Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Lianxiang Li"'
Publikováno v:
IEEE Access, Vol 12, Pp 70345-70356 (2024)
The real-time and accurate detection of premature ventricular contractions (PVC) in patients is of great significance for preventing the occurrence of high-risk events such as sudden cardiac death and guiding cardiac surgical procedures such as radio
Externí odkaz:
https://doaj.org/article/ed1254bc31b5415dbb3280748a267dfc
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
Hypothermia has been widely used to treat moderate to severe neonatal hypoxic–ischemic encephalopathy (HIE), yet evaluating the effects of hypothermia relies on clinical neurology, neuroimaging, amplitude-integrated electroencephalography, and foll
Externí odkaz:
https://doaj.org/article/54d68ab3d5f04e06b432946f5cc4e9e7
Autor:
Hongyan Lv, Baojun Qiao, Liyuan Fang, Lihong Yang, Qiuli Wang, Sujing Wu, Pengshun Ren, Lianxiang Li
Publikováno v:
Hereditas, Vol 156, Iss 1, Pp 1-10 (2019)
Abstract Objective To investigate the clinical and genetic characteristics of neonatal Crohn’s disease (CD), improve recognition of neonatal CD, and reduce the number of patients that are missed or misdiagnosed. Methods A 10-day-old Chinese girl wi
Externí odkaz:
https://doaj.org/article/8071e3c8363548cc9ffd04f20b4018f8
Publikováno v:
Hematology Reports, Vol 11, Iss 3 (2019)
Beta thalassemia is a hereditary disorder resulted from mutations in the β globin gene leading to alpha/beta imbalance, ineffective erythropoiesis, and chronic anemia. Three types have been defined, based on the degree of reduced beta-globin chain s
Externí odkaz:
https://doaj.org/article/094f5317d5bc4250956a7ffb3f3478f6
Autor:
Hongyan Lv, Fang Liu, Qiuli Wang, Zhiyong Dong, Pengshun Ren, Huiming Zhang, Xiaohui Yan, Lianxiang Li
Publikováno v:
Clinical Laboratory; 2023, Vol. 69 Issue 8, p1763-1768, 6p
Publikováno v:
Journal of biochemical and molecular toxicologyREFERENCES. 36(7)
Gastric cancer (GC) is a highly heterogeneous malignancy, characterized by high mortality and poor prognosis. Ferroptosis is a newly defined nonapoptotic programmed cell death mechanism that has been implicated in the development of various pathologi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e57e97a56c67be5cc35a89c4705e2ee
https://pubmed.ncbi.nlm.nih.gov/35315178
https://pubmed.ncbi.nlm.nih.gov/35315178
Publikováno v:
The Journal of Maternal-Fetal & Neonatal Medicine. 33:3887-3893
The aim of this study was to explore differences in serum Tau protein levels and neurodevelopmental prognoses of placental abruption or umbilical cord around neck with hypoxic-ischemic encephalopathy (HIE).Forty neonates with moderate/severe HIE divi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f72814044cc165c14f8a72f13104339
https://doi.org/10.1080/14767058.2019.1588878
https://doi.org/10.1080/14767058.2019.1588878
Autor:
Pengshun Ren, Lianxiang Li, Haihua Huo, Junxia Song, Qiuli Wang, Sujing Wu, Junqin Li, Hongyan Lv
Publikováno v:
American journal of perinatology. 39(12)
Objective Multiple randomized controlled trials have shown that hypothermia is a safe and effective treatment for neonatal moderate or severe hypoxic-ischemic encephalopathy (HIE). The neuroprotective mechanisms of hypothermia need further study. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7abf925f348aa578fac936bede004d1c
https://pubmed.ncbi.nlm.nih.gov/33454948
https://pubmed.ncbi.nlm.nih.gov/33454948
Publikováno v:
Clinical Laboratory. 66
Background Congenital thrombotic thrombocytopenic purpura (TTP) is rare and is prone to misdiagnosis or missed diagnosis in clinical. The relationship between genotype and phenotype needs further study. Methods A 15-hour-old Chinese girl develops jau
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2f820409c273df03eaf77687a331d0a
https://doi.org/10.7754/clin.lab.2019.190715
https://doi.org/10.7754/clin.lab.2019.190715
Autor:
Bao-jun Qiao, Hongyan Lv, Pengshun Ren, Liyuan Fang, Lihong Yang, Lianxiang Li, Qiuli Wang, Sujing Wu
Publikováno v:
Hereditas
Hereditas, Vol 156, Iss 1, Pp 1-10 (2019)
Hereditas, Vol 156, Iss 1, Pp 1-10 (2019)
Objective To investigate the clinical and genetic characteristics of neonatal Crohn’s disease (CD), improve recognition of neonatal CD, and reduce the number of patients that are missed or misdiagnosed. Methods A 10-day-old Chinese girl with oral u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::efa09674587c0aba1620b232e2ca634a
https://doi.org/10.1186/s41065-019-0114-8
https://doi.org/10.1186/s41065-019-0114-8