Literature DB >> 6382907

Experimental transmission of human subacute spongiform encephalopathy to small rodents. IV. Positive transmission from a typical case of Gerstmann-Sträussler-Scheinker's disease.

J Tateishi, Y Sato, H Nagara, J W Boellaard.   

Abstract

Spongiform encephalopathy was transmitted to mice from a patient belonging to the "Sch" family with Gerstmann-Sträussler-Scheinker's disease (GSS). Incubation periods in the first passage were much shorter than those in mice infected with Creutzfeldt-Jakob disease. Clinical and pathologic findings of mice infected with both diseases were almost identical. This is the first successful transmission from a typical GSS case without severe spongiform change which suggests the possible transmissible nature of this disorder.

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Year:  1984        PMID: 6382907     DOI: 10.1007/bf00695613

Source DB:  PubMed          Journal:  Acta Neuropathol        ISSN: 0001-6322            Impact factor:   17.088


  13 in total

1.  Subacute spongiform encephalopathy (Creutzfeldt-Jakob disease). The nature and progression of spongiform change.

Authors:  C L Masters; E P Richardson
Journal:  Brain       Date:  1978-06       Impact factor: 13.501

2.  Properties of the transmissible agent derived from chronic spongiform encephalopathy.

Authors:  J Tateishi; M Koga; Y Sato; R Mori
Journal:  Ann Neurol       Date:  1980-04       Impact factor: 10.422

3.  Experimental transmission of human subacute spongiform encephalopathy to small rodents. I. Clinical and histological observations.

Authors:  J Tateishi; Y Sato; M Koga; H Doi; M Ohta
Journal:  Acta Neuropathol       Date:  1980       Impact factor: 17.088

4.  Experimental transmission of human subacute spongiform encephalopathy to small rodents. II. Ultrastructural study of spongy state in the gray and white matter.

Authors:  Y Sato; M Ohta; J Tateishi
Journal:  Acta Neuropathol       Date:  1980       Impact factor: 17.088

5.  Sträussler's disease.

Authors:  F Seitelberger
Journal:  Acta Neuropathol Suppl       Date:  1981

6.  Amyloid plaques in the brains of mice with Creutzfeldt-Jakob disease.

Authors:  J Tateishi; H Nagara; K Hikita; Y Sato
Journal:  Ann Neurol       Date:  1984-03       Impact factor: 10.422

7.  Creutzfeldt-Jakob disease virus isolations from the Gerstmann-Sträussler syndrome with an analysis of the various forms of amyloid plaque deposition in the virus-induced spongiform encephalopathies.

Authors:  C L Masters; D C Gajdusek; C J Gibbs
Journal:  Brain       Date:  1981-09       Impact factor: 13.501

8.  [Subacute spongiform encephalopathy with multiform plaque formation. "Peculiar familial-hereditary disease of CNS [spinocerebellar atrophy with dementia, plaques, and plaque-like deposits in cerebellum and cerebrum" (Gerstmann, Sträussler, Scheinker)] (author's transl)].

Authors:  J W Boellaard; W Schlote
Journal:  Acta Neuropathol       Date:  1980       Impact factor: 17.088

9.  [Morbus Gerstmann-Sträussler-Scheinker. The Sch. family-a report of three cases (author's transl)].

Authors:  F Schumm; J W Boellaard; W Schlote; M Stöhr
Journal:  Arch Psychiatr Nervenkr (1970)       Date:  1981

10.  Transmission of chronic spongiform encephalopathy with kuru plaques from humans to small rodents.

Authors:  J Tateishi; M Ohta; M Koga; Y Sato; Y Kuroiwa
Journal:  Ann Neurol       Date:  1979-06       Impact factor: 10.422

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  5 in total

Review 1.  The prion strain phenomenon: molecular basis and unprecedented features.

Authors:  Rodrigo Morales; Karim Abid; Claudio Soto
Journal:  Biochim Biophys Acta       Date:  2006-12-15

2.  Prions impair bioaminergic functions through serotonin- or catecholamine-derived neurotoxins in neuronal cells.

Authors:  Sophie Mouillet-Richard; Noriyuki Nishida; Elodie Pradines; Hubert Laude; Benoît Schneider; Cécile Féraudet; Jacques Grassi; Jean-Marie Launay; Sylvain Lehmann; Odile Kellermann
Journal:  J Biol Chem       Date:  2008-07-09       Impact factor: 5.157

3.  Immunohistochemical confirmation of Creutzfeldt-Jakob disease with a long clinical course with amyloid plaque core antibodies.

Authors:  T Kitamoto; J Tateishi
Journal:  Am J Pathol       Date:  1988-06       Impact factor: 4.307

4.  Amyloid protein of Gerstmann-Sträussler-Scheinker disease (Indiana kindred) is an 11 kd fragment of prion protein with an N-terminal glycine at codon 58.

Authors:  F Tagliavini; F Prelli; J Ghiso; O Bugiani; D Serban; S B Prusiner; M R Farlow; B Ghetti; B Frangione
Journal:  EMBO J       Date:  1991-03       Impact factor: 11.598

Review 5.  Prion and Prion-Like Protein Strains: Deciphering the Molecular Basis of Heterogeneity in Neurodegeneration.

Authors:  Carlo Scialò; Elena De Cecco; Paolo Manganotti; Giuseppe Legname
Journal:  Viruses       Date:  2019-03-14       Impact factor: 5.048

  5 in total

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