Publication Name	World Journal of Gastroenterology
Manuscript ID	9478
Country	United States

Received	2014-02-13 13:30
Peer-Review Started	2014-02-13 14:21
First Decision by Editorial Office Director
Return for Revision	2014-04-21 19:46
Revised	2014-05-13 10:11
Publication Fee Transferred
Second Decision by Editor	2014-06-23 10:06
Second Decision by Editor-in-Chief
Final Decision by Editorial Office Director	2014-06-23 10:19
Articles in Press	2014-06-23 10:33
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 & 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
Key Words	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