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17 results

Corrigendum: Association between Serum Fibroblast Growth Factor 21 Levels and Bone Mineral Density in Postmenopausal Women

Choi HS, Lee HA, Kim SW, Cho EH

  • Endocrinol Metab.
  • 2018 Sep;33(3):428-428.
  • doi: 10.3803/EnM.2018.33.3.428
There were some wrong contents in the Acknowledgments section, which should be properly revised.
Corrigendum: Author's Name Correction. Study Protocol of Multicenter Prospective Cohort Study of Active Surveillance on Papillary Thyroid Microcarcinoma (MAeSTro)

Moon JH, Kim JH, Lee EK, Lee KE, Kong SH, Kim YK, Jeong WJ, Lee CY, Yoo RE, Hwangbo Y, Song YS, Kim MJ, Cho SW, Kim SJ, Chung EJ, Choi JY, Ryu CH, Lee YJ, Hah JH, Jung YS, Ryu J, Hwang Y, Park SK, Sung HK, Yi KH, Park DJ, Park YJ

  • Endocrinol Metab.
  • 2018 Sep;33(3):427-427.
  • doi: 10.3803/EnM.2018.33.3.427
Two of the authors' names were misprinted.
Letter: The Association between Persistent Hypertriglyceridemia and the Risk of Diabetes Development: The Kangbuk Samsung Health Study (Endocrinol Metab 2018;33:55–61, Yu Hyun Kwon et al.)

Rhee EJ, Kwon YH

  • Endocrinol Metab.
  • 2018 Sep;33(3):425-426.
  • doi: 10.3803/EnM.2018.33.3.425
No abstract available.
An Ectopic Cortisol-Producing Adrenocortical Adenoma Masquerading as a Liposarcoma in the Pararenal Space

Kang S, Park SS, Bae JH, Lee KE, Kim JH, Shin CS

  • Endocrinol Metab.
  • 2018 Sep;33(3):423-424.
  • doi: 10.3803/EnM.2018.33.3.423
No abstract available.
Functional Identification of Compound Heterozygous Mutations in the CYP17A1 Gene Resulting in Combined 17α-Hydroxylase/17,20-Lyase Deficiency

Mo EY, Lee JY, Kim SY, Kim MJ, Kim ES, Lee S, Han JH, Moon SD

  • Endocrinol Metab.
  • 2018 Sep;33(3):413-422.
  • doi: 10.3803/EnM.2018.33.3.413
BACKGROUND: We previously reported a patient with congenital adrenal hyperplasia (CAH) with compound heterozygous mutations in the cytochrome P450 17A1 (CYP17A1) gene. One allele had a p.His373Leu and the other...
Deficiency of Sphingosine-1-Phosphate Reduces the Expression of Prohibitin and Causes β-Cell Impairment via Mitochondrial Dysregulation

Hong SW, Lee J, Kwon H, Park SE, Rhee EJ, Park CY, Oh KW, Park SW, Lee WY

  • Endocrinol Metab.
  • 2018 Sep;33(3):403-412.
  • doi: 10.3803/EnM.2018.33.3.403
BACKGROUND: Emerging evidence suggests that sphingolipids may be involved in type 2 diabetes. However, the exact signaling defect through which disordered sphingolipid metabolism induces β-cell dysfunction remains unknown. The current...
Effects of Maternal Iodine Status during Pregnancy and Lactation on Maternal Thyroid Function and Offspring Growth and Development: A Prospective Study Protocol for the Ideal Breast Milk Cohort

Lee YA, Cho SW, Sung HK, Kim K, Song YS, Moon SJ, Oh JW, Ju DL, Choi S, Song SH, Cheon GJ, Park YJ, Shin CH, Park SK, Jun JK, Chung JK

  • Endocrinol Metab.
  • 2018 Sep;33(3):395-402.
  • doi: 10.3803/EnM.2018.33.3.395
BACKGROUND: Iodine is an intrinsic element of thyroid hormone, which is essential for childhood growth and development. The Ideal Breast Milk (IBM) cohort study aims to evaluate the effects of...
Effect of Dapagliflozin on Alanine Aminotransferase Improvement in Type 2 Diabetes Mellitus with Non-alcoholic Fatty Liver Disease

Choi DH, Jung CH, Mok JO, Kim CH, Kang SK, Kim BY

  • Endocrinol Metab.
  • 2018 Sep;33(3):387-394.
  • doi: 10.3803/EnM.2018.33.3.387
BACKGROUND: Sodium-glucose cotransporter-2 inhibitors (SGLT2i) are expected to improve the liver function of patients with non-alcoholic fatty liver disease (NAFLD) combined type 2 diabetes mellitus (T2DM) by its characteristic mechanism....
Genetic Analysis of CLCN7 in an Old Female Patient with Type II Autosomal Dominant Osteopetrosis

Kim SY, Lee Y, Kang YE, Kim JM, Joung KH, Lee JH, Kim KS, Kim HJ, Ku BJ, Shong M, Yi HS

  • Endocrinol Metab.
  • 2018 Sep;33(3):380-386.
  • doi: 10.3803/EnM.2018.33.3.380
BACKGROUND: Type II autosomal dominant osteopetrosis (ADO II) is a rare genetically heterogeneous disorder characterized by osteosclerosis and increased bone mass, predominantly involving spine, pelvis, and skull. It is closely...
Iodine Status in Filipino Women of Childbearing Age

Serafico M, Ulanday JR, Alibayan M, Gironella , Perlas LA

  • Endocrinol Metab.
  • 2018 Sep;33(3):372-379.
  • doi: 10.3803/EnM.2018.33.3.372
BACKGROUND: Iodine deficiency (ID) has become a concern not only among pregnant women, but in women of childbearing age as well. In fact, a recent report suggested that women with...
Calpain-10 and Adiponectin Gene Polymorphisms in Korean Type 2 Diabetes Patients

Nam JS, Han JW, Lee SB, You JH, Kim MJ, Kang S, Park JS, Ahn CW

  • Endocrinol Metab.
  • 2018 Sep;33(3):364-371.
  • doi: 10.3803/EnM.2018.33.3.364
BACKGROUND: Genetic variations in calpain-10 and adiponectin gene are known to influence insulin secretion and resistance in type 2 diabetes mellitus. Recently, several single nucleotide polymorphisms (SNPs) in calpain-10 and...
Factors Associated with Resolution of Hypertension after Adrenalectomy in Patients with Primary Aldosteronism

Loh WJ, Lim DS, Loh LM, Kek PC

  • Endocrinol Metab.
  • 2018 Sep;33(3):355-363.
  • doi: 10.3803/EnM.2018.33.3.355
BACKGROUND: The aim of this study was to investigate the factors associated with resolution of hypertension after adrenalectomy in patients with primary aldosteronism. A secondary aim was to describe our...
Update on the Aldosterone Resolution Score and Lateralization in Patients with Primary Aldosteronism

Cho EH

  • Endocrinol Metab.
  • 2018 Sep;33(3):352-354.
  • doi: 10.3803/EnM.2018.33.3.352
No abstract available.
Skeletal Fragility in Type 2 Diabetes Mellitus

Starup-Linde J, Hygum K, Langdahl B

  • Endocrinol Metab.
  • 2018 Sep;33(3):339-351.
  • doi: 10.3803/EnM.2018.33.3.339
Type 2 diabetes (T2D) is associated with an increased risk of fracture, which has been reported in several epidemiological studies. However, bone mineral density in T2D is increased and underestimates...
Recent Topics in Fibrodysplasia Ossificans Progressiva

Katagiri T, Tsukamoto , Nakachi Y, Kuratani M

  • Endocrinol Metab.
  • 2018 Sep;33(3):331-338.
  • doi: 10.3803/EnM.2018.33.3.331
Fibrodysplasia ossificans progressiva (FOP) is a rare genetic disease that is characterized by the formation of heterotopic bone tissues in soft tissues, such as skeletal muscle, ligament, and tendon. It...
Regulation of Osteoblast Metabolism by Wnt Signaling

Moorer MC, Riddle RC

  • Endocrinol Metab.
  • 2018 Sep;33(3):318-330.
  • doi: 10.3803/EnM.2018.33.3.318
Wnt/β-catenin signaling plays a critical role in the achievement of peak bone mass, affecting the commitment of mesenchymal progenitors to the osteoblast lineage and the anabolic capacity of osteoblasts depositing...
Therapeutic Role of Yoga in Type 2 Diabetes

Raveendran AV, Deshpandae A, Joshi SR

  • Endocrinol Metab.
  • 2018 Sep;33(3):307-317.
  • doi: 10.3803/EnM.2018.33.3.307
Yoga originated in India more than 5,000 years ago and is a means of balancing and harmonizing the body, mind, and emotions. Yoga practice is useful in the management of...

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