Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Myoclonus and PRNP[original query] |
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Clinical features of rapidly progressive Alzheimer's disease. Dementia and geriatric cognitive disorders 2010 29 (4): 371-8. Schmidt Christian, Redyk Katharina, Meissner Bettina, Krack Lennart, von Ahsen Nico, Roeber Sigrun, Kretzschmar Hans, Zerr In |
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 |
Clinical features of genetic Creutzfeldt-Jakob disease with V180I mutation in the prion protein gene. BMJ open 2014 4 (5): e004968. Qina Temu, Sanjo Nobuo, Hizume Masaki, Higuma Maya, Tomita Makoto, Atarashi Ryuichiro, Satoh Katsuya, Nozaki Ichiro, Hamaguchi Tsuyoshi, Nakamura Yosikazu, Kobayashi Atsushi, Kitamoto Tetsuyuki, Murayama Shigeo, Murai Hiroyuki, Yamada Masahito, Mizusawa Hidehi |
The associations of two SNPs in miRNA-146a and one SNP in ZBTB38-RASA2 with the disease susceptibility and the clinical features of the Chinese patients of sCJD and FFI. Prion 2017 12 12 (1): 34-41. Gao Chen, Shi Qiang, Wei Jing, Zhou Wei, Xiao Kang, Wang Jing, Shi Qi, Dong Xiao-Pi |
Genetic prion diseases presenting as frontotemporal dementia: clinical features and diagnostic challenge. Alzheimer's research & therapy 2022 6 14 (1): 90. Chen Zhongyun, Chu Min, Liu Li, Zhang Jing, Kong Yu, Xie Kexin, Cui Yue, Ye Hong, Li Junjie, Wang Lin, Wu Liyo |
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