Prion

01 21 September 2026

DOI 10.1080/19336896.2026.2729488

A case report of sporadic Creutzfeldt–Jakob disease presenting with progressive opsoclonus–myoclonus–ataxia-Plus (OMAS-Plus) phenotype

Open DOI

Richard Hulej, Pavol Skáčik, Dana Žáková et al.

Sporadic Creutzfeldt-Jakob disease (sCJD) is a rapidly progressive prion disorder whose heterogeneous manifestations may overlap with potentially treatable neurological conditions. We report an atypical sCJD phenotype dominated by progre...

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02 2 September 2026

DOI 10.1080/19336896.2026.2725518

Monte Carlo simulation of testing requirements for chronic wasting disease (CWD) surveillance via hunter-harvest in Illinois, USA

Open DOI

Jameson J. Mori, William M. Brown, Nelda A. Rivera et al.

Chronic wasting disease (CWD) is an invariably fatal neurodegenerative disease of cervids detected in wild and captive herds in the United States, Canada, Norway, Sweden, and Finland since its disc...

03 2 September 2026

DOI 10.1080/19336896.2026.2727327

Effect of decay on detection of chronic wasting disease (CWD) in lymph nodes using enzyme-linked immunosorbent assay (ELISA)

Open DOI

Jameson Mori, Daniel Barr, Benjamin Johnson et al.

Members of the family Cervidae, both wild and captive, are becoming increasingly affected by chronic wasting disease (CWD), a prion disease with high transmissibility and a 100% fatality rate [1–3]...

04 10 August 2026

DOI 10.1080/19336896.2026.2710965

Epigenetic changes associated with the progression of prion disease in Syrian hamsters ( Mesocricetus auratus )

Open DOI

Lexi E. Frank, Nicole Flack, Christopher Faulk et al.

Prion diseases are a group of fatal, transmissible neurodegenerative disorders that impact a variety of mammalian species, including humans, and are transmissible both within and across specific sp...

05 10 June 2026

DOI 10.1080/19336896.2026.2684820

Correction

Open DOI

06 27 March 2026

DOI 10.1080/19336896.2026.2645322

Early diagnosis of a case of Heidenhain variant of Creutzfeld-Jakob disease by cerebrospinal fluid real-time quaking-induced conversion test

Open DOI

Lin Li, Rong Yan, Jiawei Wang et al.

Sporadic Creutzfeldt-Jakob disease (sCJD) is a rare, rapidly progressive, and fatal neurodegenerative disorder caused by the accumulation of abnormal prion proteins in the central nervous system. The Heidenhain variant (HvCJD), a rare su...

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07 5 March 2026

DOI 10.1080/19336896.2026.2640273

In memoriam of Pawel P. Liberski (1954–2025)

Open DOI

Beata Sikorska

08 2 March 2026

DOI 10.1080/19336896.2026.2635296

Maternal chronic wasting disease infection restricts fetal head size in white-tailed deer ( Odocoileus virginianus )

Open DOI

Jameson Mori, Sara Villazan Perez-Girones, Tooba Latif et al.

Chronic wasting disease (CWD) is a fatal neurodegenerative prion disease of cervids that can be transmitted through direct physical contact, indirect contact with a contaminated environment, or vertical transmission. CWD is characterized...

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09 28 February 2026

DOI 10.1080/19336896.2026.2635298

Plaque-type dura mater graft-associated Creutzfeldt-Jakob disease: an autopsied case report

Open DOI

Daisuke Tahara, Daichi Yokoi, Nao Tahara et al.

Dura mater graft-associated Creutzfeldt-Jakob disease (dCJD) is an iatrogenic form of Creutzfeldt-Jakob disease (CJD) [1]. Cadaveric dural grafts were previously used for dural repair in neurosurge...

10 17 February 2026

DOI 10.1080/19336896.2026.2630484

Efficient induction of motor neuron disease in transgenic G93A SOD1 mice by prion-like seeding

Open DOI

Guilian Xu, Amanda Lopez, Selma Brkic et al.

Mutations in superoxide dismutase 1 (SOD1) cause paralysis in familial amyotrophic lateral sclerosis and promote its misfolding into neurotoxic aggregates. Previous studies have shown that mice expressing the ALS-causing G85R variant of ...

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