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 *

195 related articles for article (PubMed ID: 25609647)

  • 1. 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]  

  • 2. [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]  

  • 3. 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]  

  • 4. 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]  

  • 5. [Creutzfeldt-Jakob disease and psychiatry. Apropos of a case].
    Alezrah C; Monteil AL; Faillie X; Hatem O
    Encephale; 1997; 23(1):72-5. PubMed ID: 9172971
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Revisiting the Heidenhain Variant of Creutzfeldt-Jakob Disease: Evidence for Prion Type Variability Influencing Clinical Course and Laboratory Findings.
    Baiardi S; Capellari S; Ladogana A; Strumia S; Santangelo M; Pocchiari M; Parchi P
    J Alzheimers Dis; 2016; 50(2):465-76. PubMed ID: 26682685
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Creutzfeldt-Jakob disease with the V203I mutation and M129V polymorphism of the prion protein gene (PRNP) and a 17 kDa prion protein fragment.
    Jeong BH; Jeon YC; Lee YJ; Cho HJ; Park SJ; Chung DI; Kim J; Kim SH; Kim HT; Choi EK; Choi KC; Carp RI; Kim YS
    Neuropathol Appl Neurobiol; 2010 Oct; 36(6):558-63. PubMed ID: 20497338
    [No Abstract]   [Full Text] [Related]  

  • 10. Prolonged, progressive dementia with spongiform encephalopathy: a variant of Creutzfeldt-Jakob disease?
    Davanipour Z; Alter M; Coslett HB; Sobel E; Kundu S; Hoenig EM
    Neuroepidemiology; 1988; 7(2):56-65. PubMed ID: 3287204
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Movement disturbances in the differential diagnosis of Creutzfeldt-Jakob disease.
    Edler J; Mollenhauer B; Heinemann U; Varges D; Werner C; Zerr I; Schulz-Schaeffer WJ
    Mov Disord; 2009 Feb; 24(3):350-6. PubMed ID: 19053051
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. The prion diseases: Creutzfeldt-Jakob, Gerstmann-Sträussler-Scheinker, and related disorders.
    Mastrianni JA
    J Geriatr Psychiatry Neurol; 1998; 11(2):78-97. PubMed ID: 9877529
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Clinical experiences with Creutzfeldt-Jakob disease: three case studies.
    Szucs A; Várallyay P; Osztie E; Papp E; Sólyom A; Finta L; Varga D; Barcs G; Holló A; Kamondi A
    Ideggyogy Sz; 2012 Nov; 65(11-12):401-10. PubMed ID: 23289175
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Multiple prion types in the same brain: is a molecular diagnosis of CJD possible?
    Dickson DW; Brown P
    Neurology; 1999 Dec; 53(9):1903-4. PubMed ID: 10599755
    [No Abstract]   [Full Text] [Related]  

  • 17. [Case report. Creutzfeldt-Jakob encephalopathy].
    Horstmann Henz S; Ludin HP
    Ther Umsch; 1999 Feb; 56(2):118-9. PubMed ID: 10095380
    [No Abstract]   [Full Text] [Related]  

  • 18. Early-onset spastic paraparesis as presenting sign of familial Creutzfeldt-Jakob disease.
    Conte F; Giordano A; Tortora F; Caiazzo G; Ladogana A; Tedeschi G; Tessitore A
    Parkinsonism Relat Disord; 2015 Dec; 21(12):1479-80. PubMed ID: 26578040
    [No Abstract]   [Full Text] [Related]  

  • 19. [Prion diseases. Review of the literature on the light of two case reports of Creutzfeldt-Jakob disease].
    Skjaerpe KA; Tysnes OB; Mørk S
    Tidsskr Nor Laegeforen; 1996 Mar; 116(9):1081-5. PubMed ID: 8658476
    [TBL] [Abstract][Full Text] [Related]  

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

    [Next]    [New Search]
    of 10.