Results 141 to 150 of about 111,518 (268)
Clinical Case Reports, Volume 14, Issue 4, April 2026.ABSTRACT Severe polyhydramnios occurs in 1%–2% of pregnancies and may be associated with maternal diabetes, fetal structural anomalies, genetic disorders, or remain idiopathic. Among the rare etiologies is Bartter syndrome, a renal tubular defect causing impaired salt reabsorption.
Fatemeh Shariati nia +5 more
wiley +1 more source
Eosinophil Cationic Protein Shows Survival Effect on H9c2 Cardiac Myoblast Cells with Enhanced Phosphorylation of ERK and Akt/GSK-3β under Oxidative Stress [PDF]
, 2015 To assess the knowledge and attitudes of pregnant Japanese women regarding non-invasive prenatal testing (NIPT). Between March and June 2013, 557 pregnant women in the Hyogo and Hiroshima Prefectures were surveyed using an anonymous, self-completed ...
Mikamo, Shoko, Nakatsuka, Mikiya
core +1 more source
Clinical Case Reports, Volume 14, Issue 4, April 2026.ABSTRACT Early prenatal screening at 26 + 6 weeks detected Citrobacter koseri vaginal colonization in an asymptomatic high‐risk gravida. Culture‐guided IV ceftazidime (susceptible per CLSI testing) eradicated the pathogen without maternal/fetal compromise.
Mario Assenza +2 more
wiley +1 more source
Obstetrician and Gynecologist Utilization of the NIPT Expanded Testing Option [PDF]
, 2015 Noninvasive prenatal testing (NIPT) enables the detection of common fetal aneuploidies such as trisomy 21, trisomy 18, trisomy 13, and sex chromosome abnormalities via analysis of cell-free fetal DNA circulating in maternal serum.
Mayes, Sarah, BA
core
Stakeholder attitudes and needs regarding cell-free fetal DNA testing [PDF]
, 2016 PURPOSE OF REVIEW: To explore stakeholder views on cell-free DNA testing and highlight findings important for successful implementation and the provision of best practice in counseling.
Chitty, LS, Hill, M, Lewis, C
core +1 more source
Noninvasive prenatal testing to analyze the fetal genome [PDF]
Proceedings of the National Academy of Sciences, 2016 Prenatal genetic testing has changed markedly since the original introduction of amniocentesis as a means to evaluate the fetal karyotype. Because it has long been recognized that maternal age is highly associated with risk for Down syndrome, maternal age became the first screening test for aneuploidy. Later development of screening with maternal serum
openaire +2 more sources
The Homeobox Genes: Classification, Regulation, Biological Functions, and Diseases
MedComm, Volume 7, Issue 4, April 2026.Overview of the homeobox gene superfamily and its pathophysiological roles. The homeobox superfamily comprises several major classes, including ANTP, PRD, TALE, LIM, POU, and others. Among these, the HOX clusters (A–D) play critical roles in embryonic development specifically in conferring cellular identity, regulating morphogenesis, and guiding axial ...
Maedeh Dadzadi +5 more
wiley +1 more source
Taiwanese Journal of Obstetrics & Gynecology, 2018 Objective: The coexistence of maternal malignancy and pregnancy has received increasing attention in Noninvasive prenatal testing (NIPT) studies. Malignancy in pregnant women potentially affects the copy number variation (CNV) profile in NIPT results ...
Xing Ji +25 more
doaj +1 more source