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Journal Abstract Search

208 related items for PubMed ID: 1301926

  • 1. Two transthyretin variants (TTR Ala-49 and TTR Gln-89) in two Sicilian kindreds with hereditary amyloidosis.
    Almeida MR, Ferlini A, Forabosco A, Gawinowicz M, Costa PP, Salvi F, Plasmati R, Tassinari CA, Altland K, Saraiva MJ.
    Hum Mutat; 1992; 1(3):211-5. PubMed ID: 1301926
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  • 2. Screening and biochemical characterization of transthyretin variants in the Portuguese population.
    Alves IL, Altland K, Almeida MR, Winter P, Saraiva MJ.
    Hum Mutat; 1997; 9(3):226-33. PubMed ID: 9090525
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  • 3. Biochemical and clinical characterization of prealbuminCHICAGO: an apparently benign variant of serum prealbumin (transthyretin) discovered with high-resolution two-dimensional electrophoresis.
    Harrison HH, Gordon ED, Nichols WC, Benson MD.
    Am J Med Genet; 1991 Jun 15; 39(4):442-52. PubMed ID: 1877623
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  • 4. Cardiac amyloidosis: a review and report of a new transthyretin (prealbumin) variant.
    Hesse A, Altland K, Linke RP, Almeida MR, Saraiva MJ, Steinmetz A, Maisch B.
    Br Heart J; 1993 Aug 15; 70(2):111-5. PubMed ID: 8038017
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  • 6. Familial amyloidosis in a large Spanish kindred resulting from a D38V mutation in the transthyretin gene.
    Augustin S, Llige D, Andreu A, González A, Genescà J.
    Eur J Clin Invest; 2007 Aug 15; 37(8):673-8. PubMed ID: 17635579
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  • 9. Familial amyloid polyneuropathy: alanine-for-threonine substitution in the transthyretin (prealbumin) molecule.
    Koeppen AH, Wallace MR, Benson MD, Altland K.
    Muscle Nerve; 1990 Nov 15; 13(11):1065-75. PubMed ID: 2122246
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  • 11. Familial amyloidotic polyneuropathy: report of patients heterozygous for the transthyretin Gly42 gene.
    Murakami T, Yi S, Yamamoto K, Maruyama S, Araki S.
    Ann Neurol; 1992 Mar 15; 31(3):340-2. PubMed ID: 1637142
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  • 12. A new Thr49Pro transthyretin gene mutation associated with leptomeningeal amyloidosis.
    Nakagawa K, Sheikh SI, Snuderl M, Frosch MP, Greenberg SM.
    J Neurol Sci; 2008 Sep 15; 272(1-2):186-90. PubMed ID: 18579156
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  • 13. Human transthyretin (prealbumin) gene and molecular genetics of familial amyloidotic polyneuropathy.
    Sakaki Y, Yoshioka K, Tanahashi H, Furuya H, Sasaki H.
    Mol Biol Med; 1989 Apr 15; 6(2):161-8. PubMed ID: 2693890
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  • 14. 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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  • 15. A novel variant of transthyretin, 59Thr-->Lys, associated with autosomal dominant cardiac amyloidosis in an Italian family.
    Booth DR, Tan SY, Hawkins PN, Pepys MB, Frustaci A.
    Circulation; 1995 Feb 15; 91(4):962-7. PubMed ID: 7850982
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  • 16. Cardiomyopathy in Swedish patients with the Gly53Glu and His88Arg transthyretin variants.
    Holmgren G, Hellman U, Anan I, Lundgren HE, Jonasson J, Stafberg C, Fahoum S, Suhr OB.
    Amyloid; 2005 Sep 15; 12(3):184-8. PubMed ID: 16194874
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  • 17. Cardiomyopathy in a Japanese family with the Glu61Lys transthyretin variant: a new phenotype.
    Noto Y, Tokuda T, Shiga K, Tsuchiya A, Yazaki M, Matoba S, Nakagawa M.
    Amyloid; 2009 Sep 15; 16(2):99-102. PubMed ID: 20536403
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  • 18. Amyloid fibril composition and transthyretin gene structure in senile systemic amyloidosis.
    Gustavsson A, Jahr H, Tobiassen R, Jacobson DR, Sletten K, Westermark P.
    Lab Invest; 1995 Nov 15; 73(5):703-8. PubMed ID: 7474944
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  • 19. A case of late onset cardiac amyloidosis with a new transthyretin variant (lysine 92).
    Saito F, Nakazato M, Akiyama H, Kitahara Y, Date Y, Iwasaki Y, Harasawa S, Hisaki R, Horie T, Kinukawa N, Watanabe T, Sakamaki T, Yagi H, Hoshii Y, Yutani C, Kanmatsuse K.
    Hum Pathol; 2001 Feb 15; 32(2):237-9. PubMed ID: 11230714
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  • 20. Biochemical characterization of vitreous and cardiac amyloid in Ile84Ser transthyretin amyloidosis.
    Liepnieks JJ, Wilson DL, Benson MD.
    Amyloid; 2006 Sep 15; 13(3):170-7. PubMed ID: 17062384
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