Endogenous Viral Etiology of Prion Diseases [PDF]
, 2009 Transmissible spongiform encephalopathies (TSEs), or prion diseases, are a group of incurable neurodegenerative disorders, including Kuru and Creutzfeldt-Jakob disease in humans, “mad cow” disease in cattle, and scrapie in sheep. This paper
Claudiu I. Bandea
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Relationship Between Annual Airborne Pollen Levels and Occurrence of Parkinson Disease, Amyotrophic Lateral Sclerosis, Myasthenia Gravis, Multiple Sclerosis, Spinocerebellar Degeneration, Huntington’s Disease, Shy-Drager Syndrome, Moyamoya Disease and Creutzfeldt- Jakob Disease Based on the National Registry Database of Specific Intractable Disease in Japan, 1974-2014: A Retrospective Study [PDF]
, 2022 Akira Awaya, Yoshiyuki Kuroiwa
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Oxidative and Inflammatory Events in Prion Diseases: Can They Be Therapeutic Targets? [PDF]
, 2019 Prion diseases are a group of incurable infectious terminal neurodegenerative diseases caused by the aggregated misfolded PrPsc in selected mammals including humans.
Bondy, Stephen C, Prasad, Kedar N
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CSF pleocytosis and syndrome of inappropriate antidiuretic hormone secretion in Creutzfeldt-Jakob disease [PDF]
, 2016 Ali G. Hamedani +4 more
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Is variant Creutzfeldt-Jakob disease in young children misdiagnosed as Alpers' syndrome? An analysis of a national surveillance study [PDF]
, 2004 Johann te Water Naudé
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Ultrastructural study of florid plaques in variant Creutzfeldt-Jakob disease: a comparison with amyloid plaques in kuru, sporadic Creutzfeldt-Jakob disease and Gerstmann-Straussler-Scheinker disease [PDF]
, 2009 Alwasiak +52 more
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A Case of Heidenhain Variant of Creutzfeldt-Jakob Disease Mimicking A Charles Bonnet Syndrome [PDF]
, 2021 Prado-Miranda Gala +1 more
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Wernicke-Korsakoff syndrome as a rare phenotype of sporadic Creutzfeldt-Jakob disease [PDF]
, 2018 Joanna Bielewicz +5 more
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Fatal Familial Insomnia: An Overview [PDF]
, 2011 Fatal Familial Insomnia (FFI) is an insidious prion disorder that tends to manifest itself as a patient reaches middle age following a pattern consistent with autosomal dominance.
Schools, Eric
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