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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:3.3/Q1

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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
Jung Sub Lim,Se Won Lim,Ju Hyun Ahn et al. Jung Sub Lim et al.
Purpose: To construct new Korean reference curves for birth weight by sex and gestational age using contemporary Korean birth weight data and to compare them with the Lubchenco and the 2010 United States (US) intrauterine...
Min Sun Cho,Gyung Sun Cho,So Hyun Park et al. Min Sun Cho et al.
Purpose: The incidence of congenital hypothyroidism (CH) has increased in several countries. Lower cut-off in screening programs have led to an increase in the proportion of transient hypothyroidism (TH) cases diagnosed, ...
Ji Woo Lee,Hyung Jin Kim,Yun Mee Choe et al. Ji Woo Lee et al.
Purpose: Long-acting gonadotropin-releasing hormone agonists (GnRHa) are commonly used to treat central precocious puberty (CPP) in Korea. Although rare, there have been reports on the characteristic of adverse reactions ...
Hye Jin Lee,Hae Woon Jung,Gyung Min Lee et al. Hye Jin Lee et al.
Purpose: Whether parental origin of the intact X chromosome and/or the presence of Y chromosome sequences (Yseq) play a role in three-year height response to growth hormone (GH) were investigated. ...
Hae Sang Lee,Jin Soon Hwang Hae Sang Lee
Graves' disease (GD) accounts for 10%-15% of thyroid disorders in children and adolescents. The use of antithyroid drugs as the initial treatment option in GD is well accepted. An average two years remission is achieved in about 30% of chil...
Toshihiro Tajima,Akie Nakamura,Shuntaro Morikawa et al. Toshihiro Tajima et al.
Congenital central hypothyroidism (C-CH) is a rare disease in which thyroid hormone deficiency is caused by insufficient thyrotropin (TSH) stimulation of a normally-located thyroid gland. Most patients with C-CH have low free thyroxine leve...
Gyung Min Lee,Jung Min Ko,Choong Ho Shin et al. Gyung Min Lee et al.
The 46,XX testicular disorder of sex development (DSD), also known as 46,XX male syndrome, is a rare form of DSD and clinical phenotype shows complete sex reversal from female to male. The sex-determining region Y (SRY) gene can be identifi...
Jee Hyue Seo,Yong Hoon Park,Sei Won Yang et al. Jee Hyue Seo et al.
Acute suppurative thyroiditis is a rare disease because the thyroid gland is remarkably resistant to infection. We present a 2-year-old girl with refractory acute suppurative thyroiditis due to a pyriform sinus fistula (PSF). She complained...
Hong Jun Lee,Jung-Sook Yeom,Ji Sook Park et al. Hong Jun Lee et al.
There is a wide variety of genital abnormalities observed in patients with Denys-Drash syndrome (DDS). WT1 is thought to influence the genes related to genital development and mutations in this gene have been associated with DDS. DDS should...
Noorisaem Rhee,Kumi Jeong,Eun Mi Yang et al. Noorisaem Rhee et al.
Gigantism indicates excessive secretion of growth hormones (GH) during childhood when open epiphyseal growth plates allow for excessive linear growth. Case one involved a 14.7-year-old boy presented with extreme tall stature. His random ser...