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 *

162 related articles for article (PubMed ID: 11845387)

  • 1. [Clinically atypical CJD: diagnostic relevance of cerebrospinal fluid markers and molecular genetic analysis?].
    Tumani H; Windl O; Kretzschmar HA; Ludolph AC
    Dtsch Med Wochenschr; 2002 Feb; 127(7):318-20. PubMed ID: 11845387
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Psychiatric manifestations of a new variant of Creutzfeldt-Jakob disease. Apropos of a case].
    Dervaux A; Vicart S; Lopes F; Le Borgne MH
    Encephale; 2001; 27(2):194-7. PubMed ID: 11407273
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [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]  

  • 4. Total tau protein in cerebrospinal fluid and diffusion-weighted MRI as an early diagnostic marker for Creutzfeldt-Jakob disease.
    Satoh K; Shirabe S; Tsujino A; Eguchi H; Motomura M; Honda H; Tomita I; Satoh A; Tsujihata M; Matsuo H; Nakagawa M; Eguchi K
    Dement Geriatr Cogn Disord; 2007; 24(3):207-12. PubMed ID: 17690553
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [A case of probable Creutzfeldt-Jakob disease with a point mutation of prion protein gene codon 180 and atypical MRI findings].
    Kobayashi S; Ohuchi T; Maki T
    Rinsho Shinkeigaku; 1997 Aug; 37(8):671-4. PubMed ID: 9404141
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [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]  

  • 7. [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]  

  • 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. [A case of Creutzfeldt-Jakob disease with a point mutation of prion protein at codon 180].
    Tanaka T; Kinoshita I; Saitoh Y; Satoh K; Nishiura Y; Shirabe S; Kitamoto T
    No To Shinkei; 2004 Dec; 56(12):1025-8. PubMed ID: 15729879
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. [Creutzfeldt-Jakob disease with a point mutation at codon 232 of prion protein--a case report].
    Shimizu T; Tanaka K; Tanahashi N; Fukuuchi Y; Kitamoto T
    Rinsho Shinkeigaku; 1994 Jun; 34(6):590-2. PubMed ID: 7955719
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Clinical features and diagnosis of dura mater graft associated Creutzfeldt Jakob disease.
    Noguchi-Shinohara M; Hamaguchi T; Kitamoto T; Sato T; Nakamura Y; Mizusawa H; Yamada M
    Neurology; 2007 Jul; 69(4):360-7. PubMed ID: 17646628
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Current clinical diagnosis in Creutzfeldt-Jakob disease: identification of uncommon variants.
    Zerr I; Schulz-Schaeffer WJ; Giese A; Bodemer M; Schröter A; Henkel K; Tschampa HJ; Windl O; Pfahlberg A; Steinhoff BJ; Gefeller O; Kretzschmar HA; Poser S
    Ann Neurol; 2000 Sep; 48(3):323-9. PubMed ID: 10976638
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Chronological changes in MRI and CSF biochemical markers in Creutzfeldt-Jakob disease patients.
    Satoh K; Shirabe S; Eguchi H; Tsujino A; Motomura M; Satoh A; Tsujihata M; Eguchi K
    Dement Geriatr Cogn Disord; 2007; 23(6):372-81. PubMed ID: 17389797
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [CSF-analyses in clinical diagnosis of Creutzfeldt-Jakob disease. A literature review and three cases from routine clinical practice].
    Blennow K; Lind B; Andersson E; Andreasen N
    Lakartidningen; 2001 May; 98(20):2446-51. PubMed ID: 11433975
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Juvenile onset Creutzfeldt-Jakob disease with the history of neurosurgical operation].
    Sato M; Murahashi M; Hara H; Jimi T; Wakayama Y
    Rinsho Shinkeigaku; 2000 May; 40(5):428-32. PubMed ID: 11002723
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Gerstmann-Sträussler-Scheinker syndrome with a Pro102Leu mutation in the prion protein gene and atypical MRI findings, hyperthermia, tachycardia, and hyperhidrosis].
    Imaiso Y; Mitsuo K
    Rinsho Shinkeigaku; 1998; 38(10-11):920-5. PubMed ID: 10203975
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Creutzfeldt-Jakob disease: a case that initiated with psychiatric symptoms].
    Kurne A; Ertuğrul A; Anil Yağcioğlu AE; Demirci E; Yazici KM; Kansu T
    Turk Psikiyatri Derg; 2005; 16(1):55-9. PubMed ID: 15793699
    [TBL] [Abstract][Full Text] [Related]  

  • 19. An autopsied case of V180I Creutzfeldt-Jakob disease presenting with panencephalopathic-type pathology and a characteristic prion protein type.
    Iwasaki Y; Mori K; Ito M; Nagaoka M; Ieda T; Kitamoto T; Yoshida M; Hashizume Y
    Neuropathology; 2011 Oct; 31(5):540-8. PubMed ID: 21269331
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Molecular subtype-specific clinical diagnosis of prion diseases.
    Heinemann U; Krasnianski A; Meissner B; Gloeckner SF; Kretzschmar HA; Zerr I
    Vet Microbiol; 2007 Aug; 123(4):328-35. PubMed ID: 17513070
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.