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Peter F. Whitington

Researcher at Children's Memorial Hospital

Publications -  271
Citations -  17236

Peter F. Whitington is an academic researcher from Children's Memorial Hospital. The author has contributed to research in topics: Liver transplantation & Transplantation. The author has an hindex of 72, co-authored 271 publications receiving 16201 citations. Previous affiliations of Peter F. Whitington include University of California, San Francisco & University of Rochester.

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Liver transplantation in children from living related donors. Surgical techniques and results.

TL;DR: The left lateral segmentectomy presents minimal surgical trauma to the liver and should remain the primary approach for obtaining a liver graft from a living donor, and the acceptance of LRT for general clinical application in the authors' institution is led.
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Genetic predisposition to the metabolism of irinotecan (CPT-11). Role of uridine diphosphate glucuronosyltransferase isoform 1A1 in the glucuronidation of its active metabolite (SN-38) in human liver microsomes.

TL;DR: Findings indicate a genetic predisposition to the metabolism of irinotecan, suggesting that patients with low UGT1A1 activity, such as those with Gilbert's syndrome, may be at an increased risk for irinOTecan toxicity.
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Application of reduced-size liver transplants as split grafts, auxiliary orthotopic grafts, and living related segmental transplants.

TL;DR: Overall the various modalities of using graft reduction have resulted in postoperative results similar to those achieved with full-size grafts, while pretransplantation mortality has been limited to less than 2%.
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Guideline for the evaluation of cholestatic jaundice in infants: recommendations of the North American Society for Pediatric Gastroenterology, Hepatology and Nutrition.

TL;DR: This document represents the official recommendations of the North American Society for Pediatric Gastroenterology, Hepatology and Nutrition on the evaluation of cholestatic jaundice in infants and is not intended as a substitute for clinical judgment or for the care of all patients with this problem.
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A multicenter study of the outcome of biliary atresia in the United States, 1997 to 2000.

TL;DR: Efforts to improve bile flow after HPE may lead to improved outcome in children with biliary atresia, and total bilirubin in early follow-up after HPe was highly predictive of outcome.