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.


PUBMED FOR HANDHELDS

Journal Abstract Search


86 related items for PubMed ID: 1344206

  • 21. [The mystery of prion proteins: from neurodegenerative diseases to the biology of reproduction].
    Peoc'h K.
    Ann Biol Clin (Paris); 2005; 63(2):121-6. PubMed ID: 15771969
    [Abstract] [Full Text] [Related]

  • 22. Codon 219 Lys allele of PRNP is not found in sporadic Creutzfeldt-Jakob disease.
    Shibuya S, Higuchi J, Shin RW, Tateishi J, Kitamoto T.
    Ann Neurol; 1998 Jun; 43(6):826-8. PubMed ID: 9629853
    [Abstract] [Full Text] [Related]

  • 23. Isolation and characterization of the subacute spongiform virus encephalopathies of man: kuru and Creutzfeldt-Jakob disease.
    Gibbs CJ, Gajdusek DC.
    J Clin Pathol Suppl (R Coll Pathol); 1972 Jun; 6():84-96. PubMed ID: 4218244
    [No Abstract] [Full Text] [Related]

  • 24. Unusual resistance to ionizing radiation of the viruses of kuru, Creutzfeldt-Jakob disease, and scrapie.
    Gibbs CJ, Gajdusek DC, Latarjet R.
    Proc Natl Acad Sci U S A; 1978 Dec; 75(12):6268-70. PubMed ID: 104301
    [Abstract] [Full Text] [Related]

  • 25.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 26.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 27.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 28. A new point mutation of the prion protein gene in Creutzfeldt-Jakob disease.
    Pocchiari M, Salvatore M, Cutruzzolá F, Genuardi M, Allocatelli CT, Masullo C, Macchi G, Alemá G, Galgani S, Xi YG.
    Ann Neurol; 1993 Dec; 34(6):802-7. PubMed ID: 7902693
    [Abstract] [Full Text] [Related]

  • 29.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 30.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 31.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 32.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 33. [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
    [Abstract] [Full Text] [Related]

  • 34.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 35.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 36.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 37.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 38. [Familial Creutzfeldt-Jakob disease with the heterozygous point mutation at codon 200 of the prion protein gene (Glu-->Lys)--report of CJD200 brothers of Yamanashi Prefecture origin].
    Kawauchi Y, Okada M, Kuroiwa Y, Ishihara O, Akai J.
    No To Shinkei; 1997 May; 49(5):460-4. PubMed ID: 9163760
    [Abstract] [Full Text] [Related]

  • 39. Prion encephalopathies of animals and humans.
    Prusiner SB.
    Dev Biol Stand; 1993 May; 80():31-44. PubMed ID: 8270114
    [Abstract] [Full Text] [Related]

  • 40. [Clinical features of familial Creutzfeldt-Jakob disease and the E200K mutation in Spain].
    Morgado-Linares RY, Ruiz-Peña JL, Páramo MD, Díaz-Delgado M, Izquierdo G.
    Rev Neurol; 1993 May; 44(3):150-3. PubMed ID: 17285519
    [Abstract] [Full Text] [Related]


    Page: [Previous] [Next] [New Search]
    of 5.