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Journal Abstract Search

165 related items for PubMed ID: 23244293

  • 1. ATTR amyloid in the carpal tunnel ligament is frequently of wildtype transthyretin origin.
    Gioeva Z, Urban P, Meliss RR, Haag J, Axmann HD, Siebert F, Becker K, Radtke HG, Röcken C.
    Amyloid; 2013 Mar; 20(1):1-6. PubMed ID: 23244293
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  • 2. Prevalence of germline mutations in the TTR gene in a consecutive series of surgical pathology specimens with ATTR amyloid.
    Eriksson M, Büttner J, Todorov T, Yumlu S, Schönland S, Hegenbart U, Kristen AV, Dengler T, Lohse P, Helmke B, Schmidt H, Röcken C.
    Am J Surg Pathol; 2009 Jan; 33(1):58-65. PubMed ID: 18830126
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  • 3. 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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  • 4. Amyloid detection in the transverse carpal ligament of patients with hereditary ATTR V30M amyloidosis and carpal tunnel syndrome.
    Samões R, Taipa R, Valdrez K, Gonçalves I, Melo Pires M, Martins da Silva A, Coelho T.
    Amyloid; 2017 Jun; 24(2):73-77. PubMed ID: 28413892
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  • 5. Establishing and validating the fluorescent amyloid ligand h-FTAA (heptamer formyl thiophene acetic acid) to identify transthyretin amyloid deposits in carpal tunnel syndrome.
    Hahn K, Nilsson KPR, Hammarström P, Urban P, Meliss RR, Behrens HM, Krüger S, Röcken C.
    Amyloid; 2017 Jun; 24(2):78-86. PubMed ID: 28434259
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  • 8. Tenosynovial and Cardiac Amyloidosis in Patients Undergoing Carpal Tunnel Release.
    Sperry BW, Reyes BA, Ikram A, Donnelly JP, Phelan D, Jaber WA, Shapiro D, Evans PJ, Maschke S, Kilpatrick SE, Tan CD, Rodriguez ER, Monteiro C, Tang WHW, Kelly JW, Seitz WH, Hanna M.
    J Am Coll Cardiol; 2018 Oct 23; 72(17):2040-2050. PubMed ID: 30336828
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  • 13. The significance of carpal tunnel syndrome in transthyretin Val30Met familial amyloid polyneuropathy.
    Koike H, Morozumi S, Kawagashira Y, Iijima M, Yamamoto M, Hattori N, Tanaka F, Nakamura T, Hirayama M, Ando Y, Ikeda S, Sobue G.
    Amyloid; 2009 Oct 23; 16(3):142-8. PubMed ID: 19626479
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  • 14. A Swedish family with the rare Phe33Leu transthyretin mutation.
    Holmgren G, Hellman U, Jonasson J, Lundgren HE, Westermark P, Suhr OB.
    Amyloid; 2005 Sep 23; 12(3):189-92. PubMed ID: 16194875
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  • 15. 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 Sep 23; 29():19-22. PubMed ID: 28460244
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