BENJAMIN SHNEIDER to Infant
This is a "connection" page, showing publications BENJAMIN SHNEIDER has written about Infant.
Connection Strength
1.658
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A phase 2 trial of short-term intravenous N-acetylcysteine in biliary atresia after Kasai portoenterostomy. Hepatol Commun. 2025 Jul 01; 9(7).
Score: 0.079
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The association of human milk intake and outcomes in biliary atresia. J Pediatr Gastroenterol Nutr. 2025 Jan; 80(1):163-173.
Score: 0.076
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Characteristics of infections and their risk factors in children with biliary atresia. Clin Res Hepatol Gastroenterol. 2023 04; 47(4):102109.
Score: 0.067
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Serum bile acids as a prognostic biomarker in biliary atresia following Kasai portoenterostomy. Hepatology. 2023 03 01; 77(3):862-873.
Score: 0.067
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Operational Definitions for Chronic Liver Disease Manifestations and Recurring Clinical Events in Biliary Atresia. J Pediatr Gastroenterol Nutr. 2021 04 01; 72(4):584-591.
Score: 0.059
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The Fecal Microbiome in Infants With Biliary Atresia Associates With Bile Flow After Kasai Portoenterostomy. J Pediatr Gastroenterol Nutr. 2020 06; 70(6):789-795.
Score: 0.056
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Diagnostic Yield of Newborn Screening for Biliary Atresia Using Direct or Conjugated Bilirubin Measurements. JAMA. 2020 03 24; 323(12):1141-1150.
Score: 0.055
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Factors Influencing Time-to-diagnosis of Biliary Atresia. J Pediatr Gastroenterol Nutr. 2018 Jun; 66(6):850-856.
Score: 0.048
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Development of a Novel Tool to Assess the Impact of Itching in Pediatric Cholestasis. Patient. 2018 02; 11(1):69-82.
Score: 0.047
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Initial assessment of the infant with neonatal cholestasis-Is this biliary atresia? PLoS One. 2017; 12(5):e0176275.
Score: 0.045
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The Medication Level Variability Index (MLVI) Predicts Poor Liver Transplant Outcomes: A Prospective Multi-Site Study. Am J Transplant. 2017 Oct; 17(10):2668-2678.
Score: 0.045
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Cross-Sectional Analysis of Progressive Familial Intrahepatic Cholestasis in Puerto Rican Children. P R Health Sci J. 2016 Dec; 35(4):220-223.
Score: 0.044
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Possible Phenylacetate Hepatotoxicity During 4-Phenylbutyrate Therapy of Byler Disease. J Pediatr Gastroenterol Nutr. 2016 Mar; 62(3):424-8.
Score: 0.041
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Total Serum Bilirubin within 3 Months of Hepatoportoenterostomy Predicts Short-Term Outcomes in Biliary Atresia. J Pediatr. 2016 Mar; 170:211-7.e1-2.
Score: 0.041
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Total serum bilirubin predicts fat-soluble vitamin deficiency better than serum bile acids in infants with biliary atresia. J Pediatr Gastroenterol Nutr. 2014 Dec; 59(6):702-7.
Score: 0.038
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Liver transplantation for children with biliary atresia in the pediatric end-stage liver disease era: the role of insurance status. Liver Transpl. 2013 May; 19(5):543-50.
Score: 0.034
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Giant cell hepatitis and immune thrombocytopenic purpura: reversal of liver failure with rituximab therapy. J Pediatr Gastroenterol Nutr. 2012 Oct; 55(4):e128-30.
Score: 0.033
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Efficacy of fat-soluble vitamin supplementation in infants with biliary atresia. Pediatrics. 2012 Sep; 130(3):e607-14.
Score: 0.032
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Congenital hepatic fibrosis and autosomal recessive polycystic kidney disease. J Pediatr Gastroenterol Nutr. 2012 May; 54(5):580-7.
Score: 0.032
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Markedly elevated serum transaminases in glycogen storage disease type III. J Pediatr Gastroenterol Nutr. 2011 May; 52(5):621-3.
Score: 0.030
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Valproic acid-associated acute liver failure in children: case report and analysis of liver transplantation outcomes in the United States. J Pediatr. 2011 May; 158(5):802-7.
Score: 0.029
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Recurrent low gamma-glutamyl transpeptidase cholestasis following liver transplantation for bile salt export pump (BSEP) disease (posttransplant recurrent BSEP disease). Liver Transpl. 2010 Jul; 16(7):856-63.
Score: 0.028
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Biliary atresia: a transplant perspective. Liver Transpl. 2007 Nov; 13(11):1482-95.
Score: 0.023
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A multicenter study of the outcome of biliary atresia in the United States, 1997 to 2000. J Pediatr. 2006 Apr; 148(4):467-474.
Score: 0.021
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National and regional analysis of exceptions to the Pediatric End-Stage Liver Disease scoring system (2003-2004). Liver Transpl. 2006 Jan; 12(1):40-5.
Score: 0.020
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Critical analysis of the pediatric end-stage liver disease scoring system: a single center experience. Liver Transpl. 2005 Jul; 11(7):788-795.
Score: 0.020
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An ultrasound approach to visualize the "duct at the hilum" in infants undergoing evaluation for biliary atresia. J Pediatr Gastroenterol Nutr. 2025 Aug; 81(2):204-211.
Score: 0.020
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Bile acid and microbiome interactions in the developing child. J Pediatr Gastroenterol Nutr. 2025 May; 80(5):832-839.
Score: 0.019
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Diagnostic accuracy of serum matrix metalloproteinase-7 as a biomarker of biliary atresia in a large North American cohort. Hepatology. 2024 07 01; 80(1):152-162.
Score: 0.018
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Progressive familial intrahepatic cholestasis, type 1, is associated with decreased farnesoid X receptor activity. Gastroenterology. 2004 Mar; 126(3):756-64.
Score: 0.018
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Neonatal cholestasis in children with Alpha-1-AT deficiency is a risk for earlier severe liver disease with male predominance. Hepatol Commun. 2023 12 01; 7(12).
Score: 0.018
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Fat Soluble Vitamin Assessment and Supplementation in Cholestasis. Clin Liver Dis. 2022 08; 26(3):537-553.
Score: 0.016
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Risk of variceal hemorrhage and pretransplant mortality in children with biliary atresia. Hepatology. 2022 09; 76(3):712-726.
Score: 0.016
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The Epidemiology of Biliary Atresia: Exploring the Role of Developmental Factors on Birth Prevalence. J Pediatr. 2022 07; 246:89-94.e2.
Score: 0.016
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MR cholangiography in the evaluation of neonatal cholestasis: initial results. Radiology. 2002 Mar; 222(3):687-91.
Score: 0.016
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The role of quantitative Epstein-Barr virus polymerase chain reaction and preemptive immunosuppression reduction in pediatric liver transplantation: a preliminary experience. J Pediatr Gastroenterol Nutr. 2001 Oct; 33(4):445-9.
Score: 0.015
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Presentation and Outcomes of Infants With Idiopathic Cholestasis: A Multicenter Prospective Study. J Pediatr Gastroenterol Nutr. 2021 10 01; 73(4):478-484.
Score: 0.015
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Impact of Genotype, Serum Bile Acids, and Surgical Biliary Diversion on Native Liver Survival in FIC1 Deficiency. Hepatology. 2021 08; 74(2):892-906.
Score: 0.015
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Flipping over flippases. J Pediatr Gastroenterol Nutr. 2001 Jul; 33(1):102-3.
Score: 0.015
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MR cholangiography in children and young adults with biliary disease. AJR Am J Roentgenol. 1999 May; 172(5):1239-44.
Score: 0.013
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Prospective longitudinal analysis of quantitative Epstein-Barr virus polymerase chain reaction in pediatric liver transplant recipients. Transplantation. 1999 Apr 15; 67(7):1068-70.
Score: 0.013
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Accuracy of the Pediatric End-stage Liver Disease Score in Estimating Pretransplant Mortality Among Pediatric Liver Transplant Candidates. JAMA Pediatr. 2018 11 01; 172(11):1070-1077.
Score: 0.012
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Impact of Steroid Therapy on Early Growth in Infants with Biliary Atresia: The Multicenter Steroids in Biliary Atresia Randomized Trial. J Pediatr. 2018 11; 202:179-185.e4.
Score: 0.012
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A Learning Collaborative Approach Increases Specificity of Diagnosis of Acute Liver Failure in Pediatric Patients. Clin Gastroenterol Hepatol. 2018 11; 16(11):1801-1810.e3.
Score: 0.012
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Neurodevelopmental Outcome of Young Children with Biliary Atresia and Native Liver: Results from the ChiLDReN Study. J Pediatr. 2018 05; 196:139-147.e3.
Score: 0.012
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Trajectory of adherence behavior in pediatric and adolescent liver transplant recipients: The medication adherence in children who had a liver transplant cohort. Liver Transpl. 2018 01; 24(1):80-88.
Score: 0.012
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Self-Management Measurement and Prediction of Clinical Outcomes in Pediatric Transplant. J Pediatr. 2018 02; 193:128-133.e2.
Score: 0.012
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Analysis of surgical interruption of the enterohepatic circulation as a treatment for pediatric cholestasis. Hepatology. 2017 05; 65(5):1645-1654.
Score: 0.011
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Clinical Variability After Partial External Biliary Diversion in Familial Intrahepatic Cholestasis 1 Deficiency. J Pediatr Gastroenterol Nutr. 2017 03; 64(3):425-430.
Score: 0.011
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Newborn Direct or Conjugated Bilirubin Measurements As a Potential Screen for Biliary Atresia. J Pediatr Gastroenterol Nutr. 2016 06; 62(6):799-803.
Score: 0.011
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Liver Transplantation for Biliary Atresia: Is There a Difference in Outcome for Infants? J Pediatr Gastroenterol Nutr. 2016 Feb; 62(2):220-5.
Score: 0.010
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Baseline Analysis of a Young a-1-Antitrypsin Deficiency Liver Disease Cohort Reveals Frequent Portal Hypertension. J Pediatr Gastroenterol Nutr. 2015 Jul; 61(1):94-101.
Score: 0.010
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Byler disease: early natural history. J Pediatr Gastroenterol Nutr. 2015 Apr; 60(4):460-6.
Score: 0.010
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Bile acid pool dynamics in progressive familial intrahepatic cholestasis with partial external bile diversion. J Pediatr Gastroenterol Nutr. 2015 Mar; 60(3):368-74.
Score: 0.010
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Medication level variability index predicts rejection, possibly due to nonadherence, in adult liver transplant recipients. Liver Transpl. 2014 Oct; 20(10):1168-77.
Score: 0.009
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Consensus expert recommendations for the diagnosis and management of autosomal recessive polycystic kidney disease: report of an international conference. J Pediatr. 2014 Sep; 165(3):611-7.
Score: 0.009
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Use of corticosteroids after hepatoportoenterostomy for bile drainage in infants with biliary atresia: the START randomized clinical trial. JAMA. 2014 May 07; 311(17):1750-9.
Score: 0.009
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Delta 4-3-oxosteroid 5 beta-reductase deficiency causing neonatal liver failure and hemochromatosis. J Pediatr. 1994 Feb; 124(2):234-8.
Score: 0.009
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Intravenous N-acetylcysteine in pediatric patients with nonacetaminophen acute liver failure: a placebo-controlled clinical trial. Hepatology. 2013 Apr; 57(4):1542-9.
Score: 0.008
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King's College Hospital Criteria for non-acetaminophen induced acute liver failure in an international cohort of children. J Pediatr. 2013 Feb; 162(2):319-23.e1.
Score: 0.008
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A prospective analysis of cholestasis in infants supported with extracorporeal membrane oxygenation. J Pediatr Gastroenterol Nutr. 1991 Oct; 13(3):285-9.
Score: 0.008
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Increased expression of peripheral blood leukocyte genes implicate CD14+ tissue macrophages in cellular intestine allograft rejection. Am J Pathol. 2011 Oct; 179(4):1929-38.
Score: 0.008
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Differences in presentation and progression between severe FIC1 and BSEP deficiencies. J Hepatol. 2010 Jul; 53(1):170-8.
Score: 0.007
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State of research in pediatric gastroenterology, hepatology, and nutrition: 2010 and beyond. Gastroenterology. 2010 Feb; 138(2):411-6, 416.e1-2.
Score: 0.007
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Cholestasis in infants supported with extracorporeal membrane oxygenation. J Pediatr. 1989 Sep; 115(3):462-5.
Score: 0.007
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A hybrid strategy for the prevention of cytomegalovirus-related complications in pediatric liver transplantation recipients. Transplantation. 2009 May 15; 87(9):1318-24.
Score: 0.006
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Growth failure and outcomes in infants with biliary atresia: a report from the Biliary Atresia Research Consortium. Hepatology. 2007 Nov; 46(5):1632-8.
Score: 0.006
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Giant cell hepatitis and autoimmune hemolytic anemia successfully treated with rituximab. J Pediatr Gastroenterol Nutr. 2007 May; 44(5):634-6.
Score: 0.006
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Bullous pemphigoid after liver transplantation for liver failure. Liver Transpl. 2006 Nov; 12(11):1705-10.
Score: 0.005
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CMV-IVIG for prevention of Epstein Barr virus disease and posttransplant lymphoproliferative disease in pediatric liver transplant recipients. Am J Transplant. 2006 Aug; 6(8):1906-12.
Score: 0.005
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Favorable long-term outcome after liver-kidney transplant for recurrent hemolytic uremic syndrome associated with a factor H mutation. Am J Transplant. 2006 Aug; 6(8):1948-52.
Score: 0.005
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Acute liver failure in children: the first 348 patients in the pediatric acute liver failure study group. J Pediatr. 2006 May; 148(5):652-658.
Score: 0.005
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Rapamycin successfully treats post-transplant autoimmune hepatitis. Am J Transplant. 2005 May; 5(5):1085-9.
Score: 0.005
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Minor salivary gland biopsy in neonatal hemochromatosis. Arch Otolaryngol Head Neck Surg. 2004 Jun; 130(6):760-3.
Score: 0.005
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Coordinate expression of regulatory genes differentiates embryonic and perinatal forms of biliary atresia. Hepatology. 2004 Apr; 39(4):954-62.
Score: 0.005
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Sex steroid hormones, growth and puberty in children with portal hypertension. J Pediatr Endocrinol Metab. 2004 Apr; 17(4):607-13.
Score: 0.005
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Genetic induction of proinflammatory immunity in children with biliary atresia. Lancet. 2002 Nov 23; 360(9346):1653-9.
Score: 0.004
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A novel intronic mutation results in the use of a cryptic splice acceptor site within the coding region of UGT1A1, causing Crigler-Najjar syndrome type 1. Mol Genet Metab. 2002 Feb; 75(2):134-42.
Score: 0.004
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Abnormal hepatic sinusoidal bile acid transport in an Amish kindred is not linked to FIC1 and is improved by ursodiol. Gastroenterology. 2000 Jul; 119(1):188-95.
Score: 0.003
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A defect in the transport of long-chain fatty acids associated with acute liver failure. N Engl J Med. 1998 Dec 10; 339(24):1752-7.
Score: 0.003