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| Skinningsrud B, Husebye ES, Pearce SH, et al. Polymorphisms in CLEC16A and CIITA at 16p13 are associated with primary adrenal insufficiency. [JOURNAL ARTICLE] J Clin Endocrinol Metab 2008 Jul 1. Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Jennings CE, Owen CJ, Wilson V, et al. A haplotype of the CYP27B1 promoter is associated with autoimmune Addison's disease but not with Graves' disease in a UK population. [Journal Article] J Mol Endocrinol 2005 Jun; 34(3):859-63. Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Kemp EH, Ajjan RA, Husebye ES, et al. A cytotoxic T lymphocyte antigen-4 (CTLA-4) gene polymorphism is associated with autoimmune Addison's disease in English patients. [Journal Article] Clin Endocrinol (Oxf) 1998 Nov; 49(5):609-13. Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Blomhoff A, Lie BA, Myhre AG, et al. Polymorphisms in the cytotoxic T lymphocyte antigen-4 gene region confer susceptibility to Addison's disease. [Journal Article] J Clin Endocrinol Metab 2004 Jul; 89(7):3474-6. Abstract | Full Citation | Find Related Articles | | Wolff AS, Myhr KM, Vedeler CA, et al. Fcgamma Receptor Polymorphisms are not Associated with Autoimmune Addison's Disease. [Journal Article] Scand J Immunol 2007 Jun; 65(6):555-8. Abstract | Full Citation | | Maclaren NK, Riley WJ Inherited susceptibility to autoimmune Addison's disease is linked to human leukocyte antigens-DR3 and/or DR4, except when associated with type I autoimmune polyglandular syndrome. [Journal Article] J Clin Endocrinol Metab 1986 Mar; 62(3):455-9. Abstract | Full Citation | Find Related Articles | | Ghaderi M, Gambelunghe G, Tortoioli C, et al. MHC2TA single nucleotide polymorphism and genetic risk for autoimmune adrenal insufficiency. [JOURNAL ARTICLE] J Clin Endocrinol Metab 2006 Jul 18. Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Owen CJ, Kelly H, Eden JA, et al. ANALYSIS OF THE FC-RECEPTOR LIKE-3 (FCRL3) LOCUS IN CAUCASIANS WITH AUTOIMMUNE DISORDERS SUGGESTS A COMPLEX PATTERN OF DISEASE ASSOCIATION. [JOURNAL ARTICLE] J Clin Endocrinol Metab 2007 Jan 2. Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Myhre R, Klungland H, Farrer MJ, et al. Genetic association study of synphilin-1 in idiopathic Parkinson's disease. [JOURNAL ARTICLE] BMC Med Genet 2008 Mar 21; 9(1):19. Abstract | Full Citation |  |
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