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Journal Abstract Search

266 related items for PubMed ID: 22580845

  • 1. Sporadic transthyretin amyloidosis with a novel TTR gene mutation misdiagnosed as primary amyloidosis.
    Briani C, Cavallaro T, Ferrari S, Taioli F, Calamelli S, Verga L, Adami F, Fabrizi GM.
    J Neurol; 2012 Oct; 259(10):2226-8. PubMed ID: 22580845
    [No Abstract] [Full Text] [Related]

  • 2. Sporadic Cardiac Amyloidosis by Amyloidogenic Transthyretin V122I Variant.
    Nehashi T, Oikawa M, Amami K, Kanno Y, Yokokawa T, Misaka T, Yamada S, Kunii H, Nakazato K, Ishida T, Takeishi Y.
    Int Heart J; 2019 Nov 30; 60(6):1441-1443. PubMed ID: 31666456
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  • 3. Restrictive cardiomyopathy in familial amyloidosis TTR-Arg-50.
    Conraads V.
    Circulation; 2003 Sep 09; 108(10):e71. PubMed ID: 12963686
    [No Abstract] [Full Text] [Related]

  • 4. 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 09; 114(11):e33-7. PubMed ID: 17980738
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  • 7. Cardiac Amyloidosis: Overlooked, Underappreciated, and Treatable.
    Rubin J, Maurer MS.
    Annu Rev Med; 2020 Jan 27; 71():203-219. PubMed ID: 31986086
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  • 9. Late onset cardiomyopathy as presenting sign of ATTR A45G amyloidosis caused by a novel TTR mutation (p.A65G).
    Klaassen SHC, Lemmink HH, Bijzet J, Glaudemans AWJM, Bos R, Plattel W, van den Berg MP, Slart RHJA, Nienhuis HLA, van Veldhuisen DJ, Hazenberg BPC.
    Cardiovasc Pathol; 2017 Jan 27; 29():19-22. PubMed ID: 28460244
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  • 10. 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 27; 24(sup1):102. PubMed ID: 28434328
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  • 11. Variable presentations of TTR-related familial amyloid polyneuropathy in seventeen patients.
    Cappellari M, Cavallaro T, Ferrarini M, Cabrini I, Taioli F, Ferrari S, Merlini G, Obici L, Briani C, Fabrizi GM.
    J Peripher Nerv Syst; 2011 Jun 27; 16(2):119-29. PubMed ID: 21692911
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  • 12. Neuropathy Associated with Systemic Amyloidosis.
    Kaku M, Berk JL.
    Semin Neurol; 2019 Oct 27; 39(5):578-588. PubMed ID: 31639841
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  • 13. Hereditary Transthyretin Cardiac Amyloidosis in Refractory Spinal Canal Stenosis: Genetic and Pathologic Analysis.
    Higashi H, Inoue K, Ishibashi-Ueda H, Yamaguchi O.
    Can J Cardiol; 2021 Aug 27; 37(8):1289-1291. PubMed ID: 33592282
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  • 14. Novel drugs targeting transthyretin amyloidosis.
    Hanna M.
    Curr Heart Fail Rep; 2014 Mar 27; 11(1):50-7. PubMed ID: 24464360
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  • 15. Failure of Tafamidis to Halt Progression of Ala36Pro TTR Oculomeningovascular Amyloidosis.
    Salvi F, Volpe R, Pastorelli F, Bianchi A, Vella A, Rapezzi C, Mascalchi M.
    J Stroke Cerebrovasc Dis; 2018 Sep 27; 27(9):e212-e214. PubMed ID: 29779881
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  • 16. 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 27; 68(2):e49-51. PubMed ID: 23317988
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  • 20. Oculoleptomeningeal Amyloidosis Secondary to the Rare Transthyretin c.381T>G (p.Ile127Met) Mutation.
    Mathieu F, Morgan E, So J, Munoz DG, Mason W, Kongkham P.
    World Neurosurg; 2018 Mar 27; 111():190-193. PubMed ID: 29277593
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