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8/29/2014 11:57:00 AM | Browse: 579 | Download: 495
Publication Name World Journal of Gastroenterology
Manuscript ID 9478
Country/Territory United States
Received
2014-02-13 13:30
Peer-Review Started
2014-02-13 14:21
To Make the First Decision
2014-04-15 19:28
Return for Revision
2014-04-21 19:46
Revised
2014-05-13 10:11
Second Decision
2014-06-23 10:06
Accepted by Journal Editor-in-Chief
Accepted by Company Editor-in-Chief
2014-06-23 10:19
Articles in Press
2014-06-23 10:33
Publication Fee Transferred
Edit the Manuscript by Language Editor
Typeset the Manuscript
2014-08-20 13:57
Publish the Manuscript Online
2014-08-29 11:57
ISSN 1007-9327 (print) and 2219-2840 (online)
Open Access
Copyright
Article Reprints For details, please visit: http://www.wjgnet.com/bpg/gerinfo/247
Permissions For details, please visit: http://www.wjgnet.com/bpg/gerinfo/207
Publisher Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
Website http://www.wjgnet.com
Category Gastroenterology and Hepatology
Manuscript Type Topic Highlights
Article Title Beyond the Pediatric end-stage liver disease system: Solutions for infants with biliary atresia requiring liver transplant
Manuscript Source Invited Manuscript
All Author List Mary Elizabeth M Tessier, Sanjiv Harpavat, Ross W Shepherd, Girish S Hiremath, Mary L Brandt, Amy Fisher and John A Goss
Funding Agency and Grant Number
Corresponding author Correspondence to: John A Goss, MD, Department of Surgery, Baylor College of Medicine and Texas Children’s Hospital, 6620 Main Street, Suite 1450, Houston, TX 77030, United States. jgoss@bcm.tmc.edu
Keywords Biliary atresia; Liver transplantation; Pediatric liver disease; Pediatric end-stage liver disease; Kasai operation; Newborn screening; Surgical outcomes; Living-related donor transplantation; Split liver transplantation; ABO-incompatible liver transplantation
Core Tip Infants with BA can benefit by maximizing the Kasai operation’s success, through diagnosing the disease earlier, employing experienced surgeons, ensuring adequate nutrition, and administering certain medications. If they require a liver transplant despite these interventions, infants with BA can also benefit by expediting the transplant process, through the use of living-related donor, split, or ABO-incompatible liver transplants.
Publish Date 2014-08-29 11:57
Citation Tessier MEM, Harpavat S, Shepherd RW, Hiremath GS, Brandt ML, Fisher A, Goss JA. Beyond the Pediatric end-stage liver disease system: Solutions for infants with biliary atresia requiring liver transplant. World J Gastroenterol 2014; 20(32): 11062-11068
Url http://www.wjgnet.com/1007-9327/full/v20/i32/11062.htm
DOI http://dx.doi.org/10.3748/wjg.v20.i32.11062
Full Article (PDF) WJG-20-11062.pdf
Full Article (Word) WJG-20-11062.doc
Manuscript File 9478-Review.doc
Answering Reviewers 9478-Answering reviewers.pdf
Copyright License Agreement 9478-Copyright assignment.pdf
Peer-review Report 9478-Peer review.pdf
Scientific Misconduct Check 9478-CorssCheck.jpg
Scientific Editor Work List 9478-Scientific editor work list.pdf