Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Xiao-hui Qiao"'
Publikováno v:
Frontiers in Pharmacology, Vol 13 (2022)
Chronic kidney disease (CKD) is an increasingly serious public health problem in the world, but the effective therapeutic approach is quite limited at present. Cellular senescence is characterized by the irreversible cell cycle arrest, senescence-ass
Externí odkaz:
https://doaj.org/article/2ed0c416403c487dbcc95da190b58318
Publikováno v:
International Journal of Endocrinology, Vol 2018 (2018)
Objectives. The present study is aimed at evaluating the diagnostic value of combining shear wave elastography (SWE) parameters and the thyroid imaging reporting and data system (TIRADS) for differentiating between benign and malignant thyroid nodule
Externí odkaz:
https://doaj.org/article/c38d6976161e4e65bc1fea1a8d413229
Publikováno v:
Chinese Journal of Contemporary Neurology and Neurosurgery, Vol 13, Iss 3, Pp 250-254 (2013)
Externí odkaz:
https://doaj.org/article/f7091edba30948d0bb10a6c5ed6a8b46
Autor:
Tian-Ming Wang, Chen-Xi Yang, Xiao-Hui Qiao, Xing-Yuan Liu, Yi-Qing Yang, Ying-Jia Xu, Cui-Mei Zhao, Shan-Shan Wang
Publikováno v:
International Heart Journal. 62:566-574
Pulmonary arterial hypertension (PAH) refers to a rare, progressive disorder that is characterized by occlusive pulmonary vascular remodeling, resulting in increased pulmonary arterial pressure, right-sided heart failure, and eventual death. Emerging
Publikováno v:
World Journal of Pediatrics. 17:115-122
Idiopathic nephrotic syndrome is a common form of glomerular nephropathy in children, with an incidence rate of 1.15–16.9/100,000 depending on different nationalities and ethnicities. The etiological factors and mechanisms of childhood idiopathic n
Autor:
Zhi Wang, Xiao-Hui Qiao, Ying-Jia Xu, Xing-Yuan Liu, Ri-Tai Huang, Song Xue, Hai-Yan Qiu, Yi-Qing Yang
Publikováno v:
BioMed research international. 2022
As the most common form of developmental malformation affecting the heart and endothoracic great vessels, congenital heart disease (CHD) confers substantial morbidity and mortality as well as socioeconomic burden on humans globally. Aggregating convi
Publikováno v:
Transl Pediatr
Williams-Beuren syndrome (WBS) is an autosomal dominant disorder caused by a gene deletion on chromosome 7q11.23. Patients with WBS usually show a group of features such as developmental delay, cardiovascular anomalies, mental retardation, and charac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9ed7c958de8be58761bd0aa5ffe3771
https://europepmc.org/articles/PMC7804474/
https://europepmc.org/articles/PMC7804474/
Autor:
Yi-Qing Yang, Juan Wang, Ruo-Gu Li, Song Xue, Xing-Biao Qiu, Ri-Tai Huang, Xing-Yuan Liu, Xiao-Hui Qiao, Ying-Jia Xu, Yan-Jie Li, Qian Wang, Min Zhang, Xin-Kai Qu
Publikováno v:
European Journal of Medical Genetics. 61:197-203
Congenital heart defect (CHD) is the most common type of birth defect in humans and a leading cause of infant morbidity and mortality. Previous studies have demonstrated that genetic defects play a pivotal role in the pathogenesis of CHD. However, th
Publikováno v:
World Journal of Gastroenterology
Aim To describe contrast-enhanced ultrasound (CEUS) features and evaluate differential diagnosis value of CEUS and conventional ultrasound for patients with benign and malignant gallbladder lesions. Methods This study included 105 gallbladder lesions
Autor:
Jiajie Zhang, Feng Gao, Xiao-Hui Qiao, Huiping Zhang, Jin-Fang Xing, Xiao-Yun Feng, Min Bai, Fan Li, Lian-Fang Du
Publikováno v:
Journal of Medical Imaging and Health Informatics. 7:1121-1125