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Journal Abstract Search

248 related items for PubMed ID: 1685359

  • 1. 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]

  • 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. 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]

  • 4. 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]

  • 5. The first case of familial amyloidotic polyneuropathy (FAP Met30) in the Finnish population.
    Drugge U, Holmgren G, Udd B.
    Hum Hered; 1992 May; 42(3):184-8. PubMed ID: 1511998
    [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. 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]

  • 8. Amyloidotic polyneuropathy in a Jewish family. Evidence for the genetic heterogeneity of the lower limb familial amyloidotic neuropathies.
    Gafni J, Fischel B, Reif R, Yaron M, Pras M.
    Q J Med; 1985 Apr; 55(216):33-44. PubMed ID: 3859886
    [Abstract] [Full Text] [Related]

  • 9. [Treatment of familial amyloid polyneuropathy].
    Adams D, Samuel D, Slama M.
    Presse Med; 2012 Sep; 41(9 Pt 1):793-806. PubMed ID: 22341949
    [Abstract] [Full Text] [Related]

  • 10. 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]

  • 11. Familial amyloidotic polyneuropathy: description of an Italian kindred.
    Di Iorio G, Sanges G, Cerracchio A, Sampaolo S, Sannino V, Bonavita V.
    Ital J Neurol Sci; 1993 May; 14(4):303-9. PubMed ID: 8325767
    [Abstract] [Full Text] [Related]

  • 12. Studies on plasma transthyretin (prealbumin) in familial amyloidotic polyneuropathy, Portuguese type.
    Saraiva MJ, Costa PP, Goodman DS.
    J Lab Clin Med; 1983 Oct; 102(4):590-603. PubMed ID: 6311926
    [Abstract] [Full Text] [Related]

  • 13. Vitreous involvement in familial amyloidotic neuropathy: a genealogical and genetic study.
    Sandgren O, Drugge U, Holmgren G, Sousa A.
    Clin Genet; 1991 Dec; 40(6):452-60. PubMed ID: 1685700
    [Abstract] [Full Text] [Related]

  • 14. A second transthyretin mutation at position 33 (Leu/Phe) associated with familial amyloidotic polyneuropathy.
    Harding J, Skare J, Skinner M.
    Biochim Biophys Acta; 1991 Oct 21; 1097(3):183-6. PubMed ID: 1932142
    [Abstract] [Full Text] [Related]

  • 15. Vitreous amyloidosis associated with homozygosity for the transthyretin methionine-30 gene.
    Sandgren O, Holmgren G, Lundgren E.
    Arch Ophthalmol; 1990 Nov 21; 108(11):1584-6. PubMed ID: 1978774
    [Abstract] [Full Text] [Related]

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  • 17. 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 21; 122 ( Pt 10)():1951-62. PubMed ID: 10506096
    [Abstract] [Full Text] [Related]

  • 18. Outcome of liver transplantation for familial amyloidotic polyneuropathy.
    Sharma P, Perri RE, Sirven JE, Zeldenrust SR, Brandhagen DJ, Rosen CB, Douglas DD, Mulligan DC, Rakela J, Wiesner RH, Balan V.
    Liver Transpl; 2003 Dec 21; 9(12):1273-80. PubMed ID: 14625827
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  • 19.
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  • 20. Association of C3 and C4A complement types with familial amyloidotic polyneuropathy.
    Nylander PO, Beckman L, Holmgren G, Steen L.
    Hum Hered; 1990 Dec 21; 40(5):272-7. PubMed ID: 2265853
    [Abstract] [Full Text] [Related]

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