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Kuru, the First Human Prion Disease
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/9780470715406.ch5openalex-snapshot
Urgent Opportunistic Observations: The Study of Changing, Transient and Disappearing Phenomena of Medical Interest in Disrupted Primitive Human Communities
inferredcites →https://doi.org/10.1002/ana.410120102openalex-snapshot
Kuru with incubation periods exceeding two decades
inferredcites →https://doi.org/10.1002/ana.410350504openalex-snapshot
Human spongiform encephalopathy: The national institutes of health series of 300 cases of experimentally transmitted disease
inferredcites →https://doi.org/10.1002/ana.410390613openalex-snapshot
Molecular basis of phenotypic variability in sporadc creudeldt‐jakob disease
inferredcites →https://doi.org/10.1002/j.1834-4461.2006.tb03044.xopenalex-snapshot
The Promised Medicine: Fore Reflections on the Scientific Investigation ofKuru
inferredcites →https://doi.org/10.1002/j.1834-4461.2009.tb00049.xopenalex-snapshot
Frontier Journeys. Fore Experiences on the Kuru Patrols.
inferredcites →https://doi.org/10.1006/neur.1995.0024openalex-snapshot
Proliferating Cell Nuclear Antigen Immunohistochemistry in Astrocytes in Experimental Creutzfeldt-Jakob Disease and in Human Kuru, Creutzfeldt-Jakob Disease and Gerstmann-Sträussler-Scheinker Syndrome
inferredcites →https://doi.org/10.1007/0-306-46890-5openalex-snapshot
Self-Assembling Peptide Systems in Biology, Medicine and Engineering
inferredcites →https://doi.org/10.1007/0-306-46890-5_8openalex-snapshot
Molecular Casting of Infectious Amyloids, Inorganic and Organic Replication: Nucleation, Conformational Change and Self-Assembly
inferredcites →https://doi.org/10.1007/bf00686775openalex-snapshot
An unusual structure in Kuru brain
inferredcites →https://doi.org/10.1016/0022-510x(83)90044-8openalex-snapshot
A clinico-pathological study of a case of kuru
inferredcites →https://doi.org/10.1016/0304-3940(94)11131-2openalex-snapshot
Prion protein accumulation in the spinal cords of patients with sporadic and growth hormone associated Creutzfeldt-Jakob disease
inferredcites →https://doi.org/10.1016/b978-0-12-429766-1.50010-8openalex-snapshot
Unconventional Viruses Causing the Spongiform Virus Encephalopathies. A Fruitless Search for the Coat and Core
inferredcites →https://doi.org/10.1016/b978-0-12-566302-1.50012-9openalex-snapshot
10.1016/b978-0-12-566302-1.50012-9
inferredcites →https://doi.org/10.1016/j.exger.2008.05.010openalex-snapshot
Kuru: Its ramifications after fifty years
inferredcites →https://doi.org/10.1016/j.mehy.2007.12.014openalex-snapshot
A potential role for Transmissible Spongiform Encephalopathies in Neanderthal extinction
inferredcites →https://doi.org/10.1016/j.mehy.2008.04.015openalex-snapshot
Mad Neanderthal disease? Some comments on “A potential role for Transmissible Spongiform Encephalopathies in Neanderthal extinction”
inferredcites →https://doi.org/10.1016/s0022-3476(66)80483-3openalex-snapshot
Kuru in childhood: Disappearance of the disease in the younger age group
inferredcites →https://doi.org/10.1016/s0140-6736(05)62355-0openalex-snapshot
Is the neuropathology of new variant Creutzfeldt-Jakob disease and kuru similar?
inferredcites →https://doi.org/10.1016/s0140-6736(06)68930-7openalex-snapshot
Kuru in the 21st century—an acquired human prion disease with very long incubation periods
inferredcites →https://doi.org/10.1016/s0140-6736(66)92031-9openalex-snapshot
EXPERIMENTAL "KURU" IN CHIMPANZEES A Pathological Report
inferredcites →https://doi.org/10.1016/s0140-6736(67)92784-5openalex-snapshot
A TRANSMISSION MODEL FOR KURU
inferredcites →https://doi.org/10.1016/s0960-9822(03)00522-0openalex-snapshot
Human evolution: a legacy of cannibalism in our genes?
inferredcites →https://doi.org/10.1016/s1286-4579(02)01608-8openalex-snapshot
Kuru: the old epidemic in a new mirror
inferredcites →https://doi.org/10.1016/s1474-4422(08)70265-5openalex-snapshot
Genetic risk factors for variant Creutzfeldt–Jakob disease: a genome-wide association study
inferredcites →https://doi.org/10.1038/179737a0openalex-snapshot
Vacuolated Neurones in Sheep affected with Scrapie
inferredcites →https://doi.org/10.1038/180393a0openalex-snapshot
Significance of Vacuolated Neurones in the Medulla of Sheep affected with Scrapie
inferredcites →https://doi.org/10.1038/204257a0openalex-snapshot
Attempts to Demonstrate a Transmissible Agent in Kuru, Amyotrophic Lateral Sclerosis, and other Sub-Acute and Chronic Nervous System Degenerations of Man
inferredcites →https://doi.org/10.1038/209794a0openalex-snapshot
Experimental Transmission of a Kuru-like Syndrome to Chimpanzees
inferredcites →https://doi.org/10.1038/240351a0openalex-snapshot
Transmission of Kuru from Man to Rhesus Monkey (Macaca mulatta) 8½ Years after Inoculation
inferredcites →https://doi.org/10.1038/35024064openalex-snapshot
Biochemical evidence of cannibalism at a prehistoric Puebloan site in southwestern Colorado
inferredcites →https://doi.org/10.1038/383685a0openalex-snapshot
Molecular analysis of prion strain variation and the aetiology of 'new variant' CJD
inferredcites →https://doi.org/10.1038/38925openalex-snapshot
The same prion strain causes vCJD and BSE
inferredcites →https://doi.org/10.1038/nature15369openalex-snapshot
Evidence for human transmission of amyloid-β pathology and cerebral amyloid angiopathy
inferredcites →https://doi.org/10.1038/nature15704openalex-snapshot
Erratum: Evidence for human transmission of amyloid-β pathology and cerebral amyloid angiopathy
inferredcites →https://doi.org/10.1038/s41586-018-0790-yopenalex-snapshot
Transmission of amyloid-β protein pathology from cadaveric pituitary growth hormone
inferredcites →https://doi.org/10.1056/nejm195711142572005openalex-snapshot
Degenerative Disease of the Central Nervous System in New Guinea
inferredcites →https://doi.org/10.1056/nejm196702162760708openalex-snapshot
Slow-Virus Infections of the Nervous System
inferredcites →https://doi.org/10.1056/nejmoa0809716openalex-snapshot
A Novel Protective Prion Protein Variant that Colocalizes with Kuru Exposure
inferredcites →https://doi.org/10.1073/pnas.0800190105openalex-snapshot
Kuru prions and sporadic Creutzfeldt–Jakob disease prions have equivalent transmission properties in transgenic and wild-type mice
inferredcites →https://doi.org/10.1073/pnas.0905825106openalex-snapshot
The kuru infectious agent is a unique geographic isolate distinct from Creutzfeldt–Jakob disease and scrapie agents
inferredcites →https://doi.org/10.1073/pnas.95.22.13239openalex-snapshot
Phenotype-genotype studies in kuru: Implications for new variant Creutzfeldt–Jakob disease
inferredcites →https://doi.org/10.1080/19485565.1962.9987505openalex-snapshot
Kuru: An appraisal of five years of investigation
inferredcites →https://doi.org/10.1086/317935openalex-snapshot
Increased Susceptibility to Kuru of Carriers of the PRNP 129 Methionine/Methionine Genotype
inferredcites →https://doi.org/10.1093/brain/104.3.559openalex-snapshot
CREUTZFELDT-JAKOB DISEASE VIRUS ISOLATIONS FROM THE GERSTMANN-STRÄUSSLER SYNDROME
inferredcites →https://doi.org/10.1093/brain/113.1.121openalex-snapshot
REEVALUATION OF THE ULTRASTRUCTURAL PATHOLOGY OF EXPERIMENTAL CREUTZFELDT-JAKOB DISEASE
inferredcites →https://doi.org/10.1093/brain/93.1.65openalex-snapshot
A COMPREHENSIVE CINEMA RECORD OF DISAPPEARING KURU
inferredcites →https://doi.org/10.1093/brain/96.3.441openalex-snapshot
EXPERIMENTAL KURU IN THE CHIMPANZEE
inferredcites →https://doi.org/10.1093/brain/98.4.595openalex-snapshot
EXPERIMENTAL KURU IN THE SPIDER MONKEY
inferredcites →https://doi.org/10.1093/brain/awq234openalex-snapshot
Agent strain variation in human prion disease: insights from a molecular and pathological review of the National Institutes of Health series of experimentally transmitted disease
inferredcites →https://doi.org/10.1093/hmg/ddr607openalex-snapshot
Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP
inferredcites →https://doi.org/10.1093/infdis/142.2.205openalex-snapshot
Oral Transmission of Kuru, Creutzfeldt-Jakob Disease, and Scrapie to Nonhuman Primates
inferredcites →https://doi.org/10.1097/00005072-196407000-00007openalex-snapshot
NEUROPATHOLOGIC FINDINGS IN EXOTIC NEUROLOGIC DISORDERS AMONG NATIVES OF THE HIGHLANDS OF NEW GUINEA
inferredcites →https://doi.org/10.1097/00005072-196701000-00007openalex-snapshot
Further Observations on the Pathology of Kuru*
inferredcites →https://doi.org/10.1097/00005072-196907000-00001openalex-snapshot
EXPERIMENTAL KURU ENCEPHALOPATHY IN CHIMPANZEES AND SPIDER MONKEYS
inferredcites →https://doi.org/10.1098/rstb.2008.0068openalex-snapshot
A clinical study of kuru patients with long incubation periods at the end of the epidemic in Papua New Guinea
inferredcites →https://doi.org/10.1098/rstb.2008.0069openalex-snapshot
The origin of the prion agent of kuru: molecular and biological strain typing
inferredcites →https://doi.org/10.1098/rstb.2008.0070openalex-snapshot
Kuru and its contribution to medicine
inferredcites →https://doi.org/10.1098/rstb.2008.0071openalex-snapshot
The epidemiology of kuru: monitoring the epidemic from its peak to its end
inferredcites →https://doi.org/10.1098/rstb.2008.0072openalex-snapshot
Understanding kuru: the contribution of anthropology and medicine
inferredcites →https://doi.org/10.1098/rstb.2008.0085openalex-snapshot
The changing face of kuru: a personal perspective
inferredcites →https://doi.org/10.1098/rstb.2008.0086openalex-snapshot
The neuropathology of kuru and variant Creutzfeldt–Jakob disease
inferredcites →https://doi.org/10.1098/rstb.2008.0087openalex-snapshot
Genetic susceptibility, evolution and the kuru epidemic
inferredcites →https://doi.org/10.1098/rstb.2008.0091openalex-snapshot
Central and peripheral pathology of kuru: pathological analysis of a recent case and comparison with other forms of human prion disease
inferredcites →https://doi.org/10.1098/rstb.2008.0121openalex-snapshot
Lessons of kuru research: background to recent studies with some personal reflections
inferredcites →https://doi.org/10.1098/rstb.2008.4000openalex-snapshot
Some tributes to research colleagues and other contributors to our knowledge about kuru
inferredcites →https://doi.org/10.1098/rstb.2008.4002openalex-snapshot
Kuru: memories of the NIH years
inferredcites →https://doi.org/10.1098/rstb.2008.4004openalex-snapshot
Richard Hornabrook's first impressions of kuru and Okapa
inferredcites →https://doi.org/10.1098/rstb.2008.4011openalex-snapshot
Early images of kuru and the people of Okapa
inferredcites →https://doi.org/10.1098/rstb.2008.4013openalex-snapshot
Kuru likened to scrapie: the story remembered
inferredcites →https://doi.org/10.1098/rstb.2008.4029openalex-snapshot
Some recollections about kuru in a patient at Rabaul in 1978, and subsequent experiences with prion diseases
inferredcites →https://doi.org/10.1101/cshperspect.a024588openalex-snapshot
α-Synuclein: Multiple System Atrophy Prions
inferredcites →https://doi.org/10.1111/imj.1958.7.4.269openalex-snapshot
OBSERVATIONS ON KURU : I. A POSSIBLE GENETIC BASIS
inferredcites →https://doi.org/10.1111/imj.1959.8.1.16openalex-snapshot
OBSERVATIONS ON KURU. III : PATHOLOGICAL FEATURES IN FIVE CASES
inferredcites →https://doi.org/10.1111/j.1365-2990.2008.00959.xopenalex-snapshot
Ultrastructural study of florid plaques in variant Creutzfeldt–Jakob disease: a comparison with amyloid plaques in kuru, sporadic Creutzfeldt–Jakob disease and Gerstmann–Sträussler–Scheinker disease
inferredcites →https://doi.org/10.1111/j.1750-3639.1995.tb00574.xopenalex-snapshot
Neuropathology and the Scrapie‐Kuru Connection
inferredcites →https://doi.org/10.1111/j.1750-3639.1997.tb01072.xopenalex-snapshot
Pathology and Immunocytochemistry of a Kuru Brain
inferredcites →https://doi.org/10.1111/j.1750-3639.1997.tb01073.xopenalex-snapshot
Kuru: Forty Years Later, A Historical Note
inferredcites →https://doi.org/10.1111/j.1750-3639.1998.tb00165.xopenalex-snapshot
Comparative Neuropathology of Kuru with the New Variant of Creutzfeldt‐Jakob Disease: Evidence for Strain of Agent Predominating Over Genotype of Host
inferredcites →https://doi.org/10.1111/j.2164-0947.1967.tb02298.xopenalex-snapshot
CANNIBALISM IN THE KURU REGION OF NEW GUINEA*
inferredcites →https://doi.org/10.1126/science.1083320openalex-snapshot
Balancing Selection at the Prion Protein Gene Consistent with Prehistoric Kurulike Epidemics
inferredcites →https://doi.org/10.1126/science.142303openalex-snapshot
Unconventional Viruses and the Origin and Disappearance of Kuru
inferredcites →https://doi.org/10.1126/science.155.3759.212openalex-snapshot
Transmission and Passage of Experimental "Kuru" to Chimpanzees
inferredcites →https://doi.org/10.1126/science.161.3839.388openalex-snapshot
Creutzfeldt-Jakob Disease (Spongiform Encephalopathy): Transmission to the Chimpanzee
inferredcites →https://doi.org/10.1126/science.165.3897.1023openalex-snapshot
Infection as the Etiology of Spongiform Encephalopathy (Creutzfeldt-Jakob Disease)
inferredcites →https://doi.org/10.1146/annurev.anthro.30.1.363openalex-snapshot
Kuru, Prions, and Human Affairs: Thinking About Epidemics
inferredcites →https://doi.org/10.1146/annurev.anthro.33.070203.143758openalex-snapshot
Thinking About Cannibalism
inferredcites →https://doi.org/10.1159/000110837openalex-snapshot
The Natural Incubation Period of Kuru and the Episodes of Transmission in Three Clusters of Patients
inferredcites →https://doi.org/10.1159/000149399openalex-snapshot
Transmission of Kuru and Creutzfeldt-Jakob Disease to Marmoset Monkeys
inferredcites →https://doi.org/10.1159/000426423openalex-snapshot
Blood Group Genetical Studies on Kuru-Afflicted Natives of the Eastern Highlands of New Guinea, and Comparisons with Unaffected Neighboring Tribes in Papua-New Guinea
inferredcites →https://doi.org/10.1159/000459951openalex-snapshot
Experimental Kuru in the Gibbon and Sooty Mangabey and Creutzfeldt-Jakob Disease in the Pigtailed Macaque
inferredcites →https://doi.org/10.1177/1525822x05280177openalex-snapshot
Kuru Truths: Obtaining Fore Narratives
inferredcites →https://doi.org/10.1212/wnl.40.3_part_1.518openalex-snapshot
Immunohistochemical localization of prion protein in spongiform encephalopathies and normal brain tissue
inferredcites →https://doi.org/10.2174/1566524043360627openalex-snapshot
Genetic Studies in Relation to Kuru: An Overview
inferredcites →https://doi.org/10.3406/jso.1976.2756openalex-snapshot
Medical Practices and Funeral Ceremony of the Dunkwi Anga
inferredcites →https://doi.org/10.4161/pri.23061openalex-snapshot
Prions, prionoids and pathogenic proteins in Alzheimer disease
inferredcites →https://doi.org/10.4269/ajtmh.1965.14.852openalex-snapshot
Changing Patterns of Kuru: Epidemiological Changes in the Period of Increasing Contact of the Fore People with Western Civilization
inferredcites →https://doi.org/10.4324/9781315223513-2openalex-snapshot
Images of Catastrophe: The Making of an Epidemic
inferredcites →https://doi.org/10.5694/j.1326-5377.1957.tb60287.xopenalex-snapshot
KURU: CLINICAL STUDY OF A NEW SYNDROME RESEMBLING PARALYSIS AGITANS IN NATIVES OF THE EASTERN HIGHLANDS OF AUSTRALIAN NEW GUINEA
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4820084openalex-extracted
Unraveling the Structural Facets of Prp127-132 Polymorphic Variants Using Combined Molecular Dynamics/Markov Modeling
inferred← citeshttps://doi.org/10.1007/978-3-031-84089-0_36openalex-snapshot
Prion Associated Diseases
inferred← citeshttps://doi.org/10.1007/978-3-031-97055-9_11openalex-snapshot
Advancing Prion Diagnostics: RT-QuIC Applications in Peripheral Tissues
inferred← citeshttps://doi.org/10.1007/978-981-32-9449-3_14openalex-snapshot
Prion Diseases: A Concern for Mankind
inferred← citeshttps://doi.org/10.1007/978-981-99-6445-1_11openalex-snapshot
Miscellaneous CNS Viral Infections: Underappreciated Causes of Neurologic Disease
inferred← citeshttps://doi.org/10.1016/b978-0-323-85730-7.00046-1openalex-snapshot
Prion diseases: A rare group of neurodegenerative disorders
inferred← citeshttps://doi.org/10.1016/bs.acc.2024.11.003openalex-snapshot
Spotting targets with 2D-DIGE proteomics
inferred← citeshttps://doi.org/10.1016/bs.apcsb.2024.11.009openalex-snapshot
Deciphering protein aggregation: Insights into morphology, contributing factors, and molecular pathologies
inferred← citeshttps://doi.org/10.1016/j.jmb.2023.168361openalex-snapshot
Emerging Trends in Cryo-EM-based Structural Studies of Neuropathological Amyloids
inferred← citeshttps://doi.org/10.1016/j.medidd.2022.100126openalex-snapshot
The folding and misfolding mechanisms of multidomain proteins
inferred← citeshttps://doi.org/10.1016/j.micpath.2025.107789openalex-snapshot
The infectious potential of protein misfolding: insights from cross-over studies of prion diseases and common neurodegenerative disorders
inferred← citeshttps://doi.org/10.1016/j.pathol.2024.09.005openalex-snapshot
Pathological spectrum of sporadic Creutzfeldt–Jakob disease
inferred← citeshttps://doi.org/10.1016/j.wneu.2020.05.134openalex-snapshot
Letter to the Editor: ‘The Laughing Disease’—From Kuru to the Joker's Sinister Laugh and Madness
inferred← citeshttps://doi.org/10.1021/acsomega.2c00155openalex-snapshot
Chronic Wasting Disease (CWD) in Cervids and the Consequences of a Mutable Protein Conformation
inferred← citeshttps://doi.org/10.1038/s41467-019-13455-0openalex-snapshot
Estimating heritability and genetic correlations from large health datasets in the absence of genetic data
inferred← citeshttps://doi.org/10.1038/s41598-020-79050-2openalex-snapshot
Antler cannibalism in reindeer
inferred← citeshttps://doi.org/10.1039/d1cp03187bopenalex-snapshot
Structural and electronic analysis of the octarepeat region of prion protein with four Cu 2+ by polarizable MD and QM/MM simulations
inferred← citeshttps://doi.org/10.1080/19336896.2026.2623370openalex-snapshot
Prion 2025: advancing the understanding and treatment of prion diseases in dialogue with patients and families
inferred← citeshttps://doi.org/10.1155/2023/6687264openalex-snapshot
The Prion Basis of Progressive Neurodegenerative Disorders
inferred← citeshttps://doi.org/10.1177/1010539519889542openalex-snapshot
Kuru: As the Neurological Disease Fades From Memory, Shoe Advertising Takes Over
inferred← citeshttps://doi.org/10.12795/araucaria.2021.i46.21openalex-snapshot
Enfermedades priónicas: historia, diversidad e importancia socioeconómica como paradigma de las Enfermedades Raras
inferred← citeshttps://doi.org/10.1515/tnsci-2022-0315openalex-snapshot
Human prion diseases and the prion protein – what is the current state of knowledge?
inferred← citeshttps://doi.org/10.20960/revmedlab.00125openalex-snapshot
Biomarcadores diagnósticos de la enfermedad de Creutzfeld-Jakob
inferred← citeshttps://doi.org/10.2174/0115743624353499250630090143openalex-snapshot
Comprehensive Insights into Prion Diseases: Classification, Mechanisms of Action, Detection Methods, and Preventive Strategies
inferred← citeshttps://doi.org/10.2174/1568026621666211201122752openalex-snapshot
Formulating the Structural Aspects of Various Benzimidazole Cognates
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Evaluation of the application for new alternative biodiesel production process for rendered fat including Category 1 animal by‐products (BDI‐RepCat® process, AT)
inferred← citeshttps://doi.org/10.3174/ng.2000035openalex-snapshot
Prionopathies and Prionlike Protein Aberrations in Neurodegenerative Diseases
inferred← citeshttps://doi.org/10.3233/jad-215171openalex-snapshot
Prions and Neurodegenerative Diseases: A Focus on Alzheimer’s Disease
inferred← citeshttps://doi.org/10.33448/rsd-v11i9.31533openalex-snapshot
Doenças priônicas neurodegenerativas humanas: o que sabemos e sua epidemiologia no Brasil
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Kuru: The Neurodegenerative Disorder; Roles of PrPC and PrPSc in infection, Effects in Blocking Neural Synapses and its Comprehensive Observation
inferred← citeshttps://doi.org/10.33552/ann.2021.09.000717openalex-snapshot
Kuru: The Neurodegenerative Disorder; Roles of PrPC and PrPSc in infection, Effects in Blocking Neural Synapses and its Comprehensive Observation
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Oral vaccination as a potential strategy to manage chronic wasting disease in wild cervid populations
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What is the role of lipids in prion conversion and disease?
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Kin-Avoidance in Cannibalistic Homicide
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From Cell Culture to Organoids-Model Systems for Investigating Prion Strain Characteristics
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Viral Infections and Interferons in the Development of Obesity
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Perspectives on CRISPR Genome Editing to Prevent Prion Diseases in High-Risk Individuals
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The Nuclear Lamina: Protein Accumulation and Disease
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Human Prion Disorders: Review of the Current Literature and a Twenty-Year Experience of the National Surveillance Center in the Czech Republic
inferred← citeshttps://doi.org/10.3390/ijms22010007openalex-snapshot
Extracellular Amyloid Deposits in Alzheimer’s and Creutzfeldt–Jakob Disease: Similar Behavior of Different Proteins?
inferred← citeshttps://doi.org/10.3390/ijms22179198openalex-snapshot
microRNA-146a-5p, Neurotropic Viral Infection and Prion Disease (PrD)
inferred← citeshttps://doi.org/10.3390/jcm13154401openalex-snapshot
Creutzfeldt–Jakob Disease and Fatal Familial Insomnia: Demographics and In-Hospital Mortality in Spain
inferred← citeshttps://doi.org/10.3390/v11111044openalex-snapshot
Transmissibility versus Pathogenicity of Self-Propagating Protein Aggregates
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Comment on Liberski, Gajos, Sikorska, and Lindenbaum: “Kuru, the First Human Prion Disease” Viruses 2019, 11, 232
inferred← citeshttps://doi.org/10.3390/v14030630openalex-snapshot
Transport of Prions in the Peripheral Nervous System: Pathways, Cell Types, and Mechanisms
inferred← citeshttps://doi.org/10.33920/med-12-2604-01openalex-snapshot
Prion diseases: risk factors for transmission in otorhinolaryngology
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Enfermedades priónicas y enfermedades similares a priones
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Human prion diseases - state of the art 2023
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Cannibals, slow viruses, Nobel Prize and young lads: the story of Daniel Carleton Gajdusek (1923-2008), laureate of the Nobel Prize in Physiology or Medicine (1976) and honorary doctor of Comenius University in Bratislava (1996)
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Misfolded protein aggregation and altered cellular pathways in neurodegenerative diseases
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Origin Links Between Humans and Infectious Disease Agents
inferred← citeshttps://doi.org/10.4132/jptm.2022.11.14openalex-snapshot
Infections and immunity: associations with obesity and related metabolic disorders
inferred← citeshttps://doi.org/10.46419/vs.53.6.6openalex-snapshot
Praćenje transmisivnih spongiformnih encefalopatija u Republici Hrvatskoj
inferred← citeshttps://doi.org/10.46419/vs.56.1.6openalex-snapshot
Chronic wasting disease as a part of animal spongiform encephalopathies
inferred← citeshttps://doi.org/10.5114/fmpcr.2022.113010openalex-snapshot
Psychological impact of the COVID-19 pandemic on healthcare professionals in the Al Ahsa Region, Saudi Arabia
inferred← citeshttps://doi.org/10.5114/fn.2022.113561openalex-snapshot
microRNA-146a as a biomarker for transmissible spongiform encephalopathy
inferred← citeshttps://doi.org/10.54160/epilepsie.11037openalex-snapshot
Nature or nurture, of beide?
inferred← citeshttps://doi.org/10.70675/0c2f652cz02f9z4c44zb4afz9507d74679eaopenalex-snapshot
Développement d'outils thérapeutiques ciblant les agrégats d'alpha-synucléine dans les synucléinopathies
inferred← citeshttps://doi.org/10.70675/9f070729z72aez4fccz9604z8c52be1a62e6openalex-snapshot
De la fonction physiologique de la protéine prion cellulaire aux maladies neurodégénératives amyloïdes
inferred← citeshttps://doi.org/10.70675/a212ad92z3b22z4eeczb177z417025bff4efopenalex-snapshot
La protéine prion cellulaire : rôles physiologiques et implications croisées dans les maladies neurodégénératives amyloïdes
inferred← citeshttps://doi.org/10.70675/a872e5bdzc153z41f4z9472z725fd78aab48openalex-snapshot
Development of Inhibitors of Amyloid Fibril Propagation
inferred← citeshttps://doi.org/10.7759/cureus.51708openalex-snapshot
Kuru Disease: Bridging the Gap Between Prion Biology and Human Health
inferred← citeshttps://doi.org/10.7759/cureus.73063openalex-snapshot
The Role of Cells in Encoding and Storing Information: A Narrative Review of Cellular Memory
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