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Journal Abstract Search

1458 related items for PubMed ID: 3461234

  • 1. Class III alleles and high-risk MHC haplotypes in type I diabetes mellitus, Graves' disease and Hashimoto's thyroiditis.
    Skanes VM, Barnard J, Farid N, Marshall WH, Murphy L, Rideout D, Taylor R, Xidos G, Larsen B.
    Mol Biol Med; 1986 Apr; 3(2):143-57. PubMed ID: 3461234
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  • 2. Polymorphism of the fourth component of complement in Graves' disease and type I diabetes mellitus.
    Skanes V, Larsen B, Sampson-Murphy L, Farid NR.
    Clin Invest Med; 1985 Apr; 8(2):126-32. PubMed ID: 3869086
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  • 5. C4A gene deletion: association with Graves' disease.
    Ratanachaiyavong S, Lloyd L, McGregor AM.
    J Mol Endocrinol; 1989 Sep; 3(2):145-53. PubMed ID: 2570594
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  • 7. The role of HLA antigens in the manifestation and course of Graves' disease.
    Stenszky V, Kozma L, Balazś C, Bear JC, Farid NR.
    Mol Biol Med; 1986 Feb; 3(1):53-62. PubMed ID: 3485758
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  • 8. Human MHC class III (Bf, C2, C4) genes and GLO: their association with other HLA antigens and extended haplotypes in the Spanish population.
    Regueiro JR, Arnaiz-Villena A.
    Tissue Antigens; 1988 Jan; 31(1):14-25. PubMed ID: 3341017
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  • 9. The interaction of MHC and Gm in liability to autoimmune thyroid disease.
    Nagataki S.
    Mol Biol Med; 1986 Feb; 3(1):73-84. PubMed ID: 3007922
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  • 12. Extended major histocompatibility complex haplotypes in type I diabetes mellitus.
    Raum D, Awdeh Z, Yunis EJ, Alper CA, Gabbay KH.
    J Clin Invest; 1984 Aug; 74(2):449-54. PubMed ID: 6746903
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  • 13. Incomplete functional deficiencies of the fourth (C4) and second (C2) components of complement in a patient with linear frontoparietal scleroderma and his family. Deficiencies determined by a gene not linked to human leukocyte antigen system.
    Venneker GT, van Meegen M, de Kok-Nazaruk M, Hulsmans RF, de Waall LP, Bos JD, Asghar SS.
    Exp Clin Immunogenet; 1996 Aug; 13(2):104-11. PubMed ID: 9063702
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  • 15. Immunogenetic markers for autoimmune diseases of the endocrine system.
    Badenhoop K.
    Klin Wochenschr; 1990 Aug; 68 Suppl 21():10-4. PubMed ID: 1973965
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  • 16. Vitamin D 1alpha-hydroxylase (CYP1alpha) polymorphism in Graves' disease, Hashimoto's thyroiditis and type 1 diabetes mellitus.
    Pani MA, Regulla K, Segni M, Krause M, Hofmann S, Hufner M, Herwig J, Pasquino AM, Usadel KH, Badenhoop K.
    Eur J Endocrinol; 2002 Jun; 146(6):777-81. PubMed ID: 12039697
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  • 17. MHC-extended haplotypes in families of patients with Graves' disease.
    Ratanachaiyavong S, Lloyd L, Darke C, McGregor AM.
    Hum Immunol; 1993 Feb; 36(2):99-111. PubMed ID: 8096501
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  • 18. Susceptibility alleles and haplotypes of human leukocyte antigen DRB1, DQA1, and DQB1 in autoimmune polyglandular syndrome type III in Japanese population.
    Hashimoto K, Maruyama H, Nishiyama M, Asaba K, Ikeda Y, Takao T, Iwasaki Y, Kumon Y, Suehiro T, Tanimoto N, Mizobuchi M, Nakamura T.
    Horm Res; 2005 Feb; 64(5):253-60. PubMed ID: 16254435
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  • 19. [DNA typing of HLA antigen in patients with autoimmune thyroid disease using the PCR-SSOP method].
    Tamai H, Kimura A.
    Nihon Rinsho; 1994 Apr; 52(4):1018-23. PubMed ID: 8196163
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  • 20. Major histocompatibility complex haplotypes and complement C4 alleles in systemic lupus erythematosus. Results of a multicenter study.
    Hartung K, Baur MP, Coldewey R, Fricke M, Kalden JR, Lakomek HJ, Peter HH, Schendel D, Schneider PM, Seuchter SA.
    J Clin Invest; 1992 Oct; 90(4):1346-51. PubMed ID: 1401069
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