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FAMILIAL SYSTEMS DEGENERATION WITH THALAMIC NEURONAL LOSS, GLIOSIS AND OLIVARY HYPERTROPHY SIMULATING CREUTZFELOT-JAKOB DISEASE

Journal of neuropathology and experimental neurology, 1985-05, Vol.44 (3), p.328

1985

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Conformational transitions, dissociation, and unfolding of scrapie amyloid (prion) protein

The Journal of biological chemistry, 1993-09, Vol.268 (27), p.20276-20284

1993

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Human spongiform encephalopathy: The national institutes of health series of 300 cases of experimentally transmitted disease

Annals of neurology, 1994-05, Vol.35 (5), p.513-529

1994

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Neuronal cell death in transmissible spongiform encephalopathies (prion diseases) revisited: from apoptosis to autophagy

International Journal of Biochemistry and Cell Biology, 2004-12, Vol.36 (12), p.2473-2490

2004

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The distribution of infectivity in blood components and plasma derivatives in experimental models of transmissible spongiform encephalopathy

Transfusion (Philadelphia, Pa.), 1998-09, Vol.38 (9), p.810-816

1998

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Natural and Experimental Oral Infection of Nonhuman Primates by Bovine Spongiform Encephalopathy Agents

Proceedings of the National Academy of Sciences - PNAS, 1999-03, Vol.96 (7), p.4046-4051

1999

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Increased Susceptibility to Kuru of Carriers of the PRNP 129 Methionine/Methionine Genotype

The Journal of infectious diseases, 2001-01, Vol.183 (2), p.192-196

2001

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Infectivity Studies of Both Ash and Air Emissions from Simulated Incineration of Scrapie- Contaminated Tissues

Environmental science & technology, 2004-11, Vol.38 (22), p.6155-6160

2004

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Different Patterns of Truncated Prion Protein Fragments Correlate with Distinct Phenotypes in P102L Gerstmann--Straussler--Scheinker Disease

Proceedings of the National Academy of Sciences - PNAS, 1998-07, Vol.95 (14), p.8322-8327

1998

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Phenotypic Variability of Gerstmann-Straussler-Scheinker Disease is Associated with Prion Protein Heterogeneity

Journal of neuropathology and experimental neurology, 1998-10, Vol.57 (10), p.979-988

1998

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Difficult and failed intubation in obstetric anaesthesia: an observational study of airway management and complications associated with general anaesthesia for caesarean section

International journal of obstetric anesthesia, 2008-10, Vol.17 (4), p.292-297

2008

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Phenotype-Genotype Studies in Kuru: Implications for New Variant Creutzfeldt-Jakob Disease

Proceedings of the National Academy of Sciences - PNAS, 1998-10, Vol.95 (22), p.13239-13241

1998

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Transmissible Familial Creutzfeldt-Jakob Disease Associated with Five, Seven, and Eight Extra Octapeptide Coding Repeats in the PRNP Gene

Proceedings of the National Academy of Sciences - PNAS, 1991-12, Vol.88 (23), p.10926-10930

1991

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Family clustering of Viliuisk encephalomyelitis in traditional and new geographic regions

Emerging infectious diseases, 2007-09, Vol.13 (9), p.1321-1326

2007

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Fatal Familial Insomnia and Familial Creutzfeldt-Jakob Disease: Different Prion Proteins Determined by a DNA Polymorphism

Proceedings of the National Academy of Sciences - PNAS, 1994-03, Vol.91 (7), p.2839-2842

1994

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Interleukin 1 Regulates Synthesis of Amyloid β -protein Precursor mRNA in Human Endothelial Cells

Proceedings of the National Academy of Sciences - PNAS, 1989-10, Vol.86 (19), p.7606-7610

1989

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Ancestral Origins and Worldwide Distribution of the PRNP 200K Mutation Causing Familial Creutzfeldt-Jakob Disease

American journal of human genetics, 1999-04, Vol.64 (4), p.1063-1070

1999

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Fatal Familial Insomnia and Familial Creutzfeldt-Jakob Disease: Disease Phenotype Determined by a DNA Polymorphism

Science (American Association for the Advancement of Science), 1992-10, Vol.258 (5083), p.806-808

1992

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First experimental transmission of fatal familial insomnia

Nature (London), 1995-08, Vol.376 (6539), p.434-435

1995

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A prospective study of awareness and recall associated with general anaesthesia for caesarean section

International journal of obstetric anesthesia, 2008-10, Vol.17 (4), p.298-303

2008

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New Studies on the Heat Resistance of Hamster-Adapted Scrapie Agent: Threshold Survival after Ashing at 600 degrees C Suggests an Inorganic Template of Replication

Proceedings of the National Academy of Sciences - PNAS, 2000-03, Vol.97 (7), p.3418-3421

2000

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Survival of scrapie virus after 3 years' interment

The Lancet (British edition), 1991-02, Vol.337 (8736), p.269-270

1991

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Unstable triplet repeat and phenotypic variability of spinocerebellar ataxia type 1

Annals of neurology, 1996-04, Vol.39 (4), p.500-506

1996

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Transmission of Creutzfeldt-Jakob disease to a chimpanzee by electrodes contaminated during neurosurgery

Journal of neurology, neurosurgery and psychiatry, 1994-06, Vol.57 (6), p.757-758

1994

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Creutzfeldt-Jakob disease: Clinical analysis of a consecutive series of 230 neuropathologically verified cases

Annals of neurology, 1986-11, Vol.20 (5), p.597-602

1986

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FAMILIAL SYSTEMS DEGENERATION WITH THALAMIC NEURONAL LOSS, GLIOSIS AND OLIVARY HYPERTROPHY SIMULATING CREUTZFELOT-JAKOB DISEASE

Conformational transitions, dissociation, and unfolding of scrapie amyloid (prion) protein

Human spongiform encephalopathy: The national institutes of health series of 300 cases of experimentally transmitted disease

Neuronal cell death in transmissible spongiform encephalopathies (prion diseases) revisited: from apoptosis to autophagy

The distribution of infectivity in blood components and plasma derivatives in experimental models of transmissible spongiform encephalopathy

Natural and Experimental Oral Infection of Nonhuman Primates by Bovine Spongiform Encephalopathy Agents

Increased Susceptibility to Kuru of Carriers of the PRNP 129 Methionine/Methionine Genotype

Infectivity Studies of Both Ash and Air Emissions from Simulated Incineration of Scrapie- Contaminated Tissues

Different Patterns of Truncated Prion Protein Fragments Correlate with Distinct Phenotypes in P102L Gerstmann--Straussler--Scheinker Disease

Phenotypic Variability of Gerstmann-Straussler-Scheinker Disease is Associated with Prion Protein Heterogeneity

Difficult and failed intubation in obstetric anaesthesia: an observational study of airway management and complications associated with general anaesthesia for caesarean section

Phenotype-Genotype Studies in Kuru: Implications for New Variant Creutzfeldt-Jakob Disease

Transmissible Familial Creutzfeldt-Jakob Disease Associated with Five, Seven, and Eight Extra Octapeptide Coding Repeats in the PRNP Gene

Family clustering of Viliuisk encephalomyelitis in traditional and new geographic regions

Fatal Familial Insomnia and Familial Creutzfeldt-Jakob Disease: Different Prion Proteins Determined by a DNA Polymorphism

Interleukin 1 Regulates Synthesis of Amyloid β -protein Precursor mRNA in Human Endothelial Cells

Ancestral Origins and Worldwide Distribution of the PRNP 200K Mutation Causing Familial Creutzfeldt-Jakob Disease

Fatal Familial Insomnia and Familial Creutzfeldt-Jakob Disease: Disease Phenotype Determined by a DNA Polymorphism

First experimental transmission of fatal familial insomnia

A prospective study of awareness and recall associated with general anaesthesia for caesarean section

New Studies on the Heat Resistance of Hamster-Adapted Scrapie Agent: Threshold Survival after Ashing at 600 degrees C Suggests an Inorganic Template of Replication

Survival of scrapie virus after 3 years' interment

Unstable triplet repeat and phenotypic variability of spinocerebellar ataxia type 1

Transmission of Creutzfeldt-Jakob disease to a chimpanzee by electrodes contaminated during neurosurgery

Creutzfeldt-Jakob disease: Clinical analysis of a consecutive series of 230 neuropathologically verified cases

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