Lista de obras -

Abnormal prion protein in the pituitary in sporadic and variant Creutzfeldt-Jakob disease

artículo científico publicado en 2007

Correction: The Distribution of Prion Protein Allotypes Differs Between Sporadic and Iatrogenic Creutzfeldt-Jakob Disease Patients

artículo científico publicado en 2016

Detection and localization of PrPSc in the skeletal muscle of patients with variant, iatrogenic, and sporadic forms of Creutzfeldt-Jakob disease

artículo científico publicado en 2006

Detection of type 1 prion protein in variant Creutzfeldt-Jakob disease

artículo científico publicado en 2006

No major change in vCJD agent strain after secondary transmission via blood transfusion

artículo científico publicado en 2008

Peripheral tissue involvement in sporadic, iatrogenic, and variant Creutzfeldt-Jakob disease: an immunohistochemical, quantitative, and biochemical study

artículo científico publicado en 2004

Preclinical vCJD after blood transfusion in a PRNP codon 129 heterozygous patient

artículo científico publicado en 2004

Prion infectivity in the spleen of a PRNP heterozygous individual with subclinical variant Creutzfeldt-Jakob disease

artículo científico publicado en 2013

Prion protein accumulation and neuroprotection in hypoxic brain damage

artículo científico publicado en 2004

Prion protein accumulation in eyes of patients with sporadic and variant Creutzfeldt-Jakob disease

artículo científico publicado en 2003

Relative Abundance of apoE and Aβ1-42 Associated with Abnormal Prion Protein Differs between Creutzfeldt-Jakob Disease Subtypes

artículo científico publicado en 2016

The Distribution of Prion Protein Allotypes Differs Between Sporadic and Iatrogenic Creutzfeldt-Jakob Disease Patients

artículo científico publicado en 2016

The prion protein protease sensitivity, stability and seeding activity in variably protease sensitive prionopathy brain tissue suggests molecular overlaps with sporadic Creutzfeldt-Jakob disease

artículo científico publicado en 2014

Transmissions of variant Creutzfeldt-Jakob disease from brain and lymphoreticular tissue show uniform and conserved bovine spongiform encephalopathy-related phenotypic properties on primary and secondary passage in wild-type mice

artículo científico publicado en 2009

Variably protease-sensitive prionopathy in the UK: a retrospective review 1991-2008.

artículo científico publicado en 2013

Variably protease-sensitive prionopathy, a unique prion variant with inefficient transmission properties

artículo científico publicado en 2014

Lista de obras de

Abnormal prion protein in the pituitary in sporadic and variant Creutzfeldt-Jakob disease

Correction: The Distribution of Prion Protein Allotypes Differs Between Sporadic and Iatrogenic Creutzfeldt-Jakob Disease Patients

Detection and localization of PrPSc in the skeletal muscle of patients with variant, iatrogenic, and sporadic forms of Creutzfeldt-Jakob disease

Detection of type 1 prion protein in variant Creutzfeldt-Jakob disease

No major change in vCJD agent strain after secondary transmission via blood transfusion

Peripheral tissue involvement in sporadic, iatrogenic, and variant Creutzfeldt-Jakob disease: an immunohistochemical, quantitative, and biochemical study

Preclinical vCJD after blood transfusion in a PRNP codon 129 heterozygous patient

Prion infectivity in the spleen of a PRNP heterozygous individual with subclinical variant Creutzfeldt-Jakob disease

Prion protein accumulation and neuroprotection in hypoxic brain damage

Prion protein accumulation in eyes of patients with sporadic and variant Creutzfeldt-Jakob disease

Relative Abundance of apoE and Aβ1-42 Associated with Abnormal Prion Protein Differs between Creutzfeldt-Jakob Disease Subtypes

The Distribution of Prion Protein Allotypes Differs Between Sporadic and Iatrogenic Creutzfeldt-Jakob Disease Patients

The prion protein protease sensitivity, stability and seeding activity in variably protease sensitive prionopathy brain tissue suggests molecular overlaps with sporadic Creutzfeldt-Jakob disease

Transmissions of variant Creutzfeldt-Jakob disease from brain and lymphoreticular tissue show uniform and conserved bovine spongiform encephalopathy-related phenotypic properties on primary and secondary passage in wild-type mice

Variably protease-sensitive prionopathy in the UK: a retrospective review 1991-2008.

Variably protease-sensitive prionopathy, a unique prion variant with inefficient transmission properties