gamma-Glutamyltransferase

Deficit di sintesi degli acidi biliari tipo 2: un caso di colestasi in un lattante con GT basse

Danesi R, Zuccoli C, Pelucchi M, Stinco M, D'Antiga L.

2026/26 — pag. 193-194 — DOI

The paper reports the case of a two-month-old infant with persistent jaundice associated with acute cholestasis, severe cytolysis and coagulopathy. After ruling out the most common causes of neonatal cholestasis (such as biliary atresia and Alagille ...

Due colestasi a confronto

M. Massaro, E. Benelli, M.C. Pellegrin

2014/9

Approccio clinico al bambino con enzimi epatici elevati, “quasi” vent’anni dopo...

G. Maggiore

2010/1 — pag. 21-32

Isolated alteration of liver enzyme particularly in an apparently healthy child can be a diagnostic challenge for the clinician. In this review the Authors provide a guide to alteration of liver enzyme activity based on four main clinical-biochemic...

L’esplorazione bioumorale del fegato: il bilancio epatico

G. Maggiore

2009/10 — pag. 649-653

Liver function tests are a simple way to explore liver function and are a helpful tool to the clinician to confirm the clinical suspect of liver disease. Practically, evaluation of liver function includes determination of total and conjugated bilir...

Colestasi nella mononucleosi infettiva da virus di Epstein-Barr

F. Massei, G. Palla, C. Ughi, et al.

2002/5 — pag. 308-310

Although biochemical evidence of liver damage is frequent in children with EBV infectious mononucleosis, signs or symptoms related to an impaired bile flow as jaundice or pruritus are rare. The Authors report three cases observed in a two-year peri...