Results 121 to 130 of about 16,859 (216)

Diffusion MR imaging in sporadic Creutzfeldt-Jakob disease

Çukurova Üniversitesi Tıp Fakültesi Dergisi, 2014
Creutzfeldt-Jakob disease (CJD) is a rare dementing disease and is thought to caused by a prion. It is characterized by rapidly progressive dementia, ataxia, myoclonus, akinetic mutism and eventual death.
Burcak Cakir Pekoz, Ozlem Alkan, Semih Giray, senay Demir, Naime Altinkaya   +4 more
doaj  

[Sporadic Creutzfeldt-Jakob disease: phenotypic variability].

Neurologia (Barcelona, Spain), 2002
Prion disease are characterized by cerebral deposition of an abnormal protease-resistant isoform of a membrane-bound glycoprotein called prion protein. Sporadic Creutzfeldt-Jakob disease (CJDs) is the most frequent, accounting for approximately 85% of all human prion disease.
M J, Moreno, J, Romero
openaire   +1 more source

Real time quaking‐induced conversion analysis of cerebrospinal fluid in sporadic Creutzfeldt–Jakob disease

Annals of Neurology, 2012
Lynne McGuire, A. Peden, C. Orrú, Jason M. Wilham, Nigel E. Appleford, G. Mallinson, M. Andrews, Mark W. Head, B. Caughey, R. G. Will, R. Knight, A. Green   +11 more
semanticscholar   +1 more source

Detection of prions in the urine of patients affected by sporadic Creutzfeldt-Jakob disease. [PDF]

Ann Clin Transl Neurol, 2023
Pritzkow S, Ramirez F, Lyon A, Schulz PE, Appleby B, Moda F, Ramirez S, Notari S, Gambetti P, Soto C.   +9 more
europepmc   +1 more source

Sporadic Creutzfeldt-Jakob Disease With Spinal Cord Lesions: A Case Report. [PDF]

Cureus
Akanuma H, Kanai K.
europepmc   +1 more source

First Suspected Case of Sporadic Creutzfeldt-Jakob Disease in Syria. [PDF]

Int Med Case Rep J
Tarboosh H, Mansour R, Haidar N, Ghulam P, Gergy R, Nafla F.   +5 more
europepmc   +1 more source

Efficient transmission and characterization of creutzfeldt-jakob disease strains in bank voles.

PLoS Pathogens, 2006
Transmission of prions between species is limited by the "species barrier," which hampers a full characterization of human prion strains in the mouse model.
doaj   +1 more source

Alterations in cerebrospinal fluid levels of myelin- and oligodendrocyte-related proteins in sporadic Creutzfeldt-Jakob disease. [PDF]

Acta Neuropathol Commun
Maass F, Thomas C, Kurvits L, Hermann P, Schmitz M, Bähr M, Stadelmann C, Zechel S, Canaslan S, Zerr I.   +9 more
europepmc   +1 more source

An Atypical Presentation of Sporadic Creutzfeldt-Jakob Disease in the Setting of Chronic Alcohol Use Disorder. [PDF]

Case Rep Neurol Med
Holt C, Sadek AT, Woodard J, Grinstead R.   +3 more
europepmc   +1 more source

18F-DPA-714 PET/MRI reveals early and widespread neuroinflammation in sporadic Creutzfeldt-Jakob disease: a case report. [PDF]

BMJ Neurol Open
Zhu Z, Huang Q, Chen S, Zhou Q.
europepmc   +1 more source