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Journal Abstract Search

167 related items for PubMed ID: 8095120

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. Homozygosity for the transthyretin-met30-gene in two Swedish sibs with familial amyloidotic polyneuropathy.
    Holmgren G, Haettner E, Nordenson I, Sandgren O, Steen L, Lundgren E.
    Clin Genet; 1988 Nov; 34(5):333-8. PubMed ID: 3229002
    [Abstract] [Full Text] [Related]

  • 3. Vitreous amyloidosis associated with homozygosity for the transthyretin methionine-30 gene.
    Sandgren O, Holmgren G, Lundgren E.
    Arch Ophthalmol; 1990 Nov; 108(11):1584-6. PubMed ID: 1978774
    [Abstract] [Full Text] [Related]

  • 4. Asymptomatic homozygous gene carrier in a family with type I familial amyloid polyneuropathy.
    Ikeda S, Nakano T, Yanagisawa N, Nakazato M, Tsukagoshi H.
    Eur Neurol; 1992 Nov; 32(6):308-13. PubMed ID: 1490495
    [Abstract] [Full Text] [Related]

  • 5. Homozygosity for the transthyretin-Met30 gene in three Japanese siblings with type I familial amyloidotic polyneuropathy.
    Yoshinaga T, Nakazato M, Ikeda S, Ohnishi A.
    Neurology; 1992 Oct; 42(10):2045-7. PubMed ID: 1407590
    [Abstract] [Full Text] [Related]

  • 6. Homozygosity for the transthyretin-Met30-gene in seven individuals with familial amyloidosis with polyneuropathy detected by restriction enzyme analysis of amplified genomic DNA sequences.
    Holmgren G, Bergström S, Drugge U, Lundgren E, Nording-Sikström C, Sandgren O, Steen L.
    Clin Genet; 1992 Jan; 41(1):39-41. PubMed ID: 1353008
    [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
    [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
    [Abstract] [Full Text] [Related]

  • 9. 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
    [Abstract] [Full Text] [Related]

  • 10. Biochemical effect of liver transplantation in two Swedish patients with familial amyloidotic polyneuropathy (FAP-met30).
    Holmgren G, Steen L, Ekstedt J, Groth CG, Ericzon BG, Eriksson S, Andersen O, Karlberg I, Nordén G, Nakazato M.
    Clin Genet; 1991 Sep; 40(3):242-6. PubMed ID: 1685359
    [Abstract] [Full Text] [Related]

  • 11. 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
    [Abstract] [Full Text] [Related]

  • 12. Diagnosis of familial amyloidotic polyneuropathy in Sweden by RFLP analysis.
    Holmgren G, Holmberg E, Lindström A, Lindström E, Nordenson I, Sandgren O, Steen L, Svensson B, Lundgren E, von Gabain A.
    Clin Genet; 1988 Mar; 33(3):176-80. PubMed ID: 2896079
    [Abstract] [Full Text] [Related]

  • 13. 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 Mar; 435():86-100. PubMed ID: 6099706
    [Abstract] [Full Text] [Related]

  • 14. Restriction fragment length polymorphism analysis of mutated transthyretin in vitreous amyloidosis.
    Sandgren O, Holmgren G, Lundgren E, Steen L.
    Arch Ophthalmol; 1988 Jun; 106(6):790-2. PubMed ID: 2897192
    [Abstract] [Full Text] [Related]

  • 15. Familial amyloidotic polyneuropathy without familial occurrence: carrier detection by the radioimmunoassay of variant transthyretin.
    Tanaka M, Hirai S, Matsubara E, Okamoto K, Morimatsu M, Nakazato M.
    J Neurol Neurosurg Psychiatry; 1988 Apr; 51(4):576-8. PubMed ID: 3379433
    [Abstract] [Full Text] [Related]

  • 16. Geographical distribution of TTR met30 carriers in northern Sweden: discrepancy between carrier frequency and prevalence rate.
    Holmgren G, Costa PM, Andersson C, Asplund K, Steen L, Beckman L, Nylander PO, Teixeira A, Saraiva MJ, Costa PP.
    J Med Genet; 1994 May; 31(5):351-4. PubMed ID: 8064809
    [Abstract] [Full Text] [Related]

  • 17. 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]

  • 18. 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
    [Abstract] [Full Text] [Related]

  • 19. Genetic expression of a transthyretin mutation in typical and late-onset Portuguese families with familial amyloidotic polyneuropathy.
    Saraiva MJ, Costa PP, Goodman DS.
    Neurology; 1986 Nov; 36(11):1413-7. PubMed ID: 3762958
    [Abstract] [Full Text] [Related]

  • 20. Late-onset familial amyloid polyneuropathy type I (transthyretin Met30-associated familial amyloid polyneuropathy) unrelated to endemic focus in Japan. Clinicopathological and genetic features.
    Misu Ki, Hattori N, Nagamatsu M, Ikeda Si, Ando Y, Nakazato M, Takei Yi, Hanyu N, Usui Y, Tanaka F, Harada T, Inukai A, Hashizume Y, Sobue G.
    Brain; 1999 Oct; 122 ( Pt 10)():1951-62. PubMed ID: 10506096
    [Abstract] [Full Text] [Related]

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