230 related articles for article (PubMed ID: 10871543)
1. Neuropathology of Gerstmann-Sträussler-Scheinker disease.
Bugiani O; Giaccone G; Piccardo P; Morbin M; Tagliavini F; Ghetti B
Microsc Res Tech; 2000 Jul; 50(1):10-5. PubMed ID: 10871543
[TBL] [Abstract][Full Text] [Related]
2. Familial Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles.
Ghetti B; Tagliavini F; Giaccone G; Bugiani O; Frangione B; Farlow MR; Dlouhy SR
Mol Neurobiol; 1994 Feb; 8(1):41-8. PubMed ID: 7916191
[TBL] [Abstract][Full Text] [Related]
3. Hereditary prion protein amyloidoses.
Ghetti B; Tagliavini F; Takao M; Bugiani O; Piccardo P
Clin Lab Med; 2003 Mar; 23(1):65-85, viii. PubMed ID: 12733425
[TBL] [Abstract][Full Text] [Related]
4. Gerstmann-Sträussler-Scheinker disease.
Liberski PP
Adv Exp Med Biol; 2012; 724():128-37. PubMed ID: 22411239
[TBL] [Abstract][Full Text] [Related]
5. Gerstmann-Sträussler-Scheinker disease. I. Human diseases.
Liberski PP; Budka H
Folia Neuropathol; 2004; 42 Suppl B():120-40. PubMed ID: 16903147
[TBL] [Abstract][Full Text] [Related]
6. Mutant prion proteins in Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles.
Hsiao K; Dlouhy SR; Farlow MR; Cass C; Da Costa M; Conneally PM; Hodes ME; Ghetti B; Prusiner SB
Nat Genet; 1992 Apr; 1(1):68-71. PubMed ID: 1363810
[TBL] [Abstract][Full Text] [Related]
7. Gerstmann-Sträussler-Scheinker disease and the Indiana kindred.
Ghetti B; Dlouhy SR; Giaccone G; Bugiani O; Frangione B; Farlow MR; Tagliavini F
Brain Pathol; 1995 Jan; 5(1):61-75. PubMed ID: 7767492
[TBL] [Abstract][Full Text] [Related]
8. Prion protein preamyloid and amyloid deposits in Gerstmann-Sträussler-Scheinker disease, Indiana kindred.
Giaccone G; Verga L; Bugiani O; Frangione B; Serban D; Prusiner SB; Farlow MR; Ghetti B; Tagliavini F
Proc Natl Acad Sci U S A; 1992 Oct; 89(19):9349-53. PubMed ID: 1357663
[TBL] [Abstract][Full Text] [Related]
9. Hyperphosphorylated tau deposition parallels prion protein burden in a case of Gerstmann-Sträussler-Scheinker syndrome P102L mutation complicated with dementia.
Ishizawa K; Komori T; Shimazu T; Yamamoto T; Kitamoto T; Shimazu K; Hirose T
Acta Neuropathol; 2002 Oct; 104(4):342-50. PubMed ID: 12200619
[TBL] [Abstract][Full Text] [Related]
10. A 7-kDa prion protein (PrP) fragment, an integral component of the PrP region required for infectivity, is the major amyloid protein in Gerstmann-Sträussler-Scheinker disease A117V.
Tagliavini F; Lievens PM; Tranchant C; Warter JM; Mohr M; Giaccone G; Perini F; Rossi G; Salmona M; Piccardo P; Ghetti B; Beavis RC; Bugiani O; Frangione B; Prelli F
J Biol Chem; 2001 Feb; 276(8):6009-15. PubMed ID: 11087738
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Gerstmann-Sträussler-Scheinker disease (PRNP P102L): amyloid deposits are best recognized by antibodies directed to epitopes in PrP region 90-165.
Piccardo P; Ghetti B; Dickson DW; Vinters HV; Giaccone G; Bugiani O; Tagliavini F; Young K; Dlouhy SR; Seiler C
J Neuropathol Exp Neurol; 1995 Nov; 54(6):790-801. PubMed ID: 7595652
[TBL] [Abstract][Full Text] [Related]
13. Beta PP participates in PrP-amyloid plaques of Gerstmann-Sträussler-Scheinker disease, Indiana kindred.
Bugiani O; Giaccone G; Verga L; Pollo B; Frangione B; Farlow MR; Tagliavini F; Ghetti B
J Neuropathol Exp Neurol; 1993 Jan; 52(1):64-70. PubMed ID: 8093899
[TBL] [Abstract][Full Text] [Related]
14. Unusual clinical and molecular-pathological profile of gerstmann-Sträussler-Scheinker disease associated with a novel PRNP mutation (V176G).
Simpson M; Johanssen V; Boyd A; Klug G; Masters CL; Li QX; Pamphlett R; McLean C; Lewis V; Collins SJ
JAMA Neurol; 2013 Sep; 70(9):1180-5. PubMed ID: 23857164
[TBL] [Abstract][Full Text] [Related]
15. Prion proteins with different conformations accumulate in Gerstmann-Sträussler-Scheinker disease caused by A117V and F198S mutations.
Piccardo P; Liepnieks JJ; William A; Dlouhy SR; Farlow MR; Young K; Nochlin D; Bird TD; Nixon RR; Ball MJ; DeCarli C; Bugiani O; Tagliavini F; Benson MD; Ghetti B
Am J Pathol; 2001 Jun; 158(6):2201-7. PubMed ID: 11395398
[TBL] [Abstract][Full Text] [Related]
16. Amyloid protein of Gerstmann-Sträussler-Scheinker disease (Indiana kindred) is an 11 kd fragment of prion protein with an N-terminal glycine at codon 58.
Tagliavini F; Prelli F; Ghiso J; Bugiani O; Serban D; Prusiner SB; Farlow MR; Ghetti B; Frangione B
EMBO J; 1991 Mar; 10(3):513-9. PubMed ID: 1672107
[TBL] [Abstract][Full Text] [Related]
17. 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; 12(10):. PubMed ID: 36291746
[TBL] [Abstract][Full Text] [Related]
18. A novel PRNP Y218N mutation in Gerstmann-Sträussler-Scheinker disease with neurofibrillary degeneration.
Alzualde A; Indakoetxea B; Ferrer I; Moreno F; Barandiaran M; Gorostidi A; Estanga A; Ruiz I; Calero M; van Leeuwen FW; Atares B; Juste R; Rodriguez-Martínez AB; López de Munain A
J Neuropathol Exp Neurol; 2010 Aug; 69(8):789-800. PubMed ID: 20613639
[TBL] [Abstract][Full Text] [Related]
19. Neuropathological features of a case with schizophrenia and prion protein gene P102L mutation before onset of Gerstmann-Sträussler-Scheinker disease.
Sasaki K; Doh-ura K; Furuta A; Nakashima S; Morisada Y; Tateishi J; Iwaki T
Acta Neuropathol; 2003 Jul; 106(1):92-6. PubMed ID: 12682740
[TBL] [Abstract][Full Text] [Related]
20. Variant Gerstmann-Sträussler syndrome with the P105L prion gene mutation: an unusual case with nigral degeneration and widespread neurofibrillary tangles.
Yamazaki M; Oyanagi K; Mori O; Kitamura S; Ohyama M; Terashi A; Kitamoto T; Katayama Y
Acta Neuropathol; 1999 Nov; 98(5):506-11. PubMed ID: 10541874
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]