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Journal Abstract Search

71 related items for PubMed ID: 100844

  • 1. [Familial Creutzfeldt-Jakob disease. A clinical and pathological study of three cases in a family with eight affected members in three generations (author's transl)].
    Buge A, Escourolle R, Brion S, Rancurel G, Hauw JJ, Mehaut M, Gray F, Gajdusek DC.
    Rev Neurol (Paris); 1978 Mar; 134(3):165-81. PubMed ID: 100844
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  • 2. [Experimental transmission of Creutzfeldt-Jakob disease to the guinea pig (author's transl)].
    Gálvez S, Gajdusek DC, Masters CL.
    Rev Med Chil; 1980 Apr; 108(4):299-303. PubMed ID: 7001596
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  • 3. Familial Creutzfeldt-Jakob disease: three autopsy cases of the panencephalopathic type.
    Seno H, Ishino H, Inagaki T, Yamamori C, Iijima M, Tanaka S, Kobayashi S, Shimizu Y, Torii I, Harada T.
    Clin Neuropathol; 1994 Apr; 13(4):185-91. PubMed ID: 7955663
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  • 4. [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; 1994 Apr; 44(3):150-3. PubMed ID: 17285519
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  • 8. Prophylactic Oophorectomy: Reducing the U.S. Death Rate from Epithelial Ovarian Cancer. A Continuing Debate.
    Piver MS.
    Oncologist; 1996 Apr; 1(5):326-330. PubMed ID: 10388011
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  • 11. Creutzfeldt-Jakob disease of long duration: clinicopathological characteristics, transmissibility, and differential diagnosis.
    Brown P, Rodgers-Johnson P, Cathala F, Gibbs CJ, Gajdusek DC.
    Ann Neurol; 1984 Sep; 16(3):295-304. PubMed ID: 6385823
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  • 12. Autophagy is a part of ultrastructural synaptic pathology in Creutzfeldt-Jakob disease: a brain biopsy study.
    Sikorska B, Liberski PP, Giraud P, Kopp N, Brown P.
    Int J Biochem Cell Biol; 2004 Dec; 36(12):2563-73. PubMed ID: 15325593
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  • 14. Creutzfeldt-Jakob disease in France: II. Clinical characteristics of 124 consecutive verified cases during the decade 1968--1977.
    Brown P, Cathala F, Sadowsky D, Gajdusek DC.
    Ann Neurol; 1979 Nov; 6(5):430-7. PubMed ID: 391141
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  • 15. Familial myoclonic dementia masquerading as Creutzfeldt-Jakob disease.
    Little BW, Brown PW, Rodgers-Johnson P, Perl DP, Gajdusek DC.
    Ann Neurol; 1986 Aug; 20(2):231-9. PubMed ID: 3530120
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  • 16. Familial Creutzfeldt-Jakob disease with extensive degeneration of white matter. Ultrastructure of peripheral nerve.
    Vallat JM, Dumas M, Corvisier N, Leboutet MJ, Loubet A, Dumas P, Cathala F.
    J Neurol Sci; 1983 Oct; 61(2):261-75. PubMed ID: 6358417
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  • 18. Gerstmann-Sträussler-Scheinker disease with coincidental familial onset.
    Hudson AJ, Farrell MA, Kalnins R, Kaufmann JC.
    Ann Neurol; 1983 Dec; 14(6):670-8. PubMed ID: 6360030
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  • 20. Familial Ménière's disease in five generations.
    Frykholm C, Larsen HC, Dahl N, Klar J, Rask-Andersen H, Friberg U.
    Otol Neurotol; 2006 Aug; 27(5):681-6. PubMed ID: 16868516
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