نتایج جستجو برای: prolonged unconjugated hyperbilirubinemia

تعداد نتایج: 92836  

2015
Antonietta Giannattasio Giusy Ranucci Francesco Raimondi

Prolonged neonatal jaundice is defined as a jaundice lasting more than 14 days of life in the full-term infants [1,2]. Etiologically it is helpful to distinguish jaundice related to unconjugated (indirect) or conjugated (direct) hyperbilirubinemia. A prolonged unconjugated hyperbilirubinemia may be related to breastfeeding or to some pathological conditions as hemolytic diseases (due to Rh or A...

Journal: :Transplantation proceedings 1996
Y Wakizaka F Pan A S Rao S Celli H Sun T Miki A J Demetris J J Fung T E Starzl L A Valdivia

THE Gunn rat is an animal model for Crigler-Najar syndrome. a rare form of congenital unconjugated nonhemolytic hyperbilirubinemia due to the absence of glucoronyl transferase. I.e It leads to deposition of bilirubin in the basal ganglia. culminating in precocious death of the patient. Because the uptake. conjugation. and excretion of bilirubin by hepatocytes involves specific carriers and enzy...

Journal: :medical journal of islamic republic of iran 0
k sakha from the department of pediatrics, tabriz university of medical sciences, tabriz, i. r. iran. h sultani

one of the causes of neonatal hyperbilirubinemia is increased reabsorption of bilirubin from meconium in the gastrointestinal tract. this occurs when the conjugated bilirubin which is excreted into the colon is 'unconjugated by beta glucuronidase activity, present in the neonatal intestine, which hydrolyzes bilirubin diglucuronide into unconjugated bilirubin, which subsequently is reabsorb...

2017
Mitsuhiko Aiso Minami Yagi Atsushi Tanaka Kotaro Miura Ryo Miura Toshihiko Arizumi Yoriyuki Takamori Sayuri Nakahara Yoshihiro Maruo Hajime Takikawa

We experienced a case of a 19-year-old man with Gilbert syndrome with concomitant hereditary spherocytosis. The patient presented with moderate unconjugated hyperbilirubinemia, and inherited etiology was strongly suspected. The diagnosis of Gilbert syndrome was confirmed by the genetic analysis of the UGT1A1 gene, demonstrating UGT1A1*28 and compound heterozygote UGT1A1*6. In addition, since th...

Journal: :Endocrinologia japonica 1990
P Cugini H Sasaki T Kawasaki S Di Simone L Di Palma P Battisti K Uezono

This report deals with three cases of Bartter's syndrome whose symptomatology was associated with indirect hyperbilirubinemia. The bilirubin disorder was suggestive of Gilbert's syndrome, with no pathological findings being detected as far as the liver function was concerned. Furthermore, the unconjugated fraction of bilirubin increased after fasting. The therapy with indomethacin exerted benef...

Journal: :Journal of Polymers and The Environment 2022

Hyperbilirubinemia is one of most severe clinical diseases, which caused by the accumulation unconjugated bilirubin. Electrospun nanofiber membranes used as highly efficient bilirubin adsorbents have been applied to remove extra in hemoperfusion for their high surface area and easy functionalized properties. In this work, Lysine (Lys) grafted polyacrylonitrile (PAN) electrospun doped with organ...

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