Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Pengshun Ren"'
Publikováno v:
BMC Pediatrics, Vol 24, Iss 1, Pp 1-8 (2024)
Abstract Background Amniotic fluid contamination (AFC) is a risk factor for neonatal hypoxic ischemic encephalopathy (HIE); however, the correlation between AFC level and the incidence and clinical grading of HIE, in addition to relevant biomarkers o
Externí odkaz:
https://doaj.org/article/6546461ae3bf4326987eca41c549bc3f
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
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:
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
Autor:
Lihong Yang, Lianxiang Li, Zhi-ying Wang, Hongyan Lv, Qiuli Wang, Lan-Na Bu, Pengshun Ren, Xiu-Ling Gu
Publikováno v:
Clinical laboratory. 65(7)
Background Primary neonatal hypocholinesterase is rare; its genetic pattern and mutation still need to be further studied. Methods The patient and his parents are studied using next-generation sequencing technology. Results A boy one day after birth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e836e46be455a4ac48284d4825df5dba
https://pubmed.ncbi.nlm.nih.gov/31307170
https://pubmed.ncbi.nlm.nih.gov/31307170
Autor:
Lin-Hong Jin, Pengshun Ren, Xiu-Ling Gu, Lianxiang Li, Qiuli Wang, Rui-Jiang Zheng, Hongyan Lv
Publikováno v:
Clinical laboratory. 64(4)
To study the clinical and genetic features from a Chinese child with SATB2-associated syndrome (SAS) and review of literature.The girl, 2 years 3 months old, is admitted to the Department of Pediatric Rehabilitation in our hospital. This patient has
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee3d752d7d8c2253e84d5cb3137893f9
https://pubmed.ncbi.nlm.nih.gov/29739092
https://pubmed.ncbi.nlm.nih.gov/29739092