Results 101 to 110 of about 12,633 (172)

Imaging and CSF analyses effectively distinguish CJD from its mimics

, 2018
OBJECTIVE: To review clinical and investigation findings in patients referred to a specialist prion clinic who were suspected to have sporadic Creutzfeldt-Jakob disease (sCJD) and yet were found to have an alternative final diagnosis. METHODS: Review the
Hyare, H, Rudge, P, Collinge, J, Mead, S, Green, A   +4 more
core  

Recent advancements in QuIC-based diagnostic assays for sporadic and inherited prion diseases: focusing on the emerging role of ES-QuIC. [PDF]

Front Neurosci
Fox R, Myskiw J, Bailey-Elkin BA, Booth SA.   +3 more
europepmc   +1 more source

A Diagnostic Pitfall in the Era of Amyloid-Targeting Therapy: Creutzfeldt-Jakob Disease Masquerading as Biologically Defined Alzheimer's Disease. [PDF]

Psychogeriatrics
Manabe Y.
europepmc   +1 more source

Heidenhain Disease: Challenging Diagnosis of a Creutzfeldt-Jakob Variant. [PDF]

Cureus
Brambilla RS, Fortunato PN, Maffeis RC, Tapajós Bolzani CM, da Silva Júnior HM.   +4 more
europepmc   +1 more source

Probable Sporadic Creutzfeldt-Jakob Disease Presenting as Rapidly Progressive Dementia: A Case Report From Georgia. [PDF]

Cureus
Kvachadze N, Kotia G, Muradashvili M, Mrelashvili S, Basilaia N, Zambakhidze L.   +5 more
europepmc   +1 more source

EEGDecoder-x: an explainable deep learning framework for cross-subject EEG-based detection of Alzheimer's and Creutzfeldt-Jakob disease. [PDF]

Front Neurol
Suffian M, Mammone N, Ieracitano C, Tripodi GG, Pascarella A, Ferlazzo E, Morabito FC.   +6 more
europepmc   +1 more source

From a Pinched Nerve to a Fatal Prognosis: Sporadic Creutzfeldt-Jakob Disease Masquerading as Cervical Myelopathy. [PDF]

Cureus
Bayati J.
europepmc   +1 more source

Prion disease mimicking rapidly progressive Alzheimer disease: case series and systematic review. [PDF]

J Neurol
Elgenidi A, Shir D, Piura YD, Sokol LL, Duara R, Lachner C, Day GS.   +6 more
europepmc   +1 more source

Beyond Delirium: Sporadic Creutzfeldt-Jakob Disease Revealed by Progressive Neurological Decline After Diabetic Ketoacidosis. [PDF]

Cureus
Abdul Rehman F, Zeeshan M, Siddique MU, Khaan K.   +3 more
europepmc   +1 more source

Young-onset CJD: Age and disease phenotype in variant and sporadic forms

, 2006
Since 1996, there have been over 140 reports of a Creutzfeldt-Jakob disease variant (vCJD), with a striking prevalence of these cases in the UK. The main peculiarity of vCJD is its onset in young people, but other features also distinguish it from ...
Cereda C., Cova E., Ferrarese C., Corato M., Ceroni M.   +4 more
core