Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Li-Yang Ying"'
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 8 (2022)
BackgroundBerry syndrome is a challenging disease for surgeons to make early diagnosis and successful surgical correction in the neonatal period. Here, we summarized the clinical features of three neonates with berry syndrome in our center to optimiz
Externí odkaz:
https://doaj.org/article/dff6fa6fc8384099827611a0aff44887
Akademický článek
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Publikováno v:
In Radiation Measurements 2011 46(12):2107-2110
Akademický článek
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Publikováno v:
Journal of Cardiothoracic Surgery
Background Cardiac tumors which may induce sudden death are rare entities with an autopsy frequency of 0.001–0.030 %. This study aims to analyze the characteristics and outcome of pediatric patients with primary cardiac tumors treated in our center
Publikováno v:
International journal of clinical and experimental medicine. 8(10)
Objective: We discussed the correlation between SNP loci (rs198389 and rs198388) in brain natriuretic peptide gene (NPPB) and susceptibility to congenital heart diseases (CHD). Method: Multiplex SNaPshot technique was adopted for profiling of SNP gen
Autor:
Ze-wei, Zhang, Jian-ying, Deng, Li-yang, Ying, Zhan, Gao, Jie, Jin, Jian-chuan, Qi, Zheng, Tan
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 28(6)
To investigate the frequency and clinical phenotypes of 22q11.2 microdeletion in patients with non-syndromic tetralogy of Fallot (TOF).Six-eight non-syndromic TOF patients (38 males and 30 females, aged 0-11 years) were selected and evaluated by hist
Autor:
Jian-ying, DENG, Ze-wei, ZHANG, Jian-hua, LI, Yu-ning, ZHU, Jian-bin, YANG, Zhan, GAO, Li-yang, YING
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 28(2)
To evaluate multiplex ligation-dependent probe amplification (MLPA) assay detection in analysis of chromosome 22q11.2 microdeletion.Between March 2008 and September 2009, thirty-two patients including 10 males and 16 females aged between years (3.6±
Publikováno v:
Journal of pediatric surgery. 45(8)
True thymic hyperplasia is a very rare entity. We present an instance of idiopathic true massive thymic hyperplasia in a 9-month-old girl with a very large left-sided mediastinal mass noted on diagnostic imaging. Percutaneous biopsy revealed normal t
Publikováno v:
Circulation. 119(15)