Understanding the Phenotypic Heterogeneity Within the Sporadic Creutzfeldt-Jakob Disease MV1 Subtype. [PDF]
We present the clinical, pathological and prion biophysical features of three atypical cases of the MV1 subtype of sporadic Creutzfeldt–Jakob disease (sCJD). We propose that these heterozygous cases exist on a spectrum ranging from MM1‐like to VV1‐like phenotypes and recommend that subtyping be performed at pH 6.9 to avoid missing atypical or mixed ...
Nemani SK +6 more
europepmc +2 more sources
Peripheral Signatures of Multidimensional Pathology in Symptomatic and Asymptomatic Creutzfeldt-Jakob Disease. [PDF]
Chen ZY +11 more
europepmc +1 more source
Clinical findings and diagnostic tests in the MV2 subtype of sporadic CJD [PDF]
Anna Krasnianski
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Limited transmission of V180I genetic Creutzfeldt-Jakob disease in knock-in mice models. [PDF]
Teruya K, Mohri S, Kitamoto T.
europepmc +1 more source
Comparison of enamel 87Sr/86Sr and δ15Ncol in humans from CJD.
Ashley E. Sharpe (8681484) +10 more
openalex +1 more source
Brain microglia were activated in sporadic CJD but almost unchanged in fatal familial insomnia and G114V genetic CJD [PDF]
Qi Shi +10 more
openalex +1 more source
18F-DPA-714 PET/MRI reveals early and widespread neuroinflammation in sporadic Creutzfeldt-Jakob disease: a case report. [PDF]
Zhu Z, Huang Q, Chen S, Zhou Q.
europepmc +1 more source
Creutzfeldt-Jakob disease mimicking Hashimoto's encephalopathy: steroid response followed by decline. [PDF]
Wu TC +6 more
europepmc +1 more source
Human Prion Disease: Pathogenesis, Diagnosis and Public Health. [PDF]
Bellini P +6 more
europepmc +1 more source

