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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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共收录本刊相关文章索引594
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
Yun Hee Gyon,Heon-Seok Han Yun Hee Gyon
A 9-year-, 11-month-old girl was brought to the Emergency Department for sudden dyspnea caused by massive pericardial effusion. In addition to relative bradycardia despite impending cardiac tamponade, short stature, overweight, and hypercho...
Hyeoh Won Yu,Yun Jeong Lee,Won Im Cho et al. Hyeoh Won Yu et al.
Purpose: We hypothesized that overweight or obese children might develop type 1 diabetes mellitus (T1DM) early despite residual beta-cell function. Factors independently associated with preservation of C-peptide level wer...
Won Im Cho,Hyeoh Won Yu,Hye Rim Chung et al. Won Im Cho et al.
Purpose: To describe the clinical characteristics of full-term neonates with hypocalcemia and to suggest factors associated with neonatal hypocalcemia. Me...
Jun-Won Hwang,Ji-Young Seo Jun-Won Hwang
Purpose: This study investigated the relationship between height and psychopathology in community children with relatively short stature according to the parents' reports. Also, the matter of parental concern about child'...
Ji-Eun Lee Ji-Eun Lee
The growing attention to alternative glycemic biomarkers including fructosamine, glycated albumin (GA), 1,5-anhydroglucitol (1,5-AG), is attributable to the limitations of the glycated hemoglobin (HbA1c) assay. It is important to recognize ...
Min Sun Kim,Dae-Yeol Lee Min Sun Kim
Increasing evidence suggests an important role of the insulin-like growth factor (IGF)-IGF binding protein (IGFBP) axis in the maintenance of normal glucose and lipid metabolism. Significant changes occur in the local IGF-I-IGFBPs environme...
Yong Suk Shim,Woohyeok Choi,Il Tae Hwang et al. Yong Suk Shim et al.
Hypoparathyroidism, sensorineural deafness, and renal dysgenesis syndrome is an autosomal dominant disease caused by mutations in the GATA3 gene on chromosome 10p15. We identified a patient diagnosed with hypoparathyroidism who also had a f...
Byung Ho Kang,Shin-Hee Kim,Kyung A Jung et al. Byung Ho Kang et al.
Purpose: Endocrine-disrupting chemicals interfere with the endocrine system and therefore affect growth and pubertal progression. The study aim was to compare the growth and pubertal progression in wild-type female rats w...
Dong Yup Lee,Ah Reum Kwon,Jung Min Ahn et al. Dong Yup Lee et al.
Purpose: Previous studies have revealed many inconsistent results regarding the relationship between vitamin D and metabolic syndrome. The purpose of our study was to investigate the association between serum 25-hydroxyvi...
Aram Yang,Yeon Hee Lee,Soon Young Nam et al. Aram Yang et al.
Purpose: Prader-Willi syndrome (PWS) is a well-known genetic disorder, and microdeletion on chromosome 15 is the most common causal mechanism. Several previous studies have suggested that various environmental factors mig...