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Richard J Thompson

Showing results (31-40 of 82) with videos related to

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Journal of Paediatrics and Child Health|October 22, 2008
Trichobezoar in a child with undiagnosed coeliac diseaseIain J D McCallum, Cathy Van zanten, Imran Z Inam, et al.
Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association|September 12, 2022
ATP7B Genotype and Chronic Liver Disease Treatment Outcomes in Wilson Disease: Worse Survival With Loss-of-Function VariantsJeremy S Nayagam, Rebecca Jeyaraj, Pierre Foskett, et al.
Liver Transplantation : Official Publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society|March 24, 2026
Preemptive liver transplantation is essential for patients with severe BSEP deficiencyMohammad Shagrani, Sateesh Maddirevula, Kishwer Kumar, et al.
Gastroenterology|October 31, 2002
The human bile salt export pump: characterization of substrate specificity and identification of inhibitorsJane A Byrne, Sandra S Strautnieks, Giorgina Mieli-Vergani, et al.
Journal of Pediatric Gastroenterology and Nutrition|November 4, 2022
Hepatic Dry Copper Weight in Pediatric Autoimmune Liver DiseaseJeremy S Nayagam, Deepak Joshi, Richard J Thompson, et al.
The Journal of Pediatrics|February 24, 2006
VPS33B mutation with ichthyosis, cholestasis, and renal dysfunction but without arthrogryposis: incomplete ARC syndrome phenotypeLaura N Bull, Venus Mahmoodi, Alastair J Baker, et al.
Hepatology International|July 8, 2022
Complications of congenital portosystemic shunts: liver tumors are affected by shunt severity, but pulmonary and neurocognitive associations are notAthanasios Tyraskis, Mark Davenport, Annamaria Deganello, et al.
Journal of Pediatric Gastroenterology and Nutrition|May 21, 2020
Systematic Review and Meta-analysis: Partial External Biliary Diversion in Progressive Familial Intrahepatic CholestasisHenkjan J Verkade, Richard J Thompson, Henrik Arnell, et al.
Journal of Pediatric Gastroenterology and Nutrition|February 20, 2024
Clinical outcomes of ABCB4 heterozygosity in infants and children with cholestatic liver diseaseRobert Hegarty, Olivia Gurra, Jenneh Tarawally, et al.
Hepatology (Baltimore, Md.)|December 23, 2008
Missense mutations and single nucleotide polymorphisms in ABCB11 impair bile salt export pump processing and function or disrupt pre-messenger RNA splicingJane A Byrne, Sandra S Strautnieks, Gudrun Ihrke, et al.
Pageof 9

Showing results (31-40 of 82) with videos related to

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Pageof 9
Journal of Paediatrics and Child Health|October 22, 2008
Trichobezoar in a child with undiagnosed coeliac diseaseIain J D McCallum, Cathy Van zanten, Imran Z Inam, et al.
Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association|September 12, 2022
ATP7B Genotype and Chronic Liver Disease Treatment Outcomes in Wilson Disease: Worse Survival With Loss-of-Function VariantsJeremy S Nayagam, Rebecca Jeyaraj, Pierre Foskett, et al.
Liver Transplantation : Official Publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society|March 24, 2026
Preemptive liver transplantation is essential for patients with severe BSEP deficiencyMohammad Shagrani, Sateesh Maddirevula, Kishwer Kumar, et al.
Gastroenterology|October 31, 2002
The human bile salt export pump: characterization of substrate specificity and identification of inhibitorsJane A Byrne, Sandra S Strautnieks, Giorgina Mieli-Vergani, et al.
Journal of Pediatric Gastroenterology and Nutrition|November 4, 2022
Hepatic Dry Copper Weight in Pediatric Autoimmune Liver DiseaseJeremy S Nayagam, Deepak Joshi, Richard J Thompson, et al.
The Journal of Pediatrics|February 24, 2006
VPS33B mutation with ichthyosis, cholestasis, and renal dysfunction but without arthrogryposis: incomplete ARC syndrome phenotypeLaura N Bull, Venus Mahmoodi, Alastair J Baker, et al.
Hepatology International|July 8, 2022
Complications of congenital portosystemic shunts: liver tumors are affected by shunt severity, but pulmonary and neurocognitive associations are notAthanasios Tyraskis, Mark Davenport, Annamaria Deganello, et al.
Journal of Pediatric Gastroenterology and Nutrition|May 21, 2020
Systematic Review and Meta-analysis: Partial External Biliary Diversion in Progressive Familial Intrahepatic CholestasisHenkjan J Verkade, Richard J Thompson, Henrik Arnell, et al.
Journal of Pediatric Gastroenterology and Nutrition|February 20, 2024
Clinical outcomes of ABCB4 heterozygosity in infants and children with cholestatic liver diseaseRobert Hegarty, Olivia Gurra, Jenneh Tarawally, et al.
Hepatology (Baltimore, Md.)|December 23, 2008
Missense mutations and single nucleotide polymorphisms in ABCB11 impair bile salt export pump processing and function or disrupt pre-messenger RNA splicingJane A Byrne, Sandra S Strautnieks, Gudrun Ihrke, et al.
Pageof 9