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Richard J Thompson

Showing results (21-30 of 82) with videos related to

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Journal of Pediatric Gastroenterology and Nutrition|June 9, 2004
Cholestatic and metabolic liver diseases: Working Group report of the second World Congress of Pediatric Gastroenterology, Hepatology, and NutritionRichard J Thompson, Ramiro Anthero Azevedo, Cristina Galoppo, et al.
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research|October 3, 2003
The use of glyceryl trinitrate (GTN) in the treatment of chronic anal fissure in childrenJohn Simpson, Jonathan N Lund, Richard J Thompson, et al.
Plos One|December 20, 2012
ATP8B1 gene expression is driven by a housekeeping-like promoter independent of bile acids and farnesoid X receptorDita Cebecauerová, Sandra S Strautnieks, Jane A Byrne, et al.
Journal of Pediatric Surgery|September 10, 2008
Congenital bile duct anomalies (biliary atresia) and chromosome 22 aneuploidyJacqueline Allotey, Florence Lacaille, Melissa M Lees, et al.
Journal of Interventional Cardiology|September 20, 2002
Application of a cardiac arrest score in patients with sudden death and ST segment elevation for triage to angiography and interventionPeter A McCullough, Rajat Prakash, Kenneth J Tobin, et al.
The Journal of Clinical Endocrinology and Metabolism|July 11, 2002
Novel mutations responsible for autosomal recessive multisystem pseudohypoaldosteronism and sequence variants in epithelial sodium channel alpha-, beta-, and gamma-subunit genesAnjana Saxena, Israel Hanukoglu, Deepak Saxena, et al.
Human Pathology|April 4, 2016
Multiple β-catenin mutations in hepatocellular lesions arising in Abernethy malformationTracy Sorkin, Sandra Strautnieks, Pierre Foskett, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|September 19, 2007
Lack of hepatocellular CD10 along bile canaliculi is physiologic in early childhood and persistent in Alagille syndromeJane A Byrne, Natalie J Meara, Anne C Rayner, et al.
Hepatology Communications|July 27, 2022
Clinical phenotype of adult-onset liver disease in patients with variants in ABCB4, ABCB11, and ATP8B1Jeremy S Nayagam, Pierre Foskett, Sandra Strautnieks, et al.
The Journal of Pediatrics|June 25, 2018
Reduced Hepatocellular Expression of Canalicular Transport Proteins in Infants with Neonatal Cholestasis and Congenital HypopituitarismTassos Grammatikopoulos, Maesha Deheragoda, Sandra Strautnieks, et al.
Pageof 9

Showing results (21-30 of 82) with videos related to

Sort By:
Pageof 9
Journal of Pediatric Gastroenterology and Nutrition|June 9, 2004
Cholestatic and metabolic liver diseases: Working Group report of the second World Congress of Pediatric Gastroenterology, Hepatology, and NutritionRichard J Thompson, Ramiro Anthero Azevedo, Cristina Galoppo, et al.
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research|October 3, 2003
The use of glyceryl trinitrate (GTN) in the treatment of chronic anal fissure in childrenJohn Simpson, Jonathan N Lund, Richard J Thompson, et al.
Plos One|December 20, 2012
ATP8B1 gene expression is driven by a housekeeping-like promoter independent of bile acids and farnesoid X receptorDita Cebecauerová, Sandra S Strautnieks, Jane A Byrne, et al.
Journal of Pediatric Surgery|September 10, 2008
Congenital bile duct anomalies (biliary atresia) and chromosome 22 aneuploidyJacqueline Allotey, Florence Lacaille, Melissa M Lees, et al.
Journal of Interventional Cardiology|September 20, 2002
Application of a cardiac arrest score in patients with sudden death and ST segment elevation for triage to angiography and interventionPeter A McCullough, Rajat Prakash, Kenneth J Tobin, et al.
The Journal of Clinical Endocrinology and Metabolism|July 11, 2002
Novel mutations responsible for autosomal recessive multisystem pseudohypoaldosteronism and sequence variants in epithelial sodium channel alpha-, beta-, and gamma-subunit genesAnjana Saxena, Israel Hanukoglu, Deepak Saxena, et al.
Human Pathology|April 4, 2016
Multiple β-catenin mutations in hepatocellular lesions arising in Abernethy malformationTracy Sorkin, Sandra Strautnieks, Pierre Foskett, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|September 19, 2007
Lack of hepatocellular CD10 along bile canaliculi is physiologic in early childhood and persistent in Alagille syndromeJane A Byrne, Natalie J Meara, Anne C Rayner, et al.
Hepatology Communications|July 27, 2022
Clinical phenotype of adult-onset liver disease in patients with variants in ABCB4, ABCB11, and ATP8B1Jeremy S Nayagam, Pierre Foskett, Sandra Strautnieks, et al.
The Journal of Pediatrics|June 25, 2018
Reduced Hepatocellular Expression of Canalicular Transport Proteins in Infants with Neonatal Cholestasis and Congenital HypopituitarismTassos Grammatikopoulos, Maesha Deheragoda, Sandra Strautnieks, et al.
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