{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,1]],"date-time":"2026-04-01T00:01:59Z","timestamp":1775001719331,"version":"3.50.1"},"reference-count":84,"publisher":"Elsevier BV","issue":"4","license":[{"start":{"date-parts":[[2015,4,1]],"date-time":"2015-04-01T00:00:00Z","timestamp":1427846400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2014,11,10]],"date-time":"2014-11-10T00:00:00Z","timestamp":1415577600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"content-domain":{"domain":["dldjournalonline.com","clinicalkey.jp","clinicalkey.com","clinicalkey.es","clinicalkey.com.au","clinicalkey.fr","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Digestive and Liver Disease"],"published-print":{"date-parts":[[2015,4]]},"DOI":"10.1016\/j.dld.2014.11.004","type":"journal-article","created":{"date-parts":[[2014,11,16]],"date-time":"2014-11-16T18:22:47Z","timestamp":1416162167000},"page":"261-270","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":26,"title":["Liver transplantation using grafts with rare metabolic disorders"],"prefix":"10.1016","volume":"47","author":[{"given":"Astrid","family":"Schielke","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Filomena","family":"Conti","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Claire","family":"Goumard","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Fabiano","family":"Perdigao","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yvon","family":"Calmus","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Olivier","family":"Scatton","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.dld.2014.11.004_bib0005","doi-asserted-by":"crossref","first-page":"595","DOI":"10.1016\/j.jhep.2013.04.004","article-title":"Monogenic diseases that can be cured by liver transplantation","volume":"59","author":"Fagiuoli","year":"2013","journal-title":"Journal of Hepatology"},{"key":"10.1016\/j.dld.2014.11.004_bib0010","doi-asserted-by":"crossref","first-page":"1589","DOI":"10.1111\/j.1478-3231.2011.02606.x","article-title":"Hepatic iron overload following liver transplantation of a C282Y homozygous allograft: a case report and literature review","volume":"31","author":"Dwyer","year":"2011","journal-title":"Liver International"},{"key":"10.1016\/j.dld.2014.11.004_bib0015","doi-asserted-by":"crossref","first-page":"1655","DOI":"10.1002\/hep.20242","article-title":"Patient and graft survival after liver transplantation for hereditary hemochromatosis: implications for pathogenesis","volume":"39","author":"Crawford","year":"2004","journal-title":"Hepatology"},{"key":"10.1016\/j.dld.2014.11.004_bib0020","doi-asserted-by":"crossref","first-page":"433","DOI":"10.1136\/gut.52.3.433","article-title":"Heterozygous recipient and donor HFE mutations associated with a hereditary haemochromatosis phenotype after liver transplantation","volume":"52","author":"Wigg","year":"2003","journal-title":"Gut"},{"key":"10.1016\/j.dld.2014.11.004_bib0025","doi-asserted-by":"crossref","first-page":"351","DOI":"10.1016\/S0168-8278(05)80668-3","article-title":"Persistant iron overload 4 years after inadvertent transplantation of a heamochromatotic liver in a patient with primary biliary cirrhosis","volume":"16","author":"Koskinas","year":"1992","journal-title":"Journal of Hepatology"},{"key":"10.1016\/j.dld.2014.11.004_bib0030","doi-asserted-by":"crossref","first-page":"310","DOI":"10.1002\/lt.20641","article-title":"Clinicopathologic findings and outcome of liver transplantation using grafts from donors with unrecognized and unusual diseases","volume":"12","author":"Pungpapong","year":"2006","journal-title":"Liver Transplantation"},{"key":"10.1016\/j.dld.2014.11.004_bib0035","doi-asserted-by":"crossref","first-page":"138","DOI":"10.1097\/MAJ.0b013e3181719b4b","article-title":"Transplantation of a liver with the C282Y Mutation into a Recipient heterozygous for H63D results in iron overload","volume":"337","author":"Ismail","year":"2009","journal-title":"American Journal of the Medical Sciences"},{"key":"10.1016\/j.dld.2014.11.004_bib0040","doi-asserted-by":"crossref","first-page":"1882","DOI":"10.1097\/00007890-200005150-00024","article-title":"Donor liver uridine diphosphate (UDP)-glucuronosyltransferase-1A1 deficiency causing Gilbert's syndrome in liver transplant recipients","volume":"69","author":"Te","year":"2000","journal-title":"Transplantation"},{"key":"10.1016\/j.dld.2014.11.004_bib0045","doi-asserted-by":"crossref","first-page":"1743","DOI":"10.1111\/j.1600-6143.2006.01363.x","article-title":"Factor XII deficiency acquired by orthotopic liver transplantation: case report and review of the literature","volume":"6","author":"Osborn","year":"2006","journal-title":"American Journal of Transplantation"},{"key":"10.1016\/j.dld.2014.11.004_bib0050","doi-asserted-by":"crossref","first-page":"278","DOI":"10.1111\/j.1432-2277.1999.tb01214.x","article-title":"Transmission of factor VII deficiency through liver transplantation","volume":"12","author":"Guy","year":"1999","journal-title":"Transplant International"},{"key":"10.1016\/j.dld.2014.11.004_bib0055","doi-asserted-by":"crossref","first-page":"877","DOI":"10.7326\/0003-4819-115-11-877","article-title":"Factor XI deficiency acquired by liver transplantation","volume":"115","author":"Clarkson","year":"1991","journal-title":"Annals of Internal Medicine"},{"key":"10.1016\/j.dld.2014.11.004_bib0060","doi-asserted-by":"crossref","first-page":"1335","DOI":"10.1097\/MEG.0b013e32836171c4","article-title":"Heterozygous \u03b11-antitrypsin Z allele mutation in presumed healthy donor livers used for transplantation","volume":"25","author":"Roelandt","year":"2013","journal-title":"European Journal of Gastroenterology and Hepatology"},{"key":"10.1016\/j.dld.2014.11.004_bib0065","doi-asserted-by":"crossref","first-page":"715","DOI":"10.1016\/j.jaad.2008.10.012","article-title":"Alfa-1-antitrypsin deficiency panniculitis acquired after liver transplant and successfully treated with retransplant","volume":"60","author":"Fern\u00e1ndez-Torres","year":"2009","journal-title":"Journal of the American Academy of Dermatology"},{"key":"10.1016\/j.dld.2014.11.004_bib0070","doi-asserted-by":"crossref","first-page":"1918","DOI":"10.1097\/01.TP.0000131602.35978.98","article-title":"Acquired PiZZ alpha-1 antitrysine deficiency in a liver transplant recipient","volume":"77","author":"Arnal","year":"2004","journal-title":"Transplantation"},{"key":"10.1016\/j.dld.2014.11.004_bib0075","doi-asserted-by":"crossref","first-page":"873","DOI":"10.1016\/j.jaad.2010.03.030","article-title":"Acquired pseudoxanthoma elasticum presenting after liver transplantation","volume":"64","author":"Bercovitch","year":"2011","journal-title":"Journal of the American Academy of Dermatology"},{"key":"10.1016\/j.dld.2014.11.004_bib0080","doi-asserted-by":"crossref","first-page":"1084","DOI":"10.1111\/ajt.12146","article-title":"A novel mutation of the ornithine transcarbamylase gene leading to fatal hyperammonemia in a liver transplant recipient","volume":"13","author":"Mukhtar","year":"2013","journal-title":"American Journal of Transplantation"},{"key":"10.1016\/j.dld.2014.11.004_bib0085","doi-asserted-by":"crossref","first-page":"921","DOI":"10.1056\/NEJM199909163411214","article-title":"Death after transplantation of a liver from a donor with unrecognized ornithine transcarbamylase deficiency","volume":"341","author":"Pl\u00f6chl","year":"1999","journal-title":"New England Journal of Medicine"},{"key":"10.1016\/j.dld.2014.11.004_bib0090","doi-asserted-by":"crossref","first-page":"1714","DOI":"10.1002\/lt.21291","article-title":"Presentation of an acquired urea cycle disorder post liver transplantation","volume":"13","author":"Ghabril","year":"2007","journal-title":"Liver Transplantation"},{"key":"10.1016\/j.dld.2014.11.004_bib0095","doi-asserted-by":"crossref","first-page":"353","DOI":"10.1002\/lt.20363","article-title":"MARS treatment for a patient presenting with acquired hepatic glutamine synthetase deficiency after orthotopic liver transplantation","volume":"11","author":"Chiu","year":"2005","journal-title":"Liver Transplantation"},{"key":"10.1016\/j.dld.2014.11.004_bib0100","doi-asserted-by":"crossref","first-page":"132","DOI":"10.1111\/j.1399-0012.2005.00432.x","article-title":"Factor V Leiden and hepatic artery thrombosis after liver transplantation","volume":"20","author":"Dunn","year":"2006","journal-title":"Clinical Transplantation"},{"key":"10.1016\/j.dld.2014.11.004_bib0105","doi-asserted-by":"crossref","first-page":"870","DOI":"10.1053\/jlts.2003.50136","article-title":"Recurrent deep-vein thrombosis based on homozygous factor V Leiden mutation acquired after liver transplantation","volume":"9","author":"Willems","year":"2003","journal-title":"Liver Transplantation"},{"key":"10.1016\/j.dld.2014.11.004_bib0110","doi-asserted-by":"crossref","first-page":"215","DOI":"10.1097\/01.mbc.0000164432.05793.7d","article-title":"Activated protein C resistance acquired through liver transplantation","volume":"16","author":"Pushkaran","year":"2005","journal-title":"Blood Coagulation and Fibrinolysis"},{"key":"10.1016\/j.dld.2014.11.004_bib0115","doi-asserted-by":"crossref","first-page":"307","DOI":"10.1111\/j.1432-2277.1995.tb01526.x","article-title":"Heterozygous protein C deficiency and dysfibrinogenemia acquired by liver transplantation","volume":"8","author":"Cransac","year":"1995","journal-title":"Transplant International"},{"key":"10.1016\/j.dld.2014.11.004_bib0120","doi-asserted-by":"crossref","first-page":"1366","DOI":"10.1097\/00007890-199905270-00013","article-title":"Acquired protein S deficiency with multiple thrombotic complications after orthotopic liver transplant","volume":"67","author":"Schuetze","year":"1999","journal-title":"Transplantation"},{"key":"10.1016\/j.dld.2014.11.004_bib0125","doi-asserted-by":"crossref","first-page":"523","DOI":"10.1053\/jlts.2003.50095","article-title":"Acquired hemophilia A after liver transplantation: a case report","volume":"9","author":"Hisatake","year":"2003","journal-title":"Liver Transplantation"},{"key":"10.1016\/j.dld.2014.11.004_bib0130","doi-asserted-by":"crossref","first-page":"5364","DOI":"10.1182\/blood-2009-02-206979","article-title":"Extrahepatic factor VIII production in transplant recipient of hemophilia donor liver","volume":"113","author":"Madeira","year":"2009","journal-title":"Blood"},{"key":"10.1016\/j.dld.2014.11.004_bib0135","doi-asserted-by":"crossref","first-page":"2734","DOI":"10.1111\/ajt.12378","article-title":"Reversibility of acquired amyloid polyneuropathy after liver retransplantation","volume":"13","author":"Antonini","year":"2013","journal-title":"American Journal of Transplantation"},{"key":"10.1016\/j.dld.2014.11.004_bib0140","doi-asserted-by":"crossref","first-page":"81","DOI":"10.3109\/13506129.2012.668503","article-title":"Solid organ transplantation for non-TTR hereditary amyloidosis: report from the 1st International Workshop on the Hereditary Renal Amyloidoses","volume":"19","author":"Stangou","year":"2012","journal-title":"Amyloid"},{"key":"10.1016\/j.dld.2014.11.004_bib0145","doi-asserted-by":"crossref","first-page":"2998","DOI":"10.1182\/blood-2009-06-223792","article-title":"Hereditary fibrinogen A alpha-chain amyloidosis: phenotypic characterization of a systemic disease and the role of liver transplantation","volume":"115","author":"Stangou","year":"2010","journal-title":"Blood"},{"key":"10.1016\/j.dld.2014.11.004_bib0150","doi-asserted-by":"crossref","first-page":"2410","DOI":"10.1056\/NEJM200512013532220","article-title":"Domino hepatic transplantation in maple syrup urine disease","volume":"353","author":"Barshop","year":"2005","journal-title":"New England Journal of Medicine"},{"key":"10.1016\/j.dld.2014.11.004_bib0155","doi-asserted-by":"crossref","first-page":"116","DOI":"10.1016\/j.jpeds.2011.06.033","article-title":"Liver transplantation for classical maple syrup urine disease: long-term follow-up in 37 patients and comparative United Network for Organ Sharing experience","volume":"160","author":"Mazariegos","year":"2012","journal-title":"Journal of Pediatrics"},{"key":"10.1016\/j.dld.2014.11.004_bib0160","doi-asserted-by":"crossref","first-page":"806","DOI":"10.1016\/j.transproceed.2012.04.031","article-title":"Domino liver transplantation in maple syrup urine disease: a case report and review of the literature","volume":"45","author":"Badell","year":"2013","journal-title":"Transplantation Proceedings"},{"key":"10.1016\/j.dld.2014.11.004_bib0165","doi-asserted-by":"crossref","first-page":"2874","DOI":"10.1016\/j.transproceed.2008.08.096","article-title":"Organ donors with exceptional medical conditions also count!","volume":"40","author":"Frutos","year":"2008","journal-title":"Transplantation Proceedings"},{"key":"10.1016\/j.dld.2014.11.004_bib0170","doi-asserted-by":"crossref","first-page":"1345","DOI":"10.1097\/01.TP.0000093996.96158.44","article-title":"Homozygous familial hypercholesterolemia: specific indication for domino liver transplantation","volume":"76","author":"Popescu","year":"2003","journal-title":"Transplantation"},{"key":"10.1016\/j.dld.2014.11.004_bib0175","doi-asserted-by":"crossref","first-page":"565","DOI":"10.1111\/j.1399-0012.2008.00935.x","article-title":"Domino liver transplantation using a graft from a donor with familial hypercholesterolemia: seven-yr follow-up","volume":"23","author":"Popescu","year":"2009","journal-title":"Clinical Transplantation"},{"key":"10.1016\/j.dld.2014.11.004_bib0180","doi-asserted-by":"crossref","first-page":"E30","DOI":"10.1111\/j.1399-3046.2009.01133.x","article-title":"Domino liver graft from a patient with homozygous familial hypercholesterolemia","volume":"14","author":"Liu","year":"2010","journal-title":"Pediatric Transplantation"},{"key":"10.1016\/j.dld.2014.11.004_bib0185","doi-asserted-by":"crossref","first-page":"1346","DOI":"10.1097\/00007890-200105150-00030","article-title":"Domino hepatic transplantation using the liver from a patient with primary hyperoxaluria","volume":"71","author":"Donckier","year":"2001","journal-title":"Transplantation"},{"key":"10.1016\/j.dld.2014.11.004_bib0190","doi-asserted-by":"crossref","first-page":"782","DOI":"10.1097\/TP.0b013e3181eefe1f","article-title":"Early renal failure after domino liver transplantation using organs from donors with primary hyperoxaluria type 1","volume":"90","author":"Saner","year":"2010","journal-title":"Transplantation"},{"key":"10.1016\/j.dld.2014.11.004_bib0195","doi-asserted-by":"crossref","first-page":"1449","DOI":"10.7863\/jum.2005.24.10.1449","article-title":"Rapidly developing nephrocalcinosis in a patient with end-stage liver disease who received a domino liver transplant from a patient with known congenital oxalosis","volume":"24","author":"Aziz","year":"2005","journal-title":"Journal of Ultrasound in Medicine"},{"key":"10.1016\/j.dld.2014.11.004_bib0200","doi-asserted-by":"crossref","first-page":"2557","DOI":"10.1093\/ndt\/gfi019","article-title":"Early renal failure after domino hepatic transplantation using the liver from a compound heterozygous patient with primary hyperoxaluria","volume":"20","author":"Farese","year":"2005","journal-title":"Nephrology, Dialysis, Transplantation"},{"key":"10.1016\/j.dld.2014.11.004_bib0205","doi-asserted-by":"crossref","first-page":"2324","DOI":"10.1111\/j.1600-6143.2005.01014.x","article-title":"Severe course of primary hyperoxaluria and renal failure after domino hepatic transplantation","volume":"5","author":"Franchello","year":"2005","journal-title":"American Journal of Transplantation"},{"key":"10.1016\/j.dld.2014.11.004_bib0210","doi-asserted-by":"crossref","first-page":"249","DOI":"10.1034\/j.1399-3046.2002.01083.x","article-title":"Domino as a bridge to definitive liver transplantation in a neonate","volume":"6","author":"Casas-Melley","year":"2002","journal-title":"Pediatric Transplantation"},{"key":"10.1016\/j.dld.2014.11.004_bib0215","doi-asserted-by":"crossref","first-page":"418","DOI":"10.1016\/j.jpeds.2004.10.036","article-title":"Liver transplantation as definitive treatment for a factor V Leiden mutation","volume":"146","author":"Dunn","year":"2005","journal-title":"Journal of Pediatrics"},{"key":"10.1016\/j.dld.2014.11.004_bib0220","doi-asserted-by":"crossref","first-page":"571","DOI":"10.7326\/0003-4819-154-8-201104190-00015","article-title":"Liver transplantation from donors with acute intermittent porphyria","volume":"154","author":"Dowman","year":"2011","journal-title":"Annals of Internal Medicine"},{"key":"10.1016\/j.dld.2014.11.004_bib0225","doi-asserted-by":"crossref","first-page":"1584","DOI":"10.1002\/pbc.25094","article-title":"HCC prevalence and histopathological findings in liver explants of patients with hereditary tyrosinemia Type 1","volume":"61","author":"Neto","year":"2014","journal-title":"Pediatr Blood Cancer"},{"key":"10.1016\/j.dld.2014.11.004_bib0230","doi-asserted-by":"crossref","first-page":"2342","DOI":"10.1111\/j.1600-6143.2006.01507.x","article-title":"Organ transplantation in hereditary apolipoprotein AI amyloidosis","volume":"6","author":"Gillmore","year":"2006","journal-title":"American Journal of Transplantation"},{"key":"10.1016\/j.dld.2014.11.004_bib0235","doi-asserted-by":"crossref","first-page":"577","DOI":"10.1038\/modpathol.3880353","article-title":"Livers from patients with apolipoprotein A-I amyloidosis are not suitable as domino donors","volume":"14","author":"Shaz","year":"2001","journal-title":"Modern Pathology"},{"key":"10.1016\/j.dld.2014.11.004_bib0240","doi-asserted-by":"crossref","first-page":"36","DOI":"10.1111\/j.1365-2796.2011.02470.x","article-title":"Hereditary lysozyme amyloidosis \u2014 phenotypic heterogeneity and the role of solid organ transplantation","volume":"272","author":"Sattianayagam","year":"2012","journal-title":"Journal of Internal Medicine"},{"key":"10.1016\/j.dld.2014.11.004_bib0245","series-title":"Recommandations Formalis\u00e9es d\u2019Experts sur le pr\u00e9l\u00e8vement et la greffe \u00e0 partir de Donneur Vivant. Medi-Text Editions","first-page":"265","article-title":"Transplantation h\u00e9patique par Donner Vivant: crit\u00e8res de selection et bilan \u00e0 effectuer","author":"Castaing","year":"2009"},{"key":"10.1016\/j.dld.2014.11.004_bib0250","doi-asserted-by":"crossref","first-page":"166","DOI":"10.1093\/ndt\/16.1.166","article-title":"Three cases of sequential liver-kidney transplantation from living-related donors","volume":"16","author":"Nakamura","year":"2001","journal-title":"Nephrology, Dialysis, Transplantation"},{"key":"10.1016\/j.dld.2014.11.004_bib0255","doi-asserted-by":"crossref","first-page":"433","DOI":"10.1053\/jlts.2003.50072","article-title":"Primary hyperoxaluria: simultaneous combined liver and kidney transplantation from a living related donor","volume":"9","author":"Astarcioglu","year":"2003","journal-title":"Liver Transplantation"},{"key":"10.1016\/j.dld.2014.11.004_bib0260","doi-asserted-by":"crossref","first-page":"373","DOI":"10.1016\/S0041-1345(02)03911-8","article-title":"Sequential liver-kidney transplantation from a living-related donor in primary hyperoxaluria type 1","volume":"35","author":"Sato","year":"2003","journal-title":"Transplantation Proceedings"},{"key":"10.1016\/j.dld.2014.11.004_bib0265","doi-asserted-by":"crossref","first-page":"e7","DOI":"10.1016\/j.urology.2006.02.035","article-title":"Treatment of primary hyperoxaluria type 1 with sequential liver and kidney transplants from the same living donor","volume":"68","author":"Rosenblatt","year":"2006","journal-title":"Urology"},{"key":"10.1016\/j.dld.2014.11.004_bib0270","doi-asserted-by":"crossref","first-page":"735","DOI":"10.1007\/s00147-004-0791-7","article-title":"Successful living-related liver transplantation for familial hypercholesterolemia in the Middle East","volume":"17","author":"Khalifeh","year":"2005","journal-title":"Transplant International"},{"key":"10.1016\/j.dld.2014.11.004_bib0275","doi-asserted-by":"crossref","first-page":"276","DOI":"10.1111\/j.1432-2277.2003.tb00299.x","article-title":"Living-donor liver transplantation for homozygous familial hypercholesterolemia from a donor with heterozygous hypercholesterolemia","volume":"16","author":"Shirahata","year":"2003","journal-title":"Transplant International"},{"key":"10.1016\/j.dld.2014.11.004_bib0280","doi-asserted-by":"crossref","first-page":"94","DOI":"10.5551\/jat.14.94","article-title":"Long-term outcome after living donor liver transplantation for two cases of homozygous familial hypercholesterolemia from a heterozygous donor","volume":"14","author":"Kawagishi","year":"2007","journal-title":"J Atheroscler Throm"},{"key":"10.1016\/j.dld.2014.11.004_bib0285","doi-asserted-by":"crossref","first-page":"1036","DOI":"10.1111\/j.1399-3046.2010.01402.x","article-title":"Living-donor liver transplantation for carbamoyl phosphate synthetase 1 deficiency","volume":"14","author":"Kasahara","year":"2010","journal-title":"Pediatric Transplantation"},{"key":"10.1016\/j.dld.2014.11.004_bib0290","doi-asserted-by":"crossref","first-page":"6","DOI":"10.1111\/petr.12196","article-title":"Living donor liver transplantation for pediatric patients with metabolic disorders: the Japanese multicenter registry","volume":"18","author":"Kasahara","year":"2014","journal-title":"Pediatric Transplantation"},{"key":"10.1016\/j.dld.2014.11.004_bib0295","doi-asserted-by":"crossref","first-page":"623","DOI":"10.1097\/01.tp.0000167995.46778.72","article-title":"Living donor liver transplantation for noncirrhotic inheritable metabolic liver diseases: impact of the use of heterozygous donors","volume":"80","author":"Morioka","year":"2005","journal-title":"Transplantation"},{"key":"10.1016\/j.dld.2014.11.004_bib0300","doi-asserted-by":"crossref","first-page":"E196","DOI":"10.1111\/j.1399-3046.2012.01716.x","article-title":"Living donor liver transplantation from an asymptomatic mother who was a carrier for ornithine transcarbamylase deficiency","volume":"16","author":"Wakiya","year":"2012","journal-title":"Pediatric Transplantation"},{"key":"10.1016\/j.dld.2014.11.004_bib0305","doi-asserted-by":"crossref","first-page":"550","DOI":"10.1002\/lt.20131","article-title":"Feasibility of auxiliary partial orthotopic liver transplantation from living donors for patients with adult-onset type II citrullinemia","volume":"10","author":"Yazaki","year":"2004","journal-title":"Liver Transplantation"},{"key":"10.1016\/j.dld.2014.11.004_bib0310","doi-asserted-by":"crossref","first-page":"157","DOI":"10.1097\/00007890-200101150-00027","article-title":"Living-related liver transplantation for type II citrullinemia using a graft from heterozygote donor","volume":"71","author":"Kasahara","year":"2001","journal-title":"Transplantation"},{"key":"10.1016\/j.dld.2014.11.004_bib0315","first-page":"2211","article-title":"Living donor liver transplantation for type II citrullinemia from a heterozygous donor","volume":"55","author":"Hirai","year":"2008","journal-title":"Hepato-Gastroenterology"},{"key":"10.1016\/j.dld.2014.11.004_bib0320","doi-asserted-by":"crossref","first-page":"127","DOI":"10.1016\/j.jns.2009.02.003","article-title":"A case of adult onset type II citrullinemia with portal-systemic shunt","volume":"281","author":"Noto","year":"2009","journal-title":"Journal of the Neurological Sciences"},{"key":"10.1016\/j.dld.2014.11.004_bib0325","doi-asserted-by":"crossref","first-page":"522","DOI":"10.1590\/1414-431X20143830","article-title":"Successful domino liver transplantation in maple syrup urine disease using a related living donor","volume":"47","author":"Feier","year":"2014","journal-title":"Brazilian Journal of Medical and Biological Research"},{"key":"10.1016\/j.dld.2014.11.004_bib0330","doi-asserted-by":"crossref","first-page":"230","DOI":"10.1111\/j.1399-3046.2011.01607.x","article-title":"Living-donor liver transplantation for propionic acidemia","volume":"16","author":"Kasahara","year":"2012","journal-title":"Pediatric Transplantation"},{"key":"10.1016\/j.dld.2014.11.004_bib0335","doi-asserted-by":"crossref","first-page":"539","DOI":"10.1007\/s10545-010-9272-6","article-title":"UK Liver Selection and Allocation Working Party. UK experience of liver transplantation for erythropoietic protoporphyria","volume":"34","author":"Dowman","year":"2011","journal-title":"Journal of Inherited Metabolic Disease"},{"key":"10.1016\/j.dld.2014.11.004_bib0340","doi-asserted-by":"crossref","first-page":"2754","DOI":"10.1111\/j.1600-6143.2005.01084.x","article-title":"Living donor liver transplantation for pediatric patients with inheritable metabolic disorders","volume":"5","author":"Morioka","year":"2005","journal-title":"American Journal of Transplantation"},{"key":"10.1016\/j.dld.2014.11.004_bib0345","doi-asserted-by":"crossref","first-page":"216","DOI":"10.1111\/ajt.12504","article-title":"Donor hemosiderosis does not affect liver function and regeneration in the setting of living donor liver transplantation","volume":"14","author":"Shaked","year":"2014","journal-title":"American Journal of Transplantation"},{"key":"10.1016\/j.dld.2014.11.004_bib0350","doi-asserted-by":"crossref","first-page":"579","DOI":"10.1016\/j.jhep.2013.10.025","article-title":"Long term results of liver transplantation for Wilson's disease: experience in France","volume":"60","author":"Guillaud","year":"2014","journal-title":"Journal of Hepatology"},{"key":"10.1016\/j.dld.2014.11.004_bib0355","doi-asserted-by":"crossref","first-page":"201","DOI":"10.1034\/j.1399-3046.1999.00014.x","article-title":"Living related liver transplantation from heterozygote genetic carriers to children with Wilson's disease","volume":"3","author":"Asonuma","year":"1999","journal-title":"Pediatric Transplantation"},{"key":"10.1016\/j.dld.2014.11.004_bib0360","doi-asserted-by":"crossref","first-page":"261","DOI":"10.1097\/TP.0b013e3181919984","article-title":"Long-term outcomes for 32 cases of Wilson's disease after living-donor liver transplantation","volume":"87","author":"Yoshitoshi","year":"2009","journal-title":"Transplantation"},{"key":"10.1016\/j.dld.2014.11.004_bib0365","doi-asserted-by":"crossref","first-page":"169","DOI":"10.1034\/j.1399-3046.1999.00034.x","article-title":"This liver is a giver: Wilson disease and living related liver transplantation","volume":"3","author":"Rand","year":"1999","journal-title":"Pediatric Transplantation"},{"key":"10.1016\/j.dld.2014.11.004_bib0370","doi-asserted-by":"crossref","first-page":"432","DOI":"10.1111\/j.1399-0012.2011.01549.x","article-title":"Outcomes of liver transplantation for glycogen storage disease: a matched-control study and a review of literature","volume":"26","author":"Maheshwari","year":"2012","journal-title":"Clinical Transplants"},{"key":"10.1016\/j.dld.2014.11.004_bib0375","doi-asserted-by":"crossref","first-page":"285","DOI":"10.1038\/jhg.2013.17","article-title":"Current status of hepatic glycogen storage disease in Japan: clinical manifestations, treatments and long-term outcomes","volume":"58","author":"Kido","year":"2013","journal-title":"Journal of Human Genetics"},{"key":"10.1016\/j.dld.2014.11.004_bib0380","doi-asserted-by":"crossref","first-page":"848","DOI":"10.1002\/lt.21151","article-title":"Long-term results of living donor liver transplantation for glycogen storage disorders in children","volume":"13","author":"Iyer","year":"2007","journal-title":"Liver Transplantation"},{"key":"10.1016\/j.dld.2014.11.004_bib0385","doi-asserted-by":"crossref","first-page":"1867","DOI":"10.1002\/lt.21929","article-title":"Living donor liver transplantation for glycogen storage disease type Ib","volume":"15","author":"Kasahara","year":"2009","journal-title":"Liver Transplantation"},{"key":"10.1016\/j.dld.2014.11.004_bib0390","doi-asserted-by":"crossref","first-page":"2875","DOI":"10.1016\/j.transproceed.2009.07.025","article-title":"Living related liver transplantation in Crigler-Najjar syndrome type 1","volume":"41","author":"Oz\u00e7ay","year":"2009","journal-title":"Transplantation Proceedings"},{"key":"10.1016\/j.dld.2014.11.004_bib0395","doi-asserted-by":"crossref","first-page":"394","DOI":"10.1111\/j.1600-6143.2010.03397.x","article-title":"Living-related liver transplantation for siblings with progressive familial intrahepatic cholestasis 2, with novel genetic findings","volume":"11","author":"Shimizu","year":"2011","journal-title":"American Journal of Transplantation"},{"key":"10.1016\/j.dld.2014.11.004_bib0400","doi-asserted-by":"crossref","first-page":"776","DOI":"10.1111\/j.1399-0012.2010.01368.x","article-title":"Progressive familial intrahepatic cholestasis: a single-center experience of living-donor liver transplantation during two decades in Japan","volume":"25","author":"Hori","year":"2011","journal-title":"Clinical Transplantation"},{"key":"10.1016\/j.dld.2014.11.004_bib0405","doi-asserted-by":"crossref","first-page":"416","DOI":"10.1097\/00007890-199902150-00013","article-title":"Unsuspected bile duct paucity in donors for living-related liver transplantation: two case reports","volume":"67","author":"Gurkan","year":"1999","journal-title":"Transplantation"},{"key":"10.1016\/j.dld.2014.11.004_bib0410","doi-asserted-by":"crossref","first-page":"2147","DOI":"10.1097\/01.TP.0000066804.33006.17","article-title":"Living-related liver transplantation for Alagille syndrome","volume":"75","author":"Kasahara","year":"2003","journal-title":"Transplantation"},{"key":"10.1016\/j.dld.2014.11.004_bib0415","doi-asserted-by":"crossref","first-page":"161","DOI":"10.1016\/j.transproceed.2010.11.013","article-title":"Living related donor liver transplantation in children","volume":"43","author":"Tannuri","year":"2011","journal-title":"Transplantation Proceedings"},{"key":"10.1016\/j.dld.2014.11.004_bib0420","doi-asserted-by":"crossref","first-page":"851","DOI":"10.1016\/S0022-3468(99)90386-X","article-title":"Living-related liver transplantation in children: The \u2018Parisian\u2019 strategy to safely increase organ availability","volume":"34","author":"Revillon","year":"1999","journal-title":"Journal of Pediatric Surgery"}],"container-title":["Digestive and Liver Disease"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1590865814007890?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1590865814007890?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2018,9,27]],"date-time":"2018-09-27T15:55:12Z","timestamp":1538063712000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1590865814007890"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2015,4]]},"references-count":84,"journal-issue":{"issue":"4","published-print":{"date-parts":[[2015,4]]}},"alternative-id":["S1590865814007890"],"URL":"https:\/\/doi.org\/10.1016\/j.dld.2014.11.004","relation":{},"ISSN":["1590-8658"],"issn-type":[{"value":"1590-8658","type":"print"}],"subject":[],"published":{"date-parts":[[2015,4]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Liver transplantation using grafts with rare metabolic disorders","name":"articletitle","label":"Article Title"},{"value":"Digestive and Liver Disease","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.dld.2014.11.004","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"Copyright \u00a9 2014 Editrice Gastroenterologica Italiana S.r.l. Published by Elsevier Ltd.","name":"copyright","label":"Copyright"}]}}