liver transplantation

Una famiglia nel bosco

Tamburlini G. Milani P.

2026/1 — pag. 7-9 — DOI

Sclerosi epatoportale

Sparaventi C, Zago A, Di Leo G, Barbi E, Bramuzzo M.

2025/7 — pag. 453-455 — DOI

Hepatoportal sclerosis is a rare and underdiagnosed liver condition characterised by histological alterations of the portal venules and hepatic sinusoids, with periportal fibrosis and vascular narrowing. Its diagnosis is histological and requires liv...

Alla faccia del corpo estraneo (vaginale)

Bleve C

2025/5 — pag. 117-119 — DOI

A 16-year-old girl with a history of partial liver transplant at the age of 5 due to autoimmune hepatitis undergoes a routine follow-up abdominal ultrasound that reveals bladder wall thickening and pseudopolypoid lesions. Cystoscopy and biopsy initia...

Questa strana epatite dei bambini: fatti e misfatti

2022/5 — pag. 326-327 — DOI

Lattanti e trapianti

F. Fusco

2018/10 — pag. 662-663

Due colestasi a confronto

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

2014/9

Le dilatazioni cistiche delle vie biliari

M. Sciveres, F. Cirillo, S. Nastasio, G. Maggiore

2013/5 — pag. 295-301

Cystic disease of the biliary tree is a rare and heterogeneous medical condition that may be diagnosed during intrauterine life or can become symptomatic with cholestatic jaundice or acute recurrent pancreatitis before adulthood. The etiology remai...

Insufficienza epatica acuta, un’evenienza rara... ma non troppo

C. Ripoli, A.P. Pinna, M. Furno, D. Congiu, S. Pusceddu, M.L. Fenu

2012/8 — pag. 515-517

Acute liver failure is a rare and complex disease that may present with a worsening course and needs a rational diagnostic and therapeutic intervention, in order to avoid most dangerous complications such as encephalopathy and metabolic changes, wh...

Dove va (o vorrebbe andare) l’epatologia pediatrica?

G. Maggiore

2012/8 — pag. 483-485

Non è mai troppo tardi...per fare una diagnosi

G. Maggiore, S. Nastasio, G. Rossi, M. Sciveres

2012/6

L’epatopatia della malattia celiaca: uno spettrodi lesioni con una comune patogenesi?

S. Caprai, G. Maggiore

2010/6 — pag. 383-386

A wide spectrum of liver injuries in children and adults may be related to celiac disease (CD) and in particular: 1) a mild parenchymal damage characterized by absence of clinical sign or symptom of a chronic liver disease and by non-specific histo...

A volte... ritornano. Una rettocolite "difficile".

2009/4 — pag. 257-258

Atresia delle vie biliari: quali insidie per il pediatra?

R. Iorio, A.M. Salzano, F. Cirillo, G. Vallone

2009/4 — pag. 224-231

Biliary atresia (BA) is the most common pediatric cause of cirrhosis, end-stage liver disease and indication for liver transplantation. The clinical presentation is characterized by jaundice with yellow or dark urine and pale stools, which eventually...

Coma e insufficienza epatica

M. Don, F. Marchetti, P. Salierno, A.M. Franzil, M. Maschio, B. Sacher, A. Burlina, A. Ventura

2008/10 — pag. 671-677

The work describes the case of a two-and-half-year-old girl who showed a clinical picture of neurologic impairment together with laboratory signs of liver insufficiency coupled with hyperammonemia. Some comments on this clinical case and how the diag...

Atresia biliare: non è mai troppo prestoStipsi severa nei bambini: non serve lo psicologoEstremi mali, estremi rimedi: chirurgia bariatrica per l'obesità grave dei bambini?Vaccino anti-Rotavirus umano attenuato: efficace anche "al di là dal mare"Neonati e “lattantini”: meglio distesi che seduti

2008/5 — pag. 283-284

Crederci sempre, arrendersi mai!

G. Maggiore

2006/6 — pag. 385-386

La tirosinemia epatorenale

M. Spada

2005/8

Il deficit di alfa1-antitripsina in età pediatrica

L. Giglio, I. Berti, C. Trevisiol

2003/3 — pag. 155-161

Alpha 1-antitrypsin deficiency (AATD) is an autosomal recessive disease, with more than 70 genetic variants, and a frequency which varies from 1:1000 to 1:5000, depending on genetic epidemiology and screening methods. The AATD involves primarily th...

Il trapianto epatico in età pediatrica: il punto attuale di un Centro italiano

G. Torre, M. Spada, S. Riva, et al.

2002/5 — pag. 302-310

The Authors report their experience on liver transplantation in children at the Pediatric Liver Transplantation Program, Ospedali Riuniti of Bergamo. Over a five year period 156 transplantations have been performed in 141 children (15 children requ...

FEGATO: AUTOIMMUNITÅ, TRAPIANTO, INFEZIONEEpatite autoimmune: cinquant’anni e non li dimostra!

G. Maggiore, M. Sciveres

2002/5 — pag. 291-310

Autoimmune hepatitis (AIH) is an uncommon disease occurring mainly in women and characterised by the morphological changes of interface hepatitis on liver biopsy, hypergammaglobulinemia, elevated serum aminotransferases, and circulating autoantibod...

Epatiti autoimmuni attorno all’anno 2000

I. Giuseppin, S. Martelossi, L. Lepore, G. Torre, I. Bruno,A. Ventura

2001/8 — pag. 499-508

Diagnosis of autoimmune hepatitis (AH) is based on: exclusion of viral genetic or tossic etiology, presence of non-organ-specific antibodies (SMA, ANA or LKM1); increased G immunoglobulin, typical histological features; response to immunosuppressiv...

L’infezione da HCV: ancora molte incertezze

L. Zancan, G. Svegliado, G. Guariso

1999/5 — pag. 311-314

HCV infection represents an emerging problem in an era of achieved control of HBV infection. There are still many open issues that the Authors briefly discuss. They regard the mechanisms of hepatic damage leading to chronic disease in a high propor...

L’atresia delle vie biliari

D. Baronciani

1998/3 — pag. 189-190