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182 related items for PubMed ID: 17971921

  • 1. [Study on the characteristic of Surveillance Creutzfeldt-Jakob disease patients from January to August in 2006 in China].
    Gao C, Han J, Zhou W, Chen JM, Shi Q, Zhang BY, Xiang NJ, Gao YJ, Dong XP.
    Zhonghua Shi Yan He Lin Chuang Bing Du Xue Za Zhi; 2007 Sep; 21(3):205-7. PubMed ID: 17971921
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  • 6. Genetic Prion Disease: Insight from the Features and Experience of China National Surveillance for Creutzfeldt-Jakob Disease.
    Shi Q, Chen C, Xiao K, Zhou W, Gao LP, Chen DD, Wu YZ, Wang Y, Hu C, Gao C, Dong XP.
    Neurosci Bull; 2021 Nov; 37(11):1570-1582. PubMed ID: 34487324
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  • 12. Detection of 14-3-3 protein in the cerebrospinal fluid supports the diagnosis of Creutzfeldt-Jakob disease.
    Zerr I, Bodemer M, Gefeller O, Otto M, Poser S, Wiltfang J, Windl O, Kretzschmar HA, Weber T.
    Ann Neurol; 1998 Jan; 43(1):32-40. PubMed ID: 9450766
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  • 14. Report about four novel mutations in the prion protein gene.
    Schelzke G, Stoeck K, Eigenbrod S, Grasbon-Frodl E, Raddatz LM, Ponto C, Kretzschmar HA, Zerr I.
    Dement Geriatr Cogn Disord; 2013 Jan; 35(3-4):229-37. PubMed ID: 23467330
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  • 16. 14-3-3 CSF levels in sporadic Creutzfeldt-Jakob disease differ across molecular subtypes.
    Gmitterová K, Heinemann U, Bodemer M, Krasnianski A, Meissner B, Kretzschmar HA, Zerr I.
    Neurobiol Aging; 2009 Nov; 30(11):1842-50. PubMed ID: 18328602
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  • 20. Subtype and regional regulation of prion biomarkers in sporadic Creutzfeldt-Jakob disease.
    Llorens F, Zafar S, Ansoleaga B, Shafiq M, Blanco R, Carmona M, Grau-Rivera O, Nos C, Gelpí E, Del Río JA, Zerr I, Ferrer I.
    Neuropathol Appl Neurobiol; 2015 Aug; 41(5):631-45. PubMed ID: 25134744
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