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Journal Abstract Search

254 related items for PubMed ID: 18709962

  • 1. [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
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  • 3. 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
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  • 8. [Amyloidosis of the vitreous body. Possibilities of diagnosis].
    Soltau JB, Seiberth V, Knorz MC, Liesenhoff H.
    Fortschr Ophthalmol; 1991 Nov; 88(4):408-10. PubMed ID: 1786932
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  • 9. 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
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  • 11. Vitreous amyloidosis associated with homozygosity for the transthyretin methionine-30 gene.
    Sandgren O, Holmgren G, Lundgren E.
    Arch Ophthalmol; 1990 Nov; 108(11):1584-6. PubMed ID: 1978774
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  • 12. Vitreous amyloidosis without systemic or familial involvement.
    Salvador F, Mateo C, Alegre J, Reventos A, García-Arumi J, Corcostegui B.
    Int Ophthalmol; 1990 Nov; 17(6):355-7. PubMed ID: 8063479
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  • 14. RE-INTERVENTION IN DE NOVO VITREOUS OPACITIES AFTER PARS PLANA VITRECTOMY IN FAMILIAL AMYLOIDOTIC POLYNEUROPATHY TTR VAL30METPORTUGUESE PATIENTS.
    Ferreira NN, Cunha Dias DA, Afonso Carvalho RP, Pardal Monteiro Coelho MT.
    Retin Cases Brief Rep; 1990 Nov; 13(3):273-278. PubMed ID: 28333852
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  • 17. Vitreous involvement as initial presentation of hereditary transthyretin amyloidosis related to the rare TTR Ile107Met (p.Ile127Met) pathogenic variant.
    Treviño-Herrera AB, Bustamante-Vargas AP, Lisker-Cervantes A, Ríos Y Valles Valles D, Villanueva-Mendoza C, González-Duarte A, Concha-Del-Río LE.
    Ophthalmic Genet; 2022 Jun; 43(3):413-419. PubMed ID: 35038954
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  • 18. 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 Jun; 23(1):46-50. PubMed ID: 26828956
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  • 20. 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
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