1. 14-3-3 and enolase abundances in the CSF of Prion diseased rats. Issue 3 (4th July 2018) Authors: Gushue, Danielle; Herbst, Allen; Sim, Valerie; McKenzie, Debbie; Aiken, Judd M. Journal: Prion Issue: Volume 12:Issue 3/4(2018) Page Start: 253 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. 18F-FP-CIT PET/CT in a case of probable sporadic Creutzfeldt-Jakob disease with parkinsonism as initial symptom. Issue 1 (31st December 2022) Authors: Tang, Songhan; Dou, Xiaofeng; Zhang, Ying Journal: Prion Issue: Volume 16:Issue 1(2022) Page Start: 91 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. 25 years of yeast prions: Symposium honouring the 25-year anniversary of Reed Wickner's discovery of yeast prions. Issue 1 (1st January 2020) Authors: Shewmaker, Frank; Masison, Dan Journal: Prion Issue: Volume 14:Issue 1(2020) Page Start: 29 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. A case of V180I genetic Creutzfeldt-Jakob disease presenting with conspicuous facial mimicry. Issue 1 (1st January 2019) Authors: Iwasaki, Yasushi; Mori, Keiko; Ito, Masumi; Kawai, Yoshinari Journal: Prion Issue: Volume 13:Issue 1(2019) Page Start: 151 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. A case of V180I genetic mutation Creutzfeldt Jakob disease (CJD) with delusional misidentification as an initial symptom. Issue 1 (31st December 2022) Authors: Nagata, Tomoyuki; Shinagawa, Shunichiro; Kobayashi, Nobuyuki; Kondo, Kazuhiro; Shigeta, Masahiro Journal: Prion Issue: Volume 16:Issue 1(2022) Page Start: 7 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. A Chinese patient of P102L Gerstmann-Sträussler-Scheinker disease contains three other disease-associated mutations in SYNE1. Issue 2 (4th March 2018) Authors: Wang, Jing; Xiao, Kang; Zhou, Wei; Gao, Chen; Chen, Cao; Shi, Qi; Dong, Xiao-Ping Journal: Prion Issue: Volume 12:Issue 2(2018) Page Start: 150 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. A Chinese patient with the clinical features of Parkinson's disease contains a single copy of octarepeat deletion in PRNP case report. Issue 1 (1st January 2021) Authors: Shi, Qi; Shen, Xiao-Jing; Gao, Li-Ping; Xiao, Kang; Zhou, Wei; Wang, Yuan; Chen, Cao; Dong, Xiao-Ping Journal: Prion Issue: Volume 15:Issue 1(2021) Page Start: 121 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. A family with mental disorder as the first symptom finally confirmed with Gerstmann–Sträussler–Scheinker disease with P102L mutation in PRNP gene – case report. Issue 1 (31st December 2023) Authors: Chen, Zeran; Guo, Junjun; Ran, Ningjing; Zhong, Yujia; Yang, Fang; Sun, Honghui Journal: Prion Issue: Volume 17:Issue 1(2023) Page Start: 37 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. A patient with spastic paralysis finally diagnosed as V180I genetic Creutzfeldt-Jakob disease 9 years after onset. Issue 1 (1st January 2020) Authors: Nomura, Taichi; Iwata, Ikuko; Naganuma, Ryoji; Matsushima, Masaaki; Satoh, Katsuya; Kitamoto, Tetsuyuki; Yabe, Ichiro Journal: Prion Issue: Volume 14:Issue 1(2020) Page Start: 226 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. A rare case of rapidly progressive dementia with elevated RT-QuIC and negative 14-3-3 and tau proteins. Issue 3 (3rd May 2016) Authors: Trikamji, Bhavesh; Hamlin, Clive; Baldwin, Kelly J. Journal: Prion Issue: Volume 10:Issue 3(2016) Page Start: 262 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗