| 缩写名/全名 |
J PEDIATR ENDOCR MET
JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM |
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| ISSN号 | 0334-018X | ||||||||||||||||||||||||
| 研究方向 | 医学-内分泌学与代谢 | ||||||||||||||||||||||||
| 影响因子 | 2015:0.912, 2016:1.233, 2017:1.086, 2018:1.239, 2019:1.278, | ||||||||||||||||||||||||
| 出版国家 | ENGLAND | ||||||||||||||||||||||||
| 出版周期 | Monthly | ||||||||||||||||||||||||
| 年文章数 | 192 | ||||||||||||||||||||||||
| 出版年份 | 0 | ||||||||||||||||||||||||
| 是否OA | No | ||||||||||||||||||||||||
| 审稿周期(仅供参考) | 一般,3-6周 |
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| 录用比例 | 容易 | ||||||||||||||||||||||||
| 投稿链接 | http://www.degruyter.com/view/j/jpem?tab=call_for_papers | ||||||||||||||||||||||||
| 投稿官网 | http://www.degruyter.com/view/j/jpem | ||||||||||||||||||||||||
| h-index | 60 | ||||||||||||||||||||||||
| CiteScore |
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| PubMed Central (PMC)链接 | http://www.ncbi.nlm.nih.gov/nlmcatalog?term=0334-018X%5BISSN%5D | ||||||||||||||||||||||||
| 中科院SCI期刊分区 （ 2018年新版本） |
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| 中科院SCI期刊分区 （ 2020年新版本） |
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| 中国学者近期发表的论文 | |
| 1. | Aromatase excess syndrome in a Chinese boy due to a novel duplication at 15q21.2. Author: Tan X1, Wu X1, Chen J1, Wu Y1, Li S1, Chen X1, Zhang X1. Journal: J Pediatr Endocrinol Metab. 2019 Jan 28;32(1):85-88. doi: 10.1515/jpem-2018-0266. PubMed DOI |
| 2. | Comparative evaluation of neuroendocrine dysfunction in children with craniopharyngiomas before and after mass effects are removed. Author: Guo Y1, Wang Y2, Ni M2, Zhang Y2,3, Zhong L4. Journal: J Pediatr Endocrinol Metab. 2019 Feb 25;32(2):127-133. doi: 10.1515/jpem-2018-0204. PubMed DOI |
| 3. | Physical growth and development characteristics of children with Williams syndrome aged 0-24 months in Zhejiang Province. Author: Yao D1, Ji C1, Chen W1, Li M1, Zhao ZY1. Journal: J Pediatr Endocrinol Metab. 2019 Mar 26;32(3):233-237. doi: 10.1515/jpem-2018-0185. PubMed DOI |
| 4. | Maternal factors associated with neonatal vitamin D deficiency. Author: Wang C1, Gao J2, Liu N3, Yu S4, Qiu L4, Wang D1. Journal: J Pediatr Endocrinol Metab. 2019 Feb 25;32(2):167-172. doi: 10.1515/jpem-2018-0422. PubMed DOI |
| 5. | Identification of two novel TPK1 gene mutations in a Chinese patient with thiamine pyrophosphokinase deficiency undergoing whole exome sequencing. Author: Zhu L1, Wu R2, Ye Z2, Gu R1, Wang Y1, Hou Y1, Feng Z1, Ma X3. Journal: J Pediatr Endocrinol Metab. 2019 Mar 26;32(3):295-300. doi: 10.1515/jpem-2018-0363. PubMed DOI |
| 6. | A pilot study on newborn screening for congenital adrenal hyperplasia in Beijing. Author: Gong LF1, Gao X2, Yang N1, Zhao JQ1, Yang HH1, Kong YY1. Journal: J Pediatr Endocrinol Metab. 2019 Mar 26;32(3):253-258. doi: 10.1515/jpem-2018-0342. PubMed DOI |
| 7. | The diagnosis of cystinosis in patients reveals new CTNS gene mutations in the Chinese population. Author: Li XQ1, Wu D1, Liang XJ1, Li WJ1, Liu M1, Cao BY1, Su C1, Meng X1, Gong CX1. Journal: J Pediatr Endocrinol Metab. 2019 Apr 24;32(4):375-382. doi: 10.1515/jpem-2018-0263. PubMed DOI |
| 8. | Carbonated beverage consumption is associated with lower C-peptide in adolescents. Author: Ye S1, Chen H2, Ren X1, Wen J1, Du Y1, Li X1, Zhang R1, Yu L1, Zhang B1, Du D1, Sun F1. Journal: J Pediatr Endocrinol Metab. 2019 May 27;32(5):447-454. doi: 10.1515/jpem-2018-0286. PubMed DOI |
| 9. | Using height-corrected definition of metabolic syndrome in children and adolescents. Author: Ma C1, Lu Q1, Wang R1, Yin F2. Journal: J Pediatr Endocrinol Metab. 2019 May 27;32(5):429-438. doi: 10.1515/jpem-2018-0414. PubMed DOI |
| 10. | A first case report of UDP-galactose-4'-epimerase deficiency in China: genotype and phenotype. Author: Tong F, Yang R, Hong F, Qian G, Jiang P, Gao R. Journal: J Pediatr Endocrinol Metab. 2016 Mar;29(3):379-83. doi: 10.1515/jpem-2014-0462. PubMed |
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