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PUBMED FOR HANDHELDS

Journal Abstract Search


187 related items for PubMed ID: 24480837

  • 1.
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  • 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
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  • 4. 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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  • 5. 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
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  • 6. 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 16; 183():156-162. PubMed ID: 28911993
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  • 7. 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 16; 5(10):1005-1008. PubMed ID: 33422693
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  • 8. Multimodal retinal imaging of familial amyloid polyneuropathy.
    Latasiewicz M, Sala-Puigdollers A, Gonzalez-Ventosa A, Milla E, Adan Civera A.
    Ophthalmic Genet; 2019 Oct 16; 40(5):407-420. PubMed ID: 31576772
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  • 9. 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 16; 114(11):e33-7. PubMed ID: 17980738
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  • 11. An unusual transthyretin gene missense mutation (TTR Phe33Val) linked to familial amyloidotic polyneuropathy.
    Frigerio R, Fabrizi GM, Ferrarini M, Cavallaro T, Brighina L, Santoro P, Agostoni E, Cavaletti G, Rizzuto N, Ferrarese C.
    Amyloid; 2004 Jun 16; 11(2):121-4. PubMed ID: 15478468
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  • 14. 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 16; 91(12):1607-9. PubMed ID: 17522146
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  • 15. Ocular amyloid angiopathy associated with familial amyloidotic polyneuropathy caused by amyloidogenic transthyretin Y114C.
    Kawaji T, Ando Y, Nakamura M, Yamashita T, Wakita M, Ando E, Hirata A, Tanihara H.
    Ophthalmology; 2005 Dec 16; 112(12):2212. PubMed ID: 16225929
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  • 16. Clinical and pathological findings in familial amyloid polyneuropathy caused by a transthyretin E61K mutation.
    Murakami T, Nishimura H, Nagai T, Hemmi S, Kutoku Y, Ohsawa Y, Sunada Y.
    J Neurol Sci; 2017 Oct 15; 381():55-58. PubMed ID: 28991715
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  • 18. A novel transthyretin variant p.H110D (H90D) as a cause of familial amyloid polyneuropathy in a large Irish kindred.
    Jimenez-Zepeda VH, Bahlis NJ, Gilbertson J, Rendell N, Porcari R, Lachmann HJ, Gillmore JD, Hawkins PN, Rowczenio DM.
    Amyloid; 2015 Mar 15; 22(1):26-30. PubMed ID: 25430583
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  • 20. Vitreous opacities and outcome of vitreous surgery in patients with familial amyloidotic polyneuropathy.
    Koga T, Ando E, Hirata A, Fukushima M, Kimura A, Ando Y, Negi A, Tanihara H.
    Am J Ophthalmol; 2003 Feb 15; 135(2):188-93. PubMed ID: 12566023
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