These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

199 related items for PubMed ID: 2981253

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. Family studies of the genetic abnormality in transthyretin (prealbumin) in Portuguese patients with familial amyloidotic polyneuropathy.
    Saraiva MJ, Birken S, Costa PP, Goodman DS.
    Ann N Y Acad Sci; 1984; 435():86-100. PubMed ID: 6099706
    [Abstract] [Full Text] [Related]

  • 3. Presence of a plasma transthyretin (prealbumin) variant in familial amyloidotic polyneuropathy in a kindred of Greek origin.
    Saraiva MJ, Sherman W, Goodman DS.
    J Lab Clin Med; 1986 Jul; 108(1):17-22. PubMed ID: 3011930
    [Abstract] [Full Text] [Related]

  • 4. Chemical classification of hereditary amyloidosis in Brazilian families and identification of gene carriers.
    Benson MD, Dwulet FE, Scheinberg MA, Greipp P.
    J Rheumatol; 1986 Oct; 13(5):927-31. PubMed ID: 3820203
    [Abstract] [Full Text] [Related]

  • 5. Biochemical and genetic characterization of type I familial amyloidotic polyneuropathy.
    Nakazato M, Sasaki H, Furuya H, Sakaki Y, Kurihara T, Matsukura S, Kangawa K, Matsuo H.
    Ann Neurol; 1987 Jun; 21(6):596-8. PubMed ID: 3037992
    [Abstract] [Full Text] [Related]

  • 6. Quantitative detection of a variant prealbumin associated with type 1 familial amyloidotic polyneuropathy (Japanese type) by high performance liquid chromatography.
    Ikegawa S, Tanase S, Araki S, Morino Y.
    Clin Chim Acta; 1987 Aug 14; 167(2):165-72. PubMed ID: 3478158
    [Abstract] [Full Text] [Related]

  • 7. Amyloid fibril protein in familial amyloidotic polyneuropathy, Portuguese type. Definition of molecular abnormality in transthyretin (prealbumin).
    Saraiva MJ, Birken S, Costa PP, Goodman DS.
    J Clin Invest; 1984 Jul 14; 74(1):104-19. PubMed ID: 6736244
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. Familial amyloidotic polyneuropathy: transthyretin (prealbumin) variants in kindreds of Italian origin.
    Saraiva MJ, Costa PP, Almeida Mdo R, Banzhoff A, Altland K, Ferlini A, Rubboli G, Plasmati R, Tassinari CA, Romeo G.
    Hum Genet; 1988 Dec 14; 80(4):341-3. PubMed ID: 2848756
    [Abstract] [Full Text] [Related]

  • 10. Simplified method for screening populations at risk for transthyretin Met30-associated familial amyloidotic polyneuropathy.
    Saraiva MJ, Alves IL, Costa PP.
    Clin Chem; 1989 Jun 14; 35(6):1033-5. PubMed ID: 2543515
    [Abstract] [Full Text] [Related]

  • 11. [Familial amyloidotic polyneuropathy without familial occurrence but with asymptomatic carriers discovered by radioimmunoassay of variant transthyretin].
    Matsubara E, Tanaka M, Hirai S, Okamoto K, Nakazato M.
    Rinsho Shinkeigaku; 1988 Mar 14; 28(3):275-9. PubMed ID: 2841056
    [No Abstract] [Full Text] [Related]

  • 12. Radioimmunoassay for detecting abnormal prealbumin in the serum for diagnosis of familial amyloidotic polyneuropathy (Japanese type).
    Nakazato M, Kangawa K, Minamino N, Tawara S, Matsuo H, Araki S.
    Biochem Biophys Res Commun; 1984 Jul 31; 122(2):719-25. PubMed ID: 6087811
    [Abstract] [Full Text] [Related]

  • 13. Molecular detection of carriers of hereditary amyloidosis in a Swedish-American family.
    Wallace MR, Conneally PM, Long GL, Benson MD.
    Am J Med Genet; 1986 Oct 31; 25(2):335-41. PubMed ID: 2877582
    [Abstract] [Full Text] [Related]

  • 14. Mass spectrometric detection of the plasma prealbumin (transthyretin) variant associated with familial amyloidotic polyneuropathy.
    Wada Y, Matsuo T, Katakuse I, Suzuki T, Azuma T, Tsujino S, Kishimoto S, Matsuda H, Hayashi A.
    Biochim Biophys Acta; 1986 Sep 26; 873(2):316-9. PubMed ID: 3756182
    [Abstract] [Full Text] [Related]

  • 15. Biochemical characterization of familial amyloidotic polyneuropathy in various districts of Japan.
    Tanaka M, Nakazato M, Kurihara T, Matsukura S, Kangawa K, Matsuo H.
    Jpn J Med; 1987 May 26; 26(2):189-93. PubMed ID: 3041083
    [Abstract] [Full Text] [Related]

  • 16. Identification of a prealbumin variant in the serum of a Japanese patient with familial amyloidotic polyneuropathy.
    Nakazato M, Kangawa K, Minamino N, Tawara S, Matsuo H, Araki S.
    Biochem Biophys Res Commun; 1984 Jul 31; 122(2):712-8. PubMed ID: 6087810
    [Abstract] [Full Text] [Related]

  • 17. Identification of carriers of mutant prealbumin gene associated with familial amyloidotic polyneuropathy type I by Southern blot procedures: study of six pedigrees in the Arao district of Japan.
    Ide M, Mita S, Ikegawa S, Maeda S, Shimada K, Araki S.
    Hum Genet; 1986 Aug 31; 73(4):281-5. PubMed ID: 3017836
    [Abstract] [Full Text] [Related]

  • 18. Characterization of a transthyretin (prealbumin) variant associated with familial amyloidotic polyneuropathy type II (Indiana/Swiss).
    Dwulet FE, Benson MD.
    J Clin Invest; 1986 Oct 31; 78(4):880-6. PubMed ID: 3760189
    [Abstract] [Full Text] [Related]

  • 19. Diagnosis of familial amyloidotic polyneuropathy: isolation of variant prealbumin.
    Suzuki T, Azuma T, Tsujino S, Mizuno R, Kishimoto S, Wada Y, Hayashi A, Ikeda S, Yanagisawa N.
    Neurology; 1987 Apr 31; 37(4):708-11. PubMed ID: 3031544
    [Abstract] [Full Text] [Related]

  • 20. [Diagnosis of familial amyloid polyneuropathy--gene analysis with primer-directed enzymatic amplification of DNA, isolation of plasma variant prealbumin and immunohistochemical identification of tissue amyloid protein].
    Ikeda S, Nakano T, Yanagisawa N, Hanyu N, Suzuki T, Sakaki Y.
    Rinsho Shinkeigaku; 1991 Apr 31; 31(4):363-71. PubMed ID: 1655325
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 10.