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 *

179 related articles for article (PubMed ID: 20226976)

  • 1. Variant or sporadic Creutzfeldt-Jakob disease?
    Brandel JP; Galanaud D; Freeman L; Laplanche JL; Haik S
    Lancet; 2010 Mar; 375(9718):889; author reply 889-90. PubMed ID: 20226976
    [No Abstract]   [Full Text] [Related]  

  • 2. Clinical range and MRI in Creutzfeldt-Jakob disease with heterozygosity at codon 129 and prion protein type 2.
    Samman I; Schulz-Schaeffer WJ; Wöhrle JC; Sommer A; Kretzschmar HA; Hennerici M
    J Neurol Neurosurg Psychiatry; 1999 Nov; 67(5):678-81. PubMed ID: 10519881
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Human prion diseases: the Hungarian experience].
    Kovács GG; Bakos A; Mitrova E; Minárovits J; László L; Majtényi K
    Ideggyogy Sz; 2007 Nov; 60(11-12):447-52. PubMed ID: 18200749
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Variant Creutzfeldt-Jakob disease in older patients.
    el Tawil S; Mackay G; Davidson L; Summers D; Knight R; Will R
    J Neurol Neurosurg Psychiatry; 2015 Nov; 86(11):1279-80. PubMed ID: 25609647
    [No Abstract]   [Full Text] [Related]  

  • 5. Serial magnetic resonance imaging changes in sporadic Creutzfeldt-Jakob disease with valine homozygosity at codon 129 of the prion protein gene.
    Furukawa F; Ishibashi S; Sanjo N; Yamashita H; Mizusawa H
    JAMA Neurol; 2014 Sep; 71(9):1186-7. PubMed ID: 25070174
    [No Abstract]   [Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. Diffusion tensor imaging in patients with Creutzfeldt-Jakob disease.
    Fujita K; Nakane S; Harada M; Izumi Y; Kaji R
    J Neurol Neurosurg Psychiatry; 2008 Nov; 79(11):1304-6. PubMed ID: 18940995
    [No Abstract]   [Full Text] [Related]  

  • 9. The diagnosis of human prion diseases.
    Kordek R
    Folia Neuropathol; 2000; 38(4):151-60. PubMed ID: 11693717
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [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]  

  • 11. [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]  

  • 12. 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]  

  • 13. Sporadic Creutzfeldt-Jakob disease in a 18-year-old in the UK.
    Bateman D; Hilton D; Love S; Zeidler M; Beck J; Collinge J
    Lancet; 1995 Oct; 346(8983):1155-6. PubMed ID: 7475612
    [No Abstract]   [Full Text] [Related]  

  • 14. [Diffusion images on brain MRI in Creutzfeldt-Jakob disease].
    Nagaoka U; Kurita K; Hosoya T; Kitamoto T; Kato T
    Rinsho Shinkeigaku; 1999 Apr; 39(4):468-70. PubMed ID: 10391976
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Double mutations at codon 180 and codon 232 of the PRNP gene in an apparently sporadic case of Creutzfeldt-Jakob disease.
    Hitoshi S; Nagura H; Yamanouchi H; Kitamoto T
    J Neurol Sci; 1993 Dec; 120(2):208-12. PubMed ID: 8138811
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Elevated phosphorylated tau pT-181 in a possible PRNP codon 129 MV vCJD case.
    Green AJ; Andrews MM; Bishop MT; McKenzie JM; McCord Y; Pennington C; Chohan G; Knight RS
    J Neurol Neurosurg Psychiatry; 2010 Dec; 81(12):1408-9. PubMed ID: 20562404
    [No Abstract]   [Full Text] [Related]  

  • 17. Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease.
    Parchi P; Castellani R; Capellari S; Ghetti B; Young K; Chen SG; Farlow M; Dickson DW; Sima AA; Trojanowski JQ; Petersen RB; Gambetti P
    Ann Neurol; 1996 Jun; 39(6):767-78. PubMed ID: 8651649
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Genetic Creutzfeldt-Jakob disease with R208H mutation presenting as progressive supranuclear palsy.
    Matěj R; Kovacs GG; Johanidesová S; Keller J; Matějčková M; Nováková J; Sigut V; Keller O; Rusina R
    Mov Disord; 2012 Apr; 27(4):476-9. PubMed ID: 22488860
    [No Abstract]   [Full Text] [Related]  

  • 20. Variant CJD in an individual heterozygous for PRNP codon 129.
    Kaski D; Mead S; Hyare H; Cooper S; Jampana R; Overell J; Knight R; Collinge J; Rudge P
    Lancet; 2009 Dec; 374(9707):2128. PubMed ID: 20109837
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.