Results 161 to 170 of about 28,470 (248)
Abstract A substantial portion of RhD‐negative pregnant patients carry an RhD‐negative fetus and are not at risk of RhD alloimmunization. Knowing the fetal RhD genotype allows such patients to avoid unnecessary monitoring or treatment. The use of cell‐free DNA (cfDNA) to detect the fetal RhD genotype from maternal blood has been proposed to identify ...
Society for Maternal‐Fetal Medicine (SMFM) +8 more
wiley +1 more source
How to facilitate ultrasound examination of the fetal heart: the 5‐4‐3‐2‐1 method
ABSTRACT We propose a new standardized, systematic method of fetal cardiac screening, the step‐by‐step ‘5‐4‐3‐2‐1’ method. This method is based on understanding the cardiac structures through a process of navigating between the different recommended views during an abdominothoracic sweep, following a user‐friendly checklist to identify the main ...
M. Levy, B. Stos
wiley +1 more source
ABSTRACT Objective To examine the contribution of fetal growth restriction ultrasound phenotypes to adverse perinatal outcomes at term. Design Retrospective population‐based cohort study. Setting John Radcliffe Hospital, Oxford, UK where universal ultrasound at 35+1–36+6 weeks is performed. Population Congenital abnormalities and births before the scan
Elena D'Alberti +5 more
wiley +1 more source
Sex-Specific Doppler Patterns of the Umbilical Artery, Middle Cerebral Artery, and Descending Abdominal Aorta in an African Pregnancy Cohort. [PDF]
Ofori E +4 more
europepmc +1 more source
ABSTRACT Objective To determine the risk of placental dysfunction associated with different ultrasound‐based phenotypes of impaired fetal growth in dichorionic twin pregnancies. Design Retrospective cohort study. Setting Single tertiary centre. Population Patients with dichorionic twin pregnancies delivered at ≥ 320/7 (2011–2023) (N = 753).
Ala Essalah +5 more
wiley +1 more source
Vasa previa with bipartite placenta and velamentous cord insertion. [PDF]
Hafsi M +6 more
europepmc +1 more source
Our findings show early increased Netrin‐4 in mice with PWMI boosts angiogenesis and OPCs proliferation. Later, high levels hinder OPCs differentiation into mature cells, impairing myelination. It may act by stimulating ET‐1 secretion. Abstract Perinatal hypoxia–ischemia is a leading cause of preterm white matter injury (PWMI), yet mechanisms ...
Fuxing Dong +8 more
wiley +1 more source
Arterial and Venous Doppler Parameters in Fetal Growth Restriction: A Comparative Evaluation of Early- and Late-Onset Subtypes. [PDF]
Ankara Aktas H +9 more
europepmc +1 more source
Neurodevelopmental screening in toddlers or preschoolers with sickle cell disease (SCD) predicts future academic deficits. Screening sensitivity for future academic deficits is highest in preschoolers with SCD. Brief neurodevelopmental screening tools can identify high risk children for early intervention. This original article is commented on by Karst
Sarah E. Bills +5 more
wiley +1 more source
Isolated tricuspid regurgitation in structurally normal fetal hearts: a systematic review. [PDF]
Bravo-Valenzuela NJ +5 more
europepmc +1 more source

