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Journal Abstract Search

422 related items for PubMed ID: 29465889

  • 1. [Transthyretin familial amyloid polyneuropathy - three Hungarian cases with rare mutations (His88Arg and Phe33Leu)].
    Csillik A, Pozsonyi Z, Soós K, Balogh I, Bodó I, Arányi Z.
    Ideggyogy Sz; 2016 Jul 30; 69(7-8):245-253. PubMed ID: 29465889
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  • 5. Late-onset familial amyloid polyneuropathy (FAP) Val30Met without family history.
    Rudolph T, Kurz MW, Farbu E.
    Clin Med Res; 2008 Sep 30; 6(2):80-2. PubMed ID: 18606975
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  • 8. Hereditary cardiac amyloidosis associated with Pro24Ser transthyretin mutation: a case report.
    Yamamoto H, Hashimoto T, Kawamura S, Hiroe M, Yamashita T, Ando Y, Yokochi T.
    J Med Case Rep; 2018 Dec 16; 12(1):370. PubMed ID: 30553273
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  • 11. Transthyretin-related familial amyloid polyneuropathy (ATTR-FAP) in Poland - genetic and clinical presentation.
    Lipowska M, Drac H, Rowczenio D, Gilbertson J, Hawkins PN, Lasek-Bal A, Szewczuk J, Grzybowski J, Gawor M, Stępień-Wojno M, Franaszczyk M, Brydak-Godowska J, Śmierciak R, Ptasińska-Perkowska A, Chandoga J, Petrovic R, Kostera-Pruszczyk A.
    Neurol Neurochir Pol; 2020 Dec 16; 54(6):552-560. PubMed ID: 33373035
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  • 12. Clinical and genetic findings in eight Israeli patients with transthyretin-associated familial amyloid polyneuropathy.
    Leibou L, Frand J, Sadeh M, Lossos A, Kremer E, Livneh A, Yarnitsky D, Herman O, Dabby R.
    Isr Med Assoc J; 2012 Nov 16; 14(11):662-5. PubMed ID: 23240369
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  • 13. Late-onset Transthyretin (TTR)-familial Amyloid Polyneuropathy (FAP) with a Long Disease Duration from Non-endemic Areas in Japan.
    Miyake Z, Nakamagoe K, Ezawa N, Yoshinaga T, Hashimoto R, Sato T, Sekijima Y, Tamaoka A.
    Intern Med; 2019 Mar 01; 58(5):713-718. PubMed ID: 30333406
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  • 16. Diagnosis of sporadic transthyretin Val30Met familial amyloid polyneuropathy: a practical analysis.
    Koike H, Hashimoto R, Tomita M, Kawagashira Y, Iijima M, Tanaka F, Sobue G.
    Amyloid; 2011 Jun 01; 18(2):53-62. PubMed ID: 21463231
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  • 17. [A sporadic case of late-onset familial amyloid polyneuropathy type I (transthyretin Met 30-associated familial amyloid polyneuropathy) inborn habitant of Ehime prefecture].
    Harada T, Ishizaki F, Togo M, Yamashita H, Nitta K, Date Y, Nakazato M, Yamamura Y, Nakamura S.
    No To Shinkei; 2002 Jul 01; 54(7):615-9. PubMed ID: 12187722
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  • 18. Two cases of late onset familial amyloid polyneuropathy with a Glu61Lys transthyretin variant.
    Nakano Y, Tadokoro K, Ohta Y, Sato K, Takemoto M, Hishikawa N, Yamashita T, Yamashita T, Ando Y, Abe K.
    J Neurol Sci; 2018 Jul 15; 390():22-25. PubMed ID: 29801893
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  • 19. Origin of sporadic late-onset hereditary ATTR Val30Met amyloidosis in Japan.
    Ueda M, Yamashita T, Misumi Y, Masuda T, Ando Y.
    Amyloid; 2018 Sep 15; 25(3):143-147. PubMed ID: 30486687
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  • 20. Hereditary transthyretin-related amyloidosis.
    Finsterer J, Iglseder S, Wanschitz J, Topakian R, Löscher WN, Grisold W.
    Acta Neurol Scand; 2019 Feb 15; 139(2):92-105. PubMed ID: 30295933
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