Diffuse deposition of immunohistochemically labeled prion protein in the granular layer of the cerebellum in a patient with Creutzfeldt-Jakob disease

[1]  A. Aguzzi,et al.  Molecular pathology of prion diseases , 2000, Neurobiology of Aging.

[2]  S. Prusiner,et al.  Spontaneous neurodegeneration in transgenic mice with mutant prion protein , 1990, Science.

[3]  S. Prusiner,et al.  Inherited human prion diseases , 1990, Neurology.

[4]  M. Rossor,et al.  Immunocytochemical confirmation of prion protein , 1990, The Lancet.

[5]  T. Crow,et al.  Prion dementia without characteristic pathology , 1990, The Lancet.

[6]  D. Gajdusek,et al.  Immunohistochemical localization of prion protein in spongiform encephalopathies and normal brain tissue , 1990, Neurology.

[7]  T. Kitamoto,et al.  Gerstmann‐Sträussler‐Scheinker disease: Immunohistological and experimental studies , 1988, Annals of neurology.

[8]  G. B. Young,et al.  Creutzfeldt‐Jakob disease without periodic sharp wave complexes , 1988, Neurology.

[9]  T. Kitamoto,et al.  Immunohistochemical confirmation of Creutzfeldt-Jakob disease with a long clinical course with amyloid plaque core antibodies. , 1988, The American journal of pathology.

[10]  S. Prusiner,et al.  Changes in the localization of brain prion proteins during scrapie infection , 1987, Neurology.

[11]  S. Prusiner,et al.  Formic acid pretreatment enhances immunostaining of cerebral and systemic amyloids. , 1987, Laboratory investigation; a journal of technical methods and pathology.

[12]  S. Prusiner,et al.  Prions causing nervous system degeneration. , 1987, Laboratory investigation; a journal of technical methods and pathology.

[13]  S. Prusiner,et al.  Molecular cloning of a human prion protein cDNA. , 1986, DNA.

[14]  S. Hsu,et al.  Color modification of diaminobenzidine (DAB) precipitation by metallic ions and its application for double immunohistochemistry. , 1982, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[15]  S. Prusiner Novel proteinaceous infectious particles cause scrapie. , 1982, Science.

[16]  S. Prusiner,et al.  Sulfated glycosaminoglycans in amyloid plaques of prion diseases , 2004, Acta Neuropathologica.

[17]  S. Prusiner,et al.  Scrapie prion proteins are synthesized in neurons. , 1986, The American journal of pathology.