Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Hang-Yang Jin"'
Autor:
Xiao-Ping Qi, Bi-Jun Lian, Xu-Dong Fang, Fang Dong, Feng Li, Hang-Yang Jin, Ke Zhang, Kang-Er Wang, Yi Zhang
Publikováno v:
Frontiers in Surgery, Vol 9 (2023)
PurposeThis study aimed to assess the feasibility of synchronous bilateral laparoscopic or open cortical-sparing adrenalectomy (SB-LCSA or SB-OCSA) for bilateral pheochromocytomas (bPHEOs) in multiple endocrine neoplasia type 2 (MEN2).MethodsAltogeth
Externí odkaz:
https://doaj.org/article/ccdf998901e64b91ad3b5b8b41da1a91
Autor:
Xiao-Ping Qi, Ju-Ming Ma, Zhen-Fang Du, Rong-Biao Ying, Jun Fei, Hang-Yang Jin, Jian-Shan Han, Jin-Quan Wang, Xiao-Ling Chen, Chun-Yue Chen, Wen-Ting Liu, Jia-Jun Lu, Jian-Guo Zhang, Xian-Ning Zhang
Publikováno v:
PLoS ONE, Vol 6, Iss 5, p e20353 (2011)
BackgroundWhole exome sequencing provides a labor-saving and direct means of genetic diagnosis of hereditary disorders in which the pathogenic gene harbors a large cohort of exons. We set out to demonstrate a suitable example of genetic diagnosis of
Externí odkaz:
https://doaj.org/article/8fc832181772457c909b0e2d2860f7de
Publikováno v:
World Journal of Clinical Cases. 11:2267-2275
Autor:
Bi-Jun Lian, Ke Zhang, Xiao-Ping Qi, Hang-Yang Jin, Qin-Yao Qi, Fang Dong, Kang-Er Wang, Xu-Dong Fang, Feng Li, Yi Zhang
Background: laparoscopic or open cortical-sparing adrenalectomy (LCSA or OCSA; CSA) for treatment of bilateral pheochromocytomas (bPHEO) in multiple endocrine neoplasia type 2 (MEN2) offers a postoperative corticosteroid independence and is balanced
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b27a74d10a696dde3cd295c3fe9c1776
https://doi.org/10.21203/rs.3.rs-948222/v1
https://doi.org/10.21203/rs.3.rs-948222/v1
Autor:
Xiao-ping, Qi, Zhen-guang, Chen, Hang-yang, Jin, Feng, Li, Jun, Cheng, Rong-biao, Ying, Jian-qiang, Zhao, Ding-gang, Guo, Shi-yun, Luo, Gui-ping, Chen, Xian-ning, Zhang
Publikováno v:
Zhonghua yi xue za zhi. 93(28)
To explore the clinical patterns and clinical significance for RET screening in adrenal pheochromocytoma (PHEO) associated with multiple endocrine neoplasia type 2A (MEN2A).The clinical data of 32 PHEO patients with MEN2A from 13 unrelated MEN2A pedi
Autor:
Jian-qiang, Zhao, Liang, Guo, Xiao-ping, Qi, Zhen-guang, Chen, Ke-jing, Wang, Jian-lin, Lou, Xiu-hua, Yu, Jun, Cheng, Hang-yang, Jin, Xiao-long, Li, Rong-biao, Ying, Xian-ning, Zhang
Publikováno v:
Zhonghua yi xue za zhi. 93(6)
To explore the clinical characteristics, therapeutic and clinical significance for RET proto-oncogene screening in a pedigree with familial medullary thyroid carcinoma.Comprehensive medical history was obtained from 19 members in a 4-generate souther
Autor:
Xian-Ning Zhang, Yun Dai, Jin-Yu Li, Wen-Ting Liu, Feng Li, Zhen-Guang Chen, Mao Shen, Yan Zhao, Xiao-Ling Chen, Zhenfang Du, Jun Fei, Hang-Yang Jin, Xiao-Ping Qi, Ju-Ming Ma
Publikováno v:
Molecular medicine reports. 8(3)
Von Hippel-Lindau (VHL) disease is an autosomal dominant familial cancer syndrome. VHL is characterized by the development of renal cell carcinoma (RCC), hemangioblastomas of the central nervous system or retina and pheochromocytoma (PCC). RCC and PC
Autor:
Yan Zhao, Chun-Yue Chen, Ju-Ming Ma, Wen-Ting Liu, Hu-Ling Jiang, Jin-Quan Wang, Jian-Shan Han, Chang-ping Yang, Jun Fei, Xian-Ning Zhang, Xiao-Ping Qi, Xiao-Ling Chen, Hai-Ping Ke, You-Ping Yang, Qi-Zhe Song, Jun Cheng, Zhen-Guang Chen, Rong-Biao Ying, Zhenfang Du, Hang-Yang Jin
Publikováno v:
Thyroid : official journal of the American Thyroid Association. 22(12)
Genetic screening for germline mutations in the RET proto-oncogene has been extensively exploited worldwide to optimize the diagnostic and clinical management of multiple endocrine neoplasia type 2 (MEN2) patients and their relatives. However, a dist
Autor:
Feng Li, Wen-Ting Liu, Xiaoming Wei, Hai-Ping Ke, Xuanzhu Liu, Yan Zhao, Zhangzhang Lan, Ju-Ming Ma, Xiao-Ping Qi, Xian-Ning Zhang, Dong Chen, Peng-Fei Li, Wei Dong, Xiao-Ling Chen, Hu-Ling Jiang, Mingyan Fang, Qing Zhang, Zhen-Guang Chen, Zheng Su, Jun Fei, Hang-Yang Jin, Zhenfang Du
Publikováno v:
Gene. 516(1)
Mutation-based molecular diagnostics of autosomal dominant polycystic kidney disease (ADPKD) is complicated by genetic and allelic heterogeneity, large multi-exon genes, and duplication sequences of PKD1. Recently, targeted resequencing by pooling lo
Autor:
Jianguo Zhang, Wen-Ting Liu, Zhenfang Du, Hang-Yang Jin, Jun Fei, Xiao-Ping Qi, Chun-Yue Chen, Jia-Jun Lu, Jian-Shan Han, Xiao-Ling Chen, Xian-Ning Zhang, Rong-Biao Ying, Jin-Quan Wang, Ju-Ming Ma
Publikováno v:
PLoS ONE, Vol 6, Iss 5, p e20353 (2011)
PLoS ONE
PLoS ONE
BackgroundWhole exome sequencing provides a labor-saving and direct means of genetic diagnosis of hereditary disorders in which the pathogenic gene harbors a large cohort of exons. We set out to demonstrate a suitable example of genetic diagnosis of