Near-final height in 82 Chinese patients with congenital adrenal hyperplasia due to classic 21-hydroxylase deficiency: a single-center study from China

Lin Juan; Ma Huamei; Su Zhe; Li Yanhong; Chen Hongshan; Chen Qiuli; Zhang Jun; Guo Song; Du Minlian

首页> 外文期刊>Journal of pediatric endocrinology & metabolism: JPEM >Near-final height in 82 Chinese patients with congenital adrenal hyperplasia due to classic 21-hydroxylase deficiency: a single-center study from China

【24h】

Near-final height in 82 Chinese patients with congenital adrenal hyperplasia due to classic 21-hydroxylase deficiency: a single-center study from China

机译：由经典21-羟化酶缺乏症引起的82名中国先天性肾上腺皮质增生患者的接近最终高度：来自中国的单中心研究

获取原文

获取原文并翻译 | 示例

获取外文期刊封面封底 >>

开具论文收录证明 >>

文献代查 >>

团队文献服务 >>

页面导航

摘要
著录项
相似文献
相关主题

摘要

Background: The objective of this study was to identify variables that might interfere with reaching the near final height (NFH) in Congenital adrenal hyperplasia (CAH) due to classic 21-hydroxylase deficiency (21-OHD).

机译：背景：本研究的目的是确定可能因经典的21-羟化酶缺乏症（21-OHD）而导致先天性肾上腺皮质增生（CAH）达到接近最终高度（NFH）的变量。

著录项

来源
《Journal of pediatric endocrinology & metabolism: JPEM 》 |2016年第7期| 共8页
作者
Lin Juan; Ma Huamei; Su Zhe; Li Yanhong; Chen Hongshan; Chen Qiuli; Zhang Jun; Guo Song; Du Minlian;
展开▼
作者单位

展开▼
收录信息
原文格式 PDF
正文语种 eng
中图分类儿科学 ;
关键词
congenital adrenal hyperplasia; 21-hydroxylase deficiency; near final height; target height;

机译：先天性肾上腺增生;21-羟化酶缺乏症;接近最终身高;目标身高;

相似文献

外文文献
中文文献
专利

1. Near-final height in 82 Chinese patients with congenital adrenal hyperplasia due to classic 21-hydroxylase deficiency: a single-center study from China [J] . Lin Juan, Ma Huamei, Su Zhe, Journal of pediatric endocrinology & metabolism: JPEM . 2016 ,第7期

机译：由经典21-羟化酶缺乏症引起的82名中国先天性肾上腺皮质增生患者的接近最终高度：来自中国的单中心研究
2. Genotype-Phenotype Correlation in 153 Adult Patients With Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency: Analysis of the United Kingdom Congenital Adrenal Hyperplasia Adult Study Executive (CaHASE) Cohort [J] . Nils Krone, Ian T. Rose, Debbie S. Willis, The journal of clinical endocrinology and metabolism . 2013 ,第2期

机译：153名因21羟化酶缺乏症引起的先天性肾上腺皮质增生的基因型与表型的相关性：英国先天性肾上腺皮质增生成人研究执行员（CaHASE）队列的分析
3. Identification of novel and rare CYP21A2 variants in Chinese patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency [J] . Jing Xu, Pin Li Clinical Biochemistry . 2019 ,第期

机译：由于21-羟化酶缺乏，中国先天性肾上腺增生患者鉴定新型和罕见的CYP21A2变体
4. Congenital adrenal hyperplasia due to 21-hydroxylase deficiency A paradigm for prenatal diagnosis and treatment [C] . Saroj Nimkarn, Maria I. New Conference on Skeletal Biology and Medicine . 2010

机译：先天性肾上腺素增生由于21羟化酶缺乏症的产前诊断和治疗范式
5. The effect of Chinese Food Therapy on community dwelling middle-aged hypertensive patients with Yin deficiency in Hangzhou, China. [D] . Shen, Cui Zhen. 2009

机译：中国食品疗法对杭州市阴虚症社区居民中年高血压患者的影响。
6. Genotype-Phenotype Correlation in 153 Adult Patients With Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency: Analysis of the United Kingdom Congenital Adrenal Hyperplasia Adult Study Executive (CaHASE) Cohort [O] . Nils Krone, Ian T. Rose, Debbie S. Willis, -1

机译：153名因21羟化酶缺乏症导致的先天性肾上腺皮质增生的基因型与表型的相关性：英国先天性肾上腺皮质增生成人研究执行员（CaHASE）队列的分析
7. Estudo comparativo do uso de prednisolona versus acetato de hidrocortisona no tratamento da hiperplasia adrenal congênita por deficiência da 21-hidroxilase forma clássica Comparative study of prednisolone versus hydrocortisone acetate for treatment of patients with the classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency [O] . Flavia M. Leite, Carlos A. Longui, Cristiane Kochi, 2008

机译：泼尼松龙与醋酸氢化可的松治疗经典21-羟化酶缺乏症先天性肾上腺增生的比较研究泼尼松龙与醋酸氢化可的松治疗经典21-羟化酶缺乏症先天性肾上腺增生的比较研究

Near-final height in 82 Chinese patients with congenital adrenal hyperplasia due to classic 21-hydroxylase deficiency: a single-center study from China

摘要

著录项

相似文献

相关主题

期刊订阅