Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: Abnormalities and PRNP[original query] |
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The 129 codon polymorphism of the prion protein gene influences earlier cognitive performance in Down syndrome subjects. Journal of neurology 2003 Jun 250 (6): 688-92. Del Bo Roberto, Comi Giacomo Pietro, Giorda Roberto, Crimi Marco, Locatelli Federica, Martinelli-Boneschi Filippo, Pozzoli Uberto, Castelli Enrico, Bresolin Nereo, Scarlato Gugliel |
Inherited prion disease with 4-octapeptide repeat insertion: disease requires the interaction of multiple genetic risk factors. Brain : a journal of neurology 2011 Jun 134 (Pt 6): 1829-38. Kaski Diego N, Pennington Catherine, Beck Jon, Poulter Mark, Uphill James, Bishop Matthew T, Linehan Jaqueline M, O'Malley Catherine, Wadsworth Jonathan D F, Joiner Susan, Knight Richard S G, Ironside James W, Brandner Sebastian, Collinge John, Mead Sim |
PRND 3'UTR polymorphism may be associated with behavioral disturbances in Alzheimer disease. Prion 2012 Jan 6 (1): 1. Flirski M, Sieruta M, Gola?ska E, K?oszewska I, Liberski PP, Sobów T |
Clinical and laboratory features of 14 young Chinese probable sCJD patients. Prion 2017 Mar 1-8. Shi Qi, Xiao Kang, Chen Cao, Zhou Wei, Gao Chen, Wang Jing, Zhang Bao-Yun, Wang Yuan, Dong Xiao-Pi |
Development of prognostic models for survival and care status in sporadic Creutzfeldt-Jakob disease. Brain communications 2022 8 4 (4): fcac201. Nihat Ak?n, Ranson Janice M, Harris Dominique, McNiven Kirsty, Mok TzeHow, Rudge Peter, Collinge John, Llewellyn David J, Mead Sim |
Two Chinese patients of sporadic Creutzfeldt-Jacob disease with a S97N mutation in PRNP gene. Prion 2023 11 17 (1): 141-144. Dong-Lin Liang, Qi Shi, Kang Xiao, Ruhan A, Wei Zhou, Xiao-Ping Do |
Accumulation Area of a Japanese PRNP P102L Variant: The Ariake PRNP P102L Variant. Journal of clinical neurology (Seoul, Korea) 2024 1 . Kohei Suzuyama, Makoto Eriguchi, Hiromu Minagawa, Hiroyuki Honda, Keita Kai, Tetsuyuki Kitamoto, Hideo Ha |
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