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(vivi )
157 results
  • Ionic liquid as antibacterial agent for an experimental orthodontic adhesive. [Journal Article]
    Dent Mater 2019; 35(8):1155-1165Martini Garcia I, Jung Ferreira C, … Mezzomo Collares F
  • CONCLUSIONS: To reduce biofilm formation around brackets and to prevent demineralization at susceptible sites, materials have been developed with antibacterial properties. In this study, a new experimental orthodontic adhesive was formulated with an imidazolium ionic liquid (BMIM.NTf2) as antibacterial agent. The incorporation of 5 wt.% of ionic liquid decreased biofilm formation without affecting the physico-chemical properties and cytotoxicity of an experimental orthodontic resin.
  • Breast milk: To each his own. From metabolomic study, evidence of personalized nutrition in preterm infants. [Journal Article]
    Nutrition 2019; 62:158-161Perrone S, Longini M, … Buonocore G
  • CONCLUSIONS: The preterm milk metabolome pattern undergoes maturation during the first 3 wk after birth, but at the end of the third week it still does not resemble the term milk pattern. The specific changes in mothers' milk metabolomic profiles according to their offspring might reflect the different nutritional requirement of each preterm infant. This knowledge is crucial to move from standardized nutritional protocols to tailored, individualized nutrition in preterm infants.
  • Osmotic stress induces biofilm production by Staphylococcus epidermidis isolates from neonates. [Journal Article]
    Diagn Microbiol Infect Dis 2019; 94(4):337-341Ferreira RBR, Ferreira MCS, … Dos Santos KRN
  • Staphylococcus epidermidis is one of the leading causes of bloodstream infections, particularly in premature neonates, and biofilm formation is a major virulence factor. We characterized biofilm formation by 50 S. epidermidis neonatal isolates under osmotic stress and evaluated the expression of biofilm-associated genes. Phenotypical analyses of biofilm production were performed in culture medium…
  • Thyroid function in patients with Prader-Willi syndrome: an Italian multicenter study of 339 patients. [Multicenter Study]
    J Pediatr Endocrinol Metab 2019; 32(2):159-165Iughetti L, Vivi G, … Predieri B
  • Background Prader-Willi syndrome (PWS) is a genetic disorder due to loss of expression of paternally transcribed genes of the imprinted region of chromosome 15q11-13. PWS is characterized by peculiar signs and symptoms and many endocrine abnormalities have been described (growth hormone deficiency, hypogonadotropic hypogonadism). The abnormalities of thyroid function are discussed in literature a…
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