Results 51 to 60 of about 2,246,140 (208)

Chorionic Villus Sampling: Results of 135 High Risk Cases

open access: yesGynecology Obstetrics & Reproductive Medicine, 2006
OBJECTIVE: To assess the data related to the first-trimester chorionic villus sampling performed in a single tertiary center. STUDY DESIGN: Transabdominal CVS perf ormed on 135 pregnant women, aged 18 to 38 y ears, at 11 to 14 weeks’ gestation, who ...
İskender Başer   +2 more
doaj  

Vaginal host–microbe signatures linked to placental outcomes in mares

open access: yesEquine Veterinary Journal, EarlyView.
Abstract Background Ascending placentitis is a leading cause of late‐term pregnancy loss in mares. Although pathogens are presumed to ascend from the caudal reproductive tract, the association between the vaginal microbiome and placentitis has not been systematically examined.
Machteld van Heule   +7 more
wiley   +1 more source

Evaluation of the Incidence of Chorionic Villus Sampling Complications at 10-13 Weeks of Gestation for Early Diagnosis of Major Thalassemia

open access: yesMajallah-i Dānishgāh-i ̒Ulūm-i Pizishkī-i Bābul, 2010
BACKGROUND AND OBJECTIVE: Early diagnosis of thalassemia with chorionic villus sampling (CVS) has an important role in fetal evaluation. Because of increasing risk of fetal loss and other probable risks, it seems that information about the incidence of ...
R Monzavi Sani, F Savadkuhi, Z Roohani
doaj  

Complication rates after chorionic villus sampling and midtrimester amniocentesis: A 7-year national registry study

open access: yesJournal of the Formosan Medical Association, 2019
Purpose: To assess the complication rates following chorionic villus sampling (CVS) and midtrimester amniocentesis in Taiwan. Methods: This is a national registry-based cohort study from Taiwan.
Wen-Wei Hsu   +8 more
doaj   +1 more source

Prenatal screening and diagnostic strategies for fetal genetic abnormalities: Comparison of international clinical guidelines

open access: yesInternational Journal of Gynecology &Obstetrics, EarlyView.
Abstract This study compares recommendations from international clinical guidelines regarding prenatal screening and diagnostic testing for fetal genetic abnormalities, including the role of non‐invasive prenatal testing (NIPT), invasive diagnostic procedures, and advanced genomic technologies.
Geovanna Saboia Veras   +1 more
wiley   +1 more source

Infant morbidity following amniocentesis and chorionic villus sampling for prenatal karyotyping

open access: yes, 2005
Objective  To investigate whether amniocentesis and chorionic villus sampling increase the risk of postural deformities, limb reduction defects, respiratory problems in the newborn, fetal and infant mortality, prematurity, low birthweight and fetal ...
Haglund, Bengt   +2 more
core   +1 more source

Molecular Genetic Analysis and Prenatal Diagnosis of a Family With MECP2 Duplication Syndrome

open access: yesJournal of Clinical Laboratory Analysis, EarlyView.
Combined low‐pass CNV‐seq and MLPA identified an inherited Xq28 duplication encompassing MECP2 in a 15‐week male fetus and his affected older brother, transmitted from an asymptomatic mother. This integrated strategy enabled accurate pedigree analysis and prenatal diagnosis of MECP2 duplication syndrome, supporting genetic counseling and reproductive ...
FengQiu Lin   +9 more
wiley   +1 more source

Simplified Anisotropic IVIM Using Spherical Means and an Application in the Placenta

open access: yesMagnetic Resonance in Medicine, EarlyView.
ABSTRACT Purpose To reduce the complexity associated with anisotropic IVIM modeling, we derived two simplified diffusion MRI models that map the apparent diffusivity, relative proportions, and anisotropy of perfusion‐ and diffusion‐related signal components and demonstrated them in placenta scans.
Paddy J. Slator   +8 more
wiley   +1 more source

The Effect of Prenatal Invasive Tests on Neonatal Birthweight

open access: yesGynecology Obstetrics & Reproductive Medicine, 2015
OBJECTIVE: The aim of this study is to investigate the effect of prenatal invasive procedures on neonatal birth weight. STUDY DESIGN: The present study consists of three group of pregnancies; 1) Amniocentesis group (n=97), 2) Chorionic Villus Sampling ...
Atakan Tanacan   +5 more
doaj  

Hemophilia A: An Ideal Disease for Prenatal Therapy

open access: yesPrenatal Diagnosis, EarlyView.
ABSTRACT Hemophilia A (HA) is the most common inherited coagulation defect. Current state‐of‐the‐art treatment consists of frequent administration of prophylactic infusions of coagulation factor VIII (FVIII) protein or bispecific antibodies that replace the cofactor function of FVIIIa to maintain hemostasis. However, these treatments are far from ideal,
Christopher D. Porada   +2 more
wiley   +1 more source

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