Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Xianhao Wen"'
Autor:
Li Xiao, Yang Zhang, Ximing Xu, Ying Dou, Xianmin Guan, Yuxia Guo, Xianhao Wen, Yan Meng, Meiling Liao, Qinshi Hu, Jie Yu
Publikováno v:
Heliyon, Vol 9, Iss 11, Pp e22202- (2023)
Background: Hemophagocytic Lymphohistiocytosis (HLH) is a rare and life-threatening disease in children, with a high early mortality rate. This study aimed to construct machine learning model to predict the risk of early death using clinical indicato
Externí odkaz:
https://doaj.org/article/7d1a5f69a2b04c0c99f0fcc79acd3cf6
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
Osteopetrosis is characterized by increased bone density caused by decreased osteoclasts or dysfunction of their differentiation and absorption properties, usually caused by biallelic variants of the TCIRG1(OMIM:604592)and CLCN7(OMIM:602727) genes. H
Externí odkaz:
https://doaj.org/article/42ba3568a19d4b30ba16d1cab21f2900
Autor:
Li Xiao, Ximing Xu, Zhiling Zhang, Ying Dou, Xianmin Guan, Yuxia Guo, Xianhao Wen, Yali Shen, Yan Meng, Meiling Liao, Qinshi Hu, Jie Yu
Background Hemophagocytic lymphohistiocytosis (HLH) is a rapidly progressive and potentially life-threatening disorder. Identifying risk factors and timely adjustment of the given treatment regimens is critical to reducing the early mortality in HLH
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2df75bb32516f629d3ef80278a813b11
https://doi.org/10.21203/rs.3.rs-1638552/v1
https://doi.org/10.21203/rs.3.rs-1638552/v1
Autor:
Li Xiao, Ximing Xu, Zhiling Zhang, Ying Dou, Xianmin Guan, Yuxia Guo, Xianhao Wen, Yali Shen, Yan Meng, Meiling Liao, Qinshi Hu, Jie Yu
Background Hemophagocytic lymphohistiocytosis (HLH) is a rapidly progressive and potentially life-threatening disorder. Identifying risk factors and timely adjustment of the given treatment regimens is critical to reducing the early mortality in HLH
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::810087e956b7a4af053fd8e3e3e17d6f
https://doi.org/10.21203/rs.3.rs-1597772/v1
https://doi.org/10.21203/rs.3.rs-1597772/v1
Publikováno v:
Thrombosis research. 210
Purpura fulminans (PF) is a hematological emergency that can be caused by severe congenital protein C (PC) deficiency. It has been rarely reported in the Chinese population. We aimed to characterize the clinical and genetic features of Chinese pediat
Publikováno v:
Journal of Clinical Laboratory Analysis
Background The aim of this study was to design and analyze the applicability of a 21‐gene high‐throughput sequencing (HTS) panel in the molecular diagnosis of patients with hereditary thrombocytopenia (HT). Methods A custom target enrichment libr
Autor:
Yi-Mei Ma, Xianhao Wen, Yali Shen, Peng-Fei Li, Qing-Lin Kong, Ying-Hui Cui, Xi-Zhou An, Xianmin Guan, Jie Yu, Yan Meng, Yanzhen Wang, Yuxia Guo
Publikováno v:
Oncology Letters
Phosphoribosyl pyrophosphate synthetase 1 (PRPS1) is closely associated with a number of diseases; however, its influence in B-cell acute lymphoblastic leukemia (B-ALL) and the potential molecular mechanisms involved remain unclear. The present study
Publikováno v:
Medicine. 99:e19150
Chronic myeloid leukemia (CML) is relatively rare in childhood and few studies have reported the clinical use of imatinib (IM) in pediatric CML. In this study, we evaluated the efficacy and tolerability of IM in children and adolescents with CML.We i
Publikováno v:
International journal of laboratory hematology. 41(2)
Introduction To investigate the correlation of long noncoding RNA-SOX6-1 (lnc-SOX6-1) with clinicopathological features and treatment outcomes in pediatric acute myeloid leukemia (AML) patients, and further explore its function in AML cell proliferat
Publikováno v:
Seminars in thrombosis and hemostasis. 43(6)
This study aims to determine the clinical significance of positive antinuclear/antiextractable nuclear antigen (ANA/A-ENA) antibody on manifestation and therapeutic response of childhood immune thrombocytopenia (ITP). Overall, 1,330 patients aged bet