Published in J Hepatol on February 08, 2013
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Anti-CD20 monoclonal antibody (Rituximab) treatment for Epstein-Barr virus-associated, B-cell lymphoproliferative disease in pediatric liver transplant recipients. J Pediatr Gastroenterol Nutr (2002) 1.47
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Widening spectrum of liver angiosarcoma in children. J Pediatr Gastroenterol Nutr (2011) 1.42
Experience with endoscopic management of high-risk gastroesophageal varices, with and without bleeding, in children with biliary atresia. Gastroenterology (2013) 1.42
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Association rate constants rationalise the pharmacodynamics of apixaban and rivaroxaban. Thromb Haemost (2015) 1.40
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MALDI-TOF MS-based drug susceptibility testing of pathogens: the example of Candida albicans and fluconazole. Proteomics (2009) 1.26
Familial liver adenomatosis associated with hepatocyte nuclear factor 1alpha inactivation. Gastroenterology (2003) 1.22
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Heterozygous bile salt export pump deficiency: a possible genetic predisposition to transient neonatal cholestasis. J Pediatr Gastroenterol Nutr (2006) 1.16
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CFCI gene mutation and biliary atresia with polysplenia syndrome. J Pediatr Gastroenterol Nutr (2002) 1.14
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Novel mutations in TTC37 associated with tricho-hepato-enteric syndrome. Hum Mutat (2011) 1.10
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Multicenter prospective validation of the Baveno IV and Baveno II/III criteria in cirrhosis patients with variceal bleeding. Hepatology (2015) 1.08
Kleine-Levin syndrome in 120 patients: differential diagnosis and long episodes. Ann Neurol (2015) 1.06
A missense mutation in ABCB4 gene involved in progressive familial intrahepatic cholestasis type 3 leads to a folding defect that can be rescued by low temperature. Hepatology (2009) 1.06
Intractable diarrhea with "phenotypic anomalies" and tricho-hepato-enteric syndrome: two names for the same disorder. Am J Med Genet A (2007) 1.06
Sexual dimorphism in the early life programming of serum leptin levels in European adolescents: the HELENA study. J Clin Endocrinol Metab (2011) 1.06
Increased intima-media thickness of the carotid artery in childhood: a systematic review of observational studies. Eur J Pediatr (2010) 1.05
Food intake of European adolescents in the light of different food-based dietary guidelines: results of the HELENA (Healthy Lifestyle in Europe by Nutrition in Adolescence) Study. Public Health Nutr (2011) 1.05
Vitamin K antagonists in children with heart disease: height and VKORC1 genotype are the main determinants of the warfarin dose requirement. Blood (2011) 1.05
Diet and nutritional status of children with food allergies. Pediatr Allergy Immunol (2011) 1.05
Defective B-cell-negative selection and terminal differentiation in the ICF syndrome. Blood (2003) 1.05
Syndromic (phenotypic) diarrhea in early infancy. Orphanet J Rare Dis (2008) 1.05
Perforin-dependent apoptosis functionally compensates Fas deficiency in activation-induced cell death of human T lymphocytes. Blood (2007) 1.04
Altered hepatobiliary gene expressions in PFIC1: ATP8B1 gene defect is associated with CFTR downregulation. Hepatology (2006) 1.04
Effect of child health status on parents' allowing children to participate in pediatric research. BMC Med Ethics (2013) 1.03
Self-reported physical activity in European adolescents: results from the HELENA (Healthy Lifestyle in Europe by Nutrition in Adolescence) study. Public Health Nutr (2010) 1.02
GPIHBP1 C89F neomutation and hydrophobic C-terminal domain G175R mutation in two pedigrees with severe hyperchylomicronemia. J Clin Endocrinol Metab (2011) 1.02
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Gastric inflammatory myofibroblastic tumors in children: an unpredictable course. J Pediatr Gastroenterol Nutr (2002) 1.02
Feasibility of ovarian tissue cryopreservation for prepubertal females with cancer. Pediatr Blood Cancer (2007) 1.00
Anderson or chylomicron retention disease: molecular impact of five mutations in the SAR1B gene on the structure and the functionality of Sar1b protein. Mol Genet Metab (2007) 0.99
SRD5B1 (AKR1D1) gene analysis in delta(4)-3-oxosteroid 5beta-reductase deficiency: evidence for primary genetic defect. J Hepatol (2004) 0.99