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 *

171 related articles for article (PubMed ID: 15851745)

  • 21. Does PRNP gene control the clinical and pathological phenotype of human spongiform transmissible encephalopathies?
    Masullo C; Macchi G
    Clin Neuropathol; 2001; 20(1):19-25. PubMed ID: 11220690
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Familial spongiform encephalopathy associated with a novel prion protein gene mutation.
    Nitrini R; Rosemberg S; Passos-Bueno MR; da Silva LS; Iughetti P; Papadopoulos M; Carrilho PM; Caramelli P; Albrecht S; Zatz M; LeBlanc A
    Ann Neurol; 1997 Aug; 42(2):138-46. PubMed ID: 9266722
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Transmissible spongiform encephalopathies with P102L mutation of PRNP manifesting different phenotypes: clinical, neuroimaging, and electrophysiological studies in Chinese kindred in Taiwan.
    Chi NF; Lee YC; Lu YC; Wu HM; Soong BW
    J Neurol; 2010 Feb; 257(2):191-7. PubMed ID: 19696976
    [TBL] [Abstract][Full Text] [Related]  

  • 24. High prevalence of pathogenic mutations in patients with early-onset dementia detected by sequence analyses of four different genes.
    Finckh U; Müller-Thomsen T; Mann U; Eggers C; Marksteiner J; Meins W; Binetti G; Alberici A; Hock C; Nitsch RM; Gal A
    Am J Hum Genet; 2000 Jan; 66(1):110-7. PubMed ID: 10631141
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Inherited prion disease with 5-OPRI: phenotype modification by repeat length and codon 129.
    Mead S; Webb TE; Campbell TA; Beck J; Linehan JM; Rutherfoord S; Joiner S; Wadsworth JD; Heckmann J; Wroe S; Doey L; King A; Collinge J
    Neurology; 2007 Aug; 69(8):730-8. PubMed ID: 17709704
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Novel twelve-generation kindred of fatal familial insomnia from germany representing the entire spectrum of disease expression.
    Harder A; Jendroska K; Kreuz F; Wirth T; Schafranka C; Karnatz N; Théallier-Janko A; Dreier J; Lohan K; Emmerich D; Cervós-Navarro J; Windl O; Kretzschmar HA; Nürnberg P; Witkowski R
    Am J Med Genet; 1999 Dec; 87(4):311-6. PubMed ID: 10588836
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Creutzfeldt-Jakob disease with PRNP G114V mutation in a Chinese family.
    Liu Z; Jia L; Piao Y; Lu D; Wang F; Lv H; Lu Y; Jia J
    Acta Neurol Scand; 2010 Jun; 121(6):377-83. PubMed ID: 20028338
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A new point mutation of the PRNP gene in Gerstmann-Sträussler-Scheinker case in Poland.
    Bratosiewicz J; Barcikowska M; Cervenakowa L; Brown P; Gajdusek DC; Liberski PP
    Folia Neuropathol; 2000; 38(4):164-6. PubMed ID: 11693719
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Inhibition of PrPSc formation by lentiviral gene transfer of PrP containing dominant negative mutations.
    Crozet C; Lin YL; Mettling C; Mourton-Gilles C; Corbeau P; Lehmann S; Perrier V
    J Cell Sci; 2004 Nov; 117(Pt 23):5591-7. PubMed ID: 15494372
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A novel prion disease associated with diarrhea and autonomic neuropathy.
    Mead S; Gandhi S; Beck J; Caine D; Gallujipali D; Carswell C; Hyare H; Joiner S; Ayling H; Lashley T; Linehan JM; Al-Doujaily H; Sharps B; Revesz T; Sandberg MK; Reilly MM; Koltzenburg M; Forbes A; Rudge P; Brandner S; Warren JD; Wadsworth JDF; Wood NW; Holton JL; Collinge J
    N Engl J Med; 2013 Nov; 369(20):1904-14. PubMed ID: 24224623
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Prion disease.
    Takada LT; Kim MO; Metcalf S; Gala II; Geschwind MD
    Handb Clin Neurol; 2018; 148():441-464. PubMed ID: 29478593
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The evolution of views on the nosological position of transmissible spongiform encephalopathies.
    Liberski PP; Brown P; Gajdusek CD
    Folia Neuropathol; 1997; 35(4):214-25. PubMed ID: 9833398
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Clinical and genetic features of human prion diseases in Catalonia: 1993-2002.
    Sanchez-Valle R; Nos C; Yagüe J; Graus F; Domínguez A; Saiz A;
    Eur J Neurol; 2004 Oct; 11(10):649-55. PubMed ID: 15469448
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Polymorphisms within the prion (PrP) and prion-like protein (Doppel) genes in AD.
    Golanska E; Hulas-Bigoszewska K; Rutkiewicz E; Styczynska M; Peplonska B; Barcikowska M; Bratosiewicz-Wasik J; Liberski PP
    Neurology; 2004 Jan; 62(2):313-5. PubMed ID: 14745079
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Creutzfeldt-Jakob disease associated with the R208H mutation in the prion protein gene.
    Capellari S; Cardone F; Notari S; Schininà ME; Maras B; Sità D; Baruzzi A; Pocchiari M; Parchi P
    Neurology; 2005 Mar; 64(5):905-7. PubMed ID: 15753435
    [TBL] [Abstract][Full Text] [Related]  

  • 36. The genetics of prion diseases.
    Mastrianni JA
    Genet Med; 2010 Apr; 12(4):187-95. PubMed ID: 20216075
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Upstream AUGs modulate prion protein translation in vitro.
    Schröder B; Nickodemus R; Jürgens T; Bodemer W
    Acta Virol; 2002; 46(3):159-67. PubMed ID: 12580378
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Creutzfeldt-Jakob disease and related disorders: etiopathogenetic aspects.
    Barbanti P; Pocchiari M
    Funct Neurol; 1997; 12(3-4):159-64. PubMed ID: 9218970
    [No Abstract]   [Full Text] [Related]  

  • 39. ApoE distribution and family history in genetic prion diseases in Germany.
    Krasnianski A; von Ahsen N; Heinemann U; Meissner B; Kretzschmar HA; Armstrong VW; Zerr I
    J Mol Neurosci; 2008; 34(1):45-50. PubMed ID: 18157657
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Ultrastructural pathology of Creutzfeldt-Jakob disease and fatal familial insomnia.
    Liberski PP; Giraud P; Kopp N
    Folia Neuropathol; 2000; 38(4):171-3. PubMed ID: 11693721
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.