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http://dx.doi.org/10.3928/01913913-20230713-02 | DOI Listing |
Ann Ital Chir
March 2025
Department of Medical, Surgical, Neurologic, Metabolic and Ageing Sciences, Unit of Colorectal Surgery, University of Campania "Luigi Vanvitelli", 80138 Naples, Italy.
Aim: Acute myocardial infarction in pregnancy (pAMI) is a rare event that is often caused by non-classical factors rather than atherosclerosis. The management of such complications requires a multidisciplinary team, and it is important to bring together the specialties involved to ensure that these teams are coordinated and ready to respond. The management of pAMI poses unique challenges because it requires consideration of both maternal and fetal well-being.
View Article and Find Full Text PDFJ AAPOS
March 2025
Ophthalmology Department, Cairo University, Cairo, Egypt.
Purpose: To compare the functional and aesthetic outcomes of two surgical techniques used to correct severe congenital ptosis with poor levator function (LF): frontalis muscle (FM) flap advancement and frontalis sling (FS) surgery.
Methods: This prospective interventional randomized comparative study included 42 eyelids of 34 children with severe congenital ptosis and poor LF. The children were randomly divided into two groups, with 21 eyelids of 19 patients undergoing FM flap advancement, and 21 eyelids of 15 patients undergoing FS surgery.
Int J Surg Case Rep
March 2025
Department of Surgery, Medical School Hospital of Monastir, Tunisia. Electronic address:
Introduction And Importance: Retrocaval ureter is a rare congenital abnormality resulting from abnormal development of the inferior vena cava (IVC), leading to compression and obstruction of the right ureter. The condition is frequently diagnosed incidentally or presents symptoms related to hydronephrosis. The left retroaortic renal vein is another vascular anomaly with an estimated prevalence of 1.
View Article and Find Full Text PDFCongenital thrombotic thrombocytopenic purpura (cTTP) is an ultra-rare disorder characterized by thrombocytopenia, microangiopathic hemolytic anemia, and ischemic organ damage caused by pathogenic ADAMTS13 variants. ADAMTS13 containing product including fresh frozen plasma (FFP) and plasma-derived Factor VIII concentrates are commonly used to supply ADAMTS13; however, frequent hospital visits and allergic reactions are major drawbacks. A recombinant ADAMTS13 (rADAMTS13) was recently developed to address these issues.
View Article and Find Full Text PDFCongenital adrenal hyperplasia (CAH) is a defect in one of the enzymes or transport proteins involved in the synthesis of cortisol in the adrenal cortex. Virile form of CAH characterized by cortisol deficiency and hyperandrogenism. Klinefelter syndrome is one of the most frequent chromosomal diseases leading to the development of primary hypogonadism.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!