These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

384 related items for PubMed ID: 14970845

  • 21. Association of the PRNP regulatory region polymorphisms with the occurrence of sporadic Creutzfeldt-Jakob disease.
    Bratosiewicz-Wąsik J, Smoleń-Dzirba J, Watała C, Rozemuller AJ, Jansen C, Spliet W, Jansen GH, Wąsik TJ, Liberski PP.
    Folia Neuropathol; 2012; 50(1):68-73. PubMed ID: 22505365
    [Abstract] [Full Text] [Related]

  • 22. Increased frequency of positive family history of dementia in sporadic CJD.
    Krasnianski A, von Ahsen N, Heinemann U, Meissner B, Schulz-Schaeffer WJ, Kretzschmar HA, Armstrong VW, Zerr I.
    Neurobiol Aging; 2009 Apr; 30(4):615-21. PubMed ID: 17822808
    [Abstract] [Full Text] [Related]

  • 23.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 24.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 25. Regulatory sequences of the PRNP gene influence susceptibility to sporadic Creutzfeldt-Jakob disease.
    Bratosiewicz-Wasik J, Liberski PP, Golanska E, Jansen GH, Wasik TJ.
    Neurosci Lett; 2007 Jan 16; 411(3):163-7. PubMed ID: 17134829
    [Abstract] [Full Text] [Related]

  • 26. Creutzfeldt-Jakob disease patients with congophilic kuru plaques have the missense variant prion protein common to Gerstmann-Sträussler syndrome.
    Doh-ura K, Tateishi J, Kitamoto T, Sasaki H, Sakaki Y.
    Ann Neurol; 1990 Feb 16; 27(2):121-6. PubMed ID: 2180366
    [Abstract] [Full Text] [Related]

  • 27.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 28.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 29. A novel phenotype in familial Creutzfeldt-Jakob disease: prion protein gene E200K mutation coupled with valine at codon 129 and type 2 protease-resistant prion protein.
    Hainfellner JA, Parchi P, Kitamoto T, Jarius C, Gambetti P, Budka H.
    Ann Neurol; 1999 Jun 16; 45(6):812-6. PubMed ID: 10360778
    [Abstract] [Full Text] [Related]

  • 30.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 31. [A related analysis for alpha, beta fibrinogen gene haplotypes and nucleotide polymorphisms associated with the ischemic stroke in Hainan Han population].
    Liang L, Sun C, Liao XP, Xiao F, Chen XD, Huang SX, Tang XL, Wen GQ, Long ZG, Wang XY, Liu GX, Cheng S, Cai WW.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Jun 16; 23(3):316-9. PubMed ID: 16767673
    [Abstract] [Full Text] [Related]

  • 32. [Clinicopathological characteristics of Creutzfeldt-Jakob disease with a PrP V180I mutation and M129V polymorphism on different alleles].
    Iwaski Y, Sone M, Kato T, Yoshida E, Indo T, Yoshida M, Hashizume Y, Yamada M.
    Rinsho Shinkeigaku; 1999 Aug 16; 39(8):800-6. PubMed ID: 10586622
    [Abstract] [Full Text] [Related]

  • 33. Association between the PRNP 1368 polymorphism and the occurrence of sporadic Creutzfeldt-Jakob disease.
    Bratosiewicz-Wąsik J, Smoleń-Dzirba J, Rozemuller AJ, Jansen C, Spliet W, Jansen GH, Wąsik TJ, Liberski PP.
    Prion; 2012 Aug 16; 6(4):413-6. PubMed ID: 22895088
    [Abstract] [Full Text] [Related]

  • 34. RARB and STMN2 polymorphisms are not associated with sporadic Creutzfeldt-Jakob disease (CJD) in the Korean population.
    Jeong BH, Kim HJ, Lee KH, Carp RI, Kim YS.
    Mol Biol Rep; 2014 Aug 16; 41(4):2389-95. PubMed ID: 24414001
    [Abstract] [Full Text] [Related]

  • 35. [Rare form of Creutzfeldt-Jakob disease].
    Al-Hamdany S, Holm IE.
    Ugeskr Laeger; 2010 Oct 04; 172(40):2772-3. PubMed ID: 20926051
    [Abstract] [Full Text] [Related]

  • 36. Creutzfeldt-Jakob disease associated with the R208H mutation in the prion protein gene.
    Capellari S, Cardone F, Notari S, Schininà ME, Maras B, Sità D, Baruzzi A, Pocchiari M, Parchi P.
    Neurology; 2005 Mar 08; 64(5):905-7. PubMed ID: 15753435
    [Abstract] [Full Text] [Related]

  • 37. Association of sporadic Creutzfeldt-Jakob disease with homozygous genotypes at PRNP codons 129 and 219 in the Korean population.
    Jeong BH, Lee KH, Kim NH, Jin JK, Kim JI, Carp RI, Kim YS.
    Neurogenetics; 2005 Dec 08; 6(4):229-32. PubMed ID: 16217673
    [Abstract] [Full Text] [Related]

  • 38. PRNP 1368 polymorphism is not associated with sporadic Creutzfeldt-Jakob disease in the Korean population.
    Jeong BH, Lee KH, Lee YJ, Kim YH, Cho YS, Carp RI, Kim YS.
    Eur J Neurol; 2008 Aug 08; 15(8):846-50. PubMed ID: 18549395
    [Abstract] [Full Text] [Related]

  • 39. Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study.
    Mead S, Poulter M, Uphill J, Beck J, Whitfield J, Webb TE, Campbell T, Adamson G, Deriziotis P, Tabrizi SJ, Hummerich H, Verzilli C, Alpers MP, Whittaker JC, Collinge J.
    Lancet Neurol; 2009 Jan 08; 8(1):57-66. PubMed ID: 19081515
    [Abstract] [Full Text] [Related]

  • 40. Genetic risk factors associated with Creutzfeld-Jakob disease in Slovenians and a rapid typing for PRNP codon 129 single nucleotide polymorphism.
    Galvani V, Rupreht RR, Serbec VC, Vidan-Jeras B.
    Transfus Med; 2005 Jun 08; 15(3):197-207. PubMed ID: 15943704
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 20.