Results 271 to 280 of about 72,360 (281)
Paediatric and Perinatal Epidemiology, EarlyView.ABSTRACT Background Much research has focused on identifying predictors of late antenatal care initiation. Many of these predictors (e.g., young age, migration background, socioeconomic position) are impossible to modify, illustrating the need to explore other interventions.
Clair A. Enthoven +7 more
wiley +1 more source
Anti‐Ce in haemolytic disease of the foetus and newborn
Transfusion Medicine, Volume 35, Issue 3, Page 287-290, June 2025.Abstract Objectives To report a delayed case of severe haemolytic disease of the foetus and newborn (HDFN) due to Anti‐Ce. Background HDFN due to maternal antibodies is potentially fatal. As a result, antibody levels and foetal anaemia are periodically monitored and risk assessed throughout pregnancy. HDFN due to Anti‐Ce is rare.
Rebecca O'Grady +6 more
wiley +1 more source
Pyloric Stenosis in Premature Twins: A Case Report
Journal of Paediatrics and Child Health, EarlyView.
S. P. Y. Tan Tanny +4 more
wiley +1 more source
The first live term birth following uterus transplantation in Australia
Medical Journal of Australia, EarlyView.Abstract Objective To report the first live birth following uterus transplantation in Australia. Study design Case report. Setting, participant The first participant in the uterus transplantation research study program at the Royal Hospital for Women, the Prince of Wales Hospital, and Westmead Hospital in Sydney.
Rebecca Deans +21 more
wiley +1 more source
Real‐time fetal brain and placental T2* mapping at 0.55T MRI
Magnetic Resonance in Medicine, Volume 94, Issue 2, Page 615-624, August 2025.ABSTRACT Purpose To provide real‐time, organ‐specific quantitative information — specifically placental and fetal brain T2 * — to optimize and personalize fetal MRI examinations. Methods A low‐latency setup enables real‐time processing, including segmentation, T2* fitting, and centile calculation.
Jordina Aviles Verdera +9 more
wiley +1 more source
Nanopore Sequencing Solves an Elusive Case of Sotos Syndrome
American Journal of Medical Genetics Part A, Volume 197, Issue 7, July 2025.ABSTRACT Sotos syndrome is a rare genetic disorder characterized by distinctive facial features, including a broad and prominent forehead, dolichocephaly, and learning disabilities ranging from mild to severe intellectual impairment. Affected individuals often show overgrowth in height and head circumference over two standard deviations.
Pasquale Di Letto +52 more
wiley +1 more source
Clinical Pharmacology &Therapeutics, Volume 118, Issue 1, Page 206-217, July 2025.Over 10 million children in the world have epilepsy, with an unknown cause in half of the cases. The gut microbiome has been associated with various neurological disorders, and certain drugs greatly disturb the microbiome. Our aim was to study the association of prenatal and childhood exposure (before the age of two) to antibiotics, proton pump ...
Unnur Gudnadottir +4 more
wiley +1 more source
Family‐Related Factors in Children and Adolescents With Chronic Pain: A Systematic Review
European Journal of Pain, Volume 29, Issue 6, July 2025.ABSTRACT Background The aim of this systematic review is to synthesise the findings about the role of family‐related factors in chronic pain in children and adolescents. Methods We conducted a search of the following electronic databases: PubMed/MedLine, CINHAL, PsychINFO, PubPsych, Scopus and Web of Science from inception to July 2024.
Lorena Martí +3 more
wiley +1 more source
American Journal of Medical Genetics Part A, Volume 197, Issue 7, July 2025.
Toru Nagata +6 more
wiley +1 more source