Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Filiz Tiker"'
Publikováno v:
The Journal of Maternal-Fetal & Neonatal Medicine. 20:407-410
Background. The pathogenetic mechanisms of hepatic injury in perinatal asphyxia (PNA) are similar to those in ischemic hepatitis, yet liver involvement is currently not considered a component of multi-organ failure in PNA.Methods. A retrospective stu
Publikováno v:
Yeditepe Medical Journal.
Publikováno v:
Current Therapeutic Research. 67:214-225
Background:Delayed passage of first stool by a newborn after birth might be an initial sign of clinical problems, such as meconium ileus, meconium plug syndrome, and intestinal atresia. Successful treatment of these conditions depends on early diagno
Publikováno v:
Journal of Paediatrics and Child Health. 41:484-487
The aim of this study was to determine what proportion of newborns admitted with idiopathic non-hemolytic hyperbilirubinemia exhibit severe weight loss and hypernatremia.The prospective study involved 115 infants48 h old who were admitted with jaundi
Publikováno v:
Annals of Tropical Paediatrics. 22:225-228
This study investigated bilirubin levels in 282 1-month-old, healthy, term infants from the Adana region in southern Turkey. Total bilirubin was > 5 mg/dl in 20.2% of the infants and > 10 mg/dl in 6% of the group. Thyroid function and levels of alani
Autor:
Alanay, Yasemin, Avaygan, Hrispima, Camacho, Natalia, Utine, G. Eda, Boduroglu, Koray, Aktas, Dilek, Alikasifoglu, Mehmet, Tuncbilek, Ergul, Orhan, Diclehan, Bakar, Filiz Tiker, Zabel, Bernard, Superti-Furga, Andrea, Bruckner-Tuderman, Leena, Curry, Cindy J. R., Pyott, Shawna, Byers, Peter H., Eyre, David R., Baldridge, Dustin, Lee, Brendan, Merrill, Amy E.
Osteogenesis imperfecta is a clinically and genetically heterogeneous brittle bone disorder that results from defects in the synthesis, structure, or posttranslational modification of type I procollagen. Dominant forms of OI result from mutations in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=r39c86a4b39b::c0a41dcdf0842e1c5f95e2923df7bb04
https://aperta.ulakbim.gov.tr/record/25305
https://aperta.ulakbim.gov.tr/record/25305
Publikováno v:
Indian pediatrics. 44(1)
The objective of this study was to assess the efficacy of phototherapy for nonhemolytic hyperbilirubinemia and rebound bilirubin levels in breast-fed newborns as compared with mixed-fed (breast milk and formula) newborns.Prospective study of effects
Publikováno v:
Indian journal of pediatrics. 73(5)
Objectives: To determine the causes and related outcomes of early onset conjugated hyperbilirubinemia in a group of newborn infants, and to determine the incidence of sepsis in these neonates.Methods: The charts of 42 babies with conjugated hyperbili
Publikováno v:
Clinical pediatrics. 45(3)
This study was undertaken to determine the frequency and investigate the etiology of extreme hyperbilirubinemia (total serum bilirubin [TSB]>or=25 mg/dL [428 micromol/L]) in newborns admitted to a neonatal intensive care unit in southern Turkey. The
Publikováno v:
Pediatric hematology and oncology. 23(4)
A recently isolated peptide hormone, hepcidin, is thought to be the principal regulator of iron homeostasis. Hepcidin acts by limiting intestinal iron absorption and promoting iron retention in reticuloendothelial cells. Its precursor peptide form is