142 related articles for article (PubMed ID: 11071439)
1. Proton magnetic resonance spectroscopy of a patient with Gerstmann-Straussler-Scheinker disease.
Konaka K; Kaido M; Okuda Y; Aoike F; Abe K; Kitamoto T; Yanagihara T
Neuroradiology; 2000 Sep; 42(9):662-5. PubMed ID: 11071439
[TBL] [Abstract][Full Text] [Related]
2. Atypical frontotemporal dementia as a new clinical phenotype of Gerstmann-Straussler-Scheinker disease with the PrP-P102L mutation. Description of a previously unreported Italian family.
Giovagnoli AR; Di Fede G; Aresi A; Reati F; Rossi G; Tagliavini F
Neurol Sci; 2008 Dec; 29(6):405-10. PubMed ID: 19030774
[TBL] [Abstract][Full Text] [Related]
3. Serial changes in regional cerebral blood flow in Gerstmann-Sträussler-Scheinker disease caused by a Pro-to-Leu mutation at codon 105 in the prion protein gene.
Kawai H; Matsubayashi T; Yokota T; Sanjo N
Prion; 2023 Dec; 17(1):138-140. PubMed ID: 37705331
[TBL] [Abstract][Full Text] [Related]
4. [Gerstmann-Sträussler-Scheinker disease with heterozygous codon change at prion protein codon 129].
Terao Y; Hitoshi S; Shimizu J; Sakuta M; Kitamoto T
Rinsho Shinkeigaku; 1992 Aug; 32(8):880-3. PubMed ID: 1490317
[TBL] [Abstract][Full Text] [Related]
5. [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]
6. [Gerstmann-Sträussler-Scheinker syndrome with a Pro102Leu mutation in the prion protein gene and atypical MRI findings, hyperthermia, tachycardia, and hyperhidrosis].
Imaiso Y; Mitsuo K
Rinsho Shinkeigaku; 1998; 38(10-11):920-5. PubMed ID: 10203975
[TBL] [Abstract][Full Text] [Related]
7. [Case of Gerstmann-Sträussler-Scheinker syndrome (GSS-P102L) mimicking variant Creurtzfeldt-Jakob disease in clinical manifestation and MRI findings].
Kanata A; Saigoh K; Mitsui Y; Kitamoto T; Kusunoki S
Rinsho Shinkeigaku; 2008 Mar; 48(3):179-83. PubMed ID: 18409537
[TBL] [Abstract][Full Text] [Related]
8. Quantitative, functional MRI and neurophysiological markers in a case of Gerstmann-Sträussler-Scheinker syndrome.
Marino S; Morabito R; De Salvo S; Bonanno L; Bramanti A; Pollicino P; Giorgianni R; Bramanti P
Funct Neurol; 2017; 32(3):153-158. PubMed ID: 29042004
[TBL] [Abstract][Full Text] [Related]
9. A distinct phenotype of leg hyperreflexia in a Japanese family with Gerstmann-Sträussler-Scheinker syndrome (P102L).
Takazawa T; Ikeda K; Ito H; Aoyagi J; Nakamura Y; Miura K; Iwamoto K; Kano O; Kawabe K; Iwasaki Y
Intern Med; 2010; 49(4):339-42. PubMed ID: 20154442
[TBL] [Abstract][Full Text] [Related]
10. Variable phenotype in a P102L Gerstmann-Sträussler-Scheinker Italian family.
De Michele G; Pocchiari M; Petraroli R; Manfredi M; Caneve G; Coppola G; Casali C; Saccà F; Piccardo P; Salvatore E; Berardelli A; Orio M; Barbieri F; Ghetti B; Filla A
Can J Neurol Sci; 2003 Aug; 30(3):233-6. PubMed ID: 12945948
[TBL] [Abstract][Full Text] [Related]
11. An Israeli family with Gerstmann-Sträussler-Scheinker disease manifesting the codon 102 mutation in the prion protein gene.
Goldhammer Y; Gabizon R; Meiner Z; Sadeh M
Neurology; 1993 Dec; 43(12):2718-9. PubMed ID: 7902971
[TBL] [Abstract][Full Text] [Related]
12. [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]
13. Thalamic involvement determined using VSRAD advance on MRI and easy Z-score analysis of
Sugiyama A; Sato N; Kimura Y; Maekawa T; Wakasugi N; Sone D; Enokizono M; Takahashi Y; Murata M; Mizusawa H; Matsuda H
J Neurol Sci; 2017 Feb; 373():27-30. PubMed ID: 28131204
[TBL] [Abstract][Full Text] [Related]
14. A variant of Gerstmann-Sträussler-Scheinker disease carrying codon 105 mutation with codon 129 polymorphism of the prion protein gene: a clinicopathological study.
Itoh Y; Yamada M; Hayakawa M; Shozawa T; Tanaka J; Matsushita M; Kitamoto T; Tateishi J; Otomo E
J Neurol Sci; 1994 Dec; 127(1):77-86. PubMed ID: 7699395
[TBL] [Abstract][Full Text] [Related]
15. A family with mental disorder as the first symptom finally confirmed with Gerstmann-Sträussler-Scheinker disease with P102L mutation in PRNP gene - case report.
Chen Z; Guo J; Ran N; Zhong Y; Yang F; Sun H
Prion; 2023 Dec; 17(1):37-43. PubMed ID: 36847171
[TBL] [Abstract][Full Text] [Related]
16. [Familial prion disease (GSS, familial CJD, FFI)].
Arata H; Takashima H
Nihon Rinsho; 2007 Aug; 65(8):1433-7. PubMed ID: 17695280
[TBL] [Abstract][Full Text] [Related]
17. A case of Gerstmann-Sträussler-Scheinker syndrome.
Irisawa M; Amanuma M; Kozawa E; Kimura F; Araki N
Magn Reson Med Sci; 2007; 6(1):53-7. PubMed ID: 17510542
[TBL] [Abstract][Full Text] [Related]
18. Prion protein mutation at codon 102 in an Italian family with Gerstmann-Sträussler-Scheinker syndrome.
Kretzschmar HA; Kufer P; Riethmüller G; DeArmond S; Prusiner SB; Schiffer D
Neurology; 1992 Apr; 42(4):809-10. PubMed ID: 1348851
[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 Japanese family with a variant of Gerstmann-Sträussler-Scheinker disease.
Tanaka Y; Minematsu K; Moriyasu H; Yamaguchi T; Yutani C; Kitamoto T; Furukawa H
J Neurol Neurosurg Psychiatry; 1997 May; 62(5):454-7. PubMed ID: 9153600
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]