Results 151 to 160 of about 26,981 (283)

Radiological and Ultrasound Findings in Neonatal Respiratory Pathology: Perspectives in Diagnosis. [PDF]

open access: yesMaedica (Bucur)
Popa AE   +4 more
europepmc   +1 more source

Several features of newborns following intrauterine intravascular blood transfusion for fetal hemolytic disease caused by anti‐D alloimmunization

open access: yesTransfusion, EarlyView.
Abstract Background Early detection and intervention for fetal hemolytic disease are essential to prevent severe complications. This study evaluates the antenatal and postnatal clinical and laboratory characteristics of newborns who underwent intrauterine intravascular transfusion due to anti‐D‐induced hemolytic disease. Study Design and Methods Twenty
Altay Babacan   +3 more
wiley   +1 more source

Antenatal corticosteroid treatment after 34 weeks of gestation in twin pregnancies at high risk of late preterm delivery. [PDF]

open access: yesBMC Pregnancy Childbirth
Dereli ML   +10 more
europepmc   +1 more source

In utero exposure to experimental maternal asthma alters fetal airway development in sheep

open access: yesExperimental Physiology, EarlyView.
Abstract The mechanisms linking maternal asthma (MA) exposure in utero and subsequent risk of asthma in childhood are not fully understood. Pathological airway remodelling, including reticular basement membrane thickening, has been reported in infants and children who go on to develop asthma later in childhood.
Sarah J. Hammond   +11 more
wiley   +1 more source

Novel Digital Anomalies, Hippocampal Atrophy, and Mutations Expand the Genotypic and Phenotypic Spectra of CNKSR2 in the Houge Type of X‐Linked Syndromic Intellectual Development Disorder (MRXSHG)

open access: yesAmerican Journal of Medical Genetics Part A, Volume 197, Issue 5, May 2025.
ABSTRACT The Houge type of X‐linked syndromic intellectual developmental disorder (MRXSHG) encompasses a spectrum of neurodevelopmental disorders characterized by intellectual disability (ID), language/speech delay, attention issues, and epilepsy. These conditions arise from hemizygous or heterozygous deletions, along with point mutations, affecting ...
Mohammad‐Reza Ghasemi   +34 more
wiley   +1 more source

Identification of a Founder GLDN Variant Associated With “Lethal” Arthrogryposis in Nunavik Inuit: Implications for Obstetrical and Long‐Term Survivors' Management

open access: yesAmerican Journal of Medical Genetics Part A, Volume 197, Issue 5, May 2025.
ABSTRACT Biallelic variants in GLDN have recently been associated with lethal congenital contracture syndrome 11 (LCCS11), a form of fetal akinesia deformation sequence (FADS) with high neonatal mortality. In this report, we describe five individuals from two Canadian Inuit families originating from different communities in Nunavik all affected with ...
Alexa McAdam   +12 more
wiley   +1 more source

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