A Creutzfeldt‐Jakob disease case misdiagnosed with acute cerebral infarction and review of the literature

Z Xu, Y Zhao - Clinical Case Reports, 2020 - Wiley Online Library
A Creutzfeldt‐Jakob disease case misdiagnosed with acute cerebral infarction and review
of the literature - Xu - 2020 - Clinical Case Reports - Wiley Online Library Skip to Article …

Sporadic Creutzfeldt-Jakob Disease Initially Presenting With Posterior Reversible Encephalopathy Syndrome: A Case Report

JP Mikhaiel, M Parasram, T Manning… - The …, 2024 - journals.lww.com
Conclusions: This case reports highlights that sCJD can present with neuroimaging
consistent with PRES. The diagnosis of sCJD should be considered in patients with PRES …

[HTML][HTML] Creutzfeldt-Jakob disease presenting as posterior reversible encephalopathy syndrome

J Bittar, P Joshi, J Genova, K Yeboah, J Kafaie - Cureus, 2020 - ncbi.nlm.nih.gov
Creutzfeldt-Jakob disease (CJD) is the most common human prion disease presenting with
subacute cognitive decline. Common MRI findings for CJD include the T2 prolongation …

Rapidly progressive sporadic Creutzfeldt-Jakob disease: isolated Heidenhain variant or a combination with PRES?

PHA Fraiman, CM Teixeira… - Arquivos de Neuro …, 2021 - thieme-connect.com
A 70-year-old man presented with rapidly progressive cognitive impairment with ataxia and
myoclonus. Visual agnosia was noticed after blood pressure oscillations, during …

Sporadische Creutzfeldt-Jakob-Erkrankung imitiert posteriores reversibles Enzephalopathie-Syndrom

S Krüger, J Larsen, J Schaumberg - Der Nervenarzt, 2019 - Springer
DieCreutzfeldt-Jakob-Erkrankung (CJD) wurde erstmals 1920 und 1921 von Creutzfeldt und
Jakob beschrieben. Sie gehört zu den transmissiblen spongiformen Enzephalopathien …

[PDF][PDF] Fehldiagnose Depression bei Prionenerkrankung

P Burger - Swiss Medical Forum - scholar.archive.org
Hintergrund Die Creutzfeld-Jakob-Erkrankung (CJD) ist eine seltene, jedoch aufgrund ihrer
drastischen Konsequenzen und des dramatischen Verlaufs hochrelevante Erkrankung. Mit …

Heidenhain Variant of Creutzfeldt-Jakob Disease with Concurrent Findings of Posterior Reversible Encephalopathy Syndrome: A Case Report and Literature Review

JJ Guan, B Policeni, G Bathla, AA Capizzano… - …, 2021 - ingentaconnect.com
Although Creutzfeldt-Jakob disease is not yet proved to be related to the development of
posterior reversible encephalopathy syndrome, prion invasion to the endothelium has been …

[PDF][PDF] Sporadic Creutzfeldt-Jakob Disease: Case Report from a Neuroscience Institute in Bangladesh

T Esteak, MB Rashid, MA Khan, MN Uddin, M Hasan… - researchgate.net
Sporadic Creutzfeldt-Jakob disease (sCJD) is a rare neurodegenerative disorder
characterized by rapidly progressive dementia and myoclonus. Additional clinical features …

Rapidly progressive sporadic Creutzfeldt-Jakob disease: isolated Heidenhain variant or a combination with PRES?

CO Godeiro Junior, PHA Fraiman, CM Teixeira… - 2020 - repositorio.ufrn.br
Pedro Henrique Almeida FRAIMAN https://orcid. org/0000-0002-5250-8602; Carolina Militão
TEIXEIRA https://orcid. org/0000-0003-0990-5044; Juliano César Dantas DE OLIVEIRA …

Fishing in muddy waters-co-existing dual intracranial pathology in PRES: A case series and review of literature

G Bathla, RP Maheshwarappa, N Soni, S Priya… - Clinical imaging, 2020 - Elsevier
Posterior reversible encephalopathy syndrome (PRES) is a neurotoxic state often
characterized by altered mental state and is seen in various clinical settings. Although it is …