scholarly article | Q13442814 |
P356 | DOI | 10.1016/0140-6736(93)91543-U |
P953 | full work available at URL | https://api.elsevier.com/content/article/PII:014067369391543U?httpAccept=text/plain |
https://api.elsevier.com/content/article/PII:014067369391543U?httpAccept=text/xml | ||
P698 | PubMed publication ID | 7690444 |
P50 | author | Jean Emond | Q6170628 |
J. Richard Thistlethwaite, Jr. | Q61482428 | ||
Peter F. Whitington | Q124426406 | ||
P2093 | author name string | J. C. Emond | |
J. R. Thistlethwaite | |||
T. Heffron | |||
P2860 | cites work | Hepatic Bilirubin UDP-Glucuronyl Transferase Activity in Liver Disease and Gilbert's Syndrome | Q37515991 |
Liver transplantation in pediatrics: indications, contraindications, and pretransplant management | Q37638823 | ||
Dissociation from albumin: a potentially rate-limiting step in the clearance of substances by the liver | Q37679910 | ||
Application of reduced-size liver transplants as split grafts, auxiliary orthotopic grafts, and living related segmental transplants | Q43571831 | ||
Auxiliary liver transplantation in jaundiced rats with UDP-glucuronyltransferase deficiency and defective hepatobiliary transport | Q69195195 | ||
The liver in Crigler-Najjar syndrome, protoporphyria, and other metabolic disorders | Q71259523 | ||
P433 | issue | 8874 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Crigler-Najjar syndrome | Q1140000 |
P1104 | number of pages | 2 | |
P304 | page(s) | 779-780 | |
P577 | publication date | 1993-09-01 | |
1993-09-25 | |||
P1433 | published in | The Lancet | Q939416 |
P1476 | title | Orthotopic auxiliary liver transplantation for Crigler-Najjar syndrome type 1 | |
P478 | volume | 342 |
Q77535029 | Application of living related auxiliary partial liver in an adult recipient with biliary atresia |
Q73278186 | Auxiliary liver transplantation for metabolic diseases |
Q74616369 | Auxiliary liver transplantation for urea-cycle enzyme deficiencies: lessons from three cases |
Q34137843 | Auxiliary partial orthotopic liver transplantation (APOLT) in the treatment of acute liver failure |
Q47295078 | Auxiliary partial orthotopic liver transplantation as a rescue for small-for-size grafts harvested from living donors |
Q40817580 | Auxiliary partial orthotopic liver transplantation for Crigler-Najjar syndrome type I. |
Q53359972 | Auxiliary partial orthotopic liver transplantation for acute liver failure. |
Q77304074 | Crigler-Najjar syndrome in Saudi Arabia |
Q78190983 | Directing portal flow is essential for graft survival in auxiliary partial heterotopic liver transplantation in the dog |
Q45279442 | Effective oral treatment of unconjugated hyperbilirubinemia in Gunn rats |
Q45882992 | Efficacy of auxiliary partial orthotopic liver transplantation for cure of hemophilia in a canine hemophilia A model |
Q34604798 | Establishment of a new pig model for auxiliary partial orthotopic liver transplantation |
Q46664890 | Functional analysis of grafts from living donors. Implications for the treatment of older recipients. |
Q41191189 | Genetic diseases of bilirubin metabolism: the inherited unconjugated hyperbilirubinemias |
Q40929641 | Indications for and timing of liver transplantation |
Q36501763 | Liver transplantation for non-hepatotoxic inborn errors of metabolism |
Q41926237 | Liver transplantation for the treatment of urea cycle disorders |
Q34636676 | Living-related liver transplantation for Crigler-Najjar syndrome in Saudi Arabia |
Q46362879 | Long-term follow-up of auxiliary liver transplantation for fulminant hepatic failure |
Q46395086 | Long-term follow-up of auxiliary orthotopic liver transplantation for the treatment of fulminant hepatic failure |
Q35960812 | Metabolic liver disease in the pediatric patient |
Q40643172 | Organ transplantation for inherited metabolic disease |
Q34515696 | Recent advances in pediatric liver transplantation |
Q50212229 | Regeneration and Cell Recruitment in an Improved Heterotopic Auxiliary Partial Liver Transplantation Model in the Rat. |
Q38507649 | Routine use of auxiliary partial orthotopic liver transplantation for children with fulminant hepatic failure: Preliminary report |
Q78256916 | Severe late acute allograft rejection in a child after living-related auxiliary partial orthotopic liver transplantation for ornithine transcarbamylase deficiency |
Q77632316 | Strategy used to overcome graft atrophy in auxiliary partial orthotopic liver transplantation from a living donor for ornithine transcarbamylase deficiency |
Q45115760 | The hereditary hyperbilirubinaemias |
Q48238424 | Treatment of Crigler-Najjar type 1 disease: relevance of early liver transplantation |
Q77736673 | Treatment of ornithine transcarbamylase deficiency in girls by auxiliary liver transplantation: conceptual changes in a living-donor program |
Q27486937 | Hepatology. |
Search more.