Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Fenhe Zhou"'
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
BackgroundFetal growth restriction (FGR) occurs in 10% of pregnancies worldwide. Placenta dysfunction, as one of the most common causes of FGR, is associated with various poor perinatal outcomes. The main objectives of this study were to screen poten
Externí odkaz:
https://doaj.org/article/5d06f129febb4b2890a36c7ca8c0027b
Autor:
Gang Zou, Qingfang Ji, Jianping Chen, Luye Zhang, Qianqian Sun, Yaqi Shi, Yingjun Yang, Fenhe Zhou, Xing Wei, Luming Sun
Publikováno v:
Frontiers in Medicine, Vol 10 (2024)
ObjectiveThe study aimed to evaluate the pregnancy outcomes of dichorionic diamniotic twin pregnancies that were reduced to singletons at different gestational ages.Study designThis was a retrospective cohort study of twin pregnancies that underwent
Externí odkaz:
https://doaj.org/article/0af0dfdb100545cd936a3a167538fc1f
Autor:
Xing Wei, Xinyao Zhou, Jia Zhou, Gang Zou, Yingjun Yang, Fenhe Zhou, Shiyi Xiong, Jianping Chen, Luming Sun
Publikováno v:
Fetal Diagnosis and Therapy. 49:138-144
Objective: We aimed to study the value of exome sequencing (ES) in severe pleural effusion with nonimmune hydrops fetalis (NIHF) that underwent thoracoamniotic shunt (TAS). Methods: It was a retrospective study of NIHF that underwent TAS between 2012
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::587d818b00fd2253963512b5b95ceeb3
https://doi.org/10.1159/000521212
https://doi.org/10.1159/000521212
Autor:
Ya Xing, Yun Zhang, Jianping Chen, Fengyu Wu, Meizhen Yuan, Gang Zou, Yingjun Yang, Fenhe Zhou, Jia Zhou, Luming Sun
Publikováno v:
Prenatal diagnosisREFERENCES. 42(7)
To investigate the use of chromosomal microarray (CMA) and Exome sequencing (ES) in fetuses with congenital heart disease (CHD).The Fetal Medicine Unit of Shanghai First Maternity and Infant Hospital records were reviewed to ascertain all cases diagn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40348a5332286a22ac98492afeddbd09
https://pubmed.ncbi.nlm.nih.gov/35584285
https://pubmed.ncbi.nlm.nih.gov/35584285
Autor:
Xing, Wei, Yingjun, Yang, Jia, Zhou, Xinyao, Zhou, Shiyi, Xiong, Jianping, Chen, Fenhe, Zhou, Gang, Zou, Luming, Sun
Publikováno v:
Genes; Volume 13; Issue 12; Pages: 2231
(1) Background: Numerous etiologies may lead to non-immune hydrops fetalis (NIHF). However, the causes remain unclear in half of NIHF cases following current standard assessment. The application of prenatal chromosomal microarray analysis (CMA) and e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bacaa7d8192c3a45d71d509bcd25824b
https://doi.org/10.3390/genes13122231
https://doi.org/10.3390/genes13122231
Publikováno v:
Prenatal Diagnosis. 38:499-503
Objective Radiofrequency ablation (RFA) is a management alternative for complicated monochorionic twin pregnancies. The purpose of this study is to evaluate risk factors for fetal death after RFA. Methods An observational study was performed to docum
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::630037f0bf605086632d61f4c3124c55
https://doi.org/10.1002/pd.5269
https://doi.org/10.1002/pd.5269
Publikováno v:
The Journal of Maternal-Fetal & Neonatal Medicine. 31:3075-3079
To report a cohort of dichorionic triamniotic (DCTA) triplets with access to contemporary fetal interventions.Prospective study.A regional referral center for the diagnosis and management of complicated multiple pregnancies.All DCTA triplets receivin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9350c0b9863986570b737967482f1a16
https://doi.org/10.1080/14767058.2017.1363733
https://doi.org/10.1080/14767058.2017.1363733