18F-FP-CIT PET/CT in a case of probable sporadic Creutzfeldt-Jakob disease with parkinsonism as initial symptom by Songhan Tang, Xiaofeng Dou, Ying Zhang

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A family with mental disorder as the first symptom finally confirmed with Gerstmann–Sträussler–Scheinker disease with P102L mutation in PRNP gene – case report by Zeran Chen, Junjun Guo, Ningjing Ran, Yujia Zhong, Fang Yang, Honghui Sun

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The first non-prion pathogen identified: neurotropic influenza virus by Suehiro Sakaguchi, Hideyuki Hara

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Transcriptomic analysis identifies novel potential biomarkers and highlights cilium-related biological processes in the early stages of prion disease in mice by Yong-Chan Kim, Byung-Hoon Jeong

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A case report of fatal familial insomnia with cerebrospinal fluid leukocytosis during the COVID-19 epidemic and review of the literature by Zheng Wang, Yueqi Huang, Shuqi Wang, Jiefang Chen, Gesang Meiduo, Man Jin, Xiaoying Zhang

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A systemic analysis of Creutzfeldt Jakob disease cases in Asia by Urwah Rasheed, Sana Khan, Minahil Khalid, Aneeqa Noor, Saima Zafar

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Genetic assessment of apolipoprotein E polymorphism and PRNP genotypes in rapidly progressive dementias in Pakistan by Urwah Rasheed, Minahil Khalid, Aneeqa Noor, Umar Saeed, Rizwan Uppal, Saima Zafar

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Polymorphism of prion protein gene (PRNP) in Nigerian sheep by Adeniyi C. Adeola, Semiu F. Bello, Abdussamad M. Abdussamad, Akanbi I. Mark, Oscar J. Sanke, Anyebe B. Onoja, Lotanna M. Nneji, Nasiru Abdullahi, Sunday C. Olaogun, Lawal D. Rogo, Godwin F. Mangbon, Shamsudeen L. Pedro, Manasseh P. Hiinan, Muhammad M. Mukhtar, Jebi Ibrahim, Hayatu Saidu, Philip M. Dawuda, Rukayya K. Bala, Hadiza L. Abdullahi, Adebowale E. Salako, Samia Kdidi, Mohamed Habib Yahyaoui, Ting-Ting Yin

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Prion forensics: a multidisciplinary approach to investigate CWD at an illegal deer carcass disposal site by Marc D. Schwabenlander, Jason C. Bartz, Michelle Carstensen, Alberto Fameli, Linda Glaser, Roxanne J. Larsen, Manci Li, Rachel L. Shoemaker, Gage Rowden, Suzanne Stone, W. David Walter, Tiffany M. Wolf, Peter A. Larsen

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Serial changes in regional cerebral blood flow in Gerstmann–Sträussler–Scheinker disease caused by a Pro-to-Leu mutation at codon 105 in the prion protein gene by Honami Kawai, Taiki Matsubayashi, Takanori Yokota, Nobuo Sanjo

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Variability in prion protein genotypes by spatial unit to inform susceptibility to chronic wasting disease by Alberto F. Fameli, Jessie Edson, Jeremiah E. Banfield, Christopher S. Rosenberry, W. David Walter

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Correction

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Expression of the cellular prion protein by mast cells in the human carotid body by Gregory D. Sweetland, Connor Eggleston, Jason C. Bartz, Candace K. Mathiason, Anthony E. Kincaid

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Difference of geographic distributions of the Chinese patients with prion diseases in the permanent resident places and referring places by Kang Xiao, Ming-Fan Pang, Yue-Qiao Zhao, Li-Ping Gao, Yue-Zhang Wu, Yuan Wang, Qi Shi, Xiao-Ping Dong

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Prion meeting 2023: implications of a growing field by Tiago F. Outeiro, Tuane C. R. G. Vieira

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Differential involvement of amyloidogenic evolvability in oligodendropathies; Multiple Sclerosis and Multiple System Atrophy by Jianshe Wei, Gilbert Ho, Eliezer Masliah, Makoto Hashimoto

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Prion therapeutics: Lessons from the past by Kyu Hwan Shim, Niti Sharma, Seong Soo A An

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Mutations in human prion-like domains: pathogenic but not always amyloidogenic by Andrea Bartolomé-Nafría, Javier García-Pardo, Salvador Ventura

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Anti-recoverin antibody positive Heidenhain variant CJD: a case report by Chi-Ting Chung, Tun Jao, Jen-Jen Su

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Cellular prion protein distribution in the vomeronasal organ, parotid, and scent glands of white-tailed deer and mule deer by Anthony Ness, Aradhana Jacob, Kelsey Saboraki, Alicia Otero, Danielle Gushue, Diana Martinez Moreno, Melanie de Peña, Xinli Tang, Judd Aiken, Susan Lingle, Debbie McKenzie

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