Event Videos
J Pediatr Gastroenterol Nutr. 2012 May;54(5):580-7. Congenital hepatic fibrosis and autosomal recessive polycystic kidney disease. 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
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J Pediatr Gastroenterol Nutr. 2012 Mar;54(3):328-35. Published on:
Mar-2012
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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. Abstract Published on:
Apr-2012
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J Pediatr Gastroenterol Nutr. 2012 Mar;54(3):313-21.
Endocrine and bone metabolic complications in chronic liver disease and after liver transplantation in children. Högler W, Baumann U, Kelly D. Department of Endocrinology and Diabetes, Birmingham Children's Hospital, Birmingham, UK. wolfgang.hogler@bch.nhs.uk Abstract Published on:
Mar-2012
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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. 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
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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. 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
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J Pediatr Gastroenterol Nutr. 2012 Apr;54(4):540-6. Neurological complications following pediatric liver transplant. 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
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J Pediatr Gastroenterol Nutr. 2012 Jan;54(1):90-6. Published on:
Jan-2012
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J Pediatr Gastroenterol Nutr. 2012 Apr;54(4):454-62. Published on:
Apr-2012
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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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