Results 111 to 120 of about 51,743 (231)
Isocitrate Dehydrogenase Mutations in Cancer: From Bench to Bedside Applications
Mutant isocitrate dehydrogenase affects multiple cancer types. Alterations in IDH1 and IDH2 result in abnormal enzyme activity, leading to the overproduction of D‐2‐hydroxyglutarate (D‐2HG). This metabolite disrupts cellular metabolism and epigenetic regulation, driving cancer initiation, progression, and metastasis.
Yuhan Fang +6 more
wiley +1 more source
Abstract Carrier screening for genetic conditions performed preconception or during pregnancy allows identification of fetal risk for inherited autosomal recessive and X‐linked conditions. The goal is to identify at‐risk patients/couples and offer them reproductive options such as preimplantation genetic diagnosis, prenatal testing, or targeted newborn
Emily B. Rosenfeld +5 more
wiley +1 more source
The Management of Congenital Cytomegalovirus Infection in an Era of Universal Newborn CMV Screening
ABSTRACT The most common infectious disease responsible for paediatric developmental disability is congenital infection with human cytomegalovirus (cCMV). Many serious sequelae are caused by cCMV, including microcephaly, intracranial calcifications, neuronal migration defects, seizure disorders, developmental delay, and sensorineural hearing loss (SNHL)
Emily R. Harrison +2 more
wiley +1 more source
Antioxidant vitamins and hyperbilirubinemia in neonates
Objective: Low antioxidant system may contribute to the severity of neonatal hyperbilirubinemia. The aim of this research was to explore the relationship between plasma vitamin E and C levels and the severity of hyperbilirubinemia in full-term neonates ...
Obediat, Ahmad D. +3 more
doaj
Summary An 11‐year‐old, female, spayed chihuahua was diagnosed with septic bile peritonitis secondary to gall bladder rupture. Surgical treatment consisted of cholecystectomy, placement of an abdominal drain and an oesophagostomy tube. The dog developed aspiration pneumonia alongside a recurrent bile peritonitis postoperatively.
Lydia Tan Yi Shean, Phil H. Franklin
wiley +1 more source
A rare cause of hyperbilirubinemia in a newborn: bilateral adrenal hematoma
Hyperbilirubinemia is an important health problem in newborns. The most common causes are Rh and ABO incompatibility, hemolytic anemias, enzyme deficiencies, sepsis, hypothyroidism, pyloric stenosis and breast-milk jaundice.
Selahattin Katar +3 more
doaj
Heart Rate Variability in Newborns From Diabetic Mothers: Clinical Application and Significance
Risk factors for GDM contribute to a hyperglycemic intrauterine environment, which may in turn impair ANS function in the offspring. Altered ANS activity can be assessed through measures such as HRV. ABSTRACT Gestational diabetes mellitus (GDM) is one of the most common pregnancy complications, arising from inadequate insulin secretion and increased ...
Virginia Beretta +7 more
wiley +1 more source
American Journal of Hematology, Volume 101, Issue 5, Page 1070-1071, May 2026.
Ashik Zala +5 more
wiley +1 more source
1 g/h magnesium sulfate maintenance for eclampsia prevention is enough
Magnesium sulfate maintenance regimen of 1 g/h seems as effective as the 2 g/h regimen for the prevention of eclampsia, with decreased incidence of maternal side effects. Abstract We conducted two systematic reviews including only randomized controlled trials (RCTs) comparing magnesium sulfate vs placebo/no treatment, as well as 2 g/h vs 1 g/h ...
Alessandro Petrecca +3 more
wiley +1 more source
Background Severe neonatal hyperbilirubinemia could lead to kernicterus and neonatal death. This study aimed to analyze the association between single nucleotide polymorphisms in genes involved in bilirubin metabolism and the incidence of severe ...
Juan Fan +7 more
doaj +1 more source

