Overcoming oral medication allergy and cervical stenosis in an anovulatory in vitro fertilization patient: a case report. [PDF]
Romana D +4 more
europepmc +1 more source
ABSTRACT In utero interventions are transformative in addressing genetic and anatomic conditions during fetal development. Next generation sequencing enables early genetic testing, playing a pivotal role in prenatal decision‐making by supporting risk stratification, precise and timely diagnosis, which directly informs eligibility for fetal surgical and
Matthew A. Shear +7 more
wiley +1 more source
Impact of mineral oil overlay on immature oocyte maturation in an optimized in vitro culture system. [PDF]
Peng J, Hao Y, Yu Z, Chen B, Zhang Z.
europepmc +1 more source
Association Between Prepregnancy Blood Pressure and Reproductive Outcomes of In Vitro Fertilization. [PDF]
Fang Y +20 more
europepmc +1 more source
Moderate Diagnostic Yield of Exome Sequencing in Fetal Growth Restriction: Retrospective Insights
ABSTRACT Objective To determine whether invasive genetic testing should be systematically proposed in cases of FGR. Methods Descriptive retrospective study of 159 FGR cases (defined by an estimated fetal growth < 3rd percentile, regardless of Doppler findings) managed at the Toulouse Fetal Medicine Center (TFMC) during 2022–2023.
Maud Langeois +5 more
wiley +1 more source
Asthma and Infertility: A Prospective Case-Control Study on Pregnancy and Live Birth Rates in Women With Asthma Undergoing Assisted Reproduction. [PDF]
Lundberg FE +3 more
europepmc +1 more source
Attitudes Toward Prenatal Interventions in the Fanconi Anemia Community
ABSTRACT Objective In‐utero cell and gene therapies may offer prenatal treatment options for inherited diseases. Preclinical data suggests in‐utero (IU) hematopoietic stem cell transplantation (HSCT) could prevent Fanconi anemia (FA) related bone marrow failure without genotoxic conditioning or immune suppression.
Tony Lum +4 more
wiley +1 more source
Large cyclic AMP-dependent increases in tyrosine-phosphorylated proteins are not absolutely necessary for the induction of full-type hyperactivation and penetration into eggs in ejaculated boar spermatozoa in vitro. [PDF]
Ueshiba A +4 more
europepmc +1 more source
CUL3‐Related Neurodevelopmental Disorder: Expanding the Prenatal Phenotype
ABSTRACT Objective Pathogenic variants of the CUL3 gene are known to cause a neurodevelopmental disorder with a partially described prenatal phenotype. This study further characterizes and expands the spectrum of prenatal sonographic findings associated with the disorder to improve prenatal diagnosis and counseling.
Yoel Gofin +12 more
wiley +1 more source

