Cargando…

Neuropathological changes in striate and extrastriate visual cortex in variant Creutzfeldt-Jakob disease (vCJD)

Pathological changes in striate (B17, V1) and extrastriate (B18, V2) visual cortex were studied in variant Creutzfeldt-Jakob disease (vCJD). No differences in densities of vacuoles or surviving neurons were observed in B17 and B18 but densities of glial cell nuclei and deposits of prion protein (PrP...

Descripción completa

Detalles Bibliográficos
Autor principal:	Armstrong, Richard A
Formato:	Texto
Lenguaje:	English
Publicado:	Dove Medical Press 2007
Materias:	Original Research
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2704504/ https://www.ncbi.nlm.nih.gov/pubmed/19668500

Ejemplares similares

New variant of Creutzfeldt-Jakob (vCJD) disease and other human prion diseases under epidemiological surveillance in Brazil
por: Gattás, Vera Lúcia, et al.
Publicado: (2007)

vCJD risk in the Republic of Ireland
por: Harney, Michael S, et al.
Publicado: (2003)

Epidemiological evidence of higher susceptibility to vCJD in the young
por: Boëlle, Pierre-Yves, et al.
Publicado: (2004)

Updated projections of future vCJD deaths in the UK
por: Ghani, Azra C, et al.
Publicado: (2003)

Wide distribution of prion infectivity in the peripheral tissues of vCJD and sCJD patients
por: Douet, Jean-Yves, et al.
Publicado: (2021)

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

Direct neural transmission of vCJD/BSE in macaque after finger incision
por: Mikol, Jacqueline, et al.
Publicado: (2020)

No Major Change in vCJD Agent Strain after Secondary Transmission via Blood Transfusion
por: Bishop, Matthew T., et al.
Publicado: (2008)

The Various Faces of Creutzfeldt-Jakob Disease (CJD); a Case of CJD Presenting as Psychosis in a Middle-Aged Woman
por: Sodiya, Olusegun, et al.
Publicado: (2022)

Ocular Tonometry and Sporadic Creutzfeldt - Jakob Disease (sCJD): A Confirmatory Case-Control Study
por: Davanipour, Zoreh, et al.
Publicado: (2014)

Laminar Distribution of the Pathological Changes in Sporadic and Variant Creutzfeldt-Jakob Disease
por: Armstrong, R. A.
Publicado: (2010)

A case of V180I genetic mutation Creutzfeldt Jakob disease (CJD) with delusional misidentification as an initial symptom
por: Nagata, Tomoyuki, et al.
Publicado: (2021)

The natural history study of preclinical genetic Creutzfeldt-Jakob Disease (CJD): a prospective longitudinal study protocol
por: Bregman, Noa, et al.
Publicado: (2023)

Topography of Striate-Extrastriate Connections in Neonatally Enucleated Rats
por: Laing, Robyn J., et al.
Publicado: (2013)

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

Comprehensive clinical, radiological, pathological and biochemical analysis required to differentiate VV1 sporadic Creutzfeldt-Jakob disease from suspected variant CJD
por: Holper, Sarah, et al.
Publicado: (2022)

PrP(res) deposition in the retina is a common finding of sporadic, familial and iatrogenic Creutzfeldt-Jakob diseases (CJD)
por: Takao, Masaki, et al.
Publicado: (2018)

A Contemporary Risk Analysis of Iatrogenic Transmission of Creutzfeldt-Jakob Disease (CJD) via Corneal Transplantation in the United States
por: Martheswaran, Tanisha, et al.
Publicado: (2020)

Correction: The natural history study of preclinical genetic Creutzfeldt-Jakob Disease (CJD): a prospective longitudinal study protocol
por: Bregman, Noa, et al.
Publicado: (2023)

Visual Interhemispheric and Striate-Extrastriate Cortical Connections in the Rabbit: A Multiple Tracer Study
por: Andelin, Adrian K., et al.
Publicado: (2015)

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

Mitochondrial respiratory chain deficiency correlates with the severity of neuropathology in sporadic Creutzfeldt-Jakob disease
por: Flønes, Irene H., et al.
Publicado: (2020)

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

Experimental sheep BSE prions generate the vCJD phenotype when serially passaged in transgenic mice expressing human prion protein
por: Joiner, Susan, et al.
Publicado: (2018)

Remodeling of lateral geniculate nucleus projections to extrastriate area MT following long-term lesions of striate cortex
por: Atapour, Nafiseh, et al.
Publicado: (2022)

All Clinically-Relevant Blood Components Transmit Prion Disease following a Single Blood Transfusion: A Sheep Model of vCJD
por: McCutcheon, Sandra, et al.
Publicado: (2011)

Blood Transfusion and Spread of Variant Creutzfeldt-Jakob Disease
por: Dietz, Klaus, et al.
Publicado: (2007)

The first case of variant Creutzfeldt-Jakob disease in the Netherlands
por: Sánchez-Juan, P., et al.
Publicado: (2007)

Bovine spongiform encephalopathy and variant Creutzfeldt-Jakob disease.
por: Riemann, H
Publicado: (2001)

Variant Creutzfeldt-Jakob Disease Death, United States
por: Belay, Ermias D., et al.
Publicado: (2005)

The Effect of Learning on the Function of Monkey Extrastriate Visual Cortex
por: Rainer, Gregor, et al.
Publicado: (2004)

The first report of RPSA polymorphisms, also called 37/67 kDa LRP/LR gene, in sporadic Creutzfeldt-Jakob disease (CJD)
por: Yun, Jisuk, et al.
Publicado: (2011)

Elevated E200K Somatic Mutation of the Prion Protein Gene (PRNP) in the Brain Tissues of Patients with Sporadic Creutzfeldt–Jakob Disease (CJD)
por: Won, Sae-Young, et al.
Publicado: (2023)

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

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

PMCA-replicated PrP(D) in urine of vCJD patients maintains infectivity and strain characteristics of brain PrP(D): Transmission study
por: Cali, Ignazio, et al.
Publicado: (2019)

Creutzfeldt-Jakob disease with unusually extensive neuropathology in a child treated with native human growth hormone
por: Mikol, Jacqueline, et al.
Publicado: (2012)

A Rare Case of Histopathologically Confirmed Creutzfeldt–Jakob Disease from Romania, Long Route to Diagnosis—Case Report and an Overview of the Romanian CJD Situation
por: Kelemen, Krisztina, et al.
Publicado: (2022)

Source of Variant Creutzfeldt-Jakob Disease outside United Kingdom
por: Sanchez-Juan, Pascual, et al.
Publicado: (2007)

Uncertainty in the Tail of the Variant Creutzfeldt-Jakob Disease Epidemic in the UK
por: Garske, Tini, et al.
Publicado: (2010)

Cannot write session to /tmp/vufind_sessions/sess_dk1p6862p2nnksi1knd8hbiid3