Results 241 to 250 of about 61,679 (338)
Incidence of Retinopathy of Prematurity Between 2021 and 2024: Results from a Single Center. [PDF]
Kizilay O, Karaca S, Oto BB, Celik G.
europepmc +1 more source
Abstract Background For parenteral nutrition (PN)–dependent neonates, soybean oil intravenous lipid emulsions (SO‐ILEs) and mixed emulsions (SO, medium‐chain triglyceride [MCT], olive oil [OO], and fish oil [FO] ILEs) are likely not providing adequate amounts of key fatty acids (FAs) arachidonic acid (AA) and docosahexaenoic acid (DHA) and are devoid ...
Mirielle L. Pauline +11 more
wiley +1 more source
Endothelial MEMO1 Regulates Angiogenic Signaling in a Model of Retinopathy of Prematurity. [PDF]
Ramshekar A +10 more
europepmc +1 more source
ABSTRACT Aim To compare discrimination and calibration of prognostic models for pulmonary outcomes in very preterm (VPT) infants born < 32 weeks’ gestation when including the mean airway pressure (MAP), the fraction of supplemental oxygen (FiO2) and the respiratory severity score (RSS) reflecting parameters of ventilation and oxygenation during the ...
Birte Staude +6 more
wiley +1 more source
Systematic review and meta-analysis of risk prediction models for retinopathy of prematurity in preterm infants. [PDF]
Li L, Gao Y, Chen W, Han M.
europepmc +1 more source
Six Drivers of Aging Identified Among Genes Differentially Expressed With Age
A meta‐analysis of 25 transcriptomic datasets from mammalian tissues revealed 45 genes consistently upregulated or downregulated with age. Orthologs of these genes were functionally evaluated using Caenorhabditis elegans lifespan screens to reveal those with causal roles in the aging process, thus identifying six evolutionarily conserved drivers of ...
Ariella Coler‐Reilly +3 more
wiley +1 more source
Virus containment box for retinopathy of prematurity screening and laser
Sameera Nayak +4 more
openalex +1 more source
Molecular and cellular mechanisms underlying gyrate atrophy: Why is the retina primarily affected?
Abstract Gyrate atrophy of the choroid and retina (GACR; OMIM #258870) is a rare early‐onset autosomal recessive disorder, caused by bi‐allelic pathogenic variants in the gene coding for ornithine aminotransferase (OAT) resulting in hyperornithinaemia.
Mark J. N. Buijs +12 more
wiley +1 more source

