja. Mastrianni et Sb. Prusiner, THE PREVALENCE OF HERITABLE PRION DISEASE IS UNDERESTIMATED BY CLINICAL-ASSESSMENT, Neurology, 46(2), 1996, pp. 4098-4098
NEUROPATHOLOGICAL CHANGES COLOCALIZE WITH DEPOSITION OF PRPCID AND LOSS OF PRPC IN CREUTZFELDT-JAKOB-DISEASE
Authors: YANG SL MASTRIANNI JA DEARMOND SJ
Citation: Sl. Yang et al., NEUROPATHOLOGICAL CHANGES COLOCALIZE WITH DEPOSITION OF PRPCID AND LOSS OF PRPC IN CREUTZFELDT-JAKOB-DISEASE, Journal of neuropathology and experimental neurology, 55(5), 1996, pp. 123-123
COMPLETE PENETRANCE OF CREUTZFELDT-JAKOB-DISEASE IN LIBYAN JEWS CARRYING THE E200K MUTATION IN THE PRION PROTEIN GENE
Authors: SPUDICH S MASTRIANNI JA WRENSCH M GABIZON R MEINER Z KAHANA I ROSENMANN H KAHANA E PRUSINER SB
Citation: S. Spudich et al., COMPLETE PENETRANCE OF CREUTZFELDT-JAKOB-DISEASE IN LIBYAN JEWS CARRYING THE E200K MUTATION IN THE PRION PROTEIN GENE, Molecular medicine, 1(6), 1995, pp. 607-613
IDENTIFICATION OF A NEW MUTATION OF THE PRION PROTEIN GENE AT CODON-208 IN A PATIENT WITH CREUTZFELDT-JAKOB-DISEASE
Authors: MASTRIANNI JA IANNICOLA C MYERS R PRUSINER SB
Citation: Ja. Mastrianni et al., IDENTIFICATION OF A NEW MUTATION OF THE PRION PROTEIN GENE AT CODON-208 IN A PATIENT WITH CREUTZFELDT-JAKOB-DISEASE, Neurology, 45(4), 1995, pp. 201-201
PRION DISEASE (PRP-A117V) PRESENTING WITH ATAXIA INSTEAD OF DEMENTIA
Authors: MASTRIANNI JA CURTIS MT OBERHOLTZER JC DACOSTA MM DEARMOND S PRUSINER SB GARBERN JY
Citation: Ja. Mastrianni et al., PRION DISEASE (PRP-A117V) PRESENTING WITH ATAXIA INSTEAD OF DEMENTIA, Neurology, 45(11), 1995, pp. 2042-2050
ISOLATED FASCICULAR ABDUCENS NERVE PALSY AND LYME-DISEASE
Authors: MASTRIANNI JA GALETTA SL RAPS EC LIU GT VOLPE NJ
Citation: Ja. Mastrianni et al., ISOLATED FASCICULAR ABDUCENS NERVE PALSY AND LYME-DISEASE, Journal of neuro-ophthalmology, 14(1), 1994, pp. 2-5
ATAXIC GERSTMANN-STRAUSSLER-SCHEINKER DISEASE CAUSED BY A PRION PROTEIN GENE MUTATION AT CODON-117
Authors: MASTRIANNI JA CURTIS MT OBERHOLTZER JC PRUSINER SB GARBERN JY
Citation: Ja. Mastrianni et al., ATAXIC GERSTMANN-STRAUSSLER-SCHEINKER DISEASE CAUSED BY A PRION PROTEIN GENE MUTATION AT CODON-117, Neurology, 44(4), 1994, pp. 10000260-10000260
AN AMERICAN FORM OF GERSTMANN-STRAUSSLER-SCHEINKER DISEASE WITH ABUNDANT CEREBELLAR PLAQUES
Authors: CURTIS MT MASTRIANNI JA GARBERN JY OBERHOLTZER JC
Citation: Mt. Curtis et al., AN AMERICAN FORM OF GERSTMANN-STRAUSSLER-SCHEINKER DISEASE WITH ABUNDANT CEREBELLAR PLAQUES, Journal of neuropathology and experimental neurology, 52(3), 1993, pp. 294-294
Risultati: 1-14 |