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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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共收录本刊相关文章索引632条
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
Min-Ji Kim,Minji Kim,Ju Young Yoon et al. Min-Ji Kim et al.
Purpose: This study aimed to identify changes in the prevalence of obesity and related diseases among children and adolescents during the coronavirus disease 2019 (COVID-19) pandemic. ...
Kyu Hyun Park,Si-Hwa Gwag,Yu Jin Kim et al. Kyu Hyun Park et al.
Purpose: Three-month gonadotropin-releasing hormone agonists (GnRHas) are expected to achieve better compliance in patients with central precocious puberty (CPP) compared to the monthly formulation. However, 1-month depot...
Kotb Abbass Metwalley,Hekma Saad Farghaly Kotb Abbass Metwalley
Idiopathic ketotic hypoglycemia (IKH) is defined as bouts of hypoglycemia with increased blood or urine ketones in certain children after prolonged fasting or during illness. IKH is divided into physiological IKH, which is most frequently o...
Soojin Hwang,Yena Lee,Ji-Hee Yoon et al. Soojin Hwang et al.
Purpose: As the survival rate from pediatric cancers has increased significantly with advances in treatment modalities, long-term endocrine complications have also risen. This study investigated the frequencies and risks ...
Hyo-Kyoung Nam,Winnah Wu-In Lea,Zepa Yang et al. Hyo-Kyoung Nam et al.
Purpose: Bone age (BA) is needed to assess developmental status and growth disorders. We evaluated the clinical performance of a deep-learning-based BA software to estimate the chronological age (CA) of healthy Korean chi...
Manal Mustafa,Mira Almheiri Manal Mustafa
Familial chylomicronemia syndrome (FCS) is a rare autosomal recessive disease affecting lipoprotein metabolism. FCS is estimated to occur in 1 in 1-2 million individuals and can be diagnosed at any age, equally affecting all genders, races,...
Donghyun Lee,So Yun Park,Heung Sik Kim et al. Donghyun Lee et al.
Hypophosphatasia (HPP) is a rare condition characterized by abnormal bone mineralization. The manifestations of HPP vary from no symptoms to intrauterine fetal death; short stature is another indication of HPP. A 3 ½-year-old boy presented...
Rosie Lee,Mi-Seon Lee,Jung Eun Moon Rosie Lee
Kleefstra syndrome is caused by chromosome 9q34.3 deletion or heterozygous mutations in the euchromatin histone methyl transferase 1 (EHMT1) gene. It can be accompanied by intellectual disability, distinctive facial features, microcephaly, ...
Young Ju Choi,Na Yeong Lee,Moon Bae Ahn et al. Young Ju Choi et al.
Purpose: Glycated albumin (GA) is a glycemic marker reflecting the average serum glucose of the previous 2 weeks. This study aimed to evaluate the usefulness of GA as a glycemic index to complement glycosylated hemoglobin...