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 *

176 related articles for article (PubMed ID: 16736740)

  • 1. A case of familial Creutzfeldt-Jakob disease presenting with dry cough.
    Larue S; Verreault S; Gould P; Coulthart MB; Bergeron C; Dupré N
    Can J Neurol Sci; 2006 May; 33(2):243-5. PubMed ID: 16736740
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Sporadic Creutzfeldt-Jakob disease--a review.
    Sharma S; Mukherjee M; Kedage V; Muttigi MS; Rao A; Rao S
    Int J Neurosci; 2009; 119(11):1981-94. PubMed ID: 19863257
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Rapidly progressive dementia syndrome associated with a novel four extra repeat mutation in the prion protein gene.
    Yanagihara C; Yasuda M; Maeda K; Miyoshi K; Nishimura Y
    J Neurol Neurosurg Psychiatry; 2002 Jun; 72(6):788-91. PubMed ID: 12023426
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. [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]  

  • 7. Novel prion protein gene mutation in an octogenarian with Creutzfeldt-Jakob disease.
    Collins S; Boyd A; Fletcher A; Byron K; Harper C; McLean CA; Masters CL
    Arch Neurol; 2000 Jul; 57(7):1058-63. PubMed ID: 10891990
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Familial Creutzfeldt-Jakob disease presenting as epilepsia partialis continua.
    Lowden MR; Scott K; Kothari MJ
    Epileptic Disord; 2008 Dec; 10(4):271-5. PubMed ID: 19017568
    [TBL] [Abstract][Full Text] [Related]  

  • 9. An unusually presenting case of sCJD--the VV1 subtype.
    Tanev KS; Yilma M
    Clin Neurol Neurosurg; 2009 Apr; 111(3):282-91. PubMed ID: 18995952
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Creutzfeldt-Jakob disease with E200K PRNP mutation: a case report and revision of the literature.
    Mancuso M; Siciliano G; Capellari S; Orsucci D; Moretti P; Di Fede G; Suardi S; Strammiello R; Parchi P; Tagliavini F; Murri L
    Neurol Sci; 2009 Oct; 30(5):417-20. PubMed ID: 19597763
    [TBL] [Abstract][Full Text] [Related]  

  • 12. An autopsied case of Creutzfeldt-Jakob disease with mutation in the prion protein gene codon 232 and type 1+2 prion protein.
    Iwasaki Y; Yokoi F; Tatsumi S; Mimuro M; Iwai K; Kitamoto T; Yoshida M
    Neuropathology; 2013 Oct; 33(5):568-75. PubMed ID: 23320809
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Ancestral origins and worldwide distribution of the PRNP 200K mutation causing familial Creutzfeldt-Jakob disease.
    Lee HS; Sambuughin N; Cervenakova L; Chapman J; Pocchiari M; Litvak S; Qi HY; Budka H; del Ser T; Furukawa H; Brown P; Gajdusek DC; Long JC; Korczyn AD; Goldfarb LG
    Am J Hum Genet; 1999 Apr; 64(4):1063-70. PubMed ID: 10090891
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Diagnostic challenge of Creutzfeldt-Jakob disease in a patient with multimorbidity: a case-report.
    Yaqub A; Ikram MK; Blankevoort J; Ikram MA
    BMC Neurol; 2023 Oct; 23(1):346. PubMed ID: 37784069
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Creutzfeldt-Jakob disease presenting with visual symptoms: a case of the 'Heidenhain variant'.
    Verma R; Junewar V; Sahu R
    BMJ Case Rep; 2013 Jan; 2013():. PubMed ID: 23365167
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Familial Creutzfeldt-Jakob disease associated with a point mutation at codon 210 of the prion protein gene.
    Huang N; Marie SK; Kok F; Nitrini R
    Arq Neuropsiquiatr; 2001 Dec; 59(4):932-5. PubMed ID: 11733840
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Low mood, visual hallucinations, and falls - heralding the onset of rapidly progressive probable sporadic Creutzfeldt-Jakob disease in a 73-year old: a case report.
    Klotz DM; Penfold RS
    J Med Case Rep; 2018 May; 12(1):128. PubMed ID: 29734943
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Creutzfeldt-Jakob encephalopathy with mutation E200K. Report of a "sporadic" case].
    Cosacov RM; Taratuto AL; Ghiraridi G; Barrionuevo P; Diaz A; Begué C; Martinetto H
    Rev Fac Cien Med Univ Nac Cordoba; 2004; 61(1):48-53. PubMed ID: 15366237
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutation of the PRNP gene at codon 211 in familial Creutzfeldt-Jakob disease.
    Ladogana A; Almonti S; Petraroli R; Giaccaglini E; Ciarmatori C; Liù QG; Bevivino S; Squitieri F; Pocchiari M
    Am J Med Genet; 2001 Oct; 103(2):133-7. PubMed ID: 11568919
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.