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Authors: POCCHIARI M
Citation: M. Pocchiari, EARLY IDENTIFICATION OF VARIANT CREUTZFELDT-JAKOB-DISEASE - SOME PROMISING APPROACHES BUT NO CLEAR ANSWERS YET, BMJ. British medical journal, 316(7131), 1998, pp. 563-564

Authors: WILL RG ALPEROVITCH A POSER S POCCHIARI M HOFMAN A MITROVA E DESILVA R DALESSANDRO M DELASNERIELAUPRETRE N ZERR I VANDUIJN C
Citation: Rg. Will et al., DESCRIPTIVE EPIDEMIOLOGY OF CREUTZFELDT-JAKOB-DISEASE IN 6 EUROPEAN COUNTRIES, 1993-1995, Annals of neurology, 43(6), 1998, pp. 763-767

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

Authors: LEE HS SAMBUUGHIN N CERVENAKOVA L CHAPMAN J AVIV R POCCHIARI M KORCZYN A AVIV R GAJDUSEK C BROWN P LITVAK S GOLDFARB LG
Citation: Hs. Lee et al., ANCESTRAL ORIGINS OF THE PRNP E200K MUTATION CAUSING FAMILIAL CREUTZFELDT-JAKOB-DISEASE, Neurology, 50(4), 1998, pp. 3124-3124

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

Authors: SILVESTRINI MC CARDONE F MARAS B PUCCI P BARRA D BRUNORI M POCCHIARI M
Citation: Mc. Silvestrini et al., IDENTIFICATION OF THE PRION PROTEIN ALLOTYPES WHICH ACCUMULATE IN THEBRAIN OF SPORADIC AND FAMILIAL CREUTZFELDT-JAKOB-DISEASE PATIENTS, Nature medicine, 3(5), 1997, pp. 521-525

Authors: SALVATORE M SEEBER AC NACMIAS B PETRAROLI R SORBI S POCCHIARI M
Citation: M. Salvatore et al., ALPHA-1-ANTICHYMOTRYPSIN SIGNAL PEPTIDE POLYMORPHISM IN SPORADIC CREUTZFELDT-JAKOB-DISEASE, Annals of neurology, 42(3), 1997, pp. 27-27

Authors: BUDKA H HAINFELLNER JA JELLINGER K KLEINERT R MAIER H PILZ P SCIOT R MARTIN JJ BOJSENMOLLER M LAURSEN H STTEGLBJAERG P HALTIA M KOVANEN J DELISLE MB DORMONT D LASMEZAS C GRAY F HAUW JJ SEILHEAN D HELDT N MIKOL J VITAL C FONCIN JF ELHACHIMI K KOPP N BERGMANN M BILZER T CERVOSNAVARRO J DIRINGER H FEIDEN W GOEBEL HH BOHL J GULLOTTA F JENDROSKA K KRETZSCHMAR HA LINKE RP MEYERMANN R BOELLAARD JW MEHRAEIN P SCHLOTE W SCHRODER JM SCHRODER R VOLK B WALTER GF HORI A WIESTLER OD BALLOYANNIS SJ DAVAKI P PATSOURIS E GEORGSSON G FARRELL M KEOHANE C BUGIANI O MACCHI G MASULLO C COSTANZI G POCCHIARI M RIZZUTTO N SCHIFFER D TRABATTONI GR GIANGASPERO F JANSEN GH GRINDE B MORK SJ SKULLERUD K LIMA C PIMENTEL J CRUZSANCHEZ FF BERCIANO JA MARTINEZLAGE J NAVARRO C CABELLO A BRUN A KRISTENSSON K LUNDBERG PO OLSSON Y COLLINGE J ESIRI MM GRAHAM D IRONSIDE JW LANTOS PL MACKENZIE JM SCARAVILLI F WELLER RO WILL RG ALLEN IV MIRAKHUR M MAJTENYI K LIBERSKI PP PETRESCU A MITROVA E POPOVIC M AGUZZI A JANZER RC PIZZOLATO G STAMM B VANDEVELDE M MASTERS CL TATEISHI J KITAMOTO T BROWN P
Citation: H. Budka et al., THE HUMAN PRION DISEASES - FROM NEUROPATHOLOGY TO PATHOBIOLOGY AND MOLECULAR-GENETICS - FINAL REPORT OF AN EU CONCERTED ACTION, Neuropathology and applied neurobiology, 23(5), 1997, pp. 416-422

Authors: SALVATORE M SEEBER AC NACMIAS B PETRAROLI R SORBI S POCCHIARI M
Citation: M. Salvatore et al., ALPHA1 ANTICHYMOTRYPSIN SIGNAL PEPTIDE POLYMORPHISM IN SPORADIC CREUTZFELDT-JAKOB-DISEASE, Neuroscience letters, 227(2), 1997, pp. 140-142

Authors: DIRINGER H BEEKES M OZEL M SIMON D QUECK I CARDONE F POCCHIARI M IRONSIDE JW
Citation: H. Diringer et al., HIGHLY INFECTIOUS PURIFIED PREPARATIONS OF DISEASE-SPECIFIC AMYLOID OF TRANSMISSIBLE SPONGIFORM ENCEPHALOPATHIES ARE NOT DEVOID OF NUCLEIC-ACIDS OF VIRAL SIZE, Intervirology, 40(4), 1997, pp. 238-246

Authors: AGUZZI A BARBARA J BROWN P BUDKA H DIRINGER H DORMONT D FLANAGAN P HEESCHEN W HOPE J HORNLIMANN B KENNEY K MASTERS C MACNAUGHTON MR POCCHIARI M ROHWER RG SAFAR J SOMOGYI A TATEISHI J TAYLOR D VANDUIJN CM WILESMITH JW WILL R WISHER M ASHER D CUESTA JD FEEK C HASEBE K HORAUD F LOWER J MINOR P NANDAPALAN P PAVLOV A PEREZ AC RICKETTS M VICARI G VANAKEN WG BEAL R MENACHEARONSON D BRADLEY R BAILEY A CHALUMEAU HP GARLAND A BROOKS W SCHRIEBER R SPRENGERS E ANDJAPARIDZE AG BOLIS CL EMMANUEL JC GRIFFITHS E HEYMANN DL KABOYO W MESLIN FX MIYAGAWA S MARROQUIN AP SCHUDEL A ZEIDLER M
Citation: A. Aguzzi et al., MEDICINAL AND OTHER PRODUCTS AND HUMAN AND ANIMAL TRANSMISSIBLE SPONGIFORM ENCEPHALOPATHIES - MEMORANDUM FROM A WHO MEETING, Bulletin of the World Health Organization, 75(6), 1997, pp. 505-513

Authors: WIENTJENS D VANDUIJN CM DELASNERIELAUPRETRE N POCCHIARI M POSER S HOFMAN A WILL BG
Citation: D. Wientjens et al., PROGNOSIS OF CREUTZFELDT-JAKOB-DISEASE - THE EUROPEAN COLLABORATIVE STUDY, Neurology, 48(3), 1997, pp. 40005-40005

Authors: CALISSANO M PETRAROLI R POCCHIARI M
Citation: M. Calissano et al., THERAPEUTIC APPROACHES TO TRANSMISSIBLE SPONGIFORM ENCEPHALOPATHIES (TSE) - THE CASE OF AMPHOTERICIN-B, Journal of biological regulators and homeostatic agents, 10(4), 1996, pp. 69-71

Authors: BUDKA H AGUZZI A BROWN P BRUCHER JM BUGIANI O COLLINGE J DIRINGER H GULLOTTA F HALTIA M HAUW JJ IRONSIDE JW KRETZSCHMAR HA LANTOS PL MASULLO C POCCHIARI M SCHLOTE W TATEISHI J WILL RG
Citation: H. Budka et al., TISSUE HANDLING IN SUSPECTED CREUTZFELDT- JAKOB-DISEASE (CJD) AND OTHER HUMAN SPONGIFORM ENCEPHALOPATHIES (PRION DISEASES), Der Pathologe, 17(2), 1996, pp. 171-175

Authors: WILL RG IRONSIDE JW ZEIDLER M COUSENS SN ESTIBEIRO K ALPEROVITCH A POSER S POCCHIARI M HOFMAN A SMITH PG
Citation: Rg. Will et al., A NEW VARIANT OF CREUTZFELDT-JAKOB-DISEASE IN THE UK, Lancet, 347(9006), 1996, pp. 921-925

Authors: BARBANTI P FABBRINI G SALVATORE M PETRAROLI R CARDONE F MARAS B EQUESTRE M MACCHI G LENZI GL POCCHIARI M
Citation: P. Barbanti et al., POLYMORPHISM AT CODON-129 OR CODON-219 OF PRNP AND CLINICAL HETEROGENEITY IN A PREVIOUSLY UNREPORTED FAMILY WITH GERSTMANN-STRAUSSLER-SCHEINKER DISEASE (PRP-P102L MUTATION), Neurology, 47(3), 1996, pp. 734-741

Authors: WIENTJENS DPWM DELASNERIELAUPRETRE N HOFMAN A POSER S POCCHIARI M WILL R
Citation: Dpwm. Wientjens et al., INCIDENCE OF CREUTZFELDT-JAKOB-DISEASE IN EUROPE, Neurology, 46(2), 1996, pp. 4019-4019

Authors: SALVATORE M POCCHIARI M CARDONE F PETRAROLI R DALESSANDRO M GALVEZ S BROWN P MACCHI G FIESCHI C COLOSIMO C
Citation: M. Salvatore et al., CODON-200 MUTATION IN A NEW FAMILY OF CHILEAN ORIGIN WITH CREUTZFELDT-JAKOB-DISEASE, Journal of Neurology, Neurosurgery and Psychiatry, 61(1), 1996, pp. 111-112

Authors: PETRAROLI R POCCHIARI M
Citation: R. Petraroli et M. Pocchiari, CODON-219 POLYMORPHISM OF PRNP IN HEALTHY CAUCASIANS AND CREUTZFELDT-JAKOB-DISEASE PATIENTS, American journal of human genetics, 58(4), 1996, pp. 888-889

Authors: BUDKA H AGUZZI A BROWN P BRUCHER JM BUGIANI O COLLINGE J DIRINGER H GULLOTTA F HALTIA M HAUW JJ IRONSIDE JW KRETZSCHMAR HA LANTOS PL MASULLO C POCCHIARI M SCHLOTE W TATEISHI J WILL RG
Citation: H. Budka et al., TISSUE HANDLING IN SUSPECTED CREUTZFELDT-JAKOB-DISEASE (CJD) AND OTHER HUMAN SPONGIFORM ENCEPHALOPATHIES (PRION DISEASES), Brain pathology, 5(3), 1995, pp. 319-322

Authors: SALVATORE M GENUARDI M PETRAROLI R MASULLO C DALESSANDRO M POCCHIARI M
Citation: M. Salvatore et al., POLYMORPHISMS OF THE PRION PROTEIN GENE IN ITALIAN PATIENTS WITH CREUTZFELDT-JAKOB-DISEASE (VOL 94, PG 375, 1994), Human genetics, 95(5), 1995, pp. 605-605

Authors: SALVATORE M SEEBER AC NACMIAS B PETRAROLI R DALESSANDRO M SORBI S POCCHIARI M
Citation: M. Salvatore et al., APOLIPOPROTEIN-E IN SPORADIC AND FAMILIAL CREUTZFELDT-JAKOB-DISEASE, Neuroscience letters, 199(2), 1995, pp. 95-98

Authors: DELASNERIELAUPRETRE N POSER S POCCHIARI M WIENTJENS DPWM WILL R
Citation: N. Delasnerielaupretre et al., CREUTZFELDT-JAKOB-DISEASE IN EUROPE, Lancet, 346(8979), 1995, pp. 898-898

Authors: INGROSSO L LADOGANA A POCCHIARI M
Citation: L. Ingrosso et al., CONGO RED PROLONGS THE INCUBATION PERIOD IN SCRAPIE-INFECTED HAMSTERS, Journal of virology, 69(1), 1995, pp. 506-508

Authors: BARBANTI P FABBRINI G SALVATORE M PETRAROLI R POCCHIARI M MACCHI G LENZI GL
Citation: P. Barbanti et al., PHENOTYPIC HETEROGENEITY IN GERSTMANN-STRAUSSLER-SCHEINKER SYNDROME WITH CODON-102 MUTATION OF THE PRION PROTEIN GENE IS NOT RELATED TO CODON-129 POLYMORPHISM, Annals of neurology, 36(2), 1994, pp. 309-309
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