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1 r autoimmune disorders, including autoimmune thyroid disease.
2 nd 18p11, showed association with autoimmune thyroid disease.
3 is a risk factor for developing symptomatic thyroid disease.
4 erapy, family cancer history, and history of thyroid disease.
5 bone mass, spine radiography, and history of thyroid disease.
6 AITD1, a susceptibility locus for autoimmune thyroid disease.
7 rtality occurs in both overt and subclinical thyroid disease.
8 associations between serum PBBs and PCBs and thyroid disease.
9 lation between fetal cell microchimerism and thyroid disease.
10 people and in individuals with a history of thyroid disease.
11 many normal individuals without evidence of thyroid disease.
12 une disorders, notably juvenile diabetes and thyroid disease.
13 abetics and 377 clinic patients assessed for thyroid disease.
14 enal anomalies, hypertension, and autoimmune thyroid disease.
15 strategy to study PTC using a mouse model of thyroid disease.
16 failure, high-arched palate, and autoimmune thyroid disease.
17 TC1 in the peripheral blood of patients with thyroid disease.
18 oid individuals as well as for patients with thyroid disease.
19 ation and edema in the setting of autoimmune thyroid disease.
20 c hypothyroidism, and 1.3% other/unspecified thyroid disease.
21 models) for a medically confirmed history of thyroid disease.
22 t was more common for neonates of women with thyroid disease.
23 tertiles, respectively) after adjusting for thyroid disease.
24 o best care for individuals with subclinical thyroid disease.
25 oduction, and reduces the risk of autoimmune thyroid disease.
26 for primary hypothyroidism, the most common thyroid disease.
27 patients with normal, benign, and malignant thyroid disease.
28 butes to the skin changes seen in autoimmune thyroid disease.
29 ases and were not restricted to inflammatory thyroid diseases.
30 ontrolling the initiation and progression of thyroid diseases.
31 I for diagnostic and therapeutic purposes in thyroid diseases.
32 hy, retinopathy of prematurity, and neonatal thyroid diseases.
33 t of 10,827 individuals screened for various thyroid diseases.
34 surement distinguished benign from malignant thyroid diseases.
36 ncrease in PBB-153 (0.43 ng/mL), the OR (any thyroid disease)=1.12; (95% CI: 0.83, 1.52) (n=105 cases
39 ariant also increased the risk of autoimmune thyroid disease (AITD) in the RA patients, whereas the F
40 nal centers are often detected in autoimmune thyroid disease (AITD), but the mechanisms underlying ly
42 s of ankylosing spondylitis (AS), autoimmune thyroid disease (AITD), multiple sclerosis (MS) and brea
53 n melanoma, other cancers, lung/liver/kidney/thyroid disease, alcohol/drug use, income/education, hem
54 n addition to fungicides, in the etiology of thyroid disease among female spouses enrolled in the Agr
56 ion test for patients who have no history of thyroid disease and have few or no signs or symptoms of
57 s is one of very few models where autoimmune thyroid disease and hypothyroidism develop in most mice
59 MS patients had slightly higher rates of thyroid disease and pernicious anaemia than did controls
62 method for (131)I RAIU measurement in benign thyroid disease and suggests that reducing the administe
64 dividuals with PBC have a high prevalence of thyroid disease and thyroid disease is reportedly more p
69 ohepatitis; however, the association between thyroid diseases and hepatocellular carcinoma (HCC) in m
70 tment, but otherwise the association between thyroid diseases and neonatal morbidity is understudied.
71 were seen individually or in clusters in all thyroid diseases and were not restricted to inflammatory
72 plies to each autoimmune disease, autoimmune thyroid disease (and Graves' disease in particular) cont
77 n thrombosis, hepatitis C, renal impairment, thyroid disease, and liver disease from 2003 to 2013 was
78 TSHR is also a primary antigen in autoimmune thyroid disease, and some TSHR antibodies may activate t
79 ' disease, Hashimoto thyroiditis, autoimmune thyroid disease, and systemic lupus erythematosus (SLE).
80 vitamin D deficiency, female sex, substernal thyroid disease, and thyroid cancer, necessitating centr
81 A), systemic lupus erythematosus, autoimmune thyroid disease, and type 1 diabetes mellitus, all of wh
82 atitis C receiving IFNalpha develop clinical thyroid disease, and up to 40% were reported to develop
85 ltrasound-based screening programs to detect thyroid disease are advised for patients and family memb
87 The cardiovascular signs and symptoms of thyroid disease are some of the most profound and clinic
89 ith uveitis as the main outcome variable and thyroid disease as the main predictor variable, while ad
90 e for the increased female susceptibility to thyroid disease, at least on activation of the PI3K path
93 s (a) four members with both candidiasis and thyroid disease, (b) five members, including one pair of
98 test abnormalities that do not reflect true thyroid disease, but rather are a manifestation of secon
101 many late effects (eg, second malignancies, thyroid disease, cardiovascular disease, and altered rep
102 on TECs during development of an autoimmune thyroid disease characterized by TEC hyperproliferation
103 mented water develop a slow onset autoimmune thyroid disease, characterized by thyrocyte epithelial c
104 re a prominent feature of the two autoimmune thyroid diseases, chronic lymphocytic (Hashimoto's) thyr
106 study period, 29 (12.9%) had a diagnosis of thyroid disease, compared with 62 of 896 patients (6.9%)
107 type 1 diabetes mellitus and with autoimmune thyroid disease, confirming the findings of other invest
110 rlipidemia, gastroesophageal reflux disease, thyroid disease, diabetes, osteoporosis) in the 12 month
111 in thyroid function and the consequences of thyroid disease during pregnancy has rapidly grown in th
114 otyped 77 affected sib-pairs with autoimmune thyroid disease for eight polymorphic markers spanning t
115 e known significant geographic variations of thyroid disease, generalizability of these findings is u
116 curate and informative websites dedicated to thyroid disease, given the large number of patients who
117 of 115,746 participants without a history of thyroid disease, >/=20 years of age, was recruited in Ta
118 i population control group, patients who had thyroid disease had a 1.7-fold (95% CI, 1.03-2.80; P = .
119 d from a database if they had no preexisting thyroid disease, had taken amiodarone for >/=6 months, a
120 These findings suggest that a history of thyroid disease has a weak to moderate association with
121 ect of environmental radioiodine exposure on thyroid disease has been well studied, little is known r
123 s (T1D), multiple sclerosis (MS), autoimmune thyroid disease (Hashimoto thyroiditis or Graves disease
124 dverse outcomes were chronic kidney disease, thyroid disease, hypercalcemia, weight gain, hypertensio
125 id conditions included autoimmune diagnoses (thyroid disease in 14.6%, diabetes mellitus in 11.1%, in
126 vance: Early identification and treatment of thyroid disease in children and adolescents is critical
130 timation and received an HTDS evaluation for thyroid disease, including a thyroid ultrasound, physica
131 h of the evidence that untreated subclinical thyroid disease is associated with clinical symptoms and
134 e Study (HTDS) was conducted to determine if thyroid disease is increased among persons exposed as ch
139 ave a high prevalence of thyroid disease and thyroid disease is reportedly more prevalent near Superf
140 ent in fibroblasts from donors without known thyroid disease, is partially susceptible to neutralizat
141 inations of generalized vitiligo, autoimmune thyroid disease, latent autoimmune diabetes in adults, r
142 se nationwide data suggest a need for better thyroid disease management to reduce neonatal morbidity.
146 ortance of the recognition of the effects of thyroid disease on the heart also derives from the obser
149 8), arthritis (OR, 1.44; 95% CI, 1.12-1.85), thyroid disease (OR, 1.43; 95% CI, 1.02-1.99), antihista
151 disease had a higher likelihood of previous thyroid disease, particularly either Graves' disease or
152 ial diagnoses, risks of progression to overt thyroid disease, potential effects on various health out
153 form of RP3, when expressed in patients with thyroid disease, presents an unusual altered self target
154 2p for chronic mucocutaneous candidiasis and thyroid disease, previously identified using a panel of
156 have indicated that patients with autoimmune thyroid disease recognize epitopes of Tg which are not u
157 atients were recruited from 8 hospital-based thyroid-disease referral centers in Italy between 2006 a
158 e rate, 2.7 [CI, 1.3 to 5.0]) and history of thyroid disease (relative rate, 1.7 [CI, 1.1 to 2.6]) we
160 er autoimmune diseases, including autoimmune thyroid disease, rheumatoid arthritis, and type I diabet
161 f the skin, nails, and mucous membranes) and thyroid disease segregate as an autosomal dominant trait
168 nsion, coronary artery disease, uncontrolled thyroid disease, systemic inflammatory disease, diabetes
169 sk Force issued a guideline on screening for thyroid disease that included a systematic evidence revi
170 (cohorts 1 and 3) with documented autoimmune thyroid disease, the T allele frequency was higher than
172 nto either organ-specific illnesses, such as thyroid disease, type 1 diabetes, and mysasthenia gravis
173 diabetes mellitus type 1, rheumatic disease, thyroid disease, vitiligo, alopecia areata and inflammat
175 alence of self-reported clinically diagnosed thyroid disease was 12.5%, and prevalence of hypothyroid
181 women, all odds ratios (ORs) for PBB-153 and thyroid disease were positive for quintiles above the re
182 es for the care of the pregnant patient with thyroid disease were released by the Endocrine Society i
185 itis compared with patients who did not have thyroid disease when controlling for age, sex, race, smo
186 id not undergo any further investigation for thyroid disease, whereas 32 (24.1%) of 133 patients were
187 ble in the peripheral blood of patients with thyroid disease, which correlates with a diagnosis of ca
188 ients 65 years of age or older with no known thyroid disease who were recruited from primary care reg
191 assay methods, the association of autoimmune thyroid disease with DTC, the prognostic significance of
192 Data supporting associations of subclinical thyroid disease with symptoms or adverse clinical outcom
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