المؤلفون: Turcotte, Jeremiah G., 1933-

وصف الملف: application/zip

العلاقة: History - Department of Surgery - Transplantation History, 1985-2007; https://hdl.handle.net/2027.42/154014Test

الإتاحة: https://hdl.handle.net/2027.42/154014Test

المؤلفون: Turcotte, Jeremiah G., 1933-

وصف الملف: application/zip

العلاقة: Presentations - Ethics, 2004; https://hdl.handle.net/2027.42/154018Test

الإتاحة: https://hdl.handle.net/2027.42/154018Test

المؤلفون: Turcotte, Jeremiah G., 1933-

وصف الملف: application/zip

العلاقة: Personal Files - Professional Activity - Curriculum Vitae, 2006; https://hdl.handle.net/2027.42/154013Test

الإتاحة: https://hdl.handle.net/2027.42/154013Test

المؤلفون: Turcotte, Jeremiah G., 1933-

وصف الملف: application/zip

العلاقة: Personal Files; https://hdl.handle.net/2027.42/154016Test

الإتاحة: https://hdl.handle.net/2027.42/154016Test

المؤلفون: Turcotte, Jeremiah G., 1933-

وصف الملف: application/zip

العلاقة: History - Professors of Surgery - Thompson, Norman W., 1979-2003; http://hdl.handle.net/2027.42/154015Test

الإتاحة: http://hdl.handle.net/2027.42/154015Test

المؤلفون: Turcotte, Jeremiah G., 1933-

وصف الملف: application/zip

العلاقة: Presentations - Ethics, 2004; http://hdl.handle.net/2027.42/154017Test

الإتاحة: http://hdl.handle.net/2027.42/154017Test

المؤلفون: Turcotte, Jeremiah G.

المصدر: Transactions of the ... Meeting of the American Surgical Association ; volume 121, page 341-342 ; ISSN 0066-0833

الإتاحة: https://doi.org/10.1097/01.sla.0000108684.91169.b0Test
http://journals.lww.com/00153307-200301210-00036Test

المؤلفون: Kayler, Liise K., Merion, Robert M., Lee, Samuel, Sung, Randall S., Punch, Jeffrey D., Rudich, Steven M., Turcotte, Jeremiah G., Campbell, Darrell A., Holmes, Ronald, Magee, John C.

المساهمون: University of Michigan Health System, Ann Arbor, Michigan, USA, Surgery, Pediatrics, Department of Surgery, Hallym University, Seoul, Korea, Department of Surgery, Recanati-Miller Transplantation Institute, Mount Sinai School of Medicine, New York, USA

مصطلحات موضوعية: Liver Transplantation, Metabolic Disorders, Pediatric Transplantation, Metabolic Disease, Pediatrics, Health Sciences

وصف الملف: 82741 bytes; 3109 bytes; application/pdf; text/plain

العلاقة: Kayler, Liise K.; Merion, Robert M.; Lee, Samuel; Sung, Randall S.; Punch, Jeffrey D.; Rudich, Steven M.; Turcotte, Jeremiah G.; A. Campbell, Darrell; Holmes, Ronald; Magee, John C. (2002). "Long-term survival after liver transplantation in children with metabolic disorders." Pediatric Transplantation 6(4): 295-300.; http://hdl.handle.net/2027.42/72583Test; http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=12234269&dopt=citationTest; Pediatric Transplantation; Esquivel C, Iwatsuki S, Gordon R. Indications for pediatric liver transplantation. J Pediatr 1987: 111: 1039 – 1045.; Busittil R, Seu P, Millis J. Liver transplantation in children. Ann Surg 1991: 213: 48 – 57.; Burdelski M, Rogiers X. Liver transplantation in metabolic disorders. Acta Gastroenterol 1999: 62: 300305.; Iwatsuki S, Shaw JBW, Starzl T. Liver transplantation for biliary atresia. World J Surg 1984: 8: 5156.; Polson R, Rolles K, Calne R, Williams R, Marsden D. Reversal of severe neurologic manifestation of Wilson's disease following orthotopic liver transplantation. Q J Med 1987: 244: 685 – 691.; Lewis J, Bontempo F, Spero J, Ragni M, Starzl T. Liver transplantation in a hemophiliac. NEJM 1985: 312: 1189 – 1190.; Weinberg A, Mize C, Wother H. The occurrence of hepatoma in the chronic form of hereditary tyrosinemia. J Pediatr 1976: 88: 434 – 438.; Mieles L, Esquivel C, Van Thiel D, Konew B. Liver transplantation for tyrosinemia. A review of 10 cases from University of Pittsburgh. Dig Dis Sci 1990: 35: 153 – 157.; Salt A, Baines N, Rolles K, et al. Liver transplantation in tyrosinemia type I. the dilemma of timing the operation. Acta Paediatr 1992: 81: 449 – 452.; Van Spronsen F, Berger R, Smit G, et al. Tyrosinaemia type I. orthotopic liver transplantation as the only definitive answer to a metabolic as well as an oncological problem. J Inherit Metab Dis 1989: 12 ( Suppl. 2 ): 339 – 342.; Silver MM, Beverley DW, Valberg LS, et al. Perinatal hemochromatosis. clinical, morphologic, and quantitative iron studies. Am J Path 1987: 128: 538 – 554.; Cochat P, Deloraine A, Olive F, et al. Primary hyperoxaluria type 1: the therapeutic dilemma. Adv Nephrol Necker Hosp 1995: 24: 227 – 242.; Mizusawa Y, Parnham A, Falk M, et al. Potential for bilateral nephrectomy to reduce oxalate release after combined liver and kidney transplantation for primary hyperoxaluria type I. Clin Trans 1997: 11: 361 – 363.; Cochat P, Gaulier J, Koch Nogueira P, et al. Combined liver-kidney transplantation in primary hyperoxaluria type 1. Eur J Pediatr 1999: 158 ( Suppl. 2 ): S75 – S80.; Burdelski M, Ullrich K. Liver transplantation in metabolic disorders: summary of the general discussion. Eur J Pediatr 1999: 158 ( Suppl. 2 ): S95 – S96.; Msall M, Batshaw M, Suss R. Neurologic outcome in children with inborn errors of urea synthesis. N Engl J Med 1984: 310: 1500 – 1505.; Fletcher J, Couper R, Moore D, Coxon R, Dorney S. Liver transplantation for citrullinemia improves intellectual function. J Inher Metab Dis 1999: 22: 581 – 586.; Egawa H, Tanaka K, Inomata Y, et al. Auxiliary partial orthotopic liver transplantation from a living related donor: a report of two cases. Transplant Proc 1996: 2: 1071 – 7072.; Uemoto S, Yabe S, Inomata Y, et al. Coexistence of a graft with the preserved native liver in auxiliary partial orthotopic liver transplantation from a living donor for ornithine transcarbamylase deficiency. Transplantation 1997: 63: 1026 – 1028.; Crigler J, Najjar V. Congenital familial nonhemolytic jaundice with kernicterus. Pediatrics 1952: 23: 903 – 913.; Arias I. Chronic unconjugated hyperbilirubinemia without signs of overt hemolysis in adolescents and adults. J Clin Invest 1962: 41: 2233 – 2245.; Karon M, Imach D, Schwarz A. Effective phototherapy in congenital nonobstructive, nonhemolytic jaundice. N Eng J Med 1970: 282: 377 – 381.; Mowat A. Liver disorders in children: the indications for liver replacement in parenchymal and metabolic diseases. Transplant Proc 1987: 19: 3236 – 3241.; Asonuma K, Gilbert J, Stein J. Quantitation of transplanted hepatic mass necessary to cure the Gunn rat model of hyperbilirubinemia. J Pediatr Surg 1992: 27: 298 – 301.; Kiuchi T, Edamoto Y, Kaibori M, et al. Auxiliary liver transplantation for urea-cycle enzyme deficiency: Lesons from three cases. Transplan Proc 1999: 31: 528 – 529.; Leonard J. The management and outcome of propionic and methylmalonic acidemia. J Inherit Metab Dis 1995: 18: 430 – 434.; Van't Hoff W, McKiernan P, Surtees R, Leonard J. Liver transplantation for methylmalonic acidaemia. Eur J Pediatr 1999: 158 ( Suppl. 2 ): S70 – S74.; Matsui S, Mahoney M, Rosenberg L. The natural history of the inherited methylmalonic acidemias. N Engl J Med 1983: 308: 857 – 856.; Saudubray J, Touati G, Delonlay P, et al. Liver transplantation in propionic acidaemia. Eur J Pediatr 1999: 158 ( Suppl. 2 ): S65 – S69.; 30. OPTN/SRTR. Annual Report. Richmond, Virginia, 2000.

الإتاحة: https://doi.org/10.1034/j.1399-3046.2002.02009.xTest
http://hdl.handle.net/2027.42/72583Test
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=12234269&dopt=citationTest

المؤلفون: Turcotte, Jeremiah G

المصدر: Journal of the American College of Surgeons ; volume 195, issue 4, page 568-569 ; ISSN 1072-7515

الإتاحة: https://doi.org/10.1016/s1072-7515Test(02)01329-7
https://api.elsevier.com/content/article/PII:S1072751502013297?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S1072751502013297?httpAccept=text/plainTest
https://journals.lww.com/00019464-200210000-00020Test

المؤلفون: Wolf, J. Stuart, Merion, Robert M., Leichtman, Alan B., Campbell, Darrell A., Magee, John C., Punch, Jeffery D., Turcotte, Jeremiah G., Konnak, John W.

المصدر: Transplantation ; volume 72, issue 2, page 284-290 ; ISSN 0041-1337

الإتاحة: https://doi.org/10.1097/00007890-200107270-00021Test
http://journals.lww.com/00007890-200107270-00021Test