Event Videos

https://www.ncbi.nlm.nih.gov/pubmed/29290659 Liver transplant
World J Gastroenterol. 2017 Dec 14;23(46):8227-8234. doi: 10.3748/wjg.v23.i46.8227.

Zhang ZY, Jin L, Chen G, Su TH, Zhu ZJ, Sun LY, Wang ZC, Xiao GW

Abstract

AIM:
To assess the efficacy and safety of balloon dilatation for the treatment of hepatic venous outflow obstruction (HVOO) following pediatric liver transplantation.

METHODS:

Published on: 
Dec-2017

https://www.ncbi.nlm.nih.gov/pubmed/29287003 Neonatal hemochromatosis
J Pediatr Gastroenterol Nutr. 2017 Dec 28. doi: 10.1097/MPG.0000000000001880. [Epub ahead of print]

Magnetic Resonance Imaging Findings in Neonatal Hemochromatosis.
Alenezi K, Kamath BM, Siddiqui I, Tomlinson C, Chavhan GB.

Abstract

BACKGROUND:
There are limited data on utility of MRI in the assessment of suspected neonatal hemochromatosis (NH).

OBJECTIVES:
To present our experience with utilization of multi-echo sequences MRI technique in the evaluation of NH and to compare MRI findings in infants with and without NH.

METHODS:

Published on: 
Dec-2017

https://www.ncbi.nlm.nih.gov/pubmed/29162346

Liver transplant

J Pediatr. 2017 Nov 18. pii: S0022-3476(17)31323-9. doi: 10.1016/j.jpeds.2017.09.069. [Epub ahead of print]

Annunziato RA, Bucuvalas JC, Yin W, Arnand R, Alonso EM, Mazariegos GV, Venick RS, Stuber ML, Shneider BL, Shemesh E.

Abstract

OBJECTIVE:
To further refine a measure of self-management, the Responsibility and Familiarity with Illness Survey (REFILS), and to determine if this score predicts medication adherence and, thus, fewer instances of allograft rejection among pediatric liver transplant recipients.

STUDY DESIGN:

Published on: 
Nov-2017

https://www.ncbi.nlm.nih.gov/pubmed/29168311

Primary sclerosing cholangitis

Hepatol Res. 2017 Nov 22. doi: 10.1111/hepr.13004. [Epub ahead of print]
Umetsu S, Inui A, Sogo T, Komatsu H, Fujisawa T.

Abstract

BACKGROUND:
Wisteria floribunda agglutinin positive Mac-2 binding protein (WFA+ -M2BP) is a novel serum marker of hepatic fibrosis in adults with chronic hepatitis C. However, it remains unclear whether serum WFA+ -M2BP levels are associated with the progression of liverhistology in primary sclerosing cholangitis (PSC) .

METHODS:

Published on: 
Nov-2017

https://www.ncbi.nlm.nih.gov/pubmed/29287007
J Pediatr Gastroenterol Nutr. 2017 Dec 28. doi: 10.1097/MPG.0000000000001881. [Epub ahead of print]

Ee LC, Noble C, Fawcett J, Cleghorn GJ.

Abstract

OBJECTIVES:
Liver transplant patients are at risk of osteopenia and fractures but limited information is available in long-term survivors after childhood transplantation. This study aimed to assess bone mineral density (BMD) of very long-term, >5 years, survivors after liver transplantation in childhood.

METHODS:

Published on: 
Dec-2017

https://www.ncbi.nlm.nih.gov/pubmed/29174177

Cholestasis

J Pediatr Surg. 2017 Nov 23. pii: S0022-3468(17)30711-X. doi: 10.1016/j.jpedsurg.2017.10.055. [Epub ahead of print]
Erginel B, Soysal FG, Durmaz O, Celik A, Salman T.

Abstract

BACKGROUND:
Partial internal biliary diversion (PIBD) is an alternative approach for the treatment of devastating pruritus in patients with progressive familial intrahepatic cholestasis (PFIC). In these patients quality of life can be improved and progression of liver disease can be delayed while waiting for liver transplantation. The aim of our study was to evaluate six patients with PFIC who have undergone PIBD in long-term follow-up.

METHODS:

Published on: 
Nov-2017

https://www.ncbi.nlm.nih.gov/pubmed/29287014 Hepatitis C
J Pediatr Gastroenterol Nutr. 2017 Dec 28. doi: 10.1097/MPG.0000000000001872. [Epub ahead of print]

Treatment of Chronic Hepatitis C Virus Infection in Children. A Position Paper by the Hepatology Committee of European Society of Paediatric Gastroenterology, Hepatology and Nutrition.
Indolfi G, Hierro L, Dezsofi A, Jahnel J, Debray D, Hadzic N, Czubowski P, Gupte G, Mozer-Glassberg Y, van der Woerd W, Smets F, Verkade HJ, Fischler B.

Abstract

OBJECTIVES:

Published on: 
Dec-2017

https://www.ncbi.nlm.nih.gov/pubmed/29176474

Neonatal Jaundice

J Pediatr Gastroenterol Nutr. 2017 Nov 22. doi: 10.1097/MPG.0000000000001843. [Epub ahead of print]

Mitchell E, Ranganathan S, McKiernan P, Squires RH, Strauss K, Soltys K, Mazariegos G, Squires JE.

Abstract

BACKGROUND:
Crigler-Najjar syndrome type I (CNI) arises from biallelic variants of UGT1A1 that abrogate UGT1A1 activity resulting in unconjugated hyperbilirubinemia. Historically, liver parenchyma in CNI was considered structurally and histologically normal. Recent review of CNI liver explants revealed fibrosis. Our aim was to investigate the association between hepatic histology and disease phenotype in CNI.

METHODS:

Published on: 
Nov-2017

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