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Journal Abstract Search

258 related items for PubMed ID: 25130926

  • 21.
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  • 22. Myopathic phenotype of familial amyloid polyneuropathy with a rare transthyretin variant: ATTR Ala45Asp.
    Misumi Y, Doki T, Ueda M, Obayashi K, Tasaki M, Tamura A, Ando Y.
    Amyloid; 2014 Sep; 21(3):216-7. PubMed ID: 24953234
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  • 26. Hereditary amyloid neuropathy by transthyretin Val107 mutation in a patient of African origin.
    Cassereau J, Lavigne C, Letournel F, Ghali A, Verny C, Dubas F, Devière F, Nicolas G.
    J Peripher Nerv Syst; 2008 Sep; 13(3):251-4. PubMed ID: 18844793
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  • 27. Rapid detection of wild-type and mutated transthyretins.
    Tasaki M, Ueda M, Obayashi K, Motokawa H, Kinoshita Y, Suenaga G, Yanagisawa A, Toyoshima R, Misumi Y, Masuda T, Yamashita T, Ando Y.
    Ann Clin Biochem; 2016 Jul; 53(Pt 4):508-10. PubMed ID: 26342004
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  • 28. Transthyretin Cardiac Amyloidosis Due to Homozygous Val122Ile Mutation in a Caucasian Man.
    Marrero Negrín N, Medina Gil JM, García Cruz ML, Jiménez Cabrera F.
    Rev Esp Cardiol (Engl Ed); 2019 Dec; 72(12):1086-1088. PubMed ID: 31561982
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  • 29. Clinical variant of familial amyloid polyneuropathy.
    Quan D, Cohen JA.
    Muscle Nerve; 2002 Sep; 26(3):417-20. PubMed ID: 12210373
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  • 30. Description of transthyretin S50A, S52P and G47A mutations in familial amyloidosis polyneuropathy.
    González-Duarte A, Lem-Carrillo M, Cárdenas-Soto K.
    Amyloid; 2013 Dec; 20(4):221-5. PubMed ID: 24053266
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  • 32. Wild-type transthyretin significantly contributes to the formation of amyloid fibrils in familial amyloid polyneuropathy patients with amyloidogenic transthyretin Val30Met.
    Tsuchiya-Suzuki A, Yazaki M, Kametani F, Sekijima Y, Ikeda S.
    Hum Pathol; 2011 Feb; 42(2):236-43. PubMed ID: 21056899
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  • 33. Case report of a young patient with transthyretin amyloidosis associated with Gly67Ala mutation.
    Salihoglu A, Yildirim S, Ar MC, Hancer VS, Bozcan S, Yilmaz U, Serin N, Tuzuner N, Celik AF.
    Amyloid; 2019 Feb; 26(sup1):75-76. PubMed ID: 31343303
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  • 34. Hereditary transthyretin amyloidosis associated with a transthyretin variant Thr59Arg.
    Watanabe T, Obayashi K, Misumi Y, Tasaki M, Shinriki S, Ando T, Akagami T, Ueda M, Yamashita T, Hirotani S, Ando Y.
    Amyloid; 2017 Mar; 24(sup1):119. PubMed ID: 28434332
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  • 35. Vitreal deposits in Val71Ala transthyretin amyloidosis.
    Suan D, Booth DR, Kennedy IH, Downie J, Earls P, Gottlieb D, Stewart GJ, Lin MW.
    Intern Med J; 2012 Jan; 42(1):106-8. PubMed ID: 22276564
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  • 36. Late-onset and fast progressive neuropathy and cardiomyopathy in Val32Ala transthyretin gene mutation.
    Cazzato D, Dalla Bella E, Saveri P, Taroni F, Marucci G, Lauria G.
    Neurol Sci; 2019 Jun; 40(6):1267-1269. PubMed ID: 30685801
    [Abstract] [Full Text] [Related]

  • 37. Upper limb neuropathy such as carpal tunnel syndrome as an initial manifestation of ATTR Val30Met familial amyloid polyneuropathy.
    Tojo K, Tsuchiya-Suzuki A, Sekijima Y, Morita H, Sumita N, Ikeda S.
    Amyloid; 2010 Mar; 17(1):32-5. PubMed ID: 20132088
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  • 38. Cardiovascular autonomic functions in late-onset hereditary transthyretin amyloidosis with Val30Met mutation.
    Nakamura T, Koike H, Nishi R, Ikeda S, Kawagashira Y, Iijima M, Katsuno M, Sobue G.
    Amyloid; 2019 Mar; 26(sup1):6. PubMed ID: 31343341
    [No Abstract] [Full Text] [Related]

  • 39. Evolution of amyloid fibrils in hereditary transthyretin amyloidosis: an ultrastructural study.
    Koike H, Nishi R, Ikeda S, Kawagashira Y, Iijima M, Katsuno M, Sobue G.
    Amyloid; 2019 Mar; 26(sup1):26. PubMed ID: 31343346
    [No Abstract] [Full Text] [Related]

  • 40. Familial amyloid polyneuropathy in Korea: the first case report with a proven ATTR Lys35Asn gene.
    Ryu JK, Baik HW, Bae JS, Hwang TJ, Paik SY, Yu HJ, Choi BO, Takei Y, Ikeda S.
    Amyloid; 2005 Mar; 12(1):62-4. PubMed ID: 16076613
    [Abstract] [Full Text] [Related]

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