336 related articles for article (PubMed ID: 12682740)
1. 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]
2. 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]
3. 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]
4. [Patient with Gerstmann-Striussler-Scheinker syndrome (GSS P102L) presenting high intensity lesions in the cerebral cortex on diffusion weighted MRI].
Misumi M; Nishida Y; Araki S
Rinsho Shinkeigaku; 2006 Apr; 46(4):291-3. PubMed ID: 16768100
[TBL] [Abstract][Full Text] [Related]
5. [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]
6. Divergent clinical and neuropathological phenotype in a Gerstmann-Sträussler-Scheinker P102L family.
Popova SN; Tarvainen I; Capellari S; Parchi P; Hannikainen P; Pirinen E; Haapasalo H; Alafuzoff I
Acta Neurol Scand; 2012 Nov; 126(5):315-23. PubMed ID: 22211828
[TBL] [Abstract][Full Text] [Related]
7. [A case of Gerstmann-Sträussler-Scheinker syndrome (P102L) accompanied by optic atrophy].
Sugai F; Nakamori M; Nakatsuji Y; Abe K; Sakoda S
Rinsho Shinkeigaku; 2000 Sep; 40(9):926-8. PubMed ID: 11257791
[TBL] [Abstract][Full Text] [Related]
8. Gerstmann-Sträussler-Scheinker disease.
Liberski PP
Adv Exp Med Biol; 2012; 724():128-37. PubMed ID: 22411239
[TBL] [Abstract][Full Text] [Related]
9. [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]
10. Cerebral amyloid angiopathy with co-localization of prion protein and beta-amyloid in an 85-year-old patient with sporadic Creutzfeldt-Jakob disease.
Paquet C; Privat N; Kaci R; Polivka M; Dupont O; Haïk S; Laplanche JL; Hauw JJ; Gray F
Acta Neuropathol; 2008 Nov; 116(5):567-73. PubMed ID: 18551298
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Gerstmann-Sträussler-Scheinker syndrome with variable phenotype in a new kindred with PRNP-P102L mutation.
Riudavets MA; Sraka MA; Schultz M; Rojas E; Martinetto H; Begué C; Noher de Halac I; Poleggi A; Equestre M; Pocchiari M; Sevlever G; Taratuto AL
Brain Pathol; 2014 Mar; 24(2):142-7. PubMed ID: 23944754
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. Anesthetic management of a patient with Gerstmann-Sträussler-Scheinker syndrome (mutation of prion protein).
Nakamura M; Ogata M; Matsuo Y; Sata T
Anesth Analg; 2006 Apr; 102(4):1285-6. PubMed ID: 16551938
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. A family with hereditary cerebellar ataxia finally confirmed as Gerstmann-Straussler-Scheinker syndrome with P102L mutation in PRNP gene.
Long L; Cai X; Shu Y; Lu Z
Neurosciences (Riyadh); 2017 Apr; 22(2):138-142. PubMed ID: 28416787
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. [A case of variant Gerstmann-Sträussler-Scheinker disease with the mutation of codon P105L].
Kubo M; Nishimura T; Shikata E; Kokubun Y; Takasu T
Rinsho Shinkeigaku; 1995 Aug; 35(8):873-7. PubMed ID: 8665729
[TBL] [Abstract][Full Text] [Related]
20. A case of Gerstmann-Sträussler-Scheinker syndrome with the P105L prion protein gene mutation presenting with ataxia and extrapyramidal signs without spastic paraparesis.
Iwasaki Y; Kizawa M; Hori N; Kitamoto T; Sobue G
Clin Neurol Neurosurg; 2009 Sep; 111(7):606-9. PubMed ID: 19443103
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
