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Journal Abstract Search

111 related items for PubMed ID: 27051017

  • 1. Association between a point mutation at the -743-bp region of the transthyretin (TTR) gene and familial vitreous amyloidosis.
    Nie XM, Cai SJ, Xie B, Chen XW, Jiang M.
    Genet Mol Res; 2016 Mar 31; 15(1):. PubMed ID: 27051017
    [Abstract] [Full Text] [Related]

  • 2. A new Arg54Gly transthyretin gene mutation associated with vitreous amyloidosis in Chinese.
    Shi Y, Li J, Hu J, Hu J, Sun L, Li H, Shi R, Yang L, Sun Y, Li C.
    Eye Sci; 2011 Dec 31; 26(4):230-8. PubMed ID: 22187309
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  • 3. [Identification of a TTR gene mutation in a family with hereditary vitreous amyloidosis].
    Xie Y, Zhao Y, Zhou JJ, Wang X.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Feb 31; 29(1):13-5. PubMed ID: 22311483
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  • 4. Mutation p.G83R in the transthyretin gene is associated with hereditary vitreous amyloidosis in Han Chinese families.
    Zhang AM, Wang H, Sun P, Hu QX, He Y, Yao YG.
    Mol Vis; 2013 Feb 31; 19():1631-8. PubMed ID: 23901247
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  • 5. A novel transthyretin Lys70Glu (p.Lys90Glu) mutation presenting with vitreous amyloidosis and carpal tunnel syndrome.
    Raivio VE, Jonasson J, Myllykangas L, Ala-Mello S, Kankuri-Tammilehto M, Kiuru-Enari S, Westermark P, Tanskanen M, Kivelä T.
    Amyloid; 2016 Feb 31; 23(1):46-50. PubMed ID: 26828956
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  • 6. Transthyretin Ala36Pro mutation in a Chinese pedigree of familial transthyretin amyloidosis with elevated vitreous and serum vascular endothelial growth factor.
    Zou X, Dong F, Zhang S, Tian R, Sui R.
    Exp Eye Res; 2013 May 31; 110():44-9. PubMed ID: 23438977
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  • 8. Transthyretin-related hereditary amyloidosis in a Chinese family with TTR Y114C mutation.
    Zhang Y, Deng YL, Ma JF, Zheng L, Hong Z, Wang ZQ, Sheng CY, Xiao Q, Cao L, Chen SD.
    Neurodegener Dis; 2011 May 31; 8(4):187-93. PubMed ID: 21135536
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  • 10. Oculoleptomeningeal amyloidosis in a large kindred with a new transthyretin variant Tyr69His.
    Blevins G, Macaulay R, Harder S, Fladeland D, Yamashita T, Yazaki M, Hamidi Asl K, Benson MD, Donat JR.
    Neurology; 2003 May 27; 60(10):1625-30. PubMed ID: 12771253
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  • 12. Familial vitreous amyloidosis resulting from transthyretin variant Gly83Arg.
    Xie B, Cai SJ, Jiang M, Li H, Su G.
    Acta Ophthalmol; 2017 Sep 27; 95(6):e520-e521. PubMed ID: 28266151
    [No Abstract] [Full Text] [Related]

  • 13. Early onset aggressive hereditary amyloidosis: report of an Italian family with TTR Arg47 mutation.
    Salvi F, Pastorelli F, Plasmati R, Ferlini A, Grazi GL, Jovine E, Mascalchi M, Tassinari CA.
    Neurol Sci; 2005 Jun 27; 26(2):140-2. PubMed ID: 15995833
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  • 18. Familial leptomeningeal amyloidosis with a transthyretin variant Asp18Gly representing repeated subarachnoid haemorrhages with superficial siderosis.
    Jin K, Sato S, Takahashi T, Nakazaki H, Date Y, Nakazato M, Tominaga T, Itoyama Y, Ikeda S.
    J Neurol Neurosurg Psychiatry; 2004 Oct 27; 75(10):1463-6. PubMed ID: 15377697
    [Abstract] [Full Text] [Related]

  • 19. Biochemical characteristics of variant transthyretins causing hereditary leptomeningeal amyloidosis.
    Mitsuhashi S, Yazaki M, Tokuda T, Sekijima Y, Washimi Y, Shimizu Y, Ando Y, Benson MD, Ikeda S.
    Amyloid; 2005 Dec 27; 12(4):216-25. PubMed ID: 16399646
    [Abstract] [Full Text] [Related]

  • 20. Laboratory assessment of transthyretin amyloidosis.
    Benson MD, Yazaki M, Magy N.
    Clin Chem Lab Med; 2002 Dec 27; 40(12):1262-5. PubMed ID: 12553428
    [Abstract] [Full Text] [Related]

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