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Journal Abstract Search

160 related items for PubMed ID: 23438977

  • 1. 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]

  • 2. 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]

  • 3. Early onset vitreous amyloidosis in familial amyloidotic polyneuropathy with a transthyretin Glu54Gly mutation is associated with elevated vitreous VEGF.
    O'Hearn TM, Fawzi A, He S, Rao NA, Lim JI.
    Br J Ophthalmol; 2007 Dec; 91(12):1607-9. PubMed ID: 17522146
    [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. 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; 124(7):1014-1022. PubMed ID: 28412068
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. 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]

  • 8. Multimodal retinal imaging in a Chinese kindred with familial amyloid polyneuropathy secondary to transthyretin Ile107Met mutation.
    Lv W, Chen J, Chen W, Hou P, Pang CP, Chen H.
    Eye (Lond); 2014 Apr; 28(4):452-8. PubMed ID: 24480837
    [Abstract] [Full Text] [Related]

  • 9. Ocular Manifestations of Familial Transthyretin Amyloidosis.
    Reynolds MM, Veverka KK, Gertz MA, Dispenzieri A, Zeldenrust SR, Leung N, Pulido JS.
    Am J Ophthalmol; 2017 Nov; 183():156-162. PubMed ID: 28911993
    [Abstract] [Full Text] [Related]

  • 10. OCULAR MANIFESTATIONS OF ASP38ALA AND THR59LYS FAMILIAL TRANSTHYRETIN AMYLOIDOSIS.
    Choi KJ, Son KY, Kang SW, Kim D, Choi JO, Kim HJ, Kim JS, Jeon ES, Kim AY, Kang MC, Kim SJ.
    Retina; 2022 Feb 01; 42(2):396-403. PubMed ID: 34483316
    [Abstract] [Full Text] [Related]

  • 11. 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]

  • 12. Deposits on Retinal Surface Seen on OCT in Ocular Amyloidosis.
    Kakihara S, Hirano T, Matsuda Y, Takano D, Imai A, Miyahara T, Murata T.
    Ophthalmol Retina; 2021 Oct 01; 5(10):1005-1008. PubMed ID: 33422693
    [Abstract] [Full Text] [Related]

  • 13. 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 Oct 01; 19():1631-8. PubMed ID: 23901247
    [Abstract] [Full Text] [Related]

  • 14. Hereditary Transthyretin Amyloidosis in Eight Chinese Families.
    Meng LC, Lyu H, Zhang W, Liu J, Wang ZX, Yuan Y.
    Chin Med J (Engl); 2015 Nov 05; 128(21):2902-5. PubMed ID: 26521788
    [Abstract] [Full Text] [Related]

  • 15. Elderly onset vitreous opacities as the initial manifestation in hereditary transthyretin (ATTR Val30Met) carries.
    Ishida K, Nishida T, Niimi Y, Suemori S, Mochizuki K, Kawakami H, Kimura A, Hirayama T.
    Ophthalmic Genet; 2017 Nov 05; 38(4):387-391. PubMed ID: 28085522
    [Abstract] [Full Text] [Related]

  • 16. Recurrence of vitreous amyloidosis and need of surgical reintervention in Portuguese patients with familial amyloidosis ATTR V30M.
    Beirão NM, Matos E, Beirão I, Costa PP, Torres P.
    Retina; 2011 Nov 05; 31(7):1373-7. PubMed ID: 21358362
    [Abstract] [Full Text] [Related]

  • 17. 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]

  • 18. When to suspect transthyretin amyloidosis in cases of isolated vitreous opacities?
    Poignet B, Cauquil C, Barreau E, Bodaghi B, Terrada C, Adams D, Francou B, Labetoulle M, Rousseau A.
    Amyloid; 2020 Dec 01; 27(4):277-278. PubMed ID: 32500742
    [No Abstract] [Full Text] [Related]

  • 19. Ocular Manifestations in a Chinese Pedigree of Familial Amyloidotic Polyneuropathy Carrying the Transthyretin Mutation c.401A>G (p.Tyr134Cys).
    Zhuang X, Sun Z, Gao F, Wang M, Tang W, Liu W, Wang K, Wu J, Jiang R, Xu G.
    Genes (Basel); 2022 May 16; 13(5):. PubMed ID: 35627273
    [Abstract] [Full Text] [Related]

  • 20. Failure of Tafamidis to Halt Progression of Ala36Pro TTR Oculomeningovascular Amyloidosis.
    Salvi F, Volpe R, Pastorelli F, Bianchi A, Vella A, Rapezzi C, Mascalchi M.
    J Stroke Cerebrovasc Dis; 2018 Sep 16; 27(9):e212-e214. PubMed ID: 29779881
    [Abstract] [Full Text] [Related]

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