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Susceptible Genes of Autoimmune Thyroid Diseases

Akamizu T

No abstract available.
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Regulation of Gene Expression in Oocyte Growth and Maturation

Lee KA

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A Case of Adrenocortical Adenoma Causing Subclinical Cushing's Syndrome Mistaken for Liddle's Syndrome

Kim KH, Kim KH, Ryu HY, Nam SM, Lee MY, Koh JH, Shin JY, Jung SH, Chung CH

Subclinical Cushing's syndrome is defined as an autonomous cortisol hyperproduction without specific clinical signs of cortisol excess, but detectable biochemically as derangements of the hypothalamic-pituitary-adrenal axis function. We report a...
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A Case of Malignant Insulinoma Metastasized to Liver after Partial Pancreatectomy due to Insulinoma 10 Years before

Kang YI, Yang BH, Chon S, Oh S, Woo JT, Kim SW, Kim JW, Kim YS, Lee JH, Koh K

Malignant insulinomas are very rare endocrine tumours with a variable clinical course. Here, a case of a malignant insulinoma, resected from the tail of the pancreas 10 years previously, which...
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Growth Hormone Treatment in Prader-Willi Syndrome

Park JE, Lee SW, Song KE, Lee HS, Kim DJ, Chung YS, Lee KW, Kim HJ

BACKGROUND: Prader-Willi syndrome (PWS) is a congenital disorder, which is clinically characterized by a short stature, muscular hypotonia, hypogonadism, mental retardation and hyperphagia, leading to early childhood obesity. Impaired growth...
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Analysis of Clinical Features of Korean Patients with Adrenocortical Carcinoma

Yoon CH, Jung TS, Jung HS, Lee EY, Bae SJ, Kim JY, Chung JH, Min YK, Lee MS, Lee MK, Kim KW

BACKGROUND: Adrenocortical carcinoma (ACC) is an extremely rare tumor. Its early detection is difficult and its prognosis is poor. METHOD: We retrospectively analyzed the medical records of 13...
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A Case of Non-islet Cell Tumor Hypoglycemia

Chae YT, Hwang IJ, Ryu KH, Ko EH, Rue JI, Kim SK, Park SW, Kim YR, Cho YW, Choi YK, Lee SJ

Mesenchymal tumors including hemangiopericytomas, hepatocellular tumors, adrenal carcinomas, and a variety of other large tumors have been reported to produce excessive amounts of insulin-like growth factor (IGF) type II precursor,...
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A Case of Papillary Thyroid Carcinoma Combined with Metastatic Renal Cell Carcinoma in the Thyroid

Cheon KI, Lee KW, Mok JO, Kim YJ, Park HK, Kim CH, Kim SJ, Byun DW, Suh KI, Yoo MH, Kim HK, Ko YW

Metastasis to the thyroid from distant cancer is rarely diagnosed clinically and renal cell carcinoma is the most common group of neoplasm to metastasize to the thyroid. Papillary thyroid carcinoma...
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The Effect of Hormone Replacement Therapy on Carotid Intima-Media Thickness in Healthy Postmenopausal Women

Shin JY, Cha BS, Chung CH, Shim WH, Lee HC

BACKGROUND: Cardiovascular disease is the leading cause of death in postmenopausal women. The use of hormone replacement therapy (HRT) preventing for cardiovascular disease in postmenopausal women remains controversial. We investigated...
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A Case of Iodine-induced Thyrotoxicosis with Acromegaly

Kim KH, Kim KH, Ryu HY, Nam SM, Lee MY, Koh JH, Sin JY, Chung CH

Hyperthyroidism is seen in 3.5-26% of subjects with acromegaly. Hyperthyroidism can be developed by thyroid stimulating hormone (TSH) dependent mechanism in TSH-secreting adenomas with acromegaly or by TSH independent mechanism...
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Effect of High Concentration of Estradiol on Thyroid Specific Genes Expression and Cell Growth

Kim DW, Park HY, Kim DH, Kim HJ, Chung HK

BACKGROUND: Since various thyroid diseases have dominant prevalence in women, it has been suggested that female sex hormone have important role on thyroid cell physiology. Interestingly, many thyroid disorders are...
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A Case of Multiple Endocrine Neoplasia Type 1 with Papillary Thyroid Carcinoma

Kim HJ, Kim CS, Je HC, Park J, Park JS, Kong JH, Kang ES, Ahn CW, Cha BS, Lim SK, Kim KR, Lee HC, Jang HS, Hong SW

This is the first report of papillary thyroid carcinoma combined with multiple endocrine neoplasia type 1 (MEN 1). It is an hereditary syndrome characterized by neoplastic disorders such as pituitary...
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Standardization of Isolation Procedure and Analysis of Variables on Successful Isolation of Islet from the Human Pancreas

Kim SC, Han DJ, Kim IH, We YM, Kim YH, Kim JH, Back JH, Lim DG

BACKGROUND: Identifying the donor and isolation-related factors during the islet isolation would be greatly helpful to improve the result of human islet isolation for successful clinical islet transplantation. METHODS: Sixty-nine pancreata...
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A Case of Acromegaly Caused by Double Pituitary Adenomas

Kim HJ, Kim CS, Park JS, Park J, Kong JH, Nam JS, Ahn CW, Cha BS, Lim SK, Kim KR, Lee HC, Hong SW

Acromegaly is a clinical syndrome, which is caused by an excess of growth hormone (GH), most commonly secreted from a pituitary solitary adenoma. However, our patient had bilateral GH-secreting pituitary...
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