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1 n have other autoimmune disorders, including autoimmune thyroid disease.
2 female reproduction, and reduces the risk of autoimmune thyroid disease.
3 dies contributes to the skin changes seen in autoimmune thyroid disease.
4 ing 18q22 and 18p11, showed association with autoimmune thyroid disease.
5 omplex and AITD1, a susceptibility locus for autoimmune thyroid disease.
6 cular and renal anomalies, hypertension, and autoimmune thyroid disease.
7 re, ovarian failure, high-arched palate, and autoimmune thyroid disease.
8 econdary autoimmune adverse effects, such as autoimmune thyroid disease.
9 D4 T-cell counts were lower in patients with autoimmune thyroid disease.
10 to inflammation and edema in the setting of autoimmune thyroid disease.
13 N22 1858T variant also increased the risk of autoimmune thyroid disease (AITD) in the RA patients, wh
15 with germinal centers are often detected in autoimmune thyroid disease (AITD), but the mechanisms un
17 endent cases of ankylosing spondylitis (AS), autoimmune thyroid disease (AITD), multiple sclerosis (M
31 in risk applies to each autoimmune disease, autoimmune thyroid disease (and Graves' disease in parti
32 celiac disease, inflammatory bowel disease, autoimmune thyroid disease, and juvenile rheumatoid arth
34 tis, Graves' disease, Hashimoto thyroiditis, autoimmune thyroid disease, and systemic lupus erythemat
35 rthritis (RA), systemic lupus erythematosus, autoimmune thyroid disease, and type 1 diabetes mellitus
36 rapy, pregnancy in the setting of underlying autoimmune thyroid disease, and with the use of certain
39 sulin-dependent diabetes mellitus (IDDM) and autoimmune thyroid disease (ATD), share genetic risk fac
41 o increases on TECs during development of an autoimmune thyroid disease characterized by TEC hyperpro
42 NaI)-supplemented water develop a slow onset autoimmune thyroid disease, characterized by thyrocyte e
43 ulin (Tg) are a prominent feature of the two autoimmune thyroid diseases, chronic lymphocytic (Hashim
44 iated with type 1 diabetes mellitus and with autoimmune thyroid disease, confirming the findings of o
46 We have genotyped 77 affected sib-pairs with autoimmune thyroid disease for eight polymorphic markers
48 e 1 diabetes (T1D), multiple sclerosis (MS), autoimmune thyroid disease (Hashimoto thyroiditis or Gra
49 arious combinations of generalized vitiligo, autoimmune thyroid disease, latent autoimmune diabetes i
50 heumatoid arthritis, polymyalgia rheumatica, autoimmune thyroid disease, psoriasis, and all others.
51 us studies have indicated that patients with autoimmune thyroid disease recognize epitopes of Tg whic
52 igo and other autoimmune diseases, including autoimmune thyroid disease, rheumatoid arthritis, and ty
54 E patients (cohorts 1 and 3) with documented autoimmune thyroid disease, the T allele frequency was h
55 iseases, such as inflammatory bowel disease, autoimmune thyroid disease, type 1 diabetes mellitus (T1
56 cious anaemia, systemic lupus erythematosus, autoimmune thyroid disease, vitiligo, and myasthenia gra
58 with TgAb assay methods, the association of autoimmune thyroid disease with DTC, the prognostic sign