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

PUBMED FOR HANDHELDS

Journal Abstract Search

222 related items for PubMed ID: 10371520

  • 1. A subtype of sporadic prion disease mimicking fatal familial insomnia.
    Parchi P, Capellari S, Chin S, Schwarz HB, Schecter NP, Butts JD, Hudkins P, Burns DK, Powers JM, Gambetti P.
    Neurology; 1999 Jun 10; 52(9):1757-63. PubMed ID: 10371520
    [Abstract] [Full Text] [Related]

  • 2. Fatal familial insomnia and sporadic fatal insomnia.
    Cracco L, Appleby BS, Gambetti P.
    Handb Clin Neurol; 2018 Jun 10; 153():271-299. PubMed ID: 29887141
    [Abstract] [Full Text] [Related]

  • 3. Conclusions of the symposium.
    Gambetti P, Lugaresi E.
    Brain Pathol; 1998 Jul 10; 8(3):571-5. PubMed ID: 9669714
    [Abstract] [Full Text] [Related]

  • 4. Association of prion protein genotype and scrapie prion protein type with cellular prion protein charge isoform profiles in cerebrospinal fluid of humans with sporadic or familial prion diseases.
    Schmitz M, Lüllmann K, Zafar S, Ebert E, Wohlhage M, Oikonomou P, Schlomm M, Mitrova E, Beekes M, Zerr I.
    Neurobiol Aging; 2014 May 10; 35(5):1177-88. PubMed ID: 24360565
    [Abstract] [Full Text] [Related]

  • 5. [Fatal familial insomnia].
    Delisle MB, Uro-Coste E, Gray F, Vital C.
    Clin Exp Pathol; 1999 May 10; 47(3-4):176-80. PubMed ID: 10472737
    [Abstract] [Full Text] [Related]

  • 6. Fatal familial insomnia: clinical features and molecular genetics.
    Cortelli P, Gambetti P, Montagna P, Lugaresi E.
    J Sleep Res; 1999 Jun 10; 8 Suppl 1():23-9. PubMed ID: 10389103
    [Abstract] [Full Text] [Related]

  • 7. Fatal familial insomnia and familial Creutzfeldt-Jakob disease: clinical, pathological and molecular features.
    Gambetti P, Parchi P, Petersen RB, Chen SG, Lugaresi E.
    Brain Pathol; 1995 Jan 10; 5(1):43-51. PubMed ID: 7767490
    [Abstract] [Full Text] [Related]

  • 8. Familial fatal insomnia with atypical clinical features in a patient with D178N mutation and homozygosity for Met at codon 129 of the prion protein gene.
    Sun L, Li X, Lin X, Yan F, Chen K, Xiao S.
    Prion; 2015 Jan 10; 9(3):228-35. PubMed ID: 26074146
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. Hereditary Creutzfeldt-Jakob disease and fatal familial insomnia.
    Gambetti P, Parchi P, Chen SG.
    Clin Lab Med; 2003 Mar 10; 23(1):43-64. PubMed ID: 12733424
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. The D178N (cis-129M) "fatal familial insomnia" mutation associated with diverse clinicopathologic phenotypes in an Australian kindred.
    McLean CA, Storey E, Gardner RJ, Tannenberg AE, Cervenáková L, Brown P.
    Neurology; 1997 Aug 10; 49(2):552-8. PubMed ID: 9270595
    [Abstract] [Full Text] [Related]

  • 14. Identification of new molecular alterations in fatal familial insomnia.
    Llorens F, Thüne K, Schmitz M, Ansoleaga B, Frau-Méndez MA, Cramm M, Tahir W, Gotzmann N, Berjaoui S, Carmona M, Silva CJ, Fernandez-Vega I, José Zarranz J, Zerr I, Ferrer I.
    Hum Mol Genet; 2016 Jun 15; 25(12):2417-2436. PubMed ID: 27056979
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene.
    Medori R, Tritschler HJ, LeBlanc A, Villare F, Manetto V, Chen HY, Xue R, Leal S, Montagna P, Cortelli P.
    N Engl J Med; 1992 Feb 13; 326(7):444-9. PubMed ID: 1346338
    [Abstract] [Full Text] [Related]

  • 17. Fatal insomnia in a case of familial Creutzfeldt-Jakob disease with the codon 200(Lys) mutation.
    Chapman J, Arlazoroff A, Goldfarb LG, Cervenakova L, Neufeld MY, Werber E, Herbert M, Brown P, Gajdusek DC, Korczyn AD.
    Neurology; 1996 Mar 13; 46(3):758-61. PubMed ID: 8618678
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 12.