Results 81 to 90 of about 25,999 (245)

Use of the Abbott i‐STAT®1 point of care device for hCG quantification in early pregnancy

International Journal of Gynecology &Obstetrics, EarlyView.
Abstract Objectives To evaluate the use of the Abbott i‐STAT®1 point‐of‐care‐test (POCT) device for measurement of human chorionic gonadotropin (hCG) to support the management of early pregnancy complications in a remote early pregnancy unit (EPU). Methods Women attending the EPU who required an hCG blood test were invited to take part in the study ...
Caroline Joyce, Paula M. O'Shea, Rebecca Lynch, Seán J. Costelloe, Tommie V. McCarthy, John Coulter, Deirdre Hayes‐Ryan, Keelin O'Donoghue   +7 more
wiley   +1 more source

Antenatal dexamethasone for late preterm delivery: Rate of complete course and neonatal outcomes

International Journal of Gynecology &Obstetrics, EarlyView.
Abstract Objective This retrospective cohort study aimed to assess the rate of complete dexamethasone administration among late preterm deliveries and its impact on neonatal outcomes. Methods We reviewed medical records of 1500 late preterm deliveries (gestational age 34–36 + 6 weeks) between January 2018 and December 2020, analyzing baseline ...
Piyamon Srisakulpanich, Pattarawalai Talungchit, Tachjaree Panchalee, Chutima Yaiyiam   +3 more
wiley   +1 more source

Maternal gut microbiota‐derived daidzein prevents osteoporosis in female offspring following prenatal prednisone exposure

iMeta, EarlyView.
Prenatal prednisone therapy (PPT)/prenatal prednisone exposure (PPE) induces long bone dysplasia, reduced peak bone mass (PBM), and increased osteoporosis susceptibility in female offspring. Maternal gut microbiota metabolite daidzein (DAI) mediates PPE‐induced osteoporosis susceptibility in female adult offspring.
Chi Ma, Hangyuan He, Kunpeng Wang, Juanjuan Guo, Liang Liu, Yuting Chen, Bin Li, Hao Xiao, Xufeng Li, Xiaoqian Lu, Tingting Wang, Yinxian Wen, Hui Wang, Liaobin Chen   +13 more
wiley   +1 more source

Screening for foetal malformations: performance of routine ultrasonography in the population of the Swiss Canton of Vaud. [PDF]

, 2001
OBJECTIVE: To determine the sensitivity of ultrasonography in screening for foetal malformations in the pregnant women of the Swiss Canton of Vaud. STUDY DESIGN: Retrospective study over a period of five years.
Addor, M.C., Hohlfeld, P., Tran, C., Vial, Y.   +3 more
core  

Association Between Fetal Myocardial Alterations and Congenital Heart Disease Based on Post‐Mortem Myocardial MRI

iRADIOLOGY, EarlyView.
Applying myocardial parametric mapping based on post‐mortem MRI is feasible for non‐invasive tissue characterization. We speculated that the elevated T2 relaxation may be an essential myocardial tissue characterization of cyanotic congenital heart disease, potentially suggesting myocardial edema, which may provide evidence to guide appropriate ...
Weizeng Zheng, Xia Ying, Yuan Chen, Le Wang, Peiyue Jiang, Ying Jiang, Guohui Yan, Hong Wang, Yimin Zhou, Yun Liang, Yu Zou, Liqun Sun, Qiong Luo   +12 more
wiley   +1 more source

Value of Magnetic Resonance Spectroscopy for Examining Fetal Brain Development in Mid‐ to Late Pregnancy

iRADIOLOGY, EarlyView.
This study demonstrates that the ratio of tNAA to tCr increases during gestation, which correlates with an increase in the number of neurons and cellular energy metabolism in the fetal brain as gestational weeks progress. Additionally, tCho levels exhibit a progressive decrease with advancing gestational weeks, indicating the ongoing development of the
Dejuan Shan, Yi Zhang, Maobo Wang, Yanyan Liu, Yudong Wang, Lianxiang Xiao   +5 more
wiley   +1 more source

Prenatal Diagnosis and Clinical Phenotypic Heterogeneity of 22q11.2 Microdeletion Syndrome Based on a Single Center Retrospective Study

Journal of Clinical Laboratory Analysis, EarlyView.
Chromosome 22q11.2 microdeletion syndrome (22q11.2DS) is a common congenital disorder with high clinical phenotypic heterogeneity. In this study, we retrospectively investigated the incidence of prenatal diagnosis of 22q11.2DS in a single center and summarized its clinical manifestations to expand the phenotypic database ABSTRACT Objective To ...
Jia‐yan Chen, Mei‐jiao Cai, Yun‐sheng Ge   +2 more
wiley   +1 more source

Prenatal ultrasound diagnosis of poland syndrome [PDF]

, 2004
D'ARMIENTO, MARIA, MARTINELLI, PASQUALE, PALADINI, DARIO   +2 more
core   +1 more source

Klippel‐Trénaunay‐Weber Syndrome: Prenatal Diagnosis and Review of the Literature

Journal of Clinical Ultrasound, Volume 53, Issue 3, Page 535-546, March/April 2025.
This meta‐analysis demonstrates the high diagnostic accuracy of SZ‐CEUS for differentiating between malignant and benign focal liver lesions, as well as for HCC from non‐HCC lesions. The study shows better performance for smaller lesions and those with a higher proportion of malignancy.
Giuliana Orlandi, Laura Sarno, Antonio Angelino, Mariarosaria Motta, Raffaella Di Girolamo, Luigi Carbone, Marika Rovetto, Laura Letizia Mazzarelli, Gabriella Sglavo, Francesco D' Antonio, Ilenia Mappa, Daniele Di Mascio, Giuseppe Rizzo, Giuseppe Maria Maruotti   +13 more
wiley   +1 more source

Prenatal Diagnosis and Prognostic Factors in Fetuses With Arthrogryposis Multiplex Congenita—A Systematic Review

Journal of Clinical Ultrasound, EarlyView.
Arthrogryposis Multiplex Congenita (AMC) is characterized by the presence of multiple joint contractures in the fetus' body. The diagnosis of arthrogryposis is complex and often missed prenatally. This comprehensive review of the literature published over the last 20 years, with an emphasis on the role of prenatal ultrasound in predicting postnatal ...
Mario Brock Leao, Marianna Facchinetti Brock, Jorge Roberto Di Tommaso Leao, Gianpaolo Grisolia, Mario Lituania, Samantha Erin Neumann, Gabriele Tonni, Rodrigo Ruano   +7 more
wiley   +1 more source