Results 191 to 200 of about 683,972 (341)
Postoperative intestinal obstruction caused by staple-related internal hernia after laparoscopic appendectomy: a case report. [PDF]
Rodrigues FCM +3 more
europepmc +1 more source
This study introduces a biomarker‐agnostic diagnostic strategy for ovarian cancer, utilizing a machine learning‐enhanced electronic nose to analyze volatile organic compound signatures from blood plasma. By overcoming the dependence on specific biomarkers, this approach enables accurate detection, staging, and cancer type differentiation, offering a ...
Ivan Shtepliuk +4 more
wiley +1 more source
Subacute puerperal uterine inversion secondary to a large uterine myoma: a case report. [PDF]
Yang J +5 more
europepmc +1 more source
ABSTRACT Postpartum hemorrhage (PPH) remains the leading cause of preventable maternal mortality despite standard interventions. Recent fibrinogen trials failed to improve outcomes, prompting interest in coagulation factor XIII (FXIII). FXIII functions as “molecular cement,” cross‐linking fibrin and stabilizing clots.
Jeremy W. Jacobs +8 more
wiley +1 more source
Correction: Anxiety Symptoms Before and After Single-Incision Mini-Sling Surgery in Women With Stress Urinary Incontinence: A Prospective Study. [PDF]
Despoina D +7 more
europepmc +1 more source
Corrigendum to ‘Prevention of preterm birth in twin pregnancies’ American Journal of Obstetrics & Gynecology MFM/ Volume 4 (2022) 100551 [PDF]
Amanda Roman +2 more
openalex +1 more source
A Systematic Review and Meta‐Analysis of the Birth Prevalence of Turner Syndrome
ABSTRACT Turner syndrome, a chromosomal disorder, causes short stature, pubertal arrest, amenorrhea, and infertility in females. Prevalence estimates vary widely; however, reliable estimates are important for public health initiatives. Therefore, a meta‐analysis was undertaken.
David Hinds +5 more
wiley +1 more source
Correction: A case of metachronous cervical and early-stage breast cancer. [PDF]
Psilopatis I +8 more
europepmc +1 more source
ABSTRACT Spinal muscular atrophy with congenital bone fractures 2 is a rare and severe autosomal recessive neuromuscular disorder caused by pathogenic variants in ASCC1. This condition characterized by prenatal onset of severe hypotonia with fetal hypokinesia and congenital contractures results in arthrogryposis multiplex congenita, and increased ...
A. Civit +16 more
wiley +1 more source

