Cargando…

DNA methylation analysis of archival lymphoreticular tissues in Creutzfeldt–Jakob disease

Detalles Bibliográficos
Autores principales:	Guntoro, Fernando, Viré, Emmanuelle, Giordani, Chiara, Darwent, Lee, Hummerich, Holger, Linehan, Jacqueline, Sinka, Katy, Jaunmuktane, Zane, Brandner, Sebastian, Collinge, John, Mead, Simon
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Springer Berlin Heidelberg 2022
Materias:	Correspondence
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9468073/ https://www.ncbi.nlm.nih.gov/pubmed/35982321 http://dx.doi.org/10.1007/s00401-022-02481-w

Ejemplares similares

A blood miRNA signature associates with sporadic Creutzfeldt-Jakob disease diagnosis
por: Norsworthy, Penny J., et al.
Publicado: (2020)

Altered DNA methylation profiles in blood from patients with sporadic Creutzfeldt–Jakob disease
por: Dabin, Luke C., et al.
Publicado: (2020)

Familial Creutzfeldt-Jakob Disease in an Indian Kindred
por: Katrak, Sarosh M., et al.
Publicado: (2019)

Protease-resistant Prion Protein in Lymphoreticular Tumors of Variant Creutzfeldt-Jakob Disease Mice
por: Cervenakova, Larisa, et al.
Publicado: (2006)

Case report of homozygous E200D mutation of PRNP in apparently sporadic Creutzfeldt-Jakob disease
por: Hassan, Ahamad, et al.
Publicado: (2021)

Variants of PLCXD3 are not associated with variant or sporadic Creutzfeldt-Jakob disease in a large international study
por: Balendra, Rubika, et al.
Publicado: (2016)

Genetic risk factors for variant Creutzfeldt–Jakob disease: a genome-wide association study
por: Mead, Simon, et al.
Publicado: (2009)

Neuronal antibodies in patients with suspected or confirmed sporadic Creutzfeldt-Jakob disease
por: Rossi, Meghan, et al.
Publicado: (2015)

MRI findings are often missed in the diagnosis of Creutzfeldt-Jakob disease
por: Carswell, Christopher, et al.
Publicado: (2012)

Association of a null allele of SPRN with variant Creutzfeldt–Jakob disease
por: Beck, J A, et al.
Publicado: (2008)

Development of prognostic models for survival and care status in sporadic Creutzfeldt-Jakob disease
por: Nihat, Akın, et al.
Publicado: (2022)

Creutzfeldt-Jakob dementia
por: Reis, Fabiano, et al.
Publicado: (2015)

Detection of Creutzfeldt-Jakob disease prions in skin: implications for healthcare
por: Nihat, Akin, et al.
Publicado: (2018)

Prion protein gene mutation detection using long-read Nanopore sequencing
por: Kroll, François, et al.
Publicado: (2022)

Development of novel clinical examination scales for the measurement of disease severity in Creutzfeldt-Jakob disease
por: Nihat, Akin, et al.
Publicado: (2022)

Etymologia: Creutzfeldt-Jakob Disease
por: Lanska, Douglas John
Publicado: (2017)

Etymologia: Creutzfeldt-Jakob Disease
por: Henry, Ronnie, et al.
Publicado: (2017)

Is Creutzfeldt-Jakob disease transmitted in blood?
por: Ricketts, M N, et al.
Publicado: (1997)

A case of Creutzfeldt-Jakob disease.
por: Cha, J. K., et al.
Publicado: (1991)

Ocular Dipping in Creutzfeldt-Jakob Disease
por: Sierra-Hidalgo, Fernando, et al.
Publicado: (2014)

Biomarkers for sporadic Creutzfeldt–Jakob disease
por: Soomro, Sanam, et al.
Publicado: (2016)

Treating seizures in Creutzfeldt–Jakob disease()
por: Ng, Marcus C., et al.
Publicado: (2014)

Creutzfeldt-Jakob disease: recent developments
por: Mackenzie, Graeme, et al.
Publicado: (2017)

Neurosyphilis Mimicking Creutzfeldt-Jakob Disease
por: Jang, Jae-Won, et al.
Publicado: (2016)

Chorea in Sporadic Creutzfeldt-Jakob Disease
por: Tan, Ai Huey, et al.
Publicado: (2018)

The Heidenhain variant of Creutzfeldt-Jakob disease
por: Muniz, Bernardo Carvalho, et al.
Publicado: (2019)

Iatrogenic CJD due to pituitary-derived growth hormone with genetically determined incubation times of up to 40 years
por: Rudge, Peter, et al.
Publicado: (2015)

Validation of Revised International Creutzfeldt-Jakob Disease Surveillance Network Diagnostic Criteria for Sporadic Creutzfeldt-Jakob Disease
por: Watson, Neil, et al.
Publicado: (2022)

Comparative Study of Prions in Iatrogenic and Sporadic Creutzfeldt-Jakob Disease
por: Xiao, Xiangzhu, et al.
Publicado: (2014)

Early neurophysiological biomarkers and spinal cord pathology in inherited prion disease
por: Rudge, Peter, et al.
Publicado: (2019)

Cerebrospinal fluid markers in Creutzfeldt-Jakob disease
por: Skinningsrud, Anders, et al.
Publicado: (2008)

Barriers to Creutzfeldt-Jakob Disease Autopsies, California
por: Nolte, Kurt B.
Publicado: (2005)

Barriers to Creutzfeldt-Jakob Disease Autopsies, California
por: Louie, Janice K., et al.
Publicado: (2004)

Iatrogenic Creutzfeldt-Jakob Disease, Final Assessment
por: Brown, Paul, et al.
Publicado: (2012)

The neuropathology of kuru and variant Creutzfeldt–Jakob disease
por: McLean, Catriona A.
Publicado: (2008)

Hyperacusis as the initial presentation of Creutzfeldt-Jakob disease
por: Merkler, Alexander E., et al.
Publicado: (2014)

Role of the biomarkers for the diagnosis of Creutzfeldt-Jakob disease
por: Dulamea, A, et al.
Publicado: (2016)

Variant Creutzfeldt-Jakob disease in older patients
por: el Tawil, Salwa, et al.
Publicado: (2015)

Creutzfeldt–Jakob Disease: Analysis of Four Cases
por: Al Balushi, Ali, et al.
Publicado: (2016)

Diagnostic Value of Electroencephalogram in Creutzfeldt-Jakob Disease
por: Radhakrishnan, Kurupath
Publicado: (2020)

Cannot write session to /tmp/vufind_sessions/sess_31a98fb9blull2jno7gn4ni7m6