QQ客服 官方微博 反馈留言

浏览/检索结果: 共13条，第1-10条 帮助 限定条件 发表日期：2019    专题：山东大学    第一署名单位    第一作者单位    通讯作者单位     已选(0)清除 条数/页：5101520253035404550556065707580859095100   排序方式：请选择作者升序作者降序题名升序题名降序发表日期升序发表日期降序提交时间升序提交时间降序 Image quality and radiation dose of two prospective ECG-triggered protocols using 128-slice dual-source CT angiography in infants with congenital heart disease 期刊论文 INTERNATIONAL JOURNAL OF CARDIOVASCULAR IMAGING, 2019, 卷号: 35, 期号: 5, 页码: 937-945 作者:  Chen, Baojin;  Zhao, Shuo;  Gao, Yang;  Cheng, Zhaoping;  Duan, Yanhua 收藏  |  浏览/下载：19/0  |  提交时间：2019/12/11 Coronary artery  Congenital heart disease  Infant  Prospective  ECG-triggered 128-slice dual source computed tomography angiography   Genotype-phenotype correlation study and mutational and hormonal analysis in a Chinese cohort with 21-hydroxylase deficiency 期刊论文 MOLECULAR GENETICS & GENOMIC MEDICINE, 2019, 卷号: 7, 期号: 6 作者:  Xu, Chao;  Jia, Wenyu;  Cheng, Xiangdeng;  Ying, Hui;  Chen, Jing 收藏  |  浏览/下载：29/0  |  提交时间：2019/12/11 congenital adrenal hyperplasia (CAH)  CYP21A2  genotype-phenotype  associations  mutation  steroid 21-hydroxylase deficiency (21OHD)   Congenital muscular dystrophies in China 期刊论文 CLINICAL GENETICS, 2019, 卷号: 96, 期号: 3, 页码: 207-215 作者:  Ge, Lin;  Zhang, Cheng;  Wang, Zhaoxia;  Chan, Sophelia H. S.;  Zhu, Wenhua 收藏  |  浏览/下载：13/0  |  提交时间：2019/12/11 congenital muscular dystrophy  nationwide population study  prevalence   Genetic spectrum of renal disease for 1001 Chinese children based on a multicenter registration system 期刊论文 Clinical Genetics, 2019 作者:  Rao J.;  Liu X.;  Mao J.;  Tang X.;  Shen Q. 收藏  |  浏览/下载：8/0  |  提交时间：2019/12/11 chronic kidney disease (CKD)  congenital anomalies of the kidney and urinary tract (CAKUT)  genetics  nephronophthisis (NPHP)  polycystic kidney disease PKD  renal disease  singleton-WES  steroid-resistant nephrotic syndrome (SRNS)  targeted gene sequence (TGS)  trio approach for WES (trio-WES)  whole-exome sequence (WES)   Treatment of Common Congenital Hand Conditions 期刊论文 CLINICS IN PLASTIC SURGERY, 2019, 卷号: 46, 期号: 3, 页码: 489-+ 作者:  Wang, Bin;  Tian, Xiaofei;  Hu, Yong 收藏  |  浏览/下载：2/0  |  提交时间：2019/12/11 Congenital  Hand  Difference  Surgical  Treatment   Congenital ulnar nerve deficient hand: a case report 期刊论文 JOURNAL OF HAND SURGERY-EUROPEAN VOLUME, 2019, 卷号: 44, 期号: 8, 页码: 856-858 作者:  Cheng, Tianqing;  Yang, Jiangfei;  Qi, Hengtao 收藏  |  浏览/下载：4/0  |  提交时间：2019/12/11 Molecular Genetics Analysis of 70 Chinese Families With Muscular Dystrophy Using Multiplex Ligation-Dependent Probe Amplification and Next-Generation Sequencing 期刊论文 FRONTIERS IN PHARMACOLOGY, 2019, 卷号: 10 作者:  Wang, Dong;  Gao, Min;  Zhang, Kaihui;  Jin, Ruifeng;  Lv, Yuqiang 收藏  |  浏览/下载：7/0  |  提交时间：2019/12/11 muscular dystrophy  multiplex ligation-dependent probe amplification  next-generation sequencing  dystrophin (DMD)  merosin-deficient  congenital muscular dystrophy type 1A  LAMA2   Hybrid procedure for treating adult congenital heart disease with valvular heart disease in two patients 期刊论文 JOURNAL OF CARDIOTHORACIC SURGERY, 2019, 卷号: 14, 期号: 1 作者:  Li, Chun-sheng;  Lu, Zhong;  Song, Xiao-rong;  Yan, Zhong-ya 收藏  |  浏览/下载：12/0  |  提交时间：2019/12/11 Adult congenital heart disease  Hybrid procedure  Valvular heart disease   Letter regarding Groves et al. "Feasibility of low radiation dose retrospectively-gated cardiac CT for functional analysis in adult congenital heart disease" 期刊论文 INTERNATIONAL JOURNAL OF CARDIOLOGY, 2019, 卷号: 274, 页码: 402-402 作者:  Sun, Chunjuan;  Yu, Benxia;  Li, Ruisheng;  Shi, Yinghong;  Wang, Weiwei 收藏  |  浏览/下载：6/0  |  提交时间：2019/12/11 Adult congenital heart disease  Cardiac computed tomography  Systolic  function  Radiation dose   Lethal melanoma in a two-year-old child with multiple congenital melanocytic nevi 期刊论文 INDIAN JOURNAL OF DERMATOLOGY VENEREOLOGY & LEPROLOGY, 2019, 卷号: 85, 期号: 1, 页码: 89-93 作者:  Gao, Fei;  Niu, Guiye;  Zhang, Bin;  Xin, Linlin 收藏  |  浏览/下载：4/0  |  提交时间：2019/12/11