Preconceptual administration of doxycycline in women with recurrent miscarriage and chronic endometritis: protocol for the Chronic Endometritis and Recurrent Miscarriage (CERM) trial, a multicentre, double-blind, placebo-controlled, adaptive randomised trial with an embedded translational substudy. [PDF]
Odendaal J+6 more
europepmc +1 more source
Are serum progesterone levels predictive of recurrent miscarriage in future pregnancies?
Mayumi Ogasawara+4 more
openalex +1 more source
All Properties of Infertility Microbiome in a Review Article
ABSTRACT Background The microbiome is crucial for many physiological processes, including immunity, metabolism, and reproduction. Aims This review aims to contribute to a detailed understanding of the microbiome of the genital tract, which can lead to better management of dysbiosis and reproductive disorders.
Zahra Elahi+7 more
wiley +1 more source
Threatened miscarriage and recurrent miscarriage: Expert opinions on progesterone therapy and treatment challenges. [PDF]
Demir SC+5 more
europepmc +1 more source
Our study investigates the genetic basis of unexplained recurrent pregnancy loss (uRPL) in 13 Chinese patients by conducting whole‐exome sequencing (WES) on miscarriage tissue samples. The analysis identified critical variants in mucosal barrier genes and genes involved in lipid metabolism within immune cells, highlighting a link to immune ...
Zhao‐Jing Lin+11 more
wiley +1 more source
Association of Interleukin-17A rs2275913 Polymorphism with Recurrent Miscarriage: A Systematic Review and Meta-Analysis Study. [PDF]
Keshavarz Motamed A+7 more
europepmc +1 more source
Endothelial nitric oxide synthase gene polymorphism in women with idiopathic recurrent miscarriage [PDF]
Clemens Tempfer
openalex +1 more source
The importance of markers HLA6 and CD68 in placenta tissues of recurrent pregnancy loss [PDF]
Introduction: Recurrent pregnancy loss of unknown etiology is correlated with immunological factors during pregnancy. Changes in leukocyte subpopulations and HLA (Human Leukocyte Antigen) expression take place in pregnant uterus on both decidua basalis ...
Adriopoulou, Luisa+7 more
core +1 more source
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+2 more
wiley +1 more source