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Kuru (disease)
A Review on Kuru: Fatal Neurodenegerative Disease”
Transmissibility Versus Pathogenicity of Self-Propagating Protein Aggregates
Genetic Studies in Relation to Kuru: an Overview
Prions in Variably Protease-Sensitive Prionopathy: an Update
FRI BRIEFINGS Bovine Spongiform Encephalopathy
Breakthroughs in Antemortem Diagnosis of Neurodegenerative Diseases COMMENTARY Glenn C
The Epidemiology of Kuru: Monitoring the Epidemic from Its Peak to Its End Michael P
Genetic Susceptibility, Evolution and the Kuru Epidemic
Balancing Selection at the Prion Protein Gene Consistent with Prehistoric Kurulike Epidemics Simon Mead,1 Michael P
Variably Protease-Sensitive Prionopathy. Emerg Infect Dis 20: 2006–2014.)
Kuru: the Neurodegenerative Disorder; Roles of Prpc and Prpsc in Infection, Effects in Blocking Neural Synapses and Its Comprehensive Observation
Prion Diseases Kuru
Fatal Familial Insomnia
The Kuru Infectious Agent Is a Unique Geographic Isolate Distinct from Creutzfeldt–Jakob Disease and Scrapie Agents
Scrapie Importance Scrapie Is a Neurodegenerative Disease, Caused by a Prion, That Affects Sheep, and Less Frequently, Goats
Human Prion Diseases Past, Present and Future Pierluigi Gambetti M.D
Molecular Pathogenesis of Sporadic Prion Diseases in Man
Kuru in the 21St Century—An Acquired Human Prion Disease with Very Long Incubation Periods
Top View
Variably Protease-Sensitive Prionopathy Mimicking Frontotemporal Dementia
Cultural Analysis of Kuru Diseases in Australian Tribe
The Kuru Infectious Agent Is a Unique Geographic Isolate Distinct from Creutzfeldt–Jakob Disease and Scrapie Agents
Transmissible Mink Encephalopathy (TME) Is a Progressive and Fatal Mink Neurodegenerative Disease That Affects Ranched Mink (Neovison (Mustela) Vison)
Fatal Familial Insomnia: an Overview 1
Prions: Brain Wasting Killer Proteins
Transmissible Spongiform Encephalopathy Mixes by Serial Saliva and Urine by Chronic Wasting Disease-Infected Deer by Protein Misfolding Cyclic Amplification
Prion Disease
The Possession of Kuru: Medical Science and Biocolonial Exchange
Kuru, the First Human Prion Disease "2279
Brain and Immune System: KURU Disease a Toxicological Process?
Kuru Prions and Sporadic Creutzfeldt–Jakob Disease Prions Have Equivalent Transmission Properties in Transgenic and Wild-Type Mice
Further Characterization of Glycoform-Selective Prions of Variably Protease-Sensitive Prionopathy
Creutzfeldt-Jakob Disease: Further Similarities with Kuru
Historical Figures in the Discovery of Prion Diseases
TRANSMISSIBLE SPONGIFORM ENCEPHALOPATHIES in HUMANS Ermias D. Belay
Communicable Disease Surveillance and Control
Kuru and Mad Cow Disease: Understanding the Prion Theory
Phenotype-Genotype Studies in Kuru: Implications for New Variant Creutzfeldt–Jakob Disease
Prion Disease Fact Sheet
Prion Disease Overview
Prions and Public Health Office (PPHO)
The Transmission and Natural Incubation Period of Kuru in Three Clusters of Patients in Papua, New Guinea Robert Klitzman Yale University
Description Treatment Prognosis
Evaluation of Non-Resolving and Progressive Pneumonia
WHO Manual for Surveillance of Human Transmissible Spongiform Encephalopathies Including Variant Creutzfeldt-Jakob Disease
Prions in Variably Protease-Sensitive Prionopathy: an Update