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Journal Abstract Search

808 related items for PubMed ID: 16872010

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  • 3. Epidemiology of familial amyloid polyneuropathy in Japan: Identification of a novel endemic focus.
    Kato-Motozaki Y, Ono K, Shima K, Morinaga A, Machiya T, Nozaki I, Shibata-Hamaguchi A, Furukawa Y, Yanase D, Ishida C, Sakajiri K, Yamada M.
    J Neurol Sci; 2008 Jul 15; 270(1-2):133-40. PubMed ID: 18410945
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  • 4. A different amyloid formation mechanism: de novo oculoleptomeningeal amyloid deposits after liver transplantation.
    Ando Y, Terazaki H, Nakamura M, Ando E, Haraoka K, Yamashita T, Ueda M, Okabe H, Sasaki Y, Tanihara H, Uchino M, Inomata Y.
    Transplantation; 2004 Feb 15; 77(3):345-9. PubMed ID: 14966406
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  • 8. [Analyses of amyloid formation mechanism in familial amyloidotic polyneuropathy and therapeutic trial].
    Ando Y.
    Rinsho Byori; 2000 May 15; 48(5):425-9. PubMed ID: 10892290
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  • 9. Modeling familial amyloidotic polyneuropathy (Transthyretin V30M) in Drosophila melanogaster.
    Berg I, Thor S, Hammarström P.
    Neurodegener Dis; 2009 May 15; 6(3):127-38. PubMed ID: 19372706
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  • 11. SELDI-TOF mass spectrometry evaluation of variant transthyretins for diagnosis and pathogenesis of familial amyloidotic polyneuropathy.
    Ueda M, Misumi Y, Mizuguchi M, Nakamura M, Yamashita T, Sekijima Y, Ota K, Shinriki S, Jono H, Ikeda S, Suhr OB, Ando Y.
    Clin Chem; 2009 Jun 15; 55(6):1223-7. PubMed ID: 19372189
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  • 12. Biochemical characteristics of variant transthyretins causing hereditary leptomeningeal amyloidosis.
    Mitsuhashi S, Yazaki M, Tokuda T, Sekijima Y, Washimi Y, Shimizu Y, Ando Y, Benson MD, Ikeda S.
    Amyloid; 2005 Dec 15; 12(4):216-25. PubMed ID: 16399646
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  • 13. Significant deposition of wild type transthyretin-derived amyloid in the gastrointestinal tract of aged individuals.
    Ikeda S, Tojo K, Suzuki-Tsuchiya A, Akamatu T, Hashimoto T, Higuchi K.
    Amyloid; 2009 Dec 15; 16(3):174-7. PubMed ID: 19626481
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  • 14. Clinical and pathological findings of non-Val30Met TTR type familial amyloid polyneuropathy in Japan.
    Ikeda S, Takei Y, Tokuda T, Nakazato M, Ando Y.
    Amyloid; 2003 Aug 15; 10 Suppl 1():39-47. PubMed ID: 14640041
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  • 16. Complement C1Q polymorphisms modulate onset in familial amyloidotic polyneuropathy TTR Val30Met.
    Dardiotis E, Koutsou P, Zamba-Papanicolaou E, Vonta I, Hadjivassiliou M, Hadjigeorgiou G, Cariolou M, Christodoulou K, Kyriakides T.
    J Neurol Sci; 2009 Sep 15; 284(1-2):158-62. PubMed ID: 19493541
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  • 20. Molecular analysis of a variant type of familial amyloidotic polyneuropathy showing cerebellar ataxia and pyramidal tract signs.
    Furuya H, Yoshioka K, Sasaki H, Sakaki Y, Nakazato M, Matsuo H, Nakadai A, Ikeda S, Yanagisawa N.
    J Clin Invest; 1987 Dec 15; 80(6):1706-11. PubMed ID: 3479441
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