Results 231 to 240 of about 124,221 (329)
The Role of Fetal Renal Artery Doppler in Predicting Intrauterine Growth Restriction: A Case-Control Study. [PDF]
D N S +5 more
europepmc +1 more source
ABSTRACT Human newborns are able to discriminate between certain languages but not others. This ability has long been attributed to sensitivity to rhythm—the temporal regularities in speech of different languages. Here, we demonstrate through a series of computational simulations that this discrimination behavior can be achieved using no temporal ...
Ruolan Leslie Famularo +3 more
wiley +1 more source
Optimization of the hatch window by preincubation and temporal changes in extra-embryonic structures in grey partridge (Perdix perdix) hatching eggs. [PDF]
Biesek J, Wlaźlak S, Adamski M.
europepmc +1 more source
ABSTRACT To enhance clinicians' understanding of Sifrim‐Hitz‐Weiss syndrome (SIHIWES), this study investigated the clinical phenotypes, genetic characteristics, and response to growth hormone therapy in a patient. A case of a patient with global developmental delay and distinctive facial features is presented.
Jianmei Zhang +6 more
wiley +1 more source
Can Cord Entanglement Occur in Monochorionic Diamniotic Twins? A Rare Case of Spontaneous Septostomy of Dividing Membranes. [PDF]
Bolbol R +3 more
europepmc +1 more source
ABSTRACT To investigate the correlation between genetic abnormalities and fetal genitourinary (GU) anomalies in Eastern China and to provide assistance for the clinical management of fetuses with different types of GU anomalies. Five hundred forty‐five fetuses with GU anomalies were enrolled, undergoing karyotyping, copy number variation sequencing ...
Jie Liang +6 more
wiley +1 more source
Link Between Non-Invasive Intrapartum Interventions and Cardiotocography Patterns, Amniotic Fluid Color, and Immediate Neonatal Outcomes. [PDF]
Garcia-Cuadrado N +6 more
europepmc +1 more source
Novel MYL1 Intron Variant With Expanded Phenotype
ABSTRACT Congenital myopathy‐14 (CMYO14) is an ultrarare autosomal recessive disorder caused by biallelic variants in MYL1, with only four patients reported to date. We describe what is likely the fifth reported patient, a neonate with severe hypotonia, respiratory insufficiency, and skeletal anomalies showing distinct histological changes of skeletal ...
Maria Barington +7 more
wiley +1 more source
ABSTRACT Uterine fibroids, also referred to as leiomyomas, are benign uterine tumors with a lifetime prevalence of approximately 75% depending on race, age, and a variety of genetic and environmental factors. Extra‐uterine leiomyomas are uncommon, and their occurrence within the rectus abdominis muscle is exceptionally rare.
Ibrahim Salum +9 more
wiley +1 more source
Multicenter validation of a machine learning model for predicting intrapartum high fever in parturients receiving labor analgesia. [PDF]
Liu B +5 more
europepmc +1 more source

