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    1. Ferrillo, F; Plazzi, G; Nobili, L; Beelke, M; De Carli, F; Cortelli, P; Tinuper, P; Avoni, P; Vandi, S; Gambetti, P; Lugaresi, E; Montagna, P
      Absence of sleep EEG markers in fatal familial insomnia healthy carriers: a spectral analysis study

      CLINICAL NEUROPHYSIOLOGY
    2. Gasser, T; Dichgans, M; Finsterer, J; Hausmanowa-Petrusewicz, I; Jurkat-Rott, K; Klopstock, T; Leguern, E; Lehesjoki, AE; Lehmann-Horn, F; Lynch, T; Morris, H; Rossor, M; Steinlein, OK; Wood, N; Zaremba, J; Zeviani, M; Zoharn, A
      EFNS task force on molecular diagnosis of neurologic disorders - Guidelines for the molecular diagnosis of inherited neurologic diseases - Second of two parts

      EUROPEAN JOURNAL OF NEUROLOGY
    3. Kawashima, T; Doh-ura, K; Ogomori, K; Iwaki, T
      Apoptotic bodies in the cerebellum of Japanese patients with Creutzfeldt-Jakob disease

      PATHOLOGY INTERNATIONAL
    4. Schlapfer, J; Stahlberger-Saitbekova, N; Womack, JE; Gaillard, C; Dolf, G
      Assignment of six genes to bovine chromosome 13

      JOURNAL OF ANIMAL BREEDING AND GENETICS-ZEITSCHRIFT FUR TIERZUCHTUNG UND ZUCHTUNGSBIOLOGIE
    5. Plaitakis, A; Viskadouraki, AK; Tzagournissakis, M; Zaganas, I; Verghese-Nikolakaki, S; Karagiorgis, V; Panagiotides, I; Kilindireas, C; Patsouris, E; Haberler, C; Budka, H; Sklaviadis, T
      Increased incidence of sporadic Creutzfeldt-Jakob disease on the island ofCrete associated with a high rate of PRNP 129-methionine homozygosity in the local population

      ANNALS OF NEUROLOGY
    6. Saiz, A; Nos, C; Yague, J; Dominguez, A; Graus, F; Munoz, P
      The impact of the introduction of the 14-3-3 protein assay in the surveillance of sporadic Creutzfeldt-Jakob disease in Catalonia

      JOURNAL OF NEUROLOGY
    7. Satoh, JI; Kuroda, Y
      Ubiquitin C-terminal hydrolase-L1 (PGP9.5) expression in human neural celllines following induction of neuronal differentiation and exposure to cytokines, neurotrophic factors or heat stress

      NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY
    8. Vaccari, G; Petraroli, R; Agrimi, U; Eleni, C; Perfetti, MG; Di Bari, MA; Morelli, L; Ligios, C; Busani, L; Nonno, R; Di Guardo, G
      PrP genotype in Sarda breed sheep and its relevance to scrapie

      ARCHIVES OF VIROLOGY
    9. Rossi, D; Cozzio, A; Flechsig, E; Klein, MA; Rulicke, T; Aguzzi, A; Weissmann, C
      Onset of ataxia and Purkinje cell loss in PrP null mice inversely correlated with Dpl level in brain

      EMBO JOURNAL
    10. Aguzzi, A; Brandner, S; Fischer, MB; Furukawa, H; Glatzel, M; Hawkins, C; Heppner, FL; Montrasio, F; Navarro, B; Parizek, P; Pekarik, V; Prinz, M; Raeber, AJ; Rockl, C; Klein, MA
      Spongiform encephalopathies: Insights from transgenic models

      ADVANCES IN VIRUS RESEARCH, VOL 56
    11. Asante, EA; Collinge, J
      Transgenic studies of the influence of the PrP structure on TSE diseases

      ADVANCES IN PROTEIN CHEMISTRY, VOL 57
    12. Bratosiewicz, J; Liberski, PP; Kulczycki, J; Kordek, R
      Codon 129 polymorphism of the PRNP gene in normal Polish population and inCreutzfeldt-Jakob disease, and the search for new mutations in PRNP gene

      ACTA NEUROBIOLOGIAE EXPERIMENTALIS
    13. Bridges, BA
      Radiation and germline mutation at repeat sequences: Are we in the middle of a paradigm shift?

      RADIATION RESEARCH
    14. Nitrini, R; Mendonca, RA; Huang, N; LeBlanc, A; Livramento, JA; Marie, SK
      Diffusion-weighted MRI in two cases of familial Creutzfeldt-Jakob disease

      JOURNAL OF THE NEUROLOGICAL SCIENCES
    15. Sodeyama, N; Iwata, T; Ishikawa, K; Mizusawa, H; Yamada, M; Itoh, Y; Otomo, E; Matsushita, M; Komatsuzaki, Y
      Very early onset Alzheimer's disease with spastic paraparesis associated with a novel presenilin 1 mutation (Phe237Ile)

      JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    16. Lee, HS; Brown, P; Cervenakova, L; Garruto, RM; Alpers, MP; Gajdusek, DC; Goldfarb, LG
      Increased susceptibility to Kuru of carriers of the PRNP 129 methionine/methionine genotype

      JOURNAL OF INFECTIOUS DISEASES
    17. Panegyres, PK; Toufexis, K; Kakulas, BA; Cernevakova, L; Brown, P; Ghetti, B; Piccardo, P; Dlouhy, SR
      A new PRNP mutation (G131V) associated with Gerstmann-Straussler-Scheinkerdisease

      ARCHIVES OF NEUROLOGY
    18. Mead, S; Mahal, SP; Beck, J; Campbell, T; Farrall, M; Fisher, E; Collinge, J
      Sporadic - but not variant - Creutzfeldt-Jakob disease is associated with polymorphisms upstream of PRNP Exon 1

      AMERICAN JOURNAL OF HUMAN GENETICS
    19. Holm, IE; Abelskov, K; Bojsen-Moller, M; Nielsen, AL; Jorgensen, AL
      Creutzfeldt-Jakob disease segregating in a three generation Danish family

      ACTA NEUROLOGICA SCANDINAVICA
    20. Parchi, P; Capellari, S; Gambetti, P
      Intracerebral distribution of the abnormal isoform of the prion protein insporadic Creutzfeldt-Jakob disease and fatal insomnia

      MICROSCOPY RESEARCH AND TECHNIQUE
    21. Privat, N; Sazdovitch, V; Seilhean, D; Laplanche, JL; Hauw, JJ
      PrP immunohistochemistry: Different protocols, including a procedure for long formalin fixation, and a proposed schematic classification for depositsin sporadic Creutzfeldt-Jakob disease

      MICROSCOPY RESEARCH AND TECHNIQUE
    22. Leuck, CJ; McIlwaine, GG; Zeidler, M
      Creutzfeldt-Jakob disease and the eye. I. Background and patient management

      EYE
    23. Lueck, CJ; McIlwaine, GG; Zeidler, M
      Creutzfeldt-Jakob disease and the eye. II. Ophthalmic and neuro-ophthalmicfeatures

      EYE
    24. Gass, CS; Luis, CA; Meyers, TL; Kuljis, RO
      Familial Creutzfeldt-Jakob disease: A neuropsychological case study

      ARCHIVES OF CLINICAL NEUROPSYCHOLOGY
    25. Scaravilli, F; Cordery, RJ; Kretzschmar, H; Gambetti, P; Brink, B; Fritz, V; Temlett, J; Kaplan, C; Fish, D; An, SF; Schulz-Schaeffer, WJ; Rossor, MN
      Sporadic fatal insomnia: A case study

      ANNALS OF NEUROLOGY
    26. Hunter, N; Goldmann, W; Marshall, E; O'Neill, G
      Sheep and goats: natural and experimental TSEs and factors influencing incidence of disease

      ARCHIVES OF VIROLOGY
    27. Peoc'h, K; Guerin, C; Brandel, JP; Launay, JM; Laplanche, JL
      First report of polymorphisms in the prion-like protein gene (PRND): implications for human prion diseases

      NEUROSCIENCE LETTERS
    28. Premzl, M; Bozic, P; Gamulin, V
      PRNP octarepeat allele genotype frequencies among the modern and rare cattle breeds in Croatia

      ANIMAL GENETICS
    29. Petraroli, R; Vaccari, G; Pocchiari, M
      A rapid and efficient method for the detection of point mutations of the human prion protein gene (PRNP) by direct sequencing

      JOURNAL OF NEUROSCIENCE METHODS
    30. Rossi, G; Giaccone, G; Giampaolo, L; Iussich, S; Puoti, G; Frigo, H; Cavaletti, G; Frattola, L; Bugiani, O; Tagliavini, F
      Creutzfeldt-Jakob disease with a novel four extra-repeat insertional mutation in the PrP gene

      NEUROLOGY
    31. Bossers, A; de Vries, R; Smits, MA
      Susceptibility of sheep for scrapie as assessed by in vitro conversion of nine naturally occurring variants of PrP

      JOURNAL OF VIROLOGY
    32. Minghetti, L; Greco, A; Cardone, F; Puopolo, M; Ladogana, A; Almonti, S; Cunningham, C; Perry, VH; Pocchiari, M; Levi, G
      Increased brain synthesis of prostaglandin E-2 and F-2-isoprostane in human and experimental transmissible spongiform encephalopathies

      JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY
    33. Tabernero, C; Polo, JM; Sevillano, MD; Munoz, R; Berciano, RJ; Cabello, A; Baez, B; Ricoy, JR; Carpizo, R; Figols, J; Cuadrado, N; Claveria, LE
      Fatal familial insomnia: clinical, neuropathological, and genetic description of a Spanish family

      JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    34. Kaneko, K; Ball, HL; Wille, H; Zhang, H; Groth, D; Torchia, M; Tremblay, P; Safar, J; Prusiner, SB; DeArmond, SJ; Baldwin, MA; Cohen, FE
      A synthetic peptide initiates Gerstmann-Straussler-Scheinker (GSS) diseasein transgenic mice

      JOURNAL OF MOLECULAR BIOLOGY
    35. Finckh, U; Muller-Thomsen, T; Mann, U; Eggers, C; Marksteiner, J; Meins, W; Binetti, G; Alberici, A; Hock, C; Nitsch, RM; Gal, A
      High prevalence of pathogenic mutations in patients with early-onset dementia detected by sequence analyses of four different genes

      AMERICAN JOURNAL OF HUMAN GENETICS
    36. Donnelly, CA; MaWhinney, S; Anderson, RM
      A review of the BSE epidemic in British cattle

      ECOSYSTEM HEALTH
    37. Weihl, CC; Roos, RP
      Creutzfeldt-Jakob disease, new variant Creutzfeldt-Jakob disease, and bovine spongiform encephalopathy

      NEUROLOGIC CLINICS
    38. Boellaard, JW; Brown, P; Tateishi, J
      Gerstmann-Straussler-Scheinker disease - The dilemma of molecular and clinical correlations

      CLINICAL NEUROPATHOLOGY
    39. Loftus, B; Monks, E; Hanlon, J; Weavers, E; Rogers, M
      Prion protein genotypes of Suffolk-type sheep representative of natural scrapie in Ireland

      IRISH VETERINARY JOURNAL
    40. 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
      Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects

      ANNALS OF NEUROLOGY
    41. Harder, A; Jendroska, K; Kreuz, F; Wirth, T; Schafranka, C; Karnatz, N; Theallier-Janko, A; Kreier, J; Lohan, K; Emmerich, D; Cervos-Navarro, J; Windl, O; Kretzschmar, HA; Nurnberg, P; Witkowski, R
      Novel twelve-generation kindred of fatal familial insomnia from Germany representing the entire spectrum of disease expression

      AMERICAN JOURNAL OF MEDICAL GENETICS
    42. Collinge, J
      Variant Creutzfeldt-Jakob disease

      LANCET
    43. Tan, LJ; Williams, MA; Khan, MK; Champion, HC; Nielsen, NH
      Risk of transmission of bovine spongiform encephalopathy to humans in the United States - Report of the Council on Scientific Affairs

      JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
    44. Belay, ED
      Transmissible spongiform encephalopathies in humans

      ANNUAL REVIEW OF MICROBIOLOGY
    45. Rosenmann, H; Kahana, E; Korczyn, AD; Kahana, I; Chapman, J; Gabizon, R
      Preliminary evidence for anticipation in genetic E200K Creutzfeldt-Jakob disease

      NEUROLOGY
    46. Yamada, M; Tomimitsu, H; Yokota, T; Tomi, H; Sunohara, N; Mukoyama, N; Itoh, Y; Suematsu, N; Otomo, E; Okeda, R; Matsushita, M; Mizusawa, H
      Involvement of the spinal posterior horn in Gerstmann-Straussler-Scheinkerdisease (PrP P102L)

      NEUROLOGY
    47. Hardy, J
      Pathways to primary neurodegenerative disease

      MAYO CLINIC PROCEEDINGS
    48. Nagashima, T; Okawa, M; Kitamoto, T; Takahashi, H; Ishihara, Y; Ozaki, Y; Nagashima, K
      Wernicke encephalopathy-like symptoms as an early manifestation of Creutzfeldt-Jakob disease in a chronic alcoholic

      JOURNAL OF THE NEUROLOGICAL SCIENCES
    49. Laplanche, JL; El Hachimi, KH; Durieux, I; Thuillet, P; Defebvre, L; Delasnerie-Laupretre, N; Peoc'h, K; Foncin, JF; Destee, A
      Prominent psychiatric features and early onset in an inherited prion disease with a new insertional mutation in the prion protein gene

      BRAIN
    50. Almer, G; Hainfellner, JA; Brucke, T; Jellinger, K; Kleinert, R; Bayer, G; Windl, O; Kretzschmar, HA; Hill, A; Sidle, K; Collinge, J; Budka, H
      Fatal familial insomnia: a new Austrian family

      BRAIN
    51. Worrall, BB; Rowland, LP; Del Bene, M; Leung, D; Chin, SSM
      Mother with amyotrophic lateral sclerosis and daughter with Creutzfeldt-Jakob disease

      ARCHIVES OF NEUROLOGY
    52. Kropp, S; Schulz-Schaeffer, WJ; Finkenstaedt, M; Riedemann, C; Windl, O; Steinhoff, BJ; Zerr, I; Kretzschmar, HA; Poser, S
      The Heidenhain variant of Creutzfeldt-Jakob disease

      ARCHIVES OF NEUROLOGY
    53. CHATELAIN J; DELASNERIELAUPRETRE N; LEMAIRE MH; CATHALA F; LAUNAY JM; LAPLANCHE JL
      CLUSTER OF CREUTZFELDT-JAKOB-DISEASE IN FRANCE ASSOCIATED WITH THE CODON-200 MUTATION (E200K) IN THE PRION PROTEIN GENE

      European journal of neurology
    54. BUDKA H
      FATAL FAMILIAL INSOMNIA AROUND THE WORLD

      Brain pathology
    55. GAMBETTI P; LUGARESI E
      CONCLUSIONS OF THE SYMPOSIUM

      Brain pathology
    56. Engelborghs, S; Marien, P; Martin, JJ; De Deyn, PP
      Functional anatomy, vascularisation and pathology of the human thalamus

      ACTA NEUROLOGICA BELGICA
    57. Miyakawa, T; Inoue, K; Iseki, E; Kawanishi, C; Sugiyama, N; Onishi, H; Yamada, Y; Suzuki, K; Iwabuchi, K; Kosaka, K
      Japanese Creutzfeldt-Jakob disease patients exhibiting high incidence of the E200K PRNP mutation and located in the basin of a river

      NEUROLOGICAL RESEARCH
    58. FISHBEIN L
      TRANSMISSIBLE SPONGIFORM ENCEPHALOPATHIES, HYPOTHESES AND FOOD SAFETY- AN OVERVIEW

      Science of the total environment
    59. TRANCHANT C; WARTER JM
      GERSTMANN-STRAUSSLER-SCHEINKER-SYNDROME

      Revue neurologique
    60. ZERR I; GIESE A; WINDL O; KROPP S; SCHULZSCHAEFFER W; RIEDEMANN C; SKWORC K; BODEMER M; KRETZSCHMAR HA; POSER S
      PHENOTYPIC VARIABILITY IN FATAL FAMILIAL INSOMNIA (D178N-129M) GENOTYPE

      Neurology
    61. CHAPMAN J; CERVENAKOVA L; LEE HS; ESTUPINAN J; RICHARDSON S; VNENCAKJONES CL; GAJDUSEK DC; KORCZYN AD; BROWN P; GOLDFARB LG
      APOE IN NON-ALZHEIMER AMYLOIDOSES - TRANSMISSIBLE SPONGIFORM ENCEPHALOPATHIES

      Neurology
    62. ROSSI G; MACCHI G; PORRO M; GIACCONE G; BUGIANI M; SCARPINI E; SCARLATO G; MOLINI GE; SASANELLI F; BUGIANI O; TAGLIAVINI F
      FATAL FAMILIAL INSOMNIA - GENETIC, NEUROPATHOLOGIC, AND BIOCHEMICAL-STUDY OF A PATIENT FROM A NEW ITALIAN KINDRED

      Neurology
    63. DEFONZO V; BERSANI E; ALUFFIPENTINI F; CASTRIGNANO T; PARISI V
      ARE ONLY REPEATED TRIPLETS GUILTY

      Journal of theoretical biology
    64. SATOH J; KUROHARA K; YUKITAKE M; KURODA Y
      CONSTITUTIVE AND CYTOKINE-INDUCIBLE EXPRESSION OF PRION PROTEIN GENE IN HUMAN NEURAL CELL-LINES

      Journal of neuropathology and experimental neurology
    65. RABENAU HF; PREISER W; DOERR HW
      TRANSMISSIBLE SPONGIFORM ENCEPHALOPATHIES - CREUTZFELDT-JAKOB-DISEASE

      Chirurg
    66. PASTORET PP; FALIZE F; BROCHIER B; VANOPDENBOSCH E; THIRY E
      TRANSMISSIBLE SPONGIFORM ENCEPHALOPATHIES AND THEIR REGULATORY CONSEQUENCES

      Annales de medecine veterinaire
    67. LIBERSKI PP; BARCIKOWSKA M; CERVENAKOVA L; BRATOSIEWICZ J; MARCZEWSKA M; BROWN P; GAJDUSEK DC
      A CASE OF SPORADIC CREUTZFELDT-JAKOB-DISEASE WITH A GERSTMANN-STAUSSLER-SCHEINKER PHENOTYPE BUT NO ALTERATIONS IN THE PRNP GENE

      Acta Neuropathologica
    68. ROSENMANN H; VARDI J; FINKELSTEIN Y; CHAPMAN J; GABIZON R
      IDENTIFICATION IN ISRAEL OF 2 JEWISH CREUTZFELDT-JAKOB-DISEASE PATIENTS WITH A 178 MUTATION AT THEIR PRP GENE

      Acta neurologica Scandinavica
    69. INOUE S; TANAKA M; HORIUCHI M; ISHIGURO N; SHINAGAWA M
      CHARACTERIZATION OF THE BOVINE PRION PROTEIN GENE - THE EXPRESSION REQUIRES INTERACTION BETWEEN THE PROMOTER AND INTRON

      Journal of veterinary medical science
    70. SALVATORE M; SEEBER AC; NACMIAS B; PETRAROLI R; SORBI S; POCCHIARI M
      ALPHA1 ANTICHYMOTRYPSIN SIGNAL PEPTIDE POLYMORPHISM IN SPORADIC CREUTZFELDT-JAKOB-DISEASE

      Neuroscience letters
    71. LUCAS M; IZQUIERDO G; MUNOZ C; SOLANO F
      INTERNUCLEOSOMAL BREAKDOWN OF THE DNA OF BRAIN CORTEX IN HUMAN SPONGIFORM ENCEPHALOPATHY

      Neurochemistry international
    72. COLOMBIER C; GERAUD G; DELISLE MB; LAPLANCHE JL; LETRAON AP; ALIZE P; DELPLA PA
      FATAL FAMILIAL INSOMNIA - PHENOTYPIC DIFF ERENCE DETERMINED BY POLYMORPHISM AT CODON-129

      Revue neurologique
    73. ROSENMANN H; HALIMI M; KAHANA I; BIRAN I; GABIZON R
      DIFFERENTIAL ALLELIC EXPRESSION OF PRP MESSENGER-RNA IN CARRIERS OF THE E200K MUTATION

      Neurology
    74. MCLEAN CA; STOREY E; GARDNER RJM; TANNENBERG AEG; CERVENAKOVA L; BROWN P
      THE D178N (CIS-129M) FATAL FAMILIAL INSOMNIA MUTATION ASSOCIATED WITHDIVERSE CLINICOPATHOLOGICAL PHENOTYPES IN AN AUSTRALIAN KINDRED

      Neurology
    75. MACCHI G; ROSSI G; ABBAMONDI AL; GIACCONE G; MANCIA D; TAGLIAVINI F; BUGIANI O
      DIFFUSE THALAMIC DEGENERATION IN FATAL FAMILIAL INSOMNIA - A MORPHOMETRIC STUDY

      Brain research
    76. KNIAZEVA M; ORMAN R; TERRANOVA VP
      EXPRESSION OF PRP MESSENGER-RNA IS REGULATED BY A FRAGMENT OF MRP8 INHUMAN FIBROBLASTS

      Biochemical and biophysical research communications
    77. PASTORET PP; HAMERS C; BROCHIER B
      INTERSPECIES TRANSMISSION OF SPONGIFORM E NCEPHALOPATHIES

      Annales de medecine veterinaire
    78. NATHANSON N; WILESMITH J; GRIOT C
      BOVINE SPONGIFORM ENCEPHALOPATHY (BSE) - CAUSES AND CONSEQUENCES OF ACOMMON SOURCE EPIDEMIC

      American journal of epidemiology
    79. ALPEROVITCH A
      EPIDEMIOLOGY OF CREUTZFELDT-JAKOB-DISEASE - PAST AND PRESENT UNCERTAINTIES

      European journal of neurology
    80. AGUZZI A
      PATHOGENESIS OF SPONGIFORM ENCEPHALOPATHIES - AN UPDATE

      International archives of allergy and immunology
    81. COLLINS SJ; CAPPAI R; MASTERS CL
      RECENT DEVELOPMENTS IN THE TRANSMISSIBLE SPONGIFORM ENCEPHALOPATHIES - IMPLICATIONS FOR CLINICAL-PRACTICE

      Journal of clinical neuroscience
    82. SAEKI K; MATSUMOTO Y; HIROTA Y; MATSUMOTO Y; ONODERA T
      3-EXON STRUCTURE OF THE GENE ENCODING THE RAT PRION PROTEIN AND ITS EXPRESSION IN TISSUES

      Virus genes
    83. MACKNIGHT C; ROCKWOOD K
      BOVINE SPONGIFORM ENCEPHALOPATHY AND CREUTZFELDT-JAKOB-DISEASE - IMPLICATIONS FOR PHYSICIANS

      CMAJ. Canadian Medical Association journal
    84. WINDL O; DEMPSTER M; ESTIBEIRO JP; LATHE R; DESILVA R; ESMONDE T; WILL R; SPRINGBETT A; CAMPBELL TA; SIDLE KCL; PALMER MS; COLLINGE J
      GENETIC-BASIS OF CREUTZFELDT-JAKOB-DISEASE IN THE UNITED-KINGDOM - A SYSTEMATIC ANALYSIS OF PREDISPOSING MUTATIONS AND ALLELIC VARIATION INTHE PRNP GENE

      Human genetics
    85. BROWN P
      TRANSMISSIBLE CEREBRAL AMYLOIDOSIS

      Journal of neural transmission. Supplementum
    86. FIORINO AS
      SLEEP, GENES AND DEATH - FATAL FAMILIAL INSOMNIA

      Brain research reviews
    87. TABRIZI SJ; SCARAVILLI F; HOWARD RS; COLLINGE J; ROSSOR M
      CREUTZFELDT-JAKOB-DISEASE IN A YOUNG WOMAN

      Lancet
    88. NARANG H
      THE NATURE OF THE SCRAPIE AGENT - THE VIRUS THEORY .2.

      Proceedings of the Society for Experimental Biology and Medicine
    89. SILBURN P; CERVENAKOVA L; VARGHESE P; TANNENBERG A; BROWN P; BOYLE R
      FATAL FAMILIAL INSOMNIA - A 7TH FAMILY

      Neurology
    90. COCHRAN EJ; BENNETT DA; CERVENAKOVA L; KENNEY K; BERNARD B; FOSTER NL; BENSON DF; GOLDFARB LG; BROWN P
      FAMILIAL CREUTZFELDT-JAKOB-DISEASE WITH A 5-REPEAT OCTAPEPTIDE INSERTMUTATION

      Neurology
    91. BARBANTI P; FABBRINI G; SALVATORE M; PETRAROLI R; CARDONE F; MARAS B; EQUESTRE M; MACCHI G; LENZI GL; POCCHIARI M
      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
    92. GALLASSI R; MORREALE A; MONTAGNA P; CORTELLI P; AVONI P; CASTELLANI R; GAMBETTI P; LUGARESI E
      FATAL FAMILIAL INSOMNIA - BEHAVIORAL AND COGNITIVE FEATURES

      Neurology
    93. CHAPMAN J; ARLAZOROFF A; GOLDFARB LG; CERVENAKOVA L; NEUFELD MY; WERBER E; HERBERT M; BROWN P; GAJDUSEK DC; KORCZYN AD
      FATAL INSOMNIA IN A CASE OF FAMILIAL CREUTZFELDT-JAKOB-DISEASE WITH THE CODON 200(LYS) MUTATION

      Neurology
    94. LLEDO PM; TREMBLAY P; DEARMOND SJ; PRUSINER SB; NICOLL RA
      MICE DEFICIENT FOR PRION PROTEIN EXHIBIT NORMAL NEURONAL EXCITABILITYAND SYNAPTIC TRANSMISSION IN THE HIPPOCAMPUS

      Proceedings of the National Academy of Sciences of the United Statesof America
    95. COLLINS S; MASTERS CL
      IATROGENIC AND ZOONOTIC CREUTZFELDT-JAKOB-DISEASE - THE AUSTRALIAN PERSPECTIVE

      Medical journal of Australia
    96. SHYU WC; HSU YD; KAO MC; TSAO WL
      PANENCEPHALITIC CREUTZFELDT-JAKOB-DISEASE IN A CHINESE FAMILY - UNUSUAL PRESENTATION WITH PRP CODON-210 MUTATION AND IDENTIFICATION BY PCR-SSCP

      Journal of the neurological sciences
    97. SALVATORE M; POCCHIARI M; CARDONE F; PETRAROLI R; DALESSANDRO M; GALVEZ S; BROWN P; MACCHI G; FIESCHI C; COLOSIMO C
      CODON-200 MUTATION IN A NEW FAMILY OF CHILEAN ORIGIN WITH CREUTZFELDT-JAKOB-DISEASE

      Journal of Neurology, Neurosurgery and Psychiatry
    98. PETRAROLI R; POCCHIARI M
      CODON-219 POLYMORPHISM OF PRNP IN HEALTHY CAUCASIANS AND CREUTZFELDT-JAKOB-DISEASE PATIENTS

      American journal of human genetics
    99. RICHARDSON EP; MASTERS CL
      THE NOSOLOGY OF CREUTZFELDT-JAKOB-DISEASE AND CONDITIONS RELATED TO THE ACCUMULATION OF PRPCJD IN THE NERVOUS-SYSTEM

      Brain pathology
    100. GAMBETTI P; PARCHI P; PETERSEN RB; CHEN SG; LUGARESI E
      FATAL FAMILIAL INSOMNIA AND FAMILIAL CREUTZFELDT-JAKOB-DISEASE - CLINICAL, PATHOLOGICAL AND MOLECULAR-FEATURES

      Brain pathology


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Documento generato il 07/08/20 alle ore 18:27:45