Zobrazeno 1 - 10
of 60
pro vyhledávání: '"Linhuan Huang"'
Publikováno v:
BMC Endocrine Disorders, Vol 24, Iss 1, Pp 1-8 (2024)
Abstract Background Functioning adrenal adenoma during pregnancy is rare, and the diagnosis is challenging owing to unspecific symptoms and restricted investigations. The obstetric outcomes of patients who undergo surgery during pregnancy or who rece
Externí odkaz:
https://doaj.org/article/0d67ef64d0ec48b4b9d6df30df38efe1
Publikováno v:
BMC Pregnancy and Childbirth, Vol 24, Iss 1, Pp 1-6 (2024)
Abstract Background To date, there are no clinical guidelines for dichorionic diamniotic (DCDA) twins complicated with previable premature rupture of membrane (PV-ROM) before 24 weeks of gestation. The typical management options including expectant m
Externí odkaz:
https://doaj.org/article/ea538489b4a64dde904755d80cce49ce
Autor:
Shaobin Lin, Shanshan Shi, Jian Lu, Zhiming He, Danlun Li, Linhuan Huang, Xuan Huang, Yi Zhou, Yanmin Luo
Publikováno v:
Molecular Cytogenetics, Vol 17, Iss 1, Pp 1-14 (2024)
Abstract Background The contribution of genetic variants to congenital heart defects (CHDs) has been investigated in many postnatal cohorts but described in few prenatal fetus cohorts. Overall, specific genetic variants especially copy number variant
Externí odkaz:
https://doaj.org/article/d2d766d3de7b4b2e8f18ca174b1d69be
Autor:
Ruijue Zhu, Mingming Zhu, Boye Wang, Enen Chen, Danlei Cai, Yinghong Yang, Yi Liang, Chuqi Su, Ding Wang, Xiaofang Sun, Linhuan Huang, Yingjun Xie
Publikováno v:
BMC Medical Genomics, Vol 17, Iss 1, Pp 1-7 (2024)
Abstract Introduction Dent disease type I is a rare X-linked recessive renal tubular disease resulting from pathogenic variants in the CLCN5 gene. Due to the rarity of Dent disease type I and the diversity of its phenotypes, its clinical diagnosis is
Externí odkaz:
https://doaj.org/article/24b2b46efe41447c85ae44857f855aa3
Publikováno v:
BMC Pregnancy and Childbirth, Vol 23, Iss 1, Pp 1-9 (2023)
Abstract Objectives To compare the clinical outcomes of different multifetal pregnancy reduction (MFPR) programs in dichorionic (DC) triplets, and explore the association between early ultrasound characteristics and co-twin death after potassium chlo
Externí odkaz:
https://doaj.org/article/7eb46ca351854f5fb9e85cc7e621cd97
Autor:
Shuting Xia, Yingnan Ye, Jialiu Liu, Hanfei Qiu, Minhuan Lin, Zhiming He, Linhuan Huang, Malie Wang, Yanmin Luo
Publikováno v:
Biomolecules, Vol 14, Iss 8, p 988 (2024)
Epigenetic regulation is an important entry point to study the pathogenesis of selective fetal growth restriction (sFGR), and an understanding of the role of long noncoding RNAs (lncRNAs) in sFGR is lacking. Our study aimed to investigate the potenti
Externí odkaz:
https://doaj.org/article/603684c6cf2442e9b467e6784e774f12
Autor:
Minhuan Lin, Yiqing Chen, Shuting Xia, Zhiming He, Xuegao Yu, Linhuan Huang, Shaobin Lin, Binrun Liang, Ziliang Huang, Shiqiang Mei, Dong Liu, Lingling Zheng, Yanmin Luo
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Introduction: Fetal growth restriction (FGR) is a placenta-mediated pregnancy complication that predisposes fetuses to perinatal complications. Maternal plasma cell-free DNA harbors DNA originating from placental trophoblasts, which is promising for
Externí odkaz:
https://doaj.org/article/60299824cddc4a678d9d325fbb816430
Autor:
Shaobin Lin, Shanshan Shi, Linhuan Huang, Ting Lei, Danlei Cai, Wenlong Hu, Yi Zhou, Yanmin Luo
Publikováno v:
Molecular Cytogenetics, Vol 12, Iss 1, Pp 1-11 (2019)
Abstract Background This study aimed to estimate the associations of copy number variants (CNVs) with fetal kidney ultrasound anomalies. A total of 331 fetuses with kidney ultrasound anomalies who underwent prenatal chromosomal microarray analyses we
Externí odkaz:
https://doaj.org/article/3fe088c466ae4f3bb53a1ced864cdd38
Autor:
Shaobin Lin, Zhiming He, Linhuan Huang, Jialiu Liu, Ting Lei, Jianzhu Wu, Peizhi Huang, Yi Zhou, Yanmin Luo
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Familial Rubinstein-Taybi syndrome (RSTS) with recurrent RSTS siblings and apparently unaffected parents is rare; such cases might result from parental somatic and/or germline mosaicism. Parental low-level (T (p.Gln1079*) in CREBBP in the siblings vi
Externí odkaz:
https://doaj.org/article/92fc3c41f9bc49f4b3244c61bbe109e3
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 11, Pp n/a-n/a (2019)
Abstract Background Fetal femur length (FL) is an important biometric index in prenatal screening. The etiology of short femur is diverse, with some pathogenic causes leading to adverse outcomes. To improve the accuracy and practicability of diagnosi
Externí odkaz:
https://doaj.org/article/9d0e8565a437483fb858a6d698710eaa