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Journal Abstract Search

140 related items for PubMed ID: 21843040

  • 1. Vitreous amyloidosis in two large mainland Chinese kindreds resulting from transthyretin variant Lys35Thr and Leu55Arg.
    Long D, Zeng J, Wu LQ, Tang LS, Wang HL, Wang H.
    Ophthalmic Genet; 2012 Mar; 33(1):28-33. PubMed ID: 21843040
    [Abstract] [Full Text] [Related]

  • 2. 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; 110():44-9. PubMed ID: 23438977
    [Abstract] [Full Text] [Related]

  • 3. [Transthyretin Arg-83 mutation in vitreous amyloidosis].
    Chen L, Lü L, Zhang P, Li Y, Lin J.
    Yan Ke Xue Bao; 2008 Mar; 24(1):65-7. PubMed ID: 18709962
    [Abstract] [Full Text] [Related]

  • 4. Oculoleptomeningeal amyloidosis in a patient with a TTR Val30Gly mutation in the transthyretin gene.
    Roe RH, Fisher Y, Eagle RC, Fine HF, Cunningham ET.
    Ophthalmology; 2007 Nov; 114(11):e33-7. PubMed ID: 17980738
    [Abstract] [Full Text] [Related]

  • 5. A rare transthyretin mutation (Asp18Glu) associated with vitreous amyloid.
    Solano JM, Pulido JS, Salomao DR.
    Ophthalmic Genet; 2007 Jun; 28(2):73-5. PubMed ID: 17558848
    [Abstract] [Full Text] [Related]

  • 6. Transthyretin amyloidosis associated with a novel variant (Trp41Leu) presenting with vitreous opacities.
    Yazaki M, Connors LH, Eagle RC, Leff SR, Skinner M, Benson MD.
    Amyloid; 2002 Dec; 9(4):263-7. PubMed ID: 12557756
    [Abstract] [Full Text] [Related]

  • 7. 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 Dec; 19():1631-8. PubMed ID: 23901247
    [Abstract] [Full Text] [Related]

  • 8. 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; 26(4):230-8. PubMed ID: 22187309
    [Abstract] [Full Text] [Related]

  • 9. Ophthalmic manifestations in a Chinese family with familial amyloid polyneuropathy due to a TTR Gly83Arg mutation.
    Liu T, Zhang B, Jin X, Wang W, Lee J, Li J, Yuan H, Cheng X.
    Eye (Lond); 2014 Jan; 28(1):26-33. PubMed ID: 24113303
    [Abstract] [Full Text] [Related]

  • 10. Vitreous amyloidosis in familial amyloidotic polyneuropathy. Report of a case with the Val30Met transthyretin mutation.
    Ciulla TA, Tolentino F, Morrow JF, Dryja TP.
    Surv Ophthalmol; 1995 Jan; 40(3):197-206. PubMed ID: 8599155
    [Abstract] [Full Text] [Related]

  • 11. A new transthyretin mutation associated with amyloidotic vitreous opacities. Asparagine for isoleucine at position 84.
    Skinner M, Harding J, Skare I, Jones LA, Cohen AS, Milunsky A, Skare J.
    Ophthalmology; 1992 Apr; 99(4):503-8. PubMed ID: 1350083
    [Abstract] [Full Text] [Related]

  • 12. Transthyretin Ser-44 mutation in a case with vitreous amyloidosis.
    Murakami A, Fujiki K, Hasegawa S, Imamura S, Kawano H, Kanai A, Matsumoto T.
    Am J Ophthalmol; 2002 Feb; 133(2):272-3. PubMed ID: 11812437
    [Abstract] [Full Text] [Related]

  • 13. 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
    [Abstract] [Full Text] [Related]

  • 14. Vitreous Amyloidosis: Ocular, Systemic, and Genetic Insights.
    Venkatesh P, Selvan H, Singh SB, Gupta D, Kashyap S, Temkar S, Gogia V, Tripathy K, Chawla R, Vohra R.
    Ophthalmology; 2017 Jul 27; 124(7):1014-1022. PubMed ID: 28412068
    [Abstract] [Full Text] [Related]

  • 15. Unusual Vitreous Opacity in a Chinese Patient.
    Yu S, Xu Y, Liang X.
    JAMA Ophthalmol; 2019 Dec 01; 137(12):1454-1455. PubMed ID: 31621813
    [No Abstract] [Full Text] [Related]

  • 16. Vitreous amyloidosis associated with homozygosity for the transthyretin methionine-30 gene.
    Sandgren O, Holmgren G, Lundgren E.
    Arch Ophthalmol; 1990 Nov 01; 108(11):1584-6. PubMed ID: 1978774
    [Abstract] [Full Text] [Related]

  • 17. Transthyretin-related TTR hereditary amyloidosis of the vitreous body. Clinical and molecular characterization in two Italian families.
    Salvi F, Salvi G, Volpe R, Mencucci R, Plasmati R, Michelucci R, Gobbi P, Santangelo M, Ferlini A, Forabosco A.
    Ophthalmic Paediatr Genet; 1993 Mar 01; 14(1):9-16. PubMed ID: 8345958
    [Abstract] [Full Text] [Related]

  • 18. A mouse model of a novel missense mutation (Gly83Arg) in a Chinese kindred manifesting vitreous amyloidosis only.
    Ran LX, Zheng ZY, Xie B, Nie XM, Chen XW, Su G, Cai SJ.
    Exp Eye Res; 2018 Apr 01; 169():13-19. PubMed ID: 29360446
    [Abstract] [Full Text] [Related]

  • 19. Isolated vitreoretinal amyloidosis in the absence of transthyretin mutations.
    Barouch FC, Benson MD, Mukai S.
    Arch Ophthalmol; 2004 Jan 01; 122(1):123-5. PubMed ID: 14718311
    [No Abstract] [Full Text] [Related]

  • 20. Immunostaining images of vitreous transthyretin amyloid.
    Latasiewicz M, Adan A, Solé M.
    Can J Ophthalmol; 2015 Oct 01; 50(5):384-7. PubMed ID: 26455975
    [Abstract] [Full Text] [Related]

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