Sporadic Creutzfeldt-Jakob Disease in a Woman Married Into a Gerstmann-Sträussler-Scheinker Family: An Investigation of Prions Transmission via Microchimerism-Reference-Cited by-同舟云学术

Sporadic Creutzfeldt-Jakob Disease in a Woman Married Into a Gerstmann-Sträussler-Scheinker Family: An Investigation of Prions Transmission via Microchimerism

Published:2018-06-07 Issue:8 Volume:77 Page:673-684
ISSN:0022-3069
Container-title:Journal of Neuropathology & Experimental Neurology
language:en
Short-container-title:

Author:

Areškevičiūtė Aušrinė¹,Melchior Linea Cecilie¹,Broholm Helle¹,Krarup Lars-Henrik²,Lindquist Suzanne Granhøj³⁴,Johansen Peter⁴,McKenzie Neil⁵,Green Alison⁵,Nielsen Jørgen Erik³,Laursen Henning¹,Lund Eva Løbner¹

Affiliation:

1. Danish Reference Center for Prion Diseases, Department of Pathology, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark

2. Department of Neurology, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark

3. Danish Dementia Research Centre, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark

4. Department of Clinical Genetics, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark

5. National Creutzfeldt-Jakob Disease Research and Surveillance Unit, the University of Edinburgh, Edinburgh, United Kingdom

Publisher

Oxford University Press (OUP)

Subject

Cellular and Molecular Neuroscience,Clinical Neurology,Neurology,General Medicine,Pathology and Forensic Medicine

Link

http://academic.oup.com/jnen/article-pdf/77/8/673/25172169/nly043.pdf

Reference49 articles.

1. Biology and genetics of prions causing neurodegeneration;Prusiner;Annu Rev Genet,2013

2. Prion diseases;Geschwind;Continuum (Minneap Minn),2015

3. Genetic prion disease: Experience of a rapidly progressive dementia center in the United States and a review of the literature;Takada;Am J Med Genet B Genet,2017

4. Hereditary human prion diseases: An update;Schmitz;Mol Neurobiol,2017

5. De novo P102L mutation in a patient with Gerstmann-Straussler-Scheinker disease;Kojovic;Eur J Neurol,2011

Cited by 6 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Variably protease-sensitive prionopathy with methionine homozygosity at codon 129 in the prion protein gene;BMJ Case Reports;2024-02

2. Case report: A Chinese patient with spinocerebellar ataxia finally confirmed as Gerstmann-Sträussler-Scheinker syndrome with P102L mutation;Frontiers in Neurology;2023-08-03

3. The First Sporadic Creutzfeldt–Jakob Disease Case with a Rare Molecular Subtype VV1 and 1-Octapeptide Repeat Deletion in PRNP;Viruses;2021-10-14

4. Maternal micro-chimeric cells in the multiple sclerosis brain;Multiple Sclerosis and Related Disorders;2020-05

5. Molecular Characterization of the Danish Prion Diseases Cohort With Special Emphasis on Rare and Unique Cases;Journal of Neuropathology & Experimental Neurology;2019-09-03