Event Videos

http://www.ncbi.nlm.nih.gov/pubmed/25419594
Venkat VL1, Shneider BL, Magee JC, Turmelle Y, Arnon R, Bezerra JA, Hertel PM, Karpen SJ, Kerkar N, Loomes KM, Molleston J, Murray KF, Ng VL,Raghunathan T, Rosenthal P, Schwartz K, Sherker AH, Sokol RJ, Teckman J, Wang K, Whitington PF, Heubi JE; Childhood Liver Disease Research and Education Network.

Abstract

OBJECTIVE:
Fat-soluble vitamin (FSV) deficiency is a well-recognized consequence of cholestatic liver disease and reduced intestinal intraluminal bile acid. We hypothesized that serum bile acid (SBA) would predict biochemical FSV deficiency better than serum total bilirubin (TB) level in infants with biliary atresia.

METHODS:

Published on: 
Dec-2014

http://www.ncbi.nlm.nih.gov/pubmed/25141230
Lu FT1, Wu JF, Hsu HY, Ni YH, Chang MH, Chao CI, Chen HL.

Abstract

OBJECTIVES:
Low γ-glutamyl transpeptidase (GGT) level is an important marker for progressive familial intrahepatic cholestasis, yet the cutoff level and clinical application is not well defined. This study aimed to evaluate the role of GGT as a screening marker among diverse etiologies of infantile cholestasis.

METHODS:

Published on: 
Dec-2014

http://www.ncbi.nlm.nih.gov/pubmed/25003372
Kim S, Kang Y, Lee MJ, Kim MJ, Han SJ, Koh H.

Abstract

OBJECTIVES:
With the introduction of smaller probes (S1, S2), the use of transient elastography has been expanded to children. Accordingly, we aimed to address points of consideration in probe choice and interpretation of measured liver stiffness by applying and comparing FibroScan S and M probes in biliary atresia.

METHODS:

Published on: 
Nov-2014

http://www.ncbi.nlm.nih.gov/pubmed/25141228
D'Antiga L1, Dacchille P, Boniver C, Poledri S, Schiff S, Zancan L, Amodio P.

Abstract

OBJECTIVE:
In children with noncirrhotic extrahepatic portal vein obstruction (EHPVO), minimal hepatic encephalopathy (MHE) was reported in a few series, but neither is it routinely investigated nor does consensus about its diagnosis exist. In this prospective observational study we aimed at detecting the prevalence of MHE in children with EHPVO and providing a practical diagnostic protocol.

METHODS:

Published on: 
Dec-2014

http://www.ncbi.nlm.nih.gov/pubmed/25340974

Schwarz KB, Dell Olio D, Lobritto SJ, Lopez MJ, Rodriguez-Baez N, Yazigi NA, Belle SH, Zhang S, Squires RH; Pediatric Acute Liver Failure Study Group. Analysis of viral testing in non-acetaminophen pediatric acute liver failure. J Pediatr Gastroenterol Nutr. 2014 Nov; 59(5): 616-23.

Abstract

OBJECTIVE:
Viral infections are often suspected to cause pediatric acute liver failure (PALF), but large-scale studies have not been performed. We analyzed the results of viral testing among nonacetaminophen PALF study participants.

METHODS:

Published on: 
Nov-2014

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2647530/

Anne Davit-Spraul, Emmanuel Gonzales,Christiane Baussan and Emmanuel Jacquemin

Abstract

Progressive familial intrahepatic cholestasis (PFIC) refers to heterogeneous group of autosomal recessive disorders of childhood that disrupt bile formation and present with cholestasis of hepatocellular origin. The exact prevalence remains unknown, but the estimated incidence varies between 1/50,000 and 1/100,000 births.

Published on: 
Jan-2009

CLF Intro movie

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