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Journal Abstract Search

255 related items for PubMed ID: 28434328

  • 1. Transthyretin-related hereditary amyloidosis in an Argentinian family with TTR Tyr114Cys mutation.
    Aguirre MA, Nucifora EM, Rugiero M, Sorroche P, Saez MS, Giunta DH, Posadas-Martinez ML, Boietti BR.
    Amyloid; 2017 Mar; 24(sup1):102. PubMed ID: 28434328
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  • 7. 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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  • 13. Transthyretin-related hereditary amyloidosis in a Chinese family with TTR Y114C mutation.
    Zhang Y, Deng YL, Ma JF, Zheng L, Hong Z, Wang ZQ, Sheng CY, Xiao Q, Cao L, Chen SD.
    Neurodegener Dis; 2011 Sep; 8(4):187-93. PubMed ID: 21135536
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  • 15. Delayed diagnosis of transthyretin amyloidosis with a novel mutation (c.210T>A) in the transthyretin gene.
    Dekmezian MS, Tschen JA, Cho-Vega JH.
    J Am Acad Dermatol; 2013 Feb; 68(2):e49-51. PubMed ID: 23317988
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  • 20. Generation of two induced pluripotent stem cell lines from patients with cardiac amyloidosis carrying heterozygous transthyretin (TTR) mutation.
    Bonilauri B, Shin HS, Htet M, Yan CD, Witteles RM, Sallam K, Wu JC.
    Stem Cell Res; 2023 Oct; 72():103215. PubMed ID: 37788558
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