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La ricerca find articoli where soggetti phrase all words 'CREUTZFELDT-JAKOB-DISEASE' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 1405 riferimenti
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    1. Kovacs, GG; Head, MW; Hegyi, I; Bunn, TJ; Flicker, H; Hainfellner, JA; McCardle, L; Laszlo, L; Jarius, C; Ironside, JW; Budka, H
      Immunohistochemistry for the prion protein: Comparison of different monoclonal antibodies in human prion disease subtypes

      BRAIN PATHOLOGY
    2. Knight, R
      Creutzfeldt-Jakob disease: A protein disease

      PROTEOMICS
    3. Narang, HK
      A critical review of atypical cerebellum-type Creutzfeldt-Jakob disease: Its relationship to "new variant" CJD and bovine spongiform encephalopathy

      EXPERIMENTAL BIOLOGY AND MEDICINE
    4. Narang, HK
      Lingering doubts about spongiform encephalopathy and Creutzfeldt-Jakob disease

      EXPERIMENTAL BIOLOGY AND MEDICINE
    5. Hill, AVS
      The genomics and genetics of human infectious disease susceptibility

      ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS
    6. Soto, C; Saborio, GP
      Prions: disease propagation and disease therapy by conformational transmission

      TRENDS IN MOLECULAR MEDICINE
    7. Aguzzi, A; Montrasio, F; Kaeser, PS
      Prions: Health scare and biological challenge

      NATURE REVIEWS MOLECULAR CELL BIOLOGY
    8. Crozet, C; Bencsik, A; Flamant, F; Lezmi, S; Samarut, J; Baron, T
      Florid plaques in ovine PrP transgenic mice infected with an experimental ovine BSE

      EMBO REPORTS
    9. Urbach, H; Paus, S; Tschampa, HJ; Keller, E; Schild, HH
      Creutzfeldt-Jakob disease: The value of MRI.

      ROFO-FORTSCHRITTE AUF DEM GEBIET DER RONTGENSTRAHLEN UND DER BILDGEBENDEN VERFAHREN
    10. Jansen, GH; Vogelaar, CF; Elshof, SM
      Distribution of cellular prion protein in normal human cerebral cortex - Does it have relevance to Creutzfeldt-Jakob disease?

      CLINICAL CHEMISTRY AND LABORATORY MEDICINE
    11. Reiber, H; Otto, M; Trendelenburg, C; Wormek, A
      Reporting cerebrospinal fluid data: Knowledge base and interpretation software

      CLINICAL CHEMISTRY AND LABORATORY MEDICINE
    12. Brown, P
      The pathogenesis of transmissible spongiform encephalopathy: routes to thebrain and the erection of therapeutic barricades

      CELLULAR AND MOLECULAR LIFE SCIENCES
    13. Tsai, MT; Su, YC; Chen, YH; Chen, CH
      Lack of evidence to support the association of the human prion gene with schizophrenia

      MOLECULAR PSYCHIATRY
    14. Min, KT
      Drosophila as a model to study human brain degenerative diseases

      PARKINSONISM & RELATED DISORDERS
    15. Kawashima, T; Doh-ura, K; Ogomori, K; Iwaki, T
      Apoptotic bodies in the cerebellum of Japanese patients with Creutzfeldt-Jakob disease

      PATHOLOGY INTERNATIONAL
    16. Pillonel, J; Courouce, AM; Saura, C; Desenclos, JC
      Impact of the exclusion of donors having stayed in the United Kingdom on the residual risk of HIV transmission by blood transfusion.

      TRANSFUSION CLINIQUE ET BIOLOGIQUE
    17. Kim, SS; Chang, KH; Kim, KW; Han, MH; Park, SH; Nam, HW; Choi, KH; Cho, WH
      Unusual acute encephalitis involving the thalamus: Imaging features

      KOREAN JOURNAL OF RADIOLOGY
    18. Klein, MA; Kaeser, PS; Schwarz, P; Weyd, H; Xenarios, I; Zinkernagel, RM; Carroll, MC; Verbeek, JS; Botto, M; Walport, MJ; Molina, H; Kalinke, U; Acha-Orbea, H; Aguzzi, A
      Complement facilitates early prion pathogenesis

      NATURE MEDICINE
    19. Aguzzi, A
      Blood simple prion diagnostics

      NATURE MEDICINE
    20. Flechsig, E; Hegyi, I; Enari, M; Schwarz, P; Collinge, J; Weissmann, C
      Transmission of scrapie by steel-surface-bound prions

      MOLECULAR MEDICINE
    21. Jacobs, DA; Lesser, RL; Mourelatos, Z; Galetta, SL; Balcer, LJ
      The Heidenhain variant of Creutzfeldt-Jakob disease: Clinical, pathologic,and neuroimaging findings

      JOURNAL OF NEURO-OPHTHALMOLOGY
    22. Brown, DR
      Microglia and Prion disease

      MICROSCOPY RESEARCH AND TECHNIQUE
    23. MacKnight, C
      Clinical implications of bovine spongiform encephalopathy

      CLINICAL INFECTIOUS DISEASES
    24. Matsumoto, K; Nakamura, T; Fukuda, S; Sekine, T; Ueda, H; Shimizu, Y
      A gelatin coated collagen-polyglycolic acid composite membrane as a dural substitute

      ASAIO JOURNAL
    25. Grizzle, WE; Fredenburgh, J
      Avoiding biohazards in medical, veterinary and research laboratories

      BIOTECHNIC & HISTOCHEMISTRY
    26. Howe, EG
      Comment: Limiting toxic information

      JOURNAL OF CLINICAL ETHICS
    27. Tateishi, J; Kitamoto, T; Mohri, S; Satoh, S; Sato, T; Shepherd, A; Macnaughton, MR
      Scrapie removal using Planova((R)) virus removal filters

      BIOLOGICALS
    28. Negro, A; Ballarin, C; Bertoli, A; Massimino, ML; Sorgato, MC
      The metabolism and imaging in live cells of the bovine prion protein in its native form or carrying single amino acid substitutions

      MOLECULAR AND CELLULAR NEUROSCIENCE
    29. Tyler, JW; Lakritz, J; Weaver, D; Johnson, G; VanMetre, D; Smith, K; Taylor, W; Jenny, A
      The 14-3-3 cerebrospinal fluid immunoassay lacks utility in the diagnosis of clinical scrapie

      JOURNAL OF VETERINARY DIAGNOSTIC INVESTIGATION
    30. Chiesa, R; Harris, DA
      Prion diseases: What is the neurotoxic molecule?

      NEUROBIOLOGY OF DISEASE
    31. Kovacs, GG; Kurucz, I; Budka, H; Adori, C; Muller, F; Acs, P; Kloppel, S; Schatzl, HM; Mayer, RJ; Laszlo, L
      Prominent stress response of Purkinje cells in Creutzfeldt-Jakob disease

      NEUROBIOLOGY OF DISEASE
    32. Diez, M; DeArmond, SJ; Groth, D; Prusiner, SB; Hokfelt, T
      Decreased MK-801 binding in discrete hippocampal regions of prion-infectedmice

      NEUROBIOLOGY OF DISEASE
    33. Chiesa, R; Pestronk, A; Schmidt, RE; Tourtellotte, VG; Ghetti, B; Piccardo, P; Harris, DA
      Primary myopathy and accumulation of PrPSc-like molecules in peripheral tissues of transgenic mice expressing a prion protein insertional mutation

      NEUROBIOLOGY OF DISEASE
    34. Doherr, MG; Audige, L
      Monitoring and surveillance for rare health-related events: a review from the veterinary perspective

      PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES
    35. Weiss, RA
      The Leeuwenhoek Lecture 2001. Animal origins of human infectious disease

      PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES
    36. Weissmann, C; Raeber, AJ; Montrasio, F; Hegyi, I; Frigg, R; Klein, MA; Aguzzi, A
      Prions and the lymphoreticular system

      PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES
    37. Clarke, AR; Jackson, GS; Collinge, J
      The molecular biology of prion propagation

      PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES
    38. Caughey, B
      Prion protein interconversions

      PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES
    39. Peretz, D; Scott, MR; Groth, D; Williamson, RA; Burton, DR; Cohen, FE; Prusiner, SB
      Strain-specified relative conformational stability of the scrapie prion protein

      PROTEIN SCIENCE
    40. Frosh, A; Joyce, R; Johnson, A
      Iatrogenic vCJD from surgical instruments - The risk is unknown, but improved decontamination will help reduce the risk

      BRITISH MEDICAL JOURNAL
    41. Bopp, MKF; Morell, A; Indrak, K; Parkkinen, J; Mertens, H; Mohr, H; Colamartino, P; Stanescu, I; Oyonarte, S; Delaney, FM; Padilla, A
      Pathogen inactivation of labile blood products

      TRANSFUSION MEDICINE
    42. MacGregor, I
      Prion protein and developments in its detection

      TRANSFUSION MEDICINE
    43. Guenther, K; Deacon, RMJ; Perry, VH; Rawlins, JNP
      Early behavioural changes in scrapie-affected mice and the influence of dapsone

      EUROPEAN JOURNAL OF NEUROSCIENCE
    44. Lee, LM; Henderson, DK
      Emerging viral infections

      CURRENT OPINION IN INFECTIOUS DISEASES
    45. Tzivion, G; Shen, YH; Zhu, J
      14-3-3 proteins; bringing new definitions to scaffolding

      ONCOGENE
    46. Funke-Kaiser, H; Theis, S; Behrouzi, T; Thomas, A; Scheuch, K; Zollmann, FS; Paterka, M; Paul, M; Orzechowski, HD
      Functional characterization of the human prion protein promoter in neuronal and endothelial cells

      JOURNAL OF MOLECULAR MEDICINE-JMM
    47. Klewer, J; Tracogna, U; Kugler, J
      What do medical students know about cause and epidemiology of the Creutzfeldt-Jakob disease in Germany?

      GESUNDHEITSWESEN
    48. Bredehorn, T; Wilhelm, F; Wiederhold, C; Duncker, GIW
      The frequency of patients at risk for Creutzfeld-Jakob disease among potential corneal donors

      OPHTHALMOLOGE
    49. Savoiardo, M; Grisoli, M
      Imaging dementias

      EUROPEAN RADIOLOGY
    50. Quaranta, N; Feijoo, SFV; Piazza, F; Zini, C
      Closed tympanoplasty in cholesteatoma surgery: long-term (10 years) hearing results using cartilage ossiculoplasty

      EUROPEAN ARCHIVES OF OTO-RHINO-LARYNGOLOGY
    51. Masel, J; Jansen, VAA
      The measured level of prion infectivity varies in a predictable way according to the aggregation state of the infectious agent

      BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE
    52. Sapriel, G
      Prion model in yeast

      RESEARCH IN MICROBIOLOGY
    53. Nicotera, P
      A route for prion neuroinvasion

      NEURON
    54. Armstrong, RA; Lantos, PL; Cairns, NJ
      Correlations between the clustering patterns of the pathological changes in sporadic Creutzfeldt-Jakob disease

      NEUROSCIENCE RESEARCH COMMUNICATIONS
    55. Klamt, F; Dal-Pizzol, F; da Frota, MLC; Walz, R; Andrades, ME; da Silva, EG; Brentani, RR; Izquierdo, I; Moreira, JCF
      Imbalance of antioxidant defense in mice lacking cellular prion protein

      FREE RADICAL BIOLOGY AND MEDICINE
    56. Vostal, JG; Holada, K; Simak, J
      Expression of cellular prion protein on blood cells: Potential functions in cell physiology and pathophysiology of transmissible spongiform encephalopathy diseases

      TRANSFUSION MEDICINE REVIEWS
    57. Newman, B
      Blood donor suitability and allogeneic whole blood donation

      TRANSFUSION MEDICINE REVIEWS
    58. Cowen, AE
      The clinical risks of infection associated with endoscopy

      CANADIAN JOURNAL OF GASTROENTEROLOGY
    59. Mastrangelo, P; Westaway, D
      Biology of the prion gene complex

      BIOCHEMISTRY AND CELL BIOLOGY-BIOCHIMIE ET BIOLOGIE CELLULAIRE
    60. Dickson, DW
      Neuropathology of Alzheimer's disease and other dementias

      CLINICS IN GERIATRIC MEDICINE
    61. Nunery, WR
      Risk of prion transmission with the use of xenografts and allografts in surgery

      OPHTHALMIC PLASTIC AND RECONSTRUCTIVE SURGERY
    62. Masullo, C; Macchi, G
      Does PRNP gene control the clinical and pathological phenotype of human spongiform transmissible encephalopathies?

      CLINICAL NEUROPATHOLOGY
    63. Dormont, D
      Transmissible spongiform encephalopathies or prion diseases.

      MEDECINE ET MALADIES INFECTIEUSES
    64. Mastrangelo, P; Westaway, D
      The prion gene complex encoding PrPC and Doppel: insights from mutational analysis

      GENE
    65. Itoh, N; Arai, H; Urakami, K; Ishiguro, K; Ohno, H; Hampel, H; Buerger, K; Wiltfang, J; Otto, M; Kretzschmar, H; Moeller, HJ; Imagawa, M; Kohno, H; Nakashima, K; Kuzuhara, S; Sasaki, H; Imahori, K
      Large-scale, multicenter study of cerebrospinal fluid tau protein phosphorylated at serine 199 for the antemortem diagnosis of Alzheimer's disease

      ANNALS OF NEUROLOGY
    66. Matoba, M; Tonami, H; Miyaji, H; Yokota, H; Yamamoto, I
      Creutzfeldt-Jakob disease: Serial changes on diffusion-weighted MRI

      JOURNAL OF COMPUTER ASSISTED TOMOGRAPHY
    67. Myers, MJ; Friedman, SL; Farrell, DE; Dove-Pettit, DA; Bucker, MF; Kelly, S; Madzo, S; Campbell, W; Wang, RF; Paine, D; Cerniglia, CE
      Validation of a polymerase chain reaction method for the detection of rendered bovine-derived materials in feedstuffs

      JOURNAL OF FOOD PROTECTION
    68. Schroder, B; Franz, B; Hempfling, P; Selbert, M; Jurgens, T; Kretzschmar, HA; Bodemer, M; Poser, S; Zerr, I
      Polymorphisms within the prion-like protein gene (Prnd) and their implications in human prion diseases, Alzheimer's disease and other neurological disorders

      HUMAN GENETICS
    69. Ratzka, P; Schroter, A; Cepek, L; Henkel, K; Wiltfang, J; Kretzschmar, HA; Prange, H; Poser, S; Otto, M
      Unaltered apoptotic behaviour of mononuclear cells from patients with sporadic Creutzfeldt-Jakob disease

      JOURNAL OF NEUROLOGY
    70. 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
    71. Croes, EA; Jansen, GH; Lemstra, AW; Frijns, CJM; van Gool, WA; van Duijn, CM
      The first two patients with dura mater associated Creutzfeldt-Jakob disease in the Netherlands

      JOURNAL OF NEUROLOGY
    72. Hsiung, GYR; Clark, AW
      A 67-year-old woman with Parkinsonism

      CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES
    73. Chertkow, H; Bergman, H; Schipper, HM; Gauthier, S; Bouchard, R; Fontaine, S; Clarfield, AM
      Assessment of suspected dementia

      CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES
    74. Axelsson, S
      The basic reality of mind and spongiform diseases

      MEDICAL HYPOTHESES
    75. Purdey, M
      Does an ultra violet photooxidation of the manganese-loaded/copper-depleted prion protein in the retina initiate the pathogenesis of TSE?

      MEDICAL HYPOTHESES
    76. Arendt, T
      Alzheimer's disease as a disorder of mechanisms underlying structural brain self-organization

      NEUROSCIENCE
    77. Barrette, I; Poisson, G; Gendron, P; Major, F
      Pseudoknots in prion protein mRNAs confirmed by comparative sequence analysis and pattern searching

      NUCLEIC ACIDS RESEARCH
    78. Sjogren, M; Gisslen, M; Vanmechelen, E; Blennow, K
      Low cerebrospinal fluid beta-amyloid 42 in patients with acute bacterial meningitis and normalization after treatment

      NEUROSCIENCE LETTERS
    79. Peoc'h, K; Schroder, HC; Laplanche, JL; Ramljak, S; Muller, WEG
      Determination of 14-3-3 protein levels in cerebrospinal fluid from Creutzfeldt-Jakob patients by a highly sensitive capture assay

      NEUROSCIENCE LETTERS
    80. Armstrong, RA; Lantos, PL; Cairns, NJ
      The spatial patterns of prion protein deposits in Creutzfeldt-Jakob disease: comparison with beta-amyloid deposits in Alzheimer's disease

      NEUROSCIENCE LETTERS
    81. Thielen, C; Melot, F; Jolois, O; Leclereq, F; Tsunoda, R; Frobert, Y; Heinen, E; Antoine, N
      Isolation of bovine follicular dendritic cells allows the demonstration ofa particular cellular prion protein

      CELL AND TISSUE RESEARCH
    82. Davids, E; Hopf, HC
      Rapidly progressing infratentorial and supratentorial centralnervous symptoms

      AKTUELLE NEUROLOGIE
    83. Van Everbroeck, B; Pals, P; Quoilin, S; Martin, JJ; Cras, P
      The many faces of human prion diseases in Belgium and the world

      ACTA NEUROLOGICA BELGICA
    84. Aguzzi, A
      From cattle to humans: which connections?

      BIOFUTUR
    85. Haik, S; Hauw, JJ
      Tracking the prion in humans

      BIOFUTUR
    86. Adjou, KT; Seman, M
      Which therapeutic trails?

      BIOFUTUR
    87. Stoiber, J; Ruckhofer, J; Lametschwandtner, A; Muss, W; Hitzl, W; Weikinger, K; Grabner, G
      Eurosol versus fetal bovine serum-containing corneal storage medium

      CORNEA
    88. Leclerc, E; Peretz, D; Ball, H; Sakurai, H; Legname, G; Serban, A; Prusiner, SB; Burton, DR; Williamson, RA
      Immobilized prion protein undergoes spontaneous rearrangement to a conformation having features in common with the infectious form

      EMBO JOURNAL
    89. Walmsley, AR; Zeng, FN; Hooper, NM
      Membrane topology influences N-glycosylation of the prion protein

      EMBO JOURNAL
    90. Wong, C; Xiong, LW; Horiuchi, M; Raymond, L; Wehrly, K; Chesebro, B; Caughey, B
      Sulfated glycans and elevated temperature stimulate PrPSc-dependent cell-free formation of protease-resistant prion protein

      EMBO JOURNAL
    91. Gauczynski, S; Peyrin, JM; Haik, S; Leucht, C; Hundt, C; Rieger, R; Krasemann, S; Deslys, JP; Dormont, D; Lasmezas, CI; Weiss, S
      The 37-kDa/67-kDa laminin receptor acts as the cell-surface receptor for the cellular prion protein

      EMBO JOURNAL
    92. Barron, RM; Thomson, V; Jamieson, E; Melton, DW; Ironside, J; Will, R; Manson, JC
      Changing a single amino acid in the N-terminus of murine PrP alters TSE incubation time across three species barriers

      EMBO JOURNAL
    93. Brugere-Picoux, J; Brugere, H
      Bovine spongiform encephalopathy: A turning point in the evolution of the epidemic?

      REVUE DE MEDECINE INTERNE
    94. Herault, O; Binet, C; Rico, A; Degenne, M; Bernard, MC; Chassaigne, M; Sensebe, L
      Evaluation of performance of white blood cell reduction filters: An original flow cytometric method for detection and quantification of cell-derived membrane fragments

      CYTOMETRY
    95. Yetiser, S; Tosun, F; Satar, B
      Revision myringoplasty with solvent-dehydrated human dura mater (Tutoplast)

      OTOLARYNGOLOGY-HEAD AND NECK SURGERY
    96. Titlestad, IL; Ebbesen, LS; Ainsworth, AP; Lillevang, ST; Qvist, N; Georgsen, J
      Leukocyte-depletion of blood components does not significantly reduce the risk of infectious complications - Results of a double-blinded, randomized study

      INTERNATIONAL JOURNAL OF COLORECTAL DISEASE
    97. Doherr, MG; Heim, D; Fatzer, R; Cohen, CH; Vandevelde, M; Zurbriggen, A
      Targeted screening of high-risk cattle populations for BSE to augment mandatory reporting of clinical suspects

      PREVENTIVE VETERINARY MEDICINE
    98. Glatzel, M; Aguzzi, A
      The shifting biology of prions

      BRAIN RESEARCH REVIEWS
    99. Rezaie, P; Lantos, PL
      Microglia and the pathogenesis of spongiform encephalopathies

      BRAIN RESEARCH REVIEWS
    100. Ladogana, A; Almonti, S; Petraroli, R; Giaccaglini, E; Ciarmatori, C; Liu, QG; Bevivino, S; Squitieri, F; Pocchiari, M
      Mutation of the PRNP gene at codon 211 in familial Creutzfeldt-Jakob disease

      AMERICAN JOURNAL OF MEDICAL GENETICS


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Documento generato il 29/02/20 alle ore 03:09:16