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Journal Abstract Search

232 related items for 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
    [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
    [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
    [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
    [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
    [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 Sep; 38(10-11):920-5. PubMed ID: 10203975
    [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
    [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 Sep; 147(4):274-8. PubMed ID: 2063076
    [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 Sep; 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
    [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
    [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
    [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
    [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
    [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
    [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
    [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
    [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 Dec; 6():7. PubMed ID: 31890235
    [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 15; 302(1-2):85-8. PubMed ID: 21167505
    [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 15; 28(2):241-4. PubMed ID: 23436635
    [Abstract] [Full Text] [Related]

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