Results 131 to 140 of about 42,724 (240)

Society for Maternal‐Fetal Medicine Special Statement: Reducing the risk of transmitting infection during ultrasound examination—Updated 2026

open access: yesPregnancy, Volume 2, Issue 5, September 2026.
Abstract Ultrasound examinations have the potential to transmit infections between individuals. The risk can be reduced by following certain well‐described procedures to clean and disinfect ultrasound transducers between examinations. However, surveys have shown widespread lapses in the cleaning and disinfection of transducers and other equipment.
Society for Maternal‐Fetal Medicine (SMFM)   +3 more
wiley   +1 more source

Systematic evaluation of whole exome sequencing for copy number variation detection in prenatal diagnosis

open access: yes
Clinical and Translational Medicine, Volume 16, Issue 9, September 2026.
Lihua Yu   +14 more
wiley   +1 more source

Placental pathology in fetuses with and without congenital heart defects

open access: yesPregnancy, Volume 2, Issue 5, September 2026.
Abstract Introduction Placental histopathologic evaluation of pregnancies affected by congenital heart defects (CHDs) can provide insight into the mechanism connecting placental and fetal vascular systems. The objective of this study was to evaluate the prevalence of maternal vascular malperfusion (MVM) and fetal vascular malperfusion (FVM) lesions of ...
Tucker E. Doiron   +6 more
wiley   +1 more source

Placental Polyp: A Case Report

open access: yesSiriraj Medical Journal, 2005
A 28-year-old widow, gravida 1, para 1 which took place ten years earlier, presented with heavy bleeding from the vagina. Pelvic examination revealed a hemorrhagic and necrotic mass protruding from the external cervical os.
Wiset Watcharotone   +1 more
doaj  

Prenatal Genomics for Sonographers: Enhancing Confidence, Communication, and Clinical Care

open access: yesSonography, Volume 13, Issue 3, September 2026.
To access CPD test for this article click here: https://www.sonographers.org/account/login?returnUrl=/cpds/Prenatal_genomics_for_sonographers. ABSTRACT Genomic medicine is advancing rapidly, bringing significant changes to prenatal care and expanding the role of health professionals.
Deborah Wye   +2 more
wiley   +1 more source

MORPHOLOGICAL FEATURES OF PLACENTAS IN PREGNANCIES WITH FETAL GROWTH RESTRICTION SYNDROME

open access: yesПаёми Сино
Objective: To present the morphological features of placentas in pregnancies with hypertension and fetal growth restriction syndrome (FGRS) Methods: Eighty-six placentas in pregnancies with FGRS on the background of arterial hypertension are examined.
N.A. MURATNAZAROVA
doaj   +1 more source

LINE-1 retrotransposon methylation in chorionic villi of first trimester miscarriages with aneuploidy. [PDF]

open access: yesJ Assist Reprod Genet, 2021
Vasilyev SA   +11 more
europepmc   +1 more source

MicroRNA‐Mediated Placental Maladaptation in Preeclampsia Pathogenesis

open access: yesFASEB BioAdvances, Volume 8, Issue 9, September 2026.
Graphical representation of miRNA‐mediated placental maladaptation in preeclampsia. Under normal pregnancy conditions, balanced expression of beneficial miRNAs (miR‐126‐3p, miR‐18a/b‐5p, miR‐144‐3p, miR‐378a‐5p, and miR‐146a‐5p) promotes trophoblast proliferation, migration and invasion, spiral artery remodeling, angiogenesis, mitochondrial function ...
Sarbani Saha, Rupasri Ain
wiley   +1 more source

Narrative Review on Therapies That Influence Inflammatory Responses During Extremely Premature Perinatal Respiratory Transition

open access: yesActa Paediatrica, Volume 115, Issue 9, Page 1847-1860, September 2026.
ABSTRACT Aims and Methods Advances in neonatal care have extended borderline survival to 22–24 post‐conceptional weeks. Present review discusses approaches for prolonging short pregnancies and prevention of serious morbidities in extremely premature infants born before 28 weeks of pregnancy.
Mikko Hallman
wiley   +1 more source

Preimplantation Genetic Testing for Families at Risk of Haemophilia: Ten‐Year Single‐Centre Experience

open access: yesHaemophilia, Volume 32, Issue 5, Page 1239-1246, September/October 2026.
ABSTRACT Introduction Preimplantation genetic testing for monogenic diseases (PGT‐M) is a reproductive option for couples at high risk of transmitting inherited disorders. We report a ten‐year single‐centre PGT‐M experience in families at risk of hemophilia.
Mimosa Mortarino   +6 more
wiley   +1 more source

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