238 related articles for article (PubMed ID: 11186913)
1. [A case of Gerstmann-Sträussler-Scheinker disease with severe muscular atrophy and vertical gaze palsy].
Oba N; Fujimoto Y; Hirata K; Ando N; Saida K
Rinsho Shinkeigaku; 2000 Jul; 40(7):726-31. PubMed ID: 11186913
[TBL] [Abstract][Full Text] [Related]
2. [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]
3. [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]
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. [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]
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. 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]
8. [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]
9. [Conference at the Salpêtrière. June 1989. Progressive instability of gait, dysphagia and dysphonia, paraparesis with amyotrophy and mental deterioration in a 56-year-old man].
Collard M; Bakchine S; Duyckaerts C
Rev Neurol (Paris); 1991; 147(4):323-8. PubMed ID: 2063085
[No Abstract] [Full Text] [Related]
10. [A case of Gerstmann-Sträussler-Scheinker syndrome (GSS) with late onset--a haplotype analysis of Glu219Lys polymorphism in PrP gene].
Takase K; Furuya H; Murai H; Yamada T; Oh-yagi Y; Doh-ura K; Iwaki T; Tobimatsu S; Kira J
Rinsho Shinkeigaku; 2001 Jun; 41(6):318-21. PubMed ID: 11771163
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. 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]
14. [A 70-year-old man with a progressive gait disturbance and gaze palsy].
Nakamura T; Yoritaka A; Sumino S; Suzuki H; Mori H; Suda K; Takubo H; Mizuno Y
No To Shinkei; 1997 Jan; 49(1):93-100. PubMed ID: 9027910
[TBL] [Abstract][Full Text] [Related]
15. Neuropsychological function in patients with Gerstmann-Sträussler-Scheinker disease from the Indiana kindred (F198S).
Unverzagt FW; Farlow MR; Norton J; Dlouhy SR; Young K; Ghetti B
J Int Neuropsychol Soc; 1997 Mar; 3(2):169-78. PubMed ID: 9126858
[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. 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]
18. A case of Gerstmann-Straussler-Scheinker (GSS) disease with supranuclear gaze palsy.
Ufkes NA; Woodard C; Dale ML
J Clin Mov Disord; 2019; 6():7. PubMed ID: 31890235
[TBL] [Abstract][Full Text] [Related]
19. Lower limb areflexia without central and peripheral conduction abnormalities is highly suggestive of Gerstmann-Sträussler-Scheinker disease Pro102Leu.
Salsano E; Fancellu R; Di Fede G; Ciano C; Scaioli V; Nanetti L; Politi LS; Tagliavini F; Mariotti C; Pareyson D
J Neurol Sci; 2011 Mar; 302(1-2):85-8. PubMed ID: 21167505
[TBL] [Abstract][Full Text] [Related]
20. Atypical parkinsonism due to a D202N Gerstmann-Sträussler-Scheinker prion protein mutation: first in vivo diagnosed case.
Plate A; Benninghoff J; Jansen GH; Wlasich E; Eigenbrod S; Drzezga A; Jansen NL; Kretzschmar HA; Bötzel K; Rujescu D; Danek A
Mov Disord; 2013 Feb; 28(2):241-4. PubMed ID: 23436635
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]