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Journal Abstract Search


196 related items for PubMed ID: 23126592

  • 1. A transthyretin variant, Asp18Asn, associated with amyloid cardiomyopathy: a new African-American variant?
    Quarta CC, Falk RH.
    Amyloid; 2012 Dec; 19(4):204-7. PubMed ID: 23126592
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  • 3. Familial amyloidosis in a large Spanish kindred resulting from a D38V mutation in the transthyretin gene.
    Augustin S, Llige D, Andreu A, González A, Genescà J.
    Eur J Clin Invest; 2007 Aug; 37(8):673-8. PubMed ID: 17635579
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  • 4. Cardiomyopathy in Swedish patients with the Gly53Glu and His88Arg transthyretin variants.
    Holmgren G, Hellman U, Anan I, Lundgren HE, Jonasson J, Stafberg C, Fahoum S, Suhr OB.
    Amyloid; 2005 Sep; 12(3):184-8. PubMed ID: 16194874
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  • 5. Cardiac amyloidosis: a review and report of a new transthyretin (prealbumin) variant.
    Hesse A, Altland K, Linke RP, Almeida MR, Saraiva MJ, Steinmetz A, Maisch B.
    Br Heart J; 1993 Aug; 70(2):111-5. PubMed ID: 8038017
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  • 9. Progression of cardiomyopathy and neuropathy after liver transplantation in a patient with familial amyloidotic polyneuropathy caused by tyrosine-77 transthyretin variant.
    García-Herola A, Prieto M, Pascual S, Berenguer M, López-Viedma B, Mir J, Vilchez JJ, Berenguer J.
    Liver Transpl Surg; 1999 May; 5(3):246-8. PubMed ID: 10226117
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  • 11. A case of hereditary amyloidosis transthyretin variant Met 30 with amyloid cardiomyopathy, less polyneuropathy, and the presence of giant cells.
    Nakamura Y, Yutani C, Nakazato M, Date Y, Baba T, Goto Y.
    Pathol Int; 1999 Oct; 49(10):898-902. PubMed ID: 10571824
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  • 12. Isolated heart transplantation for familial transthyretin (TTR) V122I cardiac amyloidosis.
    Thenappan T, Fedson S, Rich J, Murks C, Husain A, Pogoriler J, Anderson AS.
    Amyloid; 2014 Jun; 21(2):120-3. PubMed ID: 24818650
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  • 14. [A sporadic case of late onset familial amyloidotic polyneuropathy preceded by cardiac involvement].
    Aoki K, Koike R, Yuasa T, Ikeda S, Tsuji S.
    Rinsho Shinkeigaku; 1993 Aug; 33(8):905-8. PubMed ID: 8261706
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  • 17. DISCOVERY: prevalence of transthyretin (TTR) mutations in a US-centric patient population suspected of having cardiac amyloidosis.
    Akinboboye O, Shah K, Warner AL, Damy T, Taylor HA, Gollob J, Powell C, Karsten V, Vest J, Maurer MS.
    Amyloid; 2020 Dec; 27(4):223-230. PubMed ID: 32456532
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  • 18. Transthyretin V122I (pV142I)* cardiac amyloidosis: an age-dependent autosomal dominant cardiomyopathy too common to be overlooked as a cause of significant heart disease in elderly African Americans.
    Buxbaum JN, Ruberg FL.
    Genet Med; 2017 Jul; 19(7):733-742. PubMed ID: 28102864
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