214 related articles for article (PubMed ID: 25482600)
1. Rare V180I mutation in PRNP gene of a Chinese patient with Creutzfeldt-Jakob disease.
Shi Q; Shen XJ; Zhou W; Xiao K; Zhang XM; Zhang BY; Dong XP
Prion; 2014; 8(6):411-4. PubMed ID: 25482600
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Creutzfeldt-Jakob Disease with a prion protein gene codon 180 mutation presenting asymmetric cortical high-intensity on magnetic resonance imaging.
Amano Y; Kimura N; Hanaoka T; Aso Y; Hirano T; Murai H; Satoh K; Matsubara E
Prion; 2015; 9(1):29-33. PubMed ID: 25730397
[TBL] [Abstract][Full Text] [Related]
4. [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]
5. 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]
6. 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]
7. 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]
8. A case of V180I genetic mutation Creutzfeldt Jakob disease (CJD) with delusional misidentification as an initial symptom.
Nagata T; Shinagawa S; Kobayashi N; Kondo K; Shigeta M
Prion; 2022 Dec; 16(1):7-13. PubMed ID: 34965177
[TBL] [Abstract][Full Text] [Related]
9. Spreading brain lesions in a familial Creutzfeldt-Jakob disease with V180I mutation over 4 years.
Deguchi K; Takamiya M; Deguchi S; Morimoto N; Kurata T; Ikeda Y; Abe K
BMC Neurol; 2012 Nov; 12():144. PubMed ID: 23176099
[TBL] [Abstract][Full Text] [Related]
10. Novel PRNP mutation in a patient with a slow progressive dementia syndrome.
Heinemann U; Krasnianski A; Meissner B; Grasbon-Frodl EM; Kretzschmar HA; Zerr I
Med Sci Monit; 2008 May; 14(5):CS41-43. PubMed ID: 18443555
[TBL] [Abstract][Full Text] [Related]
11. Familial Creutzfeldt-Jakob disease with V180I mutation.
Yang TI; Jung DS; Ahn BY; Jeong BH; Cho HJ; Kim YS; Na DL; Geschwind MD; Kim EJ
J Korean Med Sci; 2010 Jul; 25(7):1097-100. PubMed ID: 20592908
[TBL] [Abstract][Full Text] [Related]
12. Genetic prion disease with codon 196 PRNP mutation: clinical and pathological findings.
Schelzke G; Eigenbrod S; Romero C; Varges D; Breithaupt M; Taratuto AL; Kretzschmar HA; Zerr I
Neurobiol Aging; 2011 Apr; 32(4):756.e1-9. PubMed ID: 21232818
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. [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]
15. First case of V180I rare mutation in a Brazilian patient with Creutzfeldt-Jakob disease.
De Souza RKM; Josviak ND; Batistela MS; Santos PSF; Landemberger MC; Ramina R
Prion; 2017 Nov; 11(6):465-468. PubMed ID: 29095671
[TBL] [Abstract][Full Text] [Related]
16. Clinical features of genetic Creutzfeldt-Jakob disease with V180I mutation in the prion protein gene.
Qina T; Sanjo N; Hizume M; Higuma M; Tomita M; Atarashi R; Satoh K; Nozaki I; Hamaguchi T; Nakamura Y; Kobayashi A; Kitamoto T; Murayama S; Murai H; Yamada M; Mizusawa H
BMJ Open; 2014 May; 4(5):e004968. PubMed ID: 24838726
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. Determinants of diagnostic investigation sensitivities across the clinical spectrum of sporadic Creutzfeldt-Jakob disease.
Collins SJ; Sanchez-Juan P; Masters CL; Klug GM; van Duijn C; Poleggi A; Pocchiari M; Almonti S; Cuadrado-Corrales N; de Pedro-Cuesta J; Budka H; Gelpi E; Glatzel M; Tolnay M; Hewer E; Zerr I; Heinemann U; Kretszchmar HA; Jansen GH; Olsen E; Mitrova E; Alpérovitch A; Brandel JP; Mackenzie J; Murray K; Will RG
Brain; 2006 Sep; 129(Pt 9):2278-87. PubMed ID: 16816392
[TBL] [Abstract][Full Text] [Related]
20. Novel prion mutation (p.Tyr225Cys) in a Korean patient with atypical Creutzfeldt-Jakob disease.
Bagyinszky E; Yang Y; Giau VV; Youn YC; An SSA; Kim S
Clin Interv Aging; 2019; 14():1387-1397. PubMed ID: 31447551
[No Abstract] [Full Text] [Related]
[Next] [New Search]
