Month: <span>December 2024</span>
Month: December 2024

Metformin and risk of adverse pregnancy outcomes among pregnant women with gestational diabetes in the United Kingdom: A population-based cohort study

Diabetes Obes Metab. 2024 Dec 16. doi: 10.1111/dom.16115. Online ahead of print. ABSTRACT AIMS: Metformin is increasingly used off-label as the treatment of gestational diabetes …

Exploring congenital sucrase-isomaltase deficiency in autism spectrum disorder patients with irritable bowel syndrome symptoms: A prospective SI gene sequencing study

Autism Res. 2024 Dec 16. doi: 10.1002/aur.3293. Online ahead of print. ABSTRACT Congenital sucrase-isomaltase deficiency (CSID) is an inherited metabolic disorder causing chronic gastrointestinal symptoms …

Family planning and contraception in people with multiple sclerosis: perspectives for obstetricians, gynaecologists, and other health care professionals involved in reproductive planning

Eur J Contracept Reprod Health Care. 2024 Dec 16:1-15. doi: 10.1080/13625187.2024.2434843. Online ahead of print. ABSTRACT PURPOSE: Multiple sclerosis (MS) is often diagnosed in people …

Advancement in predictive biomarkers for gestational diabetes mellitus diagnosis and related outcomes: a scoping review

BMJ Open. 2024 Dec 15;14(12):e089937. doi: 10.1136/bmjopen-2024-089937. ABSTRACT OBJECTIVE: Gestational diabetes mellitus (GDM) is a metabolic disorder associated with adverse maternal and neonatal outcomes. While …

Processes of obstetrical care and outcomes among Ontario physicians versus non-physicians: a population-based study

BMJ Open. 2024 Dec 15;14(12):e091312. doi: 10.1136/bmjopen-2024-091312. ABSTRACT OBJECTIVE: We compared processes of antepartum, intrapartum and postpartum care and obstetrical outcomes between physicians and non-physicians. …

A Kinetic Model for Compound Heterozygous Pathogenic Variants in Tyrosyl-tRNA Synthetase Gene YARS2-Associated Neonatal Phenotype

J Biol Chem. 2024 Dec 13:108092. doi: 10.1016/j.jbc.2024.108092. Online ahead of print. ABSTRACT Human genetic disorders are often caused by mutations of compound heterozygosity, where …