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Susceptibilities of nonhuman primates to chronic wasting disease

Emerging infectious diseases, 2009-09, Vol.15 (9), p.1366-1376

2009

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Creutzfeldt‐Jakob disease and blood transfusion: safe or not safe?

Transfusion (Philadelphia, Pa.), 2017-08, Vol.57 (8), p.1851-1853

Cervenakova, Larisa

2017

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C reutzfeldt‐ J akob disease and blood transfusion: safe or not safe?

Transfusion (Philadelphia, Pa.), 2017-08, Vol.57 (8), p.1851-1853

Cervenakova, Larisa

2017

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Missense mutations in desmin associated with familial cardiac and skeletal myopathy

Nature genetics, 1998-08, Vol.19 (4), p.402-403

1998

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Keeping the record straight on the availability of gene therapy for common variable immunodeficiency

Pharmaceutical journal, 2018-03

2018

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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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Candidate cell substrates, vaccine production, and transmissible spongiform encephalopathies

Emerging infectious diseases, 2011-12, Vol.17 (12), p.2262-2269

2011

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Persistent Propagation of Variant Creutzfeldt-Jakob Disease Agent in Murine Spleen Stromal Cell Culture with Features of Mesenchymal Stem Cells

Journal of Virology, 2008-11, Vol.82 (21), p.10959-10962

2008

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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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Protein misfolding cyclic amplification (PMCA): Current status and future directions

Virus research, 2015-09, Vol.207, p.47-61

2015

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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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Protease-resistant Prion Protein in Lymphoreticular Tumors of Variant Creutzfeldt-Jakob Disease Mice

Emerging infectious diseases, 2006-03, Vol.12 (3), p.511-513

2006

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First Demonstration of Transmissible Spongiform Encephalopathy-associated Prion Protein (PrPTSE) in Extracellular Vesicles from Plasma of Mice Infected with Mouse-adapted Variant Creutzfeldt-Jakob Disease by in Vitro Amplification

The Journal of biological chemistry, 2014-10, Vol.289 (42), p.29247-29260

2014

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Industry call for COVID ‐19 convalescent plasma collections

ISBT science series, 2020-11, Vol.15 (4), p.415-416

2020

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Mechanisms of prion-induced neurodegeneration

Expert reviews in molecular medicine, 2016-04, Vol.18, p.e5-e55; e7208; e1000800; e125; e15658; e1001138; e19339; e1000383; e1672, Article e5

2016

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Access and use of immunoglobulins in supportive cancer care: A thematic analysis of a systematic review data set

The journal of medicine access, 2024-01, Vol.8, p.27550834241236596-27550834241236596

2024

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Changes in cellular prion protein expression, processing and localisation during differentiation of the neuronal cell line CAD 5

Biology of the cell, 2020-01, Vol.112 (1), p.1-21

2020

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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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Spontaneous mutations in the prion protein gene causing transmissible spongiform encephalopathy

Annals of neurology, 2002-09, Vol.52 (3), p.355-359

2002

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Are prions transported by plasma exosomes?

Transfusion and apheresis science, 2016-08, Vol.55 (1), p.70-83

2016

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Access and use of immunoglobulins in secondary supportive cancer care: A systematic literature review

The Journal of Medicine Access, 2023-01, Vol.7, p.27550834231197315-27550834231197315

2023

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The Original Gerstmann-Sträussler-Scheinker Family of Austria: Divergent Clinicopathological Phenotypes but Constant PrP Genotype

Brain pathology (Zurich, Switzerland), 1995-07, Vol.5 (3), p.201-211

1995

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Similar levels of infectivity in the blood of mice infected with human-derived vCJD and GSS strains of transmissible spongiform encephalopathy

Transfusion (Philadelphia, Pa.), 2003-12, Vol.43 (12), p.1687-1694

2003

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The above letter was sent to Dr. Brown and Ms. Cervenáková, who offer the following reply

Transfusion (Philadelphia, Pa.), 2000-06, Vol.40 (6), p.754-755

2000

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A prion lexicon (out of control)

The Lancet (British edition), 2005-01, Vol.365 (9454), p.122-122

2005

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Susceptibilities of nonhuman primates to chronic wasting disease

Creutzfeldt‐Jakob disease and blood transfusion: safe or not safe?

C reutzfeldt‐ J akob disease and blood transfusion: safe or not safe?

Missense mutations in desmin associated with familial cardiac and skeletal myopathy

Keeping the record straight on the availability of gene therapy for common variable immunodeficiency

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

Candidate cell substrates, vaccine production, and transmissible spongiform encephalopathies

Persistent Propagation of Variant Creutzfeldt-Jakob Disease Agent in Murine Spleen Stromal Cell Culture with Features of Mesenchymal Stem Cells

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

Protein misfolding cyclic amplification (PMCA): Current status and future directions

First experimental transmission of fatal familial insomnia

Protease-resistant Prion Protein in Lymphoreticular Tumors of Variant Creutzfeldt-Jakob Disease Mice

First Demonstration of Transmissible Spongiform Encephalopathy-associated Prion Protein (PrPTSE) in Extracellular Vesicles from Plasma of Mice Infected with Mouse-adapted Variant Creutzfeldt-Jakob Disease by in Vitro Amplification

Industry call for COVID ‐19 convalescent plasma collections

Mechanisms of prion-induced neurodegeneration

Access and use of immunoglobulins in supportive cancer care: A thematic analysis of a systematic review data set

Changes in cellular prion protein expression, processing and localisation during differentiation of the neuronal cell line CAD 5

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

Spontaneous mutations in the prion protein gene causing transmissible spongiform encephalopathy

Are prions transported by plasma exosomes?

Access and use of immunoglobulins in secondary supportive cancer care: A systematic literature review

The Original Gerstmann-Sträussler-Scheinker Family of Austria: Divergent Clinicopathological Phenotypes but Constant PrP Genotype

Similar levels of infectivity in the blood of mice infected with human-derived vCJD and GSS strains of transmissible spongiform encephalopathy

The above letter was sent to Dr. Brown and Ms. Cervenáková, who offer the following reply

A prion lexicon (out of control)

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