Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Yue-Huang Yang"'
Autor:
Ti-Long Huang, Bao-Hua Sang, Qing-Ling Lei, Chun-Yan Song, Yun-Bi Lin, Yu Lv, Chun-Hui Yang, Na Li, Yue-Huang Yang, Xian-Wen Zhang, Xin Tian
Publikováno v:
BMC Pediatrics, Vol 19, Iss 1, Pp 1-5 (2019)
Abstract Background Hereditary spherocytosis (HS) is a type of hemolytic anemia caused by abnormal red cell membrane skeletal proteins with few unique clinical manifestations in the neonate and infant. An ANK1 gene mutation is the most common cause o
Externí odkaz:
https://doaj.org/article/e17007d5b7c74b0cbbe914f9ae57cdf4
Autor:
Ti-Long Huang, Tian-Yao Zhang, Chun-Yan Song, Yun-Bi Lin, Bao-Hua Sang, Qing-Ling Lei, Yu Lv, Chun-Hui Yang, Na Li, Xin Tian, Yue-Huang Yang, Xian-Wen Zhang
Publikováno v:
Frontiers in Pediatrics, Vol 8 (2020)
Background: Thalassemia is an autosomal genetic disorder, found throughout the world. It is still not treatable and create socio economic problems. In this study, we investigated the prevalence and spectrum features of thalassemia in Yunnan Province,
Externí odkaz:
https://doaj.org/article/1e09795807e249619bfdef18b6adf09d
Autor:
Xin Tian, Bao-Hua Sang, Ti-Long Huang, Yu Lv, Yun-Bi Lin, Yue-Huang Yang, Chun-Yan Song, Na Li, Xian-Wen Zhang, Qing-Ling Lei, Chun-Hui Yang
Publikováno v:
BMC Pediatrics, Vol 19, Iss 1, Pp 1-5 (2019)
BMC Pediatrics
BMC Pediatrics
Background Hereditary spherocytosis (HS) is a type of hemolytic anemia caused by abnormal red cell membrane skeletal proteins with few unique clinical manifestations in the neonate and infant. An ANK1 gene mutation is the most common cause of HS. Cas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7128db5d4bf716c15de74828c5fea36
http://link.springer.com/article/10.1186/s12887-019-1436-4
http://link.springer.com/article/10.1186/s12887-019-1436-4
Autor:
Chun-Yan Song, Xian-Wen Zhang, Ti-Long Huang, Yue-Huang Yang, Tian-Yao Zhang, Na Li, Chun-Hui Yang, Yu Lv, Yun-Bi Lin, Xin Tian, Bao-Hua Sang, Qing-Ling Lei
Publikováno v:
Frontiers in Pediatrics, Vol 8 (2020)
Frontiers in Pediatrics
Frontiers in Pediatrics
Background: Thalassemia is an autosomal genetic disorder, found throughout the world. It is still not treatable and create socio economic problems. In this study, we investigated the prevalence and spectrum features of thalassemia in Yunnan Province,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa1765414ced0e0509b9ba58f76efb11
https://doi.org/10.3389/fped.2020.00159
https://doi.org/10.3389/fped.2020.00159
Autor:
Ti-Long Huang, Sang, Bao-Hua, Lei, Qing-Ling, Song, Chun-Yan, Yun-Bi Lin, Lv, Yu, Yang, Chun-Hui, Li, Na, Yue-Huang Yang, Zhang, Xian-Wen, Tian, Xin
Timeline of this case. of a de novo ANK1 mutation associated to hereditary spherocytosis: a case report. (DOCX 16 kb)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d7a64914f9f13b9657a415555d37ec5
Publikováno v:
Intervirology. 56:195-200
Enterovirus 71 (EV71) is one of the causative pathogens of hand-foot-and-mouth disease and effective antiviral agents and vaccines against this virus have, to date, not been available. MicroRNAs (miRNAs) are a recently discovered class of RNAs with t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::212c99cb89a651b60249ee85c649a42b
https://doi.org/10.1159/000348504
https://doi.org/10.1159/000348504
Autor:
San-bin, Wang, Deng-ming, Hu, Li, Li, Yue-huang, Yang, Xing-hua, Pan, Lin, Liu, Li-hui, Peng, Zheng-jun, Xie, Bo, Yin, Yang, Liang, Xiao-juan, Sun
Publikováno v:
Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi. 32(12)
To evaluate the feasibility of HLA haploidentical peripheral blood hematopoietic stem cell transplantation (PBSCT) for patients with β thalassemia major.Sixteen patients with β thalassemia major received HLA haploidentical PBSCT from parents. Two c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::82a6f919363251b073c9276863508a94
https://pubmed.ncbi.nlm.nih.gov/22339959
https://pubmed.ncbi.nlm.nih.gov/22339959