247 related articles for article (PubMed ID: 10472736)
1. Gerstmann-Sträussler-Scheinker disease and the French-Alsatian A117V variant.
Mohr M; Tranchant C; Steinmetz G; Floquet J; Grignon Y; Warter JM
Clin Exp Pathol; 1999; 47(3-4):161-75. PubMed ID: 10472736
[TBL] [Abstract][Full Text] [Related]
2. [Gerstmann-Straüssler-Scheinker syndrome].
Tranchant C; Warter JM
Rev Neurol (Paris); 1998 Feb; 154(2):152-7. PubMed ID: 9773036
[TBL] [Abstract][Full Text] [Related]
3. Gerstmann-Sträussler-Scheinker disease with A117V mutation in a second French-Alsatian family.
Heldt N; Boellaard JW; Brown P; Cervenákova L; Doerr-Schott J; Thomas C; Scherer C; Rohmer F
Clin Neuropathol; 1998; 17(4):229-34. PubMed ID: 9707339
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. 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
[TBL] [Abstract][Full Text] [Related]
7. [Mutation of codon 117 of the prion gene in Gerstmann-Sträussler-Scheinker disease].
Tranchant C; Doh-Ura K; Steinmetz G; Chevalier Y; Kitamoto T; Tateishi J; Warter JM
Rev Neurol (Paris); 1991; 147(4):274-8. PubMed ID: 2063076
[TBL] [Abstract][Full Text] [Related]
8. Familial spongiform encephalopathy associated with a novel prion protein gene mutation.
Nitrini R; Rosemberg S; Passos-Bueno MR; da Silva LS; Iughetti P; Papadopoulos M; Carrilho PM; Caramelli P; Albrecht S; Zatz M; LeBlanc A
Ann Neurol; 1997 Aug; 42(2):138-46. PubMed ID: 9266722
[TBL] [Abstract][Full Text] [Related]
9. [Gerstmann-Sträussler-Scheinker disease. Pathologal and genetic study].
Genthon R; Gray F; Salama J; Duyckaerts C; Belin C; Brucher JM; Baron H; Delaporte P
Rev Neurol (Paris); 1992; 148(5):335-42. PubMed ID: 1448647
[TBL] [Abstract][Full Text] [Related]
10. Linkage of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease to the prion protein gene.
Dlouhy SR; Hsiao K; Farlow MR; Foroud T; Conneally PM; Johnson P; Prusiner SB; Hodes ME; Ghetti B
Nat Genet; 1992 Apr; 1(1):64-7. PubMed ID: 1363809
[TBL] [Abstract][Full Text] [Related]
11. A second case of Gerstmann-Sträussler-Scheinker disease linked to the G131V mutation in the prion protein gene in a Dutch patient.
Jansen C; Parchi P; Capellari S; Strammiello R; Dopper EG; van Swieten JC; Kamphorst W; Rozemuller AJ
J Neuropathol Exp Neurol; 2011 Aug; 70(8):698-702. PubMed ID: 21760536
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Gerstmann-Sträussler-Scheinker: a new phenotype with 'curly' PrP deposits.
Colucci M; Moleres FJ; Xie ZL; Ray-Chaudhury A; Gutti S; Butefisch CM; Cervenakova L; Wang W; Goldfarb LG; Kong Q; Ghetti B; Chen SG; Gambetti P
J Neuropathol Exp Neurol; 2006 Jul; 65(7):642-51. PubMed ID: 16825951
[TBL] [Abstract][Full Text] [Related]
14. Neurofibrillary tangles in Gerstmann-Sträussler-Scheinker syndrome with the A117V prion gene mutation.
Tranchant C; Sergeant N; Wattez A; Mohr M; Warter JM; Delacourte A
J Neurol Neurosurg Psychiatry; 1997 Aug; 63(2):240-6. PubMed ID: 9285466
[TBL] [Abstract][Full Text] [Related]
15. Gerstmann-Sträussler-Scheinker disease: immunohistological and experimental studies.
Tateishi J; Kitamoto T; Hashiguchi H; Shii H
Ann Neurol; 1988 Jul; 24(1):35-40. PubMed ID: 3046469
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Gerstmann-Sträussler-Scheinker disease.
Liberski PP
Adv Exp Med Biol; 2012; 724():128-37. PubMed ID: 22411239
[TBL] [Abstract][Full Text] [Related]
18. Gerstmann-Sträussler-Scheinker disease- the dilemma of molecular and clinical correlations.
Boellaard JW; Brown P; Tateishi J
Clin Neuropathol; 1999; 18(6):271-85. PubMed ID: 10580553
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]
