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NTIS 바로가기Biomedicine & pharmacotherapy = Biomédecine & pharmacothérapie, v.45 no.9, 1991년, pp.379 - 382
Jacob, F. (Hematology-Oncology Department and Research on Cancer and Blood Disorders, Centre Hospitalier de Luxembourg, L-1210, Luxembourg, Germany) , Ries, F. , Dicato, M.
Human spongiform encephalopathies (HSE) are uncommon neurodegenerative diseases of unknown etiology. Whilst numerous observations provide arguments for an infectious disorder mediated by an unconventional agent of the so-called prion-type, the recent discovery of predisposing allelic variants sugges...
Resume - Les maladies a prion chez l'homme. Les encephalopathies spongiformes humaines sont des maladies neuro-degeneratives rares dont la pathogenie reste inconnue. Alors que de nombreuses observations plaident en faveur d'une etiologie infectieuse mediee par un agent contaminant de type prion. la decouverte recente de variants alleliques predis-posants permet d'envisager un mecanisme genetique a l'origine de ces affections.
Br Med J Baker 291 299 1985 10.1136/bmj.291.6491.299 Experimental transmission of an autosomal dominant spongigorm encephalopathy: does the infectious agent originate in the human genome?
N Engl J Med Bockman 312 2 73 1985 10.1056/NEJM198501103120202 Creutzfeldt-Jakob disease prion proteins in human brains
Neurology Brown 37 895 1987 10.1212/WNL.37.6.895 The epidemiology of Creutzfeldt-Jakob disease
Nature (Lond) Chesebro 315 331 1985 10.1038/315331a0 Identification of scrapie prion protein-specific mRNA in scrapie-infected and uninfected brain
Lancet Collinge ii 15 1989 10.1016/S0140-6736(89)90256-0 Diagnosis of Gerstmann-Straussler syndrome in familial dementia with prion protein gene analysis
Lancet Collinge 336 7 1990 10.1016/0140-6736(90)91518-F Prion dementia without characteristic pathology
Neural Neurosurg Psychiatry Cousens 53 459 1990 10.1136/jnnp.53.6.459 Creutzfeldt-Jakob disease in England and Wales
Biochem Biophys Res Commun Doh-Ura 163 2 974 1989 10.1016/0006-291X(89)92317-6 Pro-leu change at position 102 of prion protein is the most common but not the sole mutation related to Gerstmann-Straussler syndrome
N Engl J Med Duffy 290 692 1974 10.1056/NEJM197403212901220 Possible person-to-person transmission of Creutzfeldt-Jakob disease
Lancet 336 21 1990 10.1016/0140-6736(90)91523-D
Science Gajdusek 127 943 1977 10.1126/science.142303 Unconventional viruses and the origin and disappearance of Kuru
Science Gibbs 161 388 1968 10.1126/science.161.3839.388 Creutzfeldt-Jakob disease: transmission to the chimpanzee
Science Gibbs 165 1023 1969 10.1126/science.165.3897.1023 Infection as the etiology of spongiform encephalopathy
Science Gibbs 182 67 1973 10.1126/science.182.4107.67 Experimental sub-acute spongiform virus encephalopathies in primates and other laboratory animals
Lancet Goldfarb 336 174 1990 10.1016/0140-6736(90)91693-5 Identical mutation in unrelated patients with Creutz-feldt-Jakob disease
Lancet Goldfarb 336 514 1990 10.1016/0140-6736(90)92073-Q Mutation in codon 200 of scrapie amyloid protein gene in two clusters of Creutzfeldt-Jakob disease in Slovakia
Exp Neurol Goldfarb 108 247 1990 10.1016/0014-4886(90)90130-K Creutzfeldt-Jakob disease and Kuru patients lack a mutation consistently found in the Gerstmann-Straussler-Scheinker syndrome
Exp Neurol Goldgaber 106 204 1989 10.1016/0014-4886(89)90095-2 Mutations in familial Creutzfeldt-Jakob disease and Gestmann-Straussler-Scheinker's syndrome
Nature (Lond) Hsio 338 342 1989 10.1038/338342a0 Linkage of a prion protein missense variant to Gerstmann-Straussler syndrome
Lancet Jackson ii 244 1985 10.1016/S0140-6736(85)90292-2 Creutz-feldt-Jakob disease after administration of human growth hormone
Cell Kinley 35 57 1983 10.1016/0092-8674(83)90207-6 A protease-resistant protein is a structural component of the scrapie prion
Neurology Nochlin 39 910 1989 10.1212/WNL.39.7.910 Familial dementia with PrP-positive amyloid plaques
Cell Westaway 40 735 1985 10.1016/0092-8674(85)90333-2 A cellular gene encodes scrapie PrP 27-30 protein
Lancet Owen i 51 1989 10.1016/S0140-6736(89)91713-3 Insertion in prion protein gene in familial Creutzfeldt-Jakob disease
Mol Brain Res Owen 7 273 1990 10.1016/0169-328X(90)90038-F An inframe insertion in the prion protein gene in familial Creutzfeldt-Jakob disease
N Engl J Med Prusiner 317 1571 1987 10.1056/NEJM198712173172505 Prions and neurodegenerative diseases
N Engl J Med Roberts 315 123 1986 Prion-protein immunoreactivity in human transmissible dementias
Br Med J Robers 300 943 1090 Bovine spongiform encephalopathy
Sparkes 83 7358 1986 Assignment of the human and mouse prion protein genes to homologous chromosomes
J Neurosurg Thadani 69 766 1988 10.3171/jns.1988.69.5.0766 Creutzfeldt-Jakob disease probably acquired from a cadaveric dura-mater graft: case report
Neur Neurosurg Psychiatry Will 45 235 1982 10.1136/jnnp.45.3.235 Evidence for case-to-case transmission of Creutzfeldt-Jakob disease
Neurol Neurosurg Psychiatry Will 47 134 1984 10.1136/jnnp.47.2.134 A retrospective study of Creutzfeldt-Jakob disease in England and Wales 1970-1979: clinical features
Lancet Will 336 369 1990 10.1016/0140-6736(90)91907-R Prion disease (in Letters to the Editor)
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