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139 related items for PubMed ID: 37302168
1. Sleep in Gerstmann-Straüssler-Scheinker disease. Pérez-Carbonell L, Sarto J, Gaig C, Muñoz-Lopetegi A, Ruiz-García R, Naranjo L, Augé JM, Perissinotti A, Santamaria J, Iranzo A, Sánchez-Valle R. Sleep Med; 2023 Aug; 108():11-15. PubMed ID: 37302168 [Abstract] [Full Text] [Related]
2. Sleep and temperature rhythms in two sisters with P102L Gerstmann-Sträussler-Scheinker (GSS) disease. Provini F, Vetrugno R, Pierangeli G, Cortelli P, Rizzo G, Filla A, Strisciuglio C, Gallassi R, Montagna P. Sleep Med; 2009 Mar; 10(3):374-7. PubMed ID: 18550428 [Abstract] [Full Text] [Related]
3. [Creutzfeldt-Jakob disease(CJD) and Gerstmann-Sträussler-Scheinker syndrome(GSS)]. Udaka F, Fujisawa M, Kameyama M. Nihon Rinsho; 1997 Apr; 55(4):972-7. PubMed ID: 9103904 [Abstract] [Full Text] [Related]
4. Gerstmann-Sträussler-Scheinker syndrome,fatal familial insomnia, and kuru: a review of these less common human transmissible spongiform encephalopathies. Collins S, McLean CA, Masters CL. J Clin Neurosci; 2001 Sep; 8(5):387-97. PubMed ID: 11535002 [Abstract] [Full Text] [Related]
5. First familial cases of P102L Gerstmann-Sträussler-Scheinker syndrome in South Korea: diffusion-weighted imaging might reflect intrafamilial phenotypic variability. Ahn SJ, Lee HS, Moon J, Chu K. Neurol Sci; 2022 May; 43(5):3419-3422. PubMed ID: 35129726 [Abstract] [Full Text] [Related]
6. Transgenic mice recapitulate the phenotypic heterogeneity of genetic prion diseases without developing prion infectivity: Role of intracellular PrP retention in neurotoxicity. Chiesa R, Restelli E, Comerio L, Del Gallo F, Imeri L. Prion; 2016 Mar 03; 10(2):93-102. PubMed ID: 26864450 [Abstract] [Full Text] [Related]
7. Clinical Variability in P102L Gerstmann-Sträussler-Scheinker Syndrome. Tesar A, Matej R, Kukal J, Johanidesova S, Rektorova I, Vyhnalek M, Keller J, Eliasova I, Parobkova E, Smetakova M, Musova Z, Rusina R. Ann Neurol; 2019 Nov 03; 86(5):643-652. PubMed ID: 31397917 [Abstract] [Full Text] [Related]
8. Gerstmann-Sträussler-Scheinker disease. Liberski PP. Adv Exp Med Biol; 2012 Nov 03; 724():128-37. PubMed ID: 22411239 [Abstract] [Full Text] [Related]
10. Genetic and pathological features encipher the phenotypic heterogeneity of Gerstmann-Sträussler-Scheinker disease. Chen Z, Kong Y, Zhang J, Zou WQ, Wu L. Neurobiol Dis; 2024 Jun 01; 195():106497. PubMed ID: 38583641 [Abstract] [Full Text] [Related]
11. Gerstmann-Sträussler-Scheinker Disease with F198S Mutation Induces Independent Tau and Prion Protein Pathologies in Bank Voles. Bruno R, Pirisinu L, Riccardi G, D'Agostino C, De Cecco E, Legname G, Cardone F, Gambetti P, Nonno R, Agrimi U, Di Bari MA. Biomolecules; 2022 Oct 21; 12(10):. PubMed ID: 36291746 [Abstract] [Full Text] [Related]
12. Phenotypic variability of Gerstmann-Sträussler-Scheinker disease is associated with prion protein heterogeneity. Piccardo P, Dlouhy SR, Lievens PM, Young K, Bird TD, Nochlin D, Dickson DW, Vinters HV, Zimmerman TR, Mackenzie IR, Kish SJ, Ang LC, De Carli C, Pocchiari M, Brown P, Gibbs CJ, Gajdusek DC, Bugiani O, Ironside J, Tagliavini F, Ghetti B. J Neuropathol Exp Neurol; 1998 Oct 21; 57(10):979-88. PubMed ID: 9786248 [Abstract] [Full Text] [Related]
13. Ultrastructural study of florid plaques in variant Creutzfeldt-Jakob disease: a comparison with amyloid plaques in kuru, sporadic Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker disease. Sikorska B, Liberski PP, Sobów T, Budka H, Ironside JW. Neuropathol Appl Neurobiol; 2009 Feb 21; 35(1):46-59. PubMed ID: 18513219 [Abstract] [Full Text] [Related]
14. Detection of tau in Gerstmann-Sträussler-Scheinker disease (PRNP F198S) by [18F]Flortaucipir PET. Risacher SL, Farlow MR, Bateman DR, Epperson F, Tallman EF, Richardson R, Murrell JR, Unverzagt FW, Apostolova LG, Bonnin JM, Ghetti B, Saykin AJ. Acta Neuropathol Commun; 2018 Oct 29; 6(1):114. PubMed ID: 30373672 [Abstract] [Full Text] [Related]
15. [Creutzfeldt-Jakob disease and other human transmissible spongiform encephalopathies. Part II]. Zaborowski A. Psychiatr Pol; 2004 Oct 29; 38(2):297-309. PubMed ID: 15307294 [Abstract] [Full Text] [Related]
16. Early neurophysiological biomarkers and spinal cord pathology in inherited prion disease. Rudge P, Jaunmuktane Z, Hyare H, Ellis M, Koltzenburg M, Collinge J, Brandner S, Mead S. Brain; 2019 Mar 01; 142(3):760-770. PubMed ID: 30698738 [Abstract] [Full Text] [Related]
17. Dopaminergic neurodegeneration in Gerstmann-Sträussler-Scheinker (P102L) disease: insights from imaging and pathological examination. Irie KI, Honda H, Tateishi T, Mori S, Yamamoto A, Morimitsu M, Shinsuke K, Moritaka T, Kurata S, Kumazoe H, Shijo M, Sasagasako N, Taniwaki T. Front Neurol; 2024 Mar 01; 15():1452709. PubMed ID: 39376689 [Abstract] [Full Text] [Related]
18. Generation of a new infectious recombinant prion: a model to understand Gerstmann-Sträussler-Scheinker syndrome. Elezgarai SR, Fernández-Borges N, Eraña H, Sevillano AM, Charco JM, Harrathi C, Saá P, Gil D, Kong Q, Requena JR, Andréoletti O, Castilla J. Sci Rep; 2017 Aug 29; 7(1):9584. PubMed ID: 28851967 [Abstract] [Full Text] [Related]
19. Gerstmann-Sträussler-Scheinker disease and "anchorless prion protein" mice share prion conformational properties diverging from sporadic Creutzfeldt-Jakob disease. Zanusso G, Fiorini M, Ferrari S, Meade-White K, Barbieri I, Brocchi E, Ghetti B, Monaco S. J Biol Chem; 2014 Feb 21; 289(8):4870-81. PubMed ID: 24398683 [Abstract] [Full Text] [Related]
20. Normal sleep-wake and circadian rhythms in a case of Gerstmann-Sträussler-Sheinker (GSS) disease. Pierangeli G, Bono F, Aguglia U, Maltoni P, Montagna P, Lugaresi E, Quattrone A, Cortelli P. Clin Auton Res; 2004 Feb 21; 14(1):39-41. PubMed ID: 15045600 [Abstract] [Full Text] [Related] Page: [Next] [New Search]