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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

130 related articles for article (PubMed ID: 3041083)

  • 1. 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(2):189-93. PubMed ID: 3041083
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Abnormal transthyretin in asymptomatic relatives in familial amyloidotic polyneuropathy.
    Nakazato M; Tanaka M; Yamamura Y; Kurihara T; Matsukura S; Kangawa K; Matsuo H
    Arch Neurol; 1987 Dec; 44(12):1275-8. PubMed ID: 2823755
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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; 122(2):719-25. PubMed ID: 6087811
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Variant transthyretin in cerebrospinal fluid in familial amyloidotic polyneuropathy.
    Nakazato M; Kangawa K; Kurihara T; Matsukura S; Matsuo H
    J Neurol Sci; 1987 Jun; 79(1-2):111-6. PubMed ID: 3039062
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Diagnostic radioimmunoassay for familial amyloidotic polyneuropathy before clinical onset.
    Nakazato M; Kurihara T; Matsukura S; Kangawa K; Matsuo H
    J Clin Invest; 1986 May; 77(5):1699-703. PubMed ID: 3457802
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Diagnostic radioimmunoassay and DNA-analysis in Swedish and Japanese patients with familial amyloidotic polyneuropathy. Homozygosity for the TTR met30 gene.
    Holmgren G; Lundgren E; Kangawa K; Kurihara T; Matsukura S; Matsuo H; Nakazato M; Steen L
    Acta Neurol Scand; 1993 Feb; 87(2):124-7. PubMed ID: 8095120
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Type I familial amyloidotic polyneuropathy in Japan.
    Nakazato M; Shiomi K; Miyazato M; Matsukura S
    Intern Med; 1992 Dec; 31(12):1335-8. PubMed ID: 1300167
    [TBL] [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; 28(3):275-9. PubMed ID: 2841056
    [No Abstract]   [Full Text] [Related]  

  • 12. 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; 122(2):712-8. PubMed ID: 6087810
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Identification of a novel transthyretin variant (Val30----Leu) associated with familial amyloidotic polyneuropathy.
    Nakazato M; Ikeda S; Shiomi K; Matsukura S; Yoshida K; Shimizu H; Atsumi T; Kangawa K; Matsuo H
    FEBS Lett; 1992 Jul; 306(2-3):206-8. PubMed ID: 1633877
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genetic analysis of familial amyloidotic polyneuropathy, an autosomal dominant disease.
    Sakaki Y; Sasaki H; Yoshioka K; Furuya H
    Clin Chim Acta; 1989 Dec; 185(3):291-7. PubMed ID: 2559819
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [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(4):363-71. PubMed ID: 1655325
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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; 873(2):316-9. PubMed ID: 3756182
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Biochemical marker in familial amyloidotic polyneuropathy, Portuguese type. Family studies on the transthyretin (prealbumin)-methionine-30 variant.
    Saraiva MJ; Costa PP; Goodman DS
    J Clin Invest; 1985 Dec; 76(6):2171-7. PubMed ID: 3908483
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Identification of carriers of a variant plasma prealbumin (transthyretin) associated with familial amyloidotic polyneuropathy type I.
    Benson MD; Dwulet FE
    J Clin Invest; 1985 Jan; 75(1):71-5. PubMed ID: 2981253
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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; 80(4):341-3. PubMed ID: 2848756
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 80(6):1706-11. PubMed ID: 3479441
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.