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 *

93 related articles for article (PubMed ID: 23531090)

  • 1. Microsphere formation in a subtype of Creutzfeldt-Jakob disease with a V180I mutation and codon 129 MM polymorphism.
    Honda H; Ishii R; Hamano A; Itoh K; Suzuki SO; Fushiki S; Nakagawa M; Iwaki T
    Neuropathol Appl Neurobiol; 2013 Dec; 39(7):844-8. PubMed ID: 23531090
    [No Abstract]   [Full Text] [Related]  

  • 2. Polymorphism at codon 129 of PRNP affects the phenotypic expression of Creutzfeldt-Jakob disease linked to E200K mutation.
    Puoti G; Rossi G; Giaccone G; Awan T; Lievens PM; Defanti CA; Tagliavini F; Bugiani O
    Ann Neurol; 2000 Aug; 48(2):269-70. PubMed ID: 10939584
    [No Abstract]   [Full Text] [Related]  

  • 3. Fluorine 18-labeled fluorodeoxyglucose positron emission tomography in familial Creutzfeldt-Jakob disease.
    Renard D; Collombier L; Castelnovo G; Remy A; Laplanche JL; Labauge P
    Arch Neurol; 2008 Oct; 65(10):1390-1. PubMed ID: 18852360
    [No Abstract]   [Full Text] [Related]  

  • 4. [An autopsy-verified case of Creutzfeldt-Jakob disease with codon 129 polymorphism and codon 180 point mutation].
    Matsumura T; Kojima S; Kuroiwa Y; Takagi A; Unakami M; Kitamoto T
    Rinsho Shinkeigaku; 1995 Mar; 35(3):282-5. PubMed ID: 7614752
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [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; 39(8):800-6. PubMed ID: 10586622
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Familial Creutzfeldt-Jakob disease with a mutation at codon 180 presenting with an atypical phenotype.
    Yeo MJ; Lee SH; Lee SY; Jeon YC; Park SJ; Cho HJ; Choi KC; Kim YS; Kim SH
    J Clin Neurosci; 2013 Jan; 20(1):180-2. PubMed ID: 22999564
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Creutzfeldt-Jakob disease with V180I mutation and senile plaque.
    Suzuki K; Matsumura N; Suzuki T; Nakano H; Nagayama H; Yokoo H; Tamura K; Katayama Y; Sugisaki Y; Oba K
    Geriatr Gerontol Int; 2009 Jun; 9(2):210-2. PubMed ID: 19490144
    [No Abstract]   [Full Text] [Related]  

  • 8. 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; 64(5):905-7. PubMed ID: 15753435
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Creutzfeldt-Jakob disease with homozygous M232R mutation: A case report.
    Kon T; Miki Y; Arai A; Funamizu Y; Ueno T; Haga R; Nishijima H; Suzuki C; Nunomura J; Baba M; Oyama Y; Shiga Y; Kitamoto T; Tomiyama M
    J Neurol Sci; 2015 May; 352(1-2):108-9. PubMed ID: 25818675
    [No Abstract]   [Full Text] [Related]  

  • 10. Clinicopathological findings of a long-term survivor of V180I genetic Creutzfeldt-Jakob disease.
    Hayashi Y; Iwasaki Y; Waza M; Kato S; Akagi A; Kimura A; Inuzuka T; Satoh K; Kitamoto T; Yoshida M; Shimohata T
    Prion; 2020 Dec; 14(1):109-117. PubMed ID: 32178563
    [TBL] [Abstract][Full Text] [Related]  

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

  • 12. Diffusion-weighted MRI in familial Creutzfeldt-Jakob disease with the codon 200 mutation in the prion protein gene.
    Tsuboi Y; Baba Y; Doh-ura K; Imamura A; Fujioka S; Yamada T
    J Neurol Sci; 2005 May; 232(1-2):45-9. PubMed ID: 15850581
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Herpes simplex encephalitis as an initial presentation of Creutzfeldt-Jakob disease.
    Pollak L; Shabazov E; Mendlovic S; Rabey MJ
    Isr Med Assoc J; 2008 May; 10(5):392-4. PubMed ID: 18605370
    [No Abstract]   [Full Text] [Related]  

  • 14. [Inherited Creutzfeldt-Jakob disease].
    Toda H; Kishida H; Kuroiwa Y
    Nihon Rinsho; 2004 Jan; 62 Suppl():261-5. PubMed ID: 15011362
    [No Abstract]   [Full Text] [Related]  

  • 15. Creutzfeldt-Jakob disease with a novel insertion and codon 219 Lys/Lys polymorphism in PRNP.
    Nishida Y; Sodeyama N; Toru Y; Toru S; Kitamoto T; Mizusawa H
    Neurology; 2004 Nov; 63(10):1978-9. PubMed ID: 15557533
    [No Abstract]   [Full Text] [Related]  

  • 16. [Hereditary Creutzfeldt-Jakob disease caused by a mutation at codon 200].
    Bertrand A; Martinez-Almoyna L; De Broucker T
    Rev Neurol (Paris); 2005 Mar; 161(3):351-4. PubMed ID: 15800459
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cortical propagation of Creutzfeldt-Jakob disease with codon 180 mutation.
    Kobayashi S; Saito Y; Maki T; Murayama S
    Clin Neurol Neurosurg; 2010 Jul; 112(6):520-3. PubMed ID: 20409635
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [A case of codon 232 mutation-induced Creutzfeldt-Jakob disease visualized by the MRI-FLAIR images with atypical clinical symptoms].
    Saito T; Isozumi K; Komatsumoto S; Nara M; Suzuki K; Dohura K
    Rinsho Shinkeigaku; 2000 Jan; 40(1):51-4. PubMed ID: 10825802
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genotype at codon 129 and susceptibility to Creutzfeldt-Jakob disease.
    Deslys JP; Jaegly A; d'Aignaux JH; Mouthon F; de Villemeur TB; Dormont D
    Lancet; 1998 Apr; 351(9111):1251. PubMed ID: 9643750
    [No Abstract]   [Full Text] [Related]  

  • 20. [Fatal familial insomnia: phenotypic changes determined by polymorphism of the codon 129].
    Colombier C; Géraud G; Delisle MB; Laplanche JL; Pavy le Traon A; Alizé P; Delpla PA
    Rev Neurol (Paris); 1997 May; 153(4):239-43. PubMed ID: 9296141
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.