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C Magee

Showing results (421-430 of 477) with videos related to

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Clinical Transplants|October 20, 2000
Renal transplantation at the University of Michigan 1964 to 1999J C Magee, R S Sung, J G Turcotte, et al.
Hepatology Communications|December 6, 2023
Neonatal cholestasis in children with Alpha-1-AT deficiency is a risk for earlier severe liver disease with male predominanceJeffrey Teckman, Philip Rosenthal, Rosalinda V Ignacio, et al.
The Journal of Pediatrics|July 15, 2020
Longitudinal Outcomes in Young Patients with Alpha-1-Antitrypsin Deficiency with Native Liver Reveal that Neonatal Cholestasis is a Poor Predictor of Future Portal HypertensionJeffrey Teckman, Philip Rosenthal, Kieran Hawthorne, et al.
Annals of Surgery|August 27, 2011
The anatomic pattern of biliary atresia identified at time of Kasai hepatoportoenterostomy and early postoperative clearance of jaundice are significant predictors of transplant-free survivalRiccardo Superina, John C Magee, Mary L Brandt, et al.
Hepatology (Baltimore, Md.)|December 18, 2024
Interleukin 8-CXCR2-mediated neutrophil extracellular trap formation in biliary atresia associated with neutrophil extracellular trap-induced stellate cell activationYuhuan Luo, Lisa Fraser, Julia Jezykowski, et al.
The Journal of Pediatrics|July 13, 2014
Medical status of 219 children with biliary atresia surviving long-term with their native livers: results from a North American multicenter consortiumVicky Lee Ng, Barbara H Haber, John C Magee, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|May 6, 2017
Hepatic Hilar Lymph Node Reactivity at Kasai Portoenterostomy for Biliary Atresia: Correlations With Age, Outcome, and Histology of Proximal Biliary RemnantK E Bove, R Sheridan, L Fei, et al.
The American Journal of Surgical Pathology|September 25, 2018
Inflammation, Active Fibroplasia, and End-stage Fibrosis in 172 Biliary Atresia Remnants Correlate Poorly With Age at Kasai Portoenterostomy, Visceral Heterotaxy, and OutcomeKevin E Bove, Andrew D Thrasher, Robert Anders, et al.
The American Journal of Surgical Pathology|October 25, 2016
Key Histopathologic Features of Liver Biopsies That Distinguish Biliary Atresia From Other Causes of Infantile Cholestasis and Their Correlation With Outcome: A Multicenter StudyPierre Russo, John C Magee, Robert A Anders, et al.
Pediatric Radiology|July 27, 2023
Prospective study of quantitative liver MRI in cystic fibrosis: feasibility and comparison to PUSH cohort ultrasoundAlexander J Towbin, Wen Ye, Suiyuan Huang, et al.
Pageof 48

Showing results (421-430 of 477) with videos related to

Sort By:
Pageof 48
Clinical Transplants|October 20, 2000
Renal transplantation at the University of Michigan 1964 to 1999J C Magee, R S Sung, J G Turcotte, et al.
Hepatology Communications|December 6, 2023
Neonatal cholestasis in children with Alpha-1-AT deficiency is a risk for earlier severe liver disease with male predominanceJeffrey Teckman, Philip Rosenthal, Rosalinda V Ignacio, et al.
The Journal of Pediatrics|July 15, 2020
Longitudinal Outcomes in Young Patients with Alpha-1-Antitrypsin Deficiency with Native Liver Reveal that Neonatal Cholestasis is a Poor Predictor of Future Portal HypertensionJeffrey Teckman, Philip Rosenthal, Kieran Hawthorne, et al.
Annals of Surgery|August 27, 2011
The anatomic pattern of biliary atresia identified at time of Kasai hepatoportoenterostomy and early postoperative clearance of jaundice are significant predictors of transplant-free survivalRiccardo Superina, John C Magee, Mary L Brandt, et al.
Hepatology (Baltimore, Md.)|December 18, 2024
Interleukin 8-CXCR2-mediated neutrophil extracellular trap formation in biliary atresia associated with neutrophil extracellular trap-induced stellate cell activationYuhuan Luo, Lisa Fraser, Julia Jezykowski, et al.
The Journal of Pediatrics|July 13, 2014
Medical status of 219 children with biliary atresia surviving long-term with their native livers: results from a North American multicenter consortiumVicky Lee Ng, Barbara H Haber, John C Magee, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|May 6, 2017
Hepatic Hilar Lymph Node Reactivity at Kasai Portoenterostomy for Biliary Atresia: Correlations With Age, Outcome, and Histology of Proximal Biliary RemnantK E Bove, R Sheridan, L Fei, et al.
The American Journal of Surgical Pathology|September 25, 2018
Inflammation, Active Fibroplasia, and End-stage Fibrosis in 172 Biliary Atresia Remnants Correlate Poorly With Age at Kasai Portoenterostomy, Visceral Heterotaxy, and OutcomeKevin E Bove, Andrew D Thrasher, Robert Anders, et al.
The American Journal of Surgical Pathology|October 25, 2016
Key Histopathologic Features of Liver Biopsies That Distinguish Biliary Atresia From Other Causes of Infantile Cholestasis and Their Correlation With Outcome: A Multicenter StudyPierre Russo, John C Magee, Robert A Anders, et al.
Pediatric Radiology|July 27, 2023
Prospective study of quantitative liver MRI in cystic fibrosis: feasibility and comparison to PUSH cohort ultrasoundAlexander J Towbin, Wen Ye, Suiyuan Huang, et al.
Pageof 48