Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Meiping Chen"'
Autor:
Xinyu Yue, Meiping Chen, Xiaoan Ke, Hongbo Yang, Fengying Gong, Linjie Wang, Lian Duan, Hui Pan, Huijuan Zhu
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 12, Iss 9, Pp n/a-n/a (2024)
ABSTRACT Background Cornelia de Lange syndrome (CdLS) is an uncommon congenital developmental disorder distinguished by intellectual disorder and distinctive facial characteristics, with a minority of cases attributed to RAD21 variants. Methods A pat
Externí odkaz:
https://doaj.org/article/1796d05b160f4cd98a5296a325828a87
Autor:
Xiaofang Liu, Pan Zhang, Meiping Chen, Haibo Zhou, Tingting Yue, Ming Xu, Ting Cai, Juan Huang, Xiaoyang Yue, Guangdi Li, Zhiguo Zhou
Publikováno v:
Heliyon, Vol 9, Iss 12, Pp e22873- (2023)
Objectives: The spread of SARS-Cov-2 remains a global concern along with the emergence of variants. This study aims to characterize the epidemiological and clinical features of hospitalized patients who were dragonized with five different variants of
Externí odkaz:
https://doaj.org/article/0070967074be41e2b486aa6fce263b3e
Autor:
Na Yu, Lian Duan, Fang Hu, Shengmin Yang, Jie Liu, Meiping Chen, Yong Yao, Kan Deng, Feng Feng, Xin Lian, Xinxin Mao, Huijuan Zhu
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
BackgroundGrowth hormone (GH)/thyroid stimulating hormone (TSH) cosecreting pituitary adenoma (PA) is an exceedingly rare kind of bihormonal pituitary neuroendocrine tumors (PitNETs). Its clinical characteristics have rarely been reported.ObjectivesT
Externí odkaz:
https://doaj.org/article/6b8c957749a84f3d81d58199ca17fbc4
Autor:
Xiaoan Ke, Linjie Wang, Meiping Chen, Shanshan Liu, Na Yu, Lian Duan, Fengying Gong, Huijuan Zhu
Publikováno v:
BMC Endocrine Disorders, Vol 22, Iss 1, Pp 1-7 (2022)
Abstract Background Recently, side effects from Dopamine Receptor Agonist Drugs (DAs) in treating pituitary prolactinoma have raised widespread concern. This study explores the incidence and influencing factors of DAs-related side effects in Chinese
Externí odkaz:
https://doaj.org/article/cd0c75eab4b4488ba8fa599e98549aa9
Autor:
Chao Cao, Li He, Jingping Ma, Meiping Chen, Yiting Li, Qingwen Jiang, Shiyu Wu, Lili Yu, Weina Huang, Guoqing Qian, Chuanbing Zhu, Jinguo Chu, Xiaomin Chen
Publikováno v:
BMC Infectious Diseases, Vol 21, Iss 1, Pp 1-7 (2021)
Abstract Background This study was performed to investigate clinical features of patients with severe SARS-CoV-2 pneumonia and identify risk factors for converting to severe cases in those who had mild to moderate diseases at the start of the pandemi
Externí odkaz:
https://doaj.org/article/8fe4cacc08a64fabb804484980c23642
Autor:
Meiping Chen, Hui Miao, Hanting Liang, Xiaoan Ke, Hongbo Yang, Fengying Gong, Linjie Wang, Lian Duan, Shi Chen, Hui Pan, Huijuan Zhu
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
Externí odkaz:
https://doaj.org/article/d69cca47e8774306999bbd5faf95adde
Autor:
Meiping Chen, Shiyi He, Phoebe Miles, Chunlin Li, Yijun Ge, Xuechan Yu, Linfeng Wang, Weina Huang, Xue Kong, Shanni Ma, Yiting Li, Qingwen Jiang, Wen Zhang, Chao Cao
Publikováno v:
Frontiers in Cellular and Infection Microbiology, Vol 12 (2022)
Perturbation of the microbiome has numerous associations with the phenotypes and progression in chronic airways disease. However, the differences in the nasal microbiome in asthma and allergic rhinitis (AR) have not been defined. We examined whether
Externí odkaz:
https://doaj.org/article/2219c619380144b78f93f65df9edee0e
Autor:
Meiping Chen, Hui Miao, Hanting Liang, Xiaoan Ke, Hongbo Yang, Fengying Gong, Linjie Wang, Lian Duan, Shi Chen, Hui Pan, Huijuan Zhu
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
ContextClinical genetic evaluation has been demonstrated as an important tool to elucidate the causes of growth disorders. Genetic defects of collagen formation (the collagenopathies) have been reported to be associated with short stature and skeleta
Externí odkaz:
https://doaj.org/article/e624e7dc48ea4de5b87862c06635124d
Autor:
Shanshan Liu, Meiping Chen, Hongbo Yang, Shi Chen, Linjie Wang, Lian Duan, Huijuan Zhu, Hui Pan
Publikováno v:
Frontiers in Endocrinology, Vol 12 (2021)
Background18q- syndrome is a rare chromosomal disease caused by the deletion of the long arm of chromosome 18. Some cases with 18q- syndrome can be combined with growth hormone deficiency (GHD), but data on the efficacy of recombinant human growth ho
Externí odkaz:
https://doaj.org/article/110fc3bcd98e4d188cd267a9a8bec31e
Autor:
Meiping Chen, Xiaoan Ke, Hanting Liang, Fengying Gong, Hongbo Yang, Linjie Wang, Lian Duan, Hui Pan, Dongyan Cao, Huijuan Zhu
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 12, Pp n/a-n/a (2021)
Abstract Background Ring chromosome 15 [r (15)] is an uncommon finding with various clinical manifestations. A common phenotype for these patients has not been established and data on the efficacy of recombinant human growth hormone (rhGH) treatment
Externí odkaz:
https://doaj.org/article/30ad1b26dff648b295b61a07a03c5f47