163 related articles for article (PubMed ID: 18409537)
1. [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]
2. [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]
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. 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]
5. [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]
6. Clinical Variability in P102L Gerstmann-Sträussler-Scheinker Syndrome.
Tesar A; Matej R; Kukal J; Johanidesova S; Rektorova I; Vyhnalek M; Keller J; Eliasova I; Parobkova E; Smetakova M; Musova Z; Rusina R
Ann Neurol; 2019 Nov; 86(5):643-652. PubMed ID: 31397917
[TBL] [Abstract][Full Text] [Related]
7. [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]
8. Gerstmann-Sträussler-Scheinker syndrome with the P102L pathogenic mutation presenting as familial Creutzfeldt-Jakob disease: a case report and review of the literature.
Rusina R; Fiala J; Holada K; Matějčková M; Nováková J; Ampapa R; Koukolík F; Matěj R
Neurocase; 2013; 19(1):41-53. PubMed ID: 22494260
[TBL] [Abstract][Full Text] [Related]
9. A Chinese patient of P102L Gerstmann-Sträussler-Scheinker disease contains three other disease-associated mutations in SYNE1.
Wang J; Xiao K; Zhou W; Gao C; Chen C; Shi Q; Dong XP
Prion; 2018 Mar; 12(2):150-155. PubMed ID: 29509064
[TBL] [Abstract][Full Text] [Related]
10. [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]
11. 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]
12. 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]
13. 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]
14. 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]
15. [A case of Gerstmann-Sträussler-Scheinker disease presented with numbness in the lower extremities].
Ando R; Nagai M; Iwaki H; Yabe H; Nishikawa N; Nomoto M
Rinsho Shinkeigaku; 2016; 56(1):7-11. PubMed ID: 26616483
[TBL] [Abstract][Full Text] [Related]
16. Early neurophysiological biomarkers and spinal cord pathology in inherited prion disease.
Rudge P; Jaunmuktane Z; Hyare H; Ellis M; Koltzenburg M; Collinge J; Brandner S; Mead S
Brain; 2019 Mar; 142(3):760-770. PubMed ID: 30698738
[TBL] [Abstract][Full Text] [Related]
17. [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]
18. Gerstmann-Straeussler-Scheinker disease with P102L prion protein gene mutation presenting with rapidly progressive clinical course.
Iwasaki Y; Mori K; Ito M; Nokura K; Tatsumi S; Mimuro M; Kitamoto T; Yoshida M
Clin Neuropathol; 2014; 33(5):344-53. PubMed ID: 24986180
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Different patterns of truncated prion protein fragments correlate with distinct phenotypes in P102L Gerstmann-Sträussler-Scheinker disease.
Parchi P; Chen SG; Brown P; Zou W; Capellari S; Budka H; Hainfellner J; Reyes PF; Golden GT; Hauw JJ; Gajdusek DC; Gambetti P
Proc Natl Acad Sci U S A; 1998 Jul; 95(14):8322-7. PubMed ID: 9653185
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
