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J Pediatr Gastroenterol Nutr. 2012 May;54(5):580-7.

Congenital hepatic fibrosis and autosomal recessive polycystic kidney disease.
Srinath A, Shneider BL.
Division of Pediatric Gastroenterology, Hepatology, and Nutrition, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, PA 15224, USA.

Abstract

OBJECTIVES: The published natural history of congenital hepatic fibrosis (CHF) was examined to inform clinical decision making in autosomal recessive polycystic kidney disease (ARPKD).

Published on: 
May-2012

J Pediatr Gastroenterol Nutr. 2012 Apr;54(4):552-7.

Intracranial hemorrhage associated with vitamin K-deficiency bleeding in patients with biliary atresia: focus on long-term outcomes.
Alatas FS, Hayashida M, Matsuura T, Saeki I, Yanagi Y, Taguchi T.
Department of Pediatric Surgery, Reproductive and Developmental Medicine, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.

Abstract

Published on: 
Apr-2012

J Pediatr Gastroenterol Nutr. 2012 Apr;54(4):547-51.

Long-term outcomes of isolated liver transplantation for short bowel syndrome and intestinal failure-associated liver disease.
Taha AM, Sharif K, Johnson T, Clarke S, Murphy MS, Gupte GL.
Liver Unit, Department of Dietetics, Birmingham Children's Hospital, Steelhouse Lane, Birmingham, UK.

Abstract

BACKGROUND AND AIM: A select group of children with short bowel syndrome (SBS) and intestinal failure-associated liver disease (IFALD) fulfill the criteria for isolated liver transplantation (iLTx). Long-term results in this group of patients have not been reported.

Published on: 
Apr-2012

J Pediatr Gastroenterol Nutr. 2012 Jan;54(1):97-100.

Predictive effect of serial serum alanine aminotransferase levels on spontaneous HBeAg seroconversion in chronic genotype B and C HBV-infected children.
Wu JF, Su YR, Chen CH, Chen HL, Ni YH, Hsu HY, Wang JL, Chang MH.
Department of Pediatrics, National Taiwan University Hospital, Taipei, Taiwan.

Abstract

OBJECTIVE: The present study aimed to investigate the association between serial serum alanine aminotransferase (ALT) and spontaneous hepatitis B e antigen (HBeAg) seroconversion age in chronic hepatitis B virus (HBV)-infected children.

Published on: 
Jan-2012

J Pediatr Gastroenterol Nutr. 2012 Apr;54(4):540-6.

Neurological complications following pediatric liver transplant.
Ghosh PS, Hupertz V, Ghosh D.
Pediatric Neurology Center, Department of Pediatric Gastroenterology and Hepatology, Cleveland Clinic, Cleveland, OH 44195, USA. e-ghoshd2@ccf.org

Abstract

OBJECTIVE: We studied neurological complications (NCs) after liver transplantation (LT) in children.

METHODS: We performed an institutional review board-approved retrospective review of patients with LT ≤21 years during a period of 30 years (1980-2010). NCs were classified as early (within 3 months post-LT) and delayed (beyond 3 months post-LT).

Published on: 
Apr-2012

J Pediatr Gastroenterol Nutr. 2012 Jan;54(1):90-6.
 
Correlation of vitamin E, uric acid, and diet composition with histologic features of pediatric NAFLD.
Vos MB, Colvin R, Belt P, Molleston JP, Murray KF, Rosenthal P, Schwimmer JB, Tonascia J, Unalp A, Lavine JE; NASH CRN Research Group.
Pediatrics, Emory University, Atlanta, GA, USA.
 
Abstract
 
OBJECTIVES: Nonalcoholic fatty liver disease (NAFLD) is the most common chronic liver disease in children in the United States. Although changes in diet are often recommended to improve NAFLD, little is known regarding the influence of diet on histologic features of the disease.
 

Published on: 
Jan-2012

J Pediatr Gastroenterol Nutr. 2012 Apr;54(4):454-62.
 
Targeted MRI contrast agents for pediatric hepatobiliary disease.
Courtier JL, Perito ER, Rhee S, Tsai P, Heyman MB, MacKenzie JD.
Department of Radiology and Biomedical Imaging, UCSF Benioff Children's Hospital, University of California-San Francisco, 505 Parnassus Ave., San Francisco, CA 94143, USA.
 
Abstract
 

Published on: 
Apr-2012

J Pediatr Gastroenterol Nutr. 2012 Jan;54(1):83-9. Congenital hepatic fibrosis and portal hypertension in autosomal dominant polycystic kidney disease. O'Brien K, Font-Montgomery E, Lukose L, Bryant J, Piwnica-Worms K, Edwards H, Riney L, Garcia A, Daryanani K, Choyke P, Mohan P, Heller T, Gahl WA, Gunay-Aygun M. Section on Human Biochemical Genetics, Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA.

Abstract

Published on: 
Aug-2011

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