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Journal Abstract Search

258 related items for PubMed ID: 25130926

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  • 3. Effects of liver transplantation and tafamidis in hereditary transthyretin amyloidosis caused by transthyretin Leu55Pro mutation: a case report.
    Kon T, Misumi Y, Nishijima H, Honda M, Suzuki C, Baba M, Inomata Y, Obayashi K, Ando Y, Tomiyama M.
    Amyloid; 2015; 22(3):203-4. PubMed ID: 26123280
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  • 4. Amyloid Polyneuropathy and Myocardial Amyloidosis 10 Years after Domino Liver Transplantation from a Patient with a Transthyretin Ser50Arg Mutation.
    Matsushima M, Yabe I, Tsuda M, Sakakibara M, Shimamura T, Sasaki H.
    Intern Med; 2017 Dec 01; 56(23):3231-3235. PubMed ID: 28943540
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  • 9. Monitoring effectiveness and safety of Tafamidis in transthyretin amyloidosis in Italy: a longitudinal multicenter study in a non-endemic area.
    Cortese A, Vita G, Luigetti M, Russo M, Bisogni G, Sabatelli M, Manganelli F, Santoro L, Cavallaro T, Fabrizi GM, Schenone A, Grandis M, Gemelli C, Mauro A, Pradotto LG, Gentile L, Stancanelli C, Lozza A, Perlini S, Piscosquito G, Calabrese D, Mazzeo A, Obici L, Pareyson D.
    J Neurol; 2016 May 01; 263(5):916-924. PubMed ID: 26984605
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  • 11. 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 01; 114(11):e33-7. PubMed ID: 17980738
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  • 12. A case of transthyretin amyloidosis with myopathy, neuropathy, and cardiomyopathy resulting from an exceedingly rare mutation transthyretin Ala120Ser (c.418G > T, p.Ala140Ser).
    Patel K, Tagoe C, Bieri P, Weidenheim K, Tauras JM.
    Amyloid; 2018 Sep 01; 25(3):211-212. PubMed ID: 30039724
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  • 13. [Transthyretin familial amyloid polyneuropathy - three Hungarian cases with rare mutations (His88Arg and Phe33Leu)].
    Csillik A, Pozsonyi Z, Soós K, Balogh I, Bodó I, Arányi Z.
    Ideggyogy Sz; 2016 Jul 30; 69(7-8):245-253. PubMed ID: 29465889
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  • 14. Cardiac Involvement in a Patient Cohort With Val30Met Mutation Transthyretin Amyloidosis.
    Ripoll-Vera T, Buades J, Cisneros E, Gómez Y, Núñez J, Raya M.
    Rev Esp Cardiol (Engl Ed); 2019 Jan 30; 72(1):92-94. PubMed ID: 29223374
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  • 18. Hereditary ATTR Amyloidosis with Cardiomyopathy Caused by the Novel Variant Transthyretin Y114S (p.Y134S).
    Nakase T, Yamashita T, Matsuo Y, Nomura T, Sasada K, Masuda T, Misumi Y, Takamatsu K, Oda S, Furukawa Y, Obayashi K, Matsui H, Ando Y, Ueda M.
    Intern Med; 2019 Sep 15; 58(18):2695-2698. PubMed ID: 31178489
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  • 19. A late-onset case of hereditary transthyretin amyloidosis with a novel compound heterozygous mutation.
    Matsumoto S, Ueda M, Yamashita T, Amano T, Misumi Y, Tasaki M, Masuda T, Mizukami M, Furuya H, Ando Y.
    Amyloid; 2017 Mar 15; 24(sup1):97-98. PubMed ID: 28434367
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