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M Hertel

Showing results (31-40 of 41) with videos related to

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The Journal of Pediatrics|June 11, 2015
Quality of Life and Its Determinants in a Multicenter Cohort of Children with Alagille SyndromeBinita M Kamath, Zhen Chen, Rene Romero, et al.
Journal of Pediatric Gastroenterology and Nutrition|February 5, 2015
Baseline Analysis of a Young α-1-Antitrypsin Deficiency Liver Disease Cohort Reveals Frequent Portal HypertensionJeffrey H Teckman, Philip Rosenthal, Robert Abel, et al.
Journal of Pediatric Gastroenterology and Nutrition|November 25, 2014
Total serum bilirubin predicts fat-soluble vitamin deficiency better than serum bile acids in infants with biliary atresiaVeena L Venkat, Benjamin L Shneider, John C Magee, et al.
Journal of Pediatric Gastroenterology and Nutrition|July 26, 2021
Presentation and Outcomes of Infants With Idiopathic Cholestasis: A Multicenter Prospective StudyPaula M Hertel, Kieran Hawthorne, Sehee Kim, et al.
Hepatology (Baltimore, Md.)|August 1, 2018
Bone Density in Children With Chronic Liver Disease Correlates With Growth and CholestasisKathleen M Loomes, Cathie Spino, Nathan P Goodrich, et al.
The Journal of Pediatrics|September 25, 2018
Impact of Steroid Therapy on Early Growth in Infants with Biliary Atresia: The Multicenter Steroids in Biliary Atresia Randomized TrialEstella M Alonso, Wen Ye, Kieran Hawthorne, et al.
JAMA|May 6, 2014
Use of corticosteroids after hepatoportoenterostomy for bile drainage in infants with biliary atresia: the START randomized clinical trialJorge A Bezerra, Cathie Spino, John C Magee, et al.
Journal of Pediatric Gastroenterology and Nutrition|May 21, 2021
Mutation Analysis and Disease Features at Presentation in a Multi-Center Cohort of Children With Monogenic CholestasisPaula M Hertel, Laura N Bull, Richard J Thompson, et al.
Hepatology (Baltimore, Md.)|December 28, 2016
Analysis of surgical interruption of the enterohepatic circulation as a treatment for pediatric cholestasisKasper S Wang, Greg Tiao, Lee M Bass, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 24, 2024
Homozygous missense variants in YKT6 result in loss of function and are associated with developmental delay, with or without severe infantile liver disease and risk for hepatocellular carcinomaMengqi Ma, Mythily Ganapathi, Yiming Zheng, et al.
Pageof 5

Showing results (31-40 of 41) with videos related to

Sort By:
Pageof 5
The Journal of Pediatrics|June 11, 2015
Quality of Life and Its Determinants in a Multicenter Cohort of Children with Alagille SyndromeBinita M Kamath, Zhen Chen, Rene Romero, et al.
Journal of Pediatric Gastroenterology and Nutrition|February 5, 2015
Baseline Analysis of a Young α-1-Antitrypsin Deficiency Liver Disease Cohort Reveals Frequent Portal HypertensionJeffrey H Teckman, Philip Rosenthal, Robert Abel, et al.
Journal of Pediatric Gastroenterology and Nutrition|November 25, 2014
Total serum bilirubin predicts fat-soluble vitamin deficiency better than serum bile acids in infants with biliary atresiaVeena L Venkat, Benjamin L Shneider, John C Magee, et al.
Journal of Pediatric Gastroenterology and Nutrition|July 26, 2021
Presentation and Outcomes of Infants With Idiopathic Cholestasis: A Multicenter Prospective StudyPaula M Hertel, Kieran Hawthorne, Sehee Kim, et al.
Hepatology (Baltimore, Md.)|August 1, 2018
Bone Density in Children With Chronic Liver Disease Correlates With Growth and CholestasisKathleen M Loomes, Cathie Spino, Nathan P Goodrich, et al.
The Journal of Pediatrics|September 25, 2018
Impact of Steroid Therapy on Early Growth in Infants with Biliary Atresia: The Multicenter Steroids in Biliary Atresia Randomized TrialEstella M Alonso, Wen Ye, Kieran Hawthorne, et al.
JAMA|May 6, 2014
Use of corticosteroids after hepatoportoenterostomy for bile drainage in infants with biliary atresia: the START randomized clinical trialJorge A Bezerra, Cathie Spino, John C Magee, et al.
Journal of Pediatric Gastroenterology and Nutrition|May 21, 2021
Mutation Analysis and Disease Features at Presentation in a Multi-Center Cohort of Children With Monogenic CholestasisPaula M Hertel, Laura N Bull, Richard J Thompson, et al.
Hepatology (Baltimore, Md.)|December 28, 2016
Analysis of surgical interruption of the enterohepatic circulation as a treatment for pediatric cholestasisKasper S Wang, Greg Tiao, Lee M Bass, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 24, 2024
Homozygous missense variants in YKT6 result in loss of function and are associated with developmental delay, with or without severe infantile liver disease and risk for hepatocellular carcinomaMengqi Ma, Mythily Ganapathi, Yiming Zheng, et al.
Pageof 5