Results 221 to 230 of about 347,112 (305)
Open fetal surgery for correction of myelomeningocele and umbilical cord presentation at hysterotomy: report of a rare complication. [PDF]
Souza ASR +6 more
europepmc +1 more source
Magnetic soft robots offer promise in biomedicine due to their wireless actuation and rapid response, but current fabrication methods are complex and have limited cellular compatibility. A new, contactless bioassembly strategy using hydrodynamic instabilities is introduced, enabling customizable, centimeter‐scale robots.
Wei Gao +5 more
wiley +1 more source
Galen vein malformation-intrauterine treatment. [PDF]
Cavalheiro S +9 more
europepmc +1 more source
Cancer cells progressively spread over intermediate epithelial‐to‐mesenchymal transition states that cause nuclear enlargement and circular redistribution of filamentous vimentin are classified by deformability cytometry coupled to a multi‐region deep learning model with convolutional feature extraction and attention‐based regional aggregation.
Javad Jarmoshti +8 more
wiley +1 more source
Prenatal diagnosis of a fetus with cri-du-chat syndrome accompanied by 18q duplication: a case description. [PDF]
Song J, Tang Z, Lin X, Yang L.
europepmc +1 more source
ABSTRACT Although circulating nucleated red blood cells (cNRBCs) have previously been detected in patients with sickle cell disease (SCD), their prevalence and clinical significance during steady‐state disease have not been established. We retrospectively analyzed 270 adults with an SS or Sβ0‐thalassemia genotype.
Ugo Boccadifuoco +7 more
wiley +1 more source
Prenatal Diagnosis and Postnatal Management of Congenital Cervicofacial Cystic Lymphangioma Associated With Multiple Fetal Anomalies: A Case Report. [PDF]
Mouna A +3 more
europepmc +1 more source
Assessment of Growth in Cardio‐Facio‐Cutaneous Syndrome
ABSTRACT Cardio‐facio‐cutaneous (CFC) syndrome is a rare, multiple congenital anomaly disorder in which individuals commonly experience faltering growth; however, systematic analysis of growth parameters in this disorder has not been performed. We recruited 69 participants with CFC through CFC International and collected data on assessing height ...
Kari Johnston +6 more
wiley +1 more source
Periconceptional GLP-1 Receptor Agonist Exposure: Lower Observed Risk or Lower Certainty? [PDF]
Singh R, Singh A, Singh AK.
europepmc +1 more source
Heterozygous Variants in LRP1 Cause a Neurodevelopmental Disorder With Congenital Heart Defects
ABSTRACT LRP1 encodes the low‐density lipoprotein (LDL) receptor‐related protein 1 (LRP1), a transmembrane protein involved in endocytosis and activation of multiple signaling pathways. LRP1 variants have been implicated in the pathogenesis of congenital heart defects (CHD), Alzheimer's disease, and neurodevelopmental disorders (NDD).
Alyssa L. Rippert +31 more
wiley +1 more source

