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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

176 related articles for article (PubMed ID: 17965961)

  • 1. Two different clinical phenotypes of Creutzfeldt-Jakob disease with a M232R substitution.
    Shiga Y; Satoh K; Kitamoto T; Kanno S; Nakashima I; Sato S; Fujihara K; Takata H; Nobukuni K; Kuroda S; Takano H; Umeda Y; Konno H; Nagasato K; Satoh A; Matsuda Y; Hidaka M; Takahashi H; Sano Y; Kim K; Konishi T; Doh-ura K; Sato T; Sasaki K; Nakamura Y; Yamada M; Mizusawa H; Itoyama Y
    J Neurol; 2007 Nov; 254(11):1509-17. PubMed ID: 17965961
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Creutzfeldt-Jakob disease with an M232R substitution: report of a patient showing slowly progressive disease with abundant plaque-like PrP deposits in the cerebellum.
    Shimizu H; Yamada M; Matsubara N; Takano H; Umeda Y; Kawase Y; Kitamoto T; Nishizawa M; Takahashi H
    Neuropathology; 2009 Dec; 29(6):735-43. PubMed ID: 19422537
    [TBL] [Abstract][Full Text] [Related]  

  • 3. An autopsied case of Creutzfeldt-Jakob disease with mutation in the prion protein gene codon 232 and type 1+2 prion protein.
    Iwasaki Y; Yokoi F; Tatsumi S; Mimuro M; Iwai K; Kitamoto T; Yoshida M
    Neuropathology; 2013 Oct; 33(5):568-75. PubMed ID: 23320809
    [TBL] [Abstract][Full Text] [Related]  

  • 4. An autopsied case of panencephalopathic-type Creutzfeldt-Jakob disease with mutation in the prion protein gene at codon 232 and type 1 prion protein.
    Hama T; Iwasaki Y; Niwa H; Yoshida M; Hashizume Y; Kitamoto T; Murakami N; Sobue G
    Neuropathology; 2009 Dec; 29(6):727-34. PubMed ID: 19422533
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Iatrogenic CJD due to pituitary-derived growth hormone with genetically determined incubation times of up to 40 years.
    Rudge P; Jaunmuktane Z; Adlard P; Bjurstrom N; Caine D; Lowe J; Norsworthy P; Hummerich H; Druyeh R; Wadsworth JD; Brandner S; Hyare H; Mead S; Collinge J
    Brain; 2015 Nov; 138(Pt 11):3386-99. PubMed ID: 26268531
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutation in the prion protein gene at codon 232 in Japanese patients with Creutzfeldt-Jakob disease: a clinicopathological, immunohistochemical and transmission study.
    Hoque MZ; Kitamoto T; Furukawa H; Muramoto T; Tateishi J
    Acta Neuropathol; 1996 Nov; 92(5):441-6. PubMed ID: 8922054
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic Creutzfeldt-Jakob disease-M232R with the cooccurrence of multiple prion strains, M1 + M2C + M2T: Report of an autopsy case.
    Shintaku M; Nakamura T; Kaneda D; Shinde A; Kusaka H; Takeuchi A; Kitamoto T
    Neuropathology; 2021 Jun; 41(3):206-213. PubMed ID: 33586250
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Creutzfeldt-Jakob disease associated with a V203I homozygous mutation in the prion protein gene.
    Komatsu J; Sakai K; Hamaguchi T; Sugiyama Y; Iwasa K; Yamada M
    Prion; 2014; 8(5):336-8. PubMed ID: 25495585
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The epidemiological, clinical, and laboratory features of sporadic Creutzfeldt-Jakob disease patients in China: surveillance data from 2006 to 2010.
    Gao C; Shi Q; Tian C; Chen C; Han J; Zhou W; Zhang BY; Jiang HY; Zhang J; Dong XP
    PLoS One; 2011; 6(8):e24231. PubMed ID: 21904617
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [A case of Creutzfeldt-Jakob disease with a double mutation (V180I/M232R) in the PRNP gene].
    Koh K; Takaki R; Miwa M; Nagasaka T; Shindo K; Takiyama Y
    Rinsho Shinkeigaku; 2015; 55(6):424-7. PubMed ID: 26103817
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Creutzfeldt-Jakob disease with the M232R mutation in the prion protein gene in two cases showing different disease courses: a clinicopathological study.
    Takeda N; Yokota O; Terada S; Haraguchi T; Nobukuni K; Mizuki R; Honda H; Yoshida H; Kishimoto Y; Oshima E; Ishizu H; Satoh K; Kitamoto T; Ihara Y; Uchitomi Y
    J Neurol Sci; 2012 Jan; 312(1-2):108-16. PubMed ID: 21983261
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mutations at codons 178, 200-129, and 232 contributed to the inherited prion diseases in Korean patients.
    Choi BY; Kim SY; Seo SY; An SS; Kim S; Park SE; Lee SH; Choi YJ; Kim SJ; Kim CK; Park JS; Ju YR
    BMC Infect Dis; 2009 Aug; 9():132. PubMed ID: 19698114
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Panencephalopathic Creutzfeldt-Jakob disease with distinct pattern of prion protein deposition in a patient with D178N mutation and homozygosity for valine at codon 129 of the prion protein Gene.
    Marcon G; Indaco A; Di Fede G; Suardi S; Finato N; Moretti V; Micoli S; Fociani P; Zerbi P; Pincherle A; Redaelli V; Tagliavini F; Giaccone G
    Brain Pathol; 2014 Mar; 24(2):148-51. PubMed ID: 24118545
    [TBL] [Abstract][Full Text] [Related]  

  • 14. MM1-type sporadic Creutzfeldt-Jakob disease with unusually prolonged disease duration presenting with panencephalopathic-type pathology.
    Hoshino A; Iwasaki Y; Izumi M; Kimura S; Ibi T; Kitamoto T; Yoshida M; Hashizume Y; Sahashi K
    Neuropathology; 2008 Jun; 28(3):326-32. PubMed ID: 18248577
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Rare E196K mutation in the PRNP gene of a patient exhibiting behavioral abnormalities.
    Béjot Y; Osseby GV; Caillier M; Moreau T; Laplanche JL; Giroud M
    Clin Neurol Neurosurg; 2010 Apr; 112(3):244-7. PubMed ID: 20005032
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The first Chinese case of Creutzfeldt-Jakob disease patient with R208H mutation in PRNP.
    Chen C; Shi Q; Tian C; Li Q; Zhou W; Gao C; Han J; Dong XP
    Prion; 2011; 5(3):232-4. PubMed ID: 21791975
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A point mutation in GPI-attachment signal peptide accelerates the development of prion disease.
    Kobayashi A; Hirata T; Shimazaki T; Munesue Y; Aoshima K; Kimura T; Nio-Kobayashi J; Hasebe R; Takeuchi A; Matsuura Y; Kusumi S; Koga D; Iwasaki Y; Kinoshita T; Mohri S; Kitamoto T
    Acta Neuropathol; 2023 May; 145(5):637-650. PubMed ID: 36879070
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Novel prion protein gene mutation at codon 196 (E196A) in a septuagenarian with Creutzfeldt-Jakob disease.
    Zhang H; Wang M; Wu L; Zhang H; Jin T; Wu J; Sun L
    J Clin Neurosci; 2014 Jan; 21(1):175-8. PubMed ID: 23787189
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Rare V203I mutation in the PRNP gene of a Chinese patient with Creutzfeldt-Jakob disease.
    Shi Q; Chen C; Wang XJ; Zhou W; Wang JC; Zhang BY; Gao C; Gao C; Han J; Dong XP
    Prion; 2013; 7(3):259-62. PubMed ID: 23764840
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Novel prion protein gene mutation in an octogenarian with Creutzfeldt-Jakob disease.
    Collins S; Boyd A; Fletcher A; Byron K; Harper C; McLean CA; Masters CL
    Arch Neurol; 2000 Jul; 57(7):1058-63. PubMed ID: 10891990
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.