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期刊名:Annals of pediatric endocrinology & metabolism

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ISSN:2287-1012

e-ISSN:2287-1292

IF/分区:2.4/Q2

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Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Dong Soo Kang,Jiyun Park,Jae Kyung Kim et al. Dong Soo Kang et al.
Purpose: Glycosylated hemoglobin (HbA1c) is often used as an indicator of glucose control. It usually reflects the average glucose levels over two to three months, and is correlated with the development of long-term diabe...
Mi Kyung Son,Ha Young Yoo,Byung Ok Kwak et al. Mi Kyung Son et al.
Purpose: Although microalbuminuria is considered as an early marker of nephropathy in diabetic adults, available information in diabetic adolescents is limited. The aim of this study was to investigate prevalence and freq...
Kye Shik Shim Kye Shik Shim
The complex networks of nutritional, cellular, paracrine, and endocrine factors are closely related with pubertal growth and epiphyseal fusion. Important influencing factors include chondrocyte differentiation capacity, multiple molecular p...
Taninee Sahakitrungruang Taninee Sahakitrungruang
Congenital adrenal hyperplasia (CAH) is one of the most common inherited metabolic disorders. It comprises a group of autosomal recessive disorders caused by the mutations in the genes encoding for steroidogenic enzymes that involved cortis...
Jae Hee Lee,Eun Young Kim Jae Hee Lee
Resistance to thyroid hormone (RTH) is a rare inherited syndrome characterized by diminished response of the target tissue to thyroid hormone caused, in the majority of cases, by mutation of the thyroid hormone receptor beta (THRβ) gene. D...
Yong Hee Hong,Young Lim Shin Yong Hee Hong
Approximately 50% of patients with Turner syndrome (TS) have complete loss of one X chromosome, whereas the rest of the patients with TS display mosaicism or structural abnormalities of the X chromosome. Most well-known common features are ...
Myo-Jing Kim,Young-Eun Kim,Chang-Seok Ki et al. Myo-Jing Kim et al.
Autosomal dominant neurohypophyseal diabetes insipidus is a rare form of central diabetes insipidus that is caused by mutations in the vasopressin-neurophysin II (AVP-NPII) gene. It is characterized by persistent polydipsia and polyuria ind...
Mo Kyung Jung,Kyung Chul Song,Ah Reum Kwon et al. Mo Kyung Jung et al.
Purpose: There is controversy surrounding the growth outcomes of treatment with gonadotropin-releasing hormone agonist (GnRHa) in central precocious puberty (CPP). We analyzed height preservation after treatment with GnRH...
Han Sol Song,Won Bok Choi,Joon Sup Song et al. Han Sol Song et al.
Purpose: The gonadotropin-releasing hormone agonist (GnRHa) is widely used to treat patients with precocious puberty. However, its effect on growth is often difficult to predict because of the diverse nature of its causes...
Sung Chul Yoon,Choong Ho Shin,Sei Won Yang et al. Sung Chul Yoon et al.
Purpose: The diagnosis of pituitary stalk lesion has been based on clinical feature, radiologic assessment for its critical location and role. This study aimed to investigate clinical symptoms, endocrine disturbance, magn...