Abstract This study investigates the longitudinal impact of socioeconomic instability on teen pregnancy and sexually transmitted infection (STI) diagnosis among adolescents and young adults (AYA) living in an agricultural region and examines pathways including supportive family and social structures, decision making autonomy in romantic relationships ...
Marie C. D. Stoner +11 more
wiley +1 more source
Cellular and Molecular Effects of Steroid Sex Hormones on the Vocal Folds: A Scoping Review [PDF]
Serena Pu +4 more
openalex +1 more source
Are sex discordant outcomes in COVID-19 related to sex hormones?
Jonathan D. Strope +2 more
openalex +2 more sources
Fetal hormonal programming of sex differences in depression: linking women's mental health with sex differences in the brain across the lifespan [PDF]
Jill M. Goldstein +3 more
openalex +1 more source
ABSTRACT Myhre syndrome is an ultrarare genetic disease characterized by short stature, distinct craniofacial features, cardiovascular and respiratory fibrosis and stenosis, neurodevelopmental delays, autism, intellectual disability, and hearing loss. The natural history of Myhre syndrome is still not fully understood due to a small patient population ...
Mary K. Young +6 more
wiley +1 more source
<i>In vitro</i> modeling of the female gut microbiome: effects of sex hormones and psychotropic drugs. [PDF]
Leao L +4 more
europepmc +1 more source
Identification of Compound Heterozygous CYP11A1 Variants via Reanalysis of Clinical Sequencing Data
ABSTRACT A molecular diagnosis is currently achievable in approximately 50% of patients assessed by clinical geneticists at tertiary care centres. Next‐Generation Sequencing Panels contain a defined group of genes associated with a clinically defined set of phenotypes.
Ana Acosta Bedón +10 more
wiley +1 more source
Impact of sex hormones on postoperative outcomes in plastic surgery: a narrative review. [PDF]
Lv X +5 more
europepmc +1 more source
Respiratory Involvement in HIST1H1E‐Related Rahman Syndrome: A Case of Severe Mixed Apnea
ABSTRACT Rahman syndrome (HIST1H1E‐related neurodevelopmental syndrome, OMIM #617537) is a rare autosomal‐dominant condition caused by truncating variants in the C‐terminal domain of the HIST1H1E gene. It is characterized by macrocephaly, hypotonia, craniofacial anomalies, and multisystem anomalies.
Nada Barakat +4 more
wiley +1 more source
Associations between sex hormones and obesity-related indicators: results from the NHANES and Mendelian randomization study. [PDF]
Yuan Y +6 more
europepmc +1 more source

