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Journal Abstract Search

137 related items for PubMed ID: 8345958

  • 1. 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; 14(1):9-16. PubMed ID: 8345958
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  • 5. 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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  • 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
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  • 9. 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
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  • 10. Two transthyretin variants (TTR Ala-49 and TTR Gln-89) in two Sicilian kindreds with hereditary amyloidosis.
    Almeida MR, Ferlini A, Forabosco A, Gawinowicz M, Costa PP, Salvi F, Plasmati R, Tassinari CA, Altland K, Saraiva MJ.
    Hum Mutat; 1992 Apr; 1(3):211-5. PubMed ID: 1301926
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  • 13. 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
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  • 14. 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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  • 17. Biochemical characterization of vitreous and cardiac amyloid in Ile84Ser transthyretin amyloidosis.
    Liepnieks JJ, Wilson DL, Benson MD.
    Amyloid; 2006 Sep; 13(3):170-7. PubMed ID: 17062384
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  • 19. Cytodiagnosis and protein typing of amyloid from a vitreous washing: initial diagnostic workup of hereditary amyloidosis.
    Coppock JD, Dusenbery AC, Elghawy O, Fellenstein LA, Frierson HF, Shildkrot Y.
    J Am Soc Cytopathol; 2020 Sep; 9(3):173-176. PubMed ID: 32113804
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  • 20. [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; 29(1):13-5. PubMed ID: 22311483
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