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BENJAMIN SHNEIDER to Infant, Newborn

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This is a "connection" page, showing publications BENJAMIN SHNEIDER has written about Infant, Newborn.
BENJAMIN SHNEIDER
Connection Strength
1.030
Infant, Newborn
  1. The association of human milk intake and outcomes in biliary atresia. J Pediatr Gastroenterol Nutr. 2025 Jan; 80(1):163-173.
    View in: PubMed
    Score: 0.095
  2. Diagnostic Yield of Newborn Screening for Biliary Atresia Using Direct or Conjugated Bilirubin Measurements. JAMA. 2020 03 24; 323(12):1141-1150.
    View in: PubMed
    Score: 0.069
  3. Factors Influencing Time-to-diagnosis of Biliary Atresia. J Pediatr Gastroenterol Nutr. 2018 Jun; 66(6):850-856.
    View in: PubMed
    Score: 0.061
  4. Development of a Novel Tool to Assess the Impact of Itching in Pediatric Cholestasis. Patient. 2018 02; 11(1):69-82.
    View in: PubMed
    Score: 0.059
  5. Initial assessment of the infant with neonatal cholestasis-Is this biliary atresia? PLoS One. 2017; 12(5):e0176275.
    View in: PubMed
    Score: 0.056
  6. Newborn Bilirubin Screening for Biliary Atresia. N Engl J Med. 2016 Aug 11; 375(6):605-6.
    View in: PubMed
    Score: 0.054
  7. Total Serum Bilirubin within 3 Months of Hepatoportoenterostomy Predicts Short-Term Outcomes in Biliary Atresia. J Pediatr. 2016 Mar; 170:211-7.e1-2.
    View in: PubMed
    Score: 0.051
  8. 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.
    View in: PubMed
    Score: 0.048
  9. 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.
    View in: PubMed
    Score: 0.042
  10. Congenital hepatic fibrosis and autosomal recessive polycystic kidney disease. J Pediatr Gastroenterol Nutr. 2012 May; 54(5):580-7.
    View in: PubMed
    Score: 0.040
  11. Biliary atresia: a transplant perspective. Liver Transpl. 2007 Nov; 13(11):1482-95.
    View in: PubMed
    Score: 0.029
  12. 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.
    View in: PubMed
    Score: 0.023
  13. 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).
    View in: PubMed
    Score: 0.022
  14. Fat Soluble Vitamin Assessment and Supplementation in Cholestasis. Clin Liver Dis. 2022 08; 26(3):537-553.
    View in: PubMed
    Score: 0.020
  15. The Epidemiology of Biliary Atresia: Exploring the Role of Developmental Factors on Birth Prevalence. J Pediatr. 2022 07; 246:89-94.e2.
    View in: PubMed
    Score: 0.020
  16. MR cholangiography in the evaluation of neonatal cholestasis: initial results. Radiology. 2002 Mar; 222(3):687-91.
    View in: PubMed
    Score: 0.020
  17. Genetic counseling in neonatal hemochromatosis. J Pediatr Gastroenterol Nutr. 2002 Mar; 34(3):328.
    View in: PubMed
    Score: 0.020
  18. Newborn Screening for Biliary Atresia: a Review of Current Methods. Curr Gastroenterol Rep. 2021 Nov 24; 23(12):28.
    View in: PubMed
    Score: 0.019
  19. 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.
    View in: PubMed
    Score: 0.019
  20. Presentation and Outcomes of Infants With Idiopathic Cholestasis: A Multicenter Prospective Study. J Pediatr Gastroenterol Nutr. 2021 10 01; 73(4):478-484.
    View in: PubMed
    Score: 0.019
  21. Flipping over flippases. J Pediatr Gastroenterol Nutr. 2001 Jul; 33(1):102-3.
    View in: PubMed
    Score: 0.019
  22. Neonatal hemochromatosis: the importance of early recognition of liver failure. J Pediatr. 2000 Apr; 136(4):537-41.
    View in: PubMed
    Score: 0.017
  23. Biliary Atresia as a Disease Starting In Utero: Implications for Treatment, Diagnosis, and Pathogenesis. J Pediatr Gastroenterol Nutr. 2019 10; 69(4):396-403.
    View in: PubMed
    Score: 0.017
  24. 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.
    View in: PubMed
    Score: 0.016
  25. 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.
    View in: PubMed
    Score: 0.015
  26. Hepatic basolateral sodium-dependent-bile acid transporter expression in two unusual cases of hypercholanemia and in extrahepatic biliary atresia. Hepatology. 1997 May; 25(5):1176-83.
    View in: PubMed
    Score: 0.014
  27. Newborn Direct or Conjugated Bilirubin Measurements As a Potential Screen for Biliary Atresia. J Pediatr Gastroenterol Nutr. 2016 06; 62(6):799-803.
    View in: PubMed
    Score: 0.013
  28. 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.
    View in: PubMed
    Score: 0.012
  29. Byler disease: early natural history. J Pediatr Gastroenterol Nutr. 2015 Apr; 60(4):460-6.
    View in: PubMed
    Score: 0.012
  30. 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.
    View in: PubMed
    Score: 0.012
  31. Delta 4-3-oxosteroid 5 beta-reductase deficiency causing neonatal liver failure and hemochromatosis. J Pediatr. 1994 Feb; 124(2):234-8.
    View in: PubMed
    Score: 0.011
  32. Intravenous N-acetylcysteine in pediatric patients with nonacetaminophen acute liver failure: a placebo-controlled clinical trial. Hepatology. 2013 Apr; 57(4):1542-9.
    View in: PubMed
    Score: 0.011
  33. Differences in presentation and progression between severe FIC1 and BSEP deficiencies. J Hepatol. 2010 Jul; 53(1):170-8.
    View in: PubMed
    Score: 0.009
  34. State of research in pediatric gastroenterology, hepatology, and nutrition: 2010 and beyond. Gastroenterology. 2010 Feb; 138(2):411-6, 416.e1-2.
    View in: PubMed
    Score: 0.008
  35. Cholestasis in infants supported with extracorporeal membrane oxygenation. J Pediatr. 1989 Sep; 115(3):462-5.
    View in: PubMed
    Score: 0.008
  36. Exposure to di(2-ethylhexyl)phthalate in infants receiving extracorporeal membrane oxygenation. N Engl J Med. 1989 Jun 08; 320(23):1563.
    View in: PubMed
    Score: 0.008
  37. Growth failure and outcomes in infants with biliary atresia: a report from the Biliary Atresia Research Consortium. Hepatology. 2007 Nov; 46(5):1632-8.
    View in: PubMed
    Score: 0.007
  38. 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.
    View in: PubMed
    Score: 0.007
  39. Rapamycin successfully treats post-transplant autoimmune hepatitis. Am J Transplant. 2005 May; 5(5):1085-9.
    View in: PubMed
    Score: 0.006
  40. Minor salivary gland biopsy in neonatal hemochromatosis. Arch Otolaryngol Head Neck Surg. 2004 Jun; 130(6):760-3.
    View in: PubMed
    Score: 0.006
  41. Coordinate expression of regulatory genes differentiates embryonic and perinatal forms of biliary atresia. Hepatology. 2004 Apr; 39(4):954-62.
    View in: PubMed
    Score: 0.006
  42. Genetic induction of proinflammatory immunity in children with biliary atresia. Lancet. 2002 Nov 23; 360(9346):1653-9.
    View in: PubMed
    Score: 0.005
  43. 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.
    View in: PubMed
    Score: 0.005
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.