Beyond the Pediatric end-stage liver disease system: Solutions for infants with biliary atresia requiring liver transplant

doi:10.3748/wjg.v20.i32.11062

Advanced Search

BPG is committed to discovery and dissemination of knowledge

Home / Archive / Volume 20, Issue 32

This Article

Academic Content and Language Evaluation of This Article

Citation of this article

Corresponding Author of This Article

Research Domain of This Article

Article-Type of This Article

Open-Access Policy of This Article

Times Cited Counts in Google of This Article

Number of Hits and Downloads for This Article

Total Article Views (6786)

All Articles published online

The chart showing PDF series, WORD series, HTML series, Figures (1-2) series.

Item

Count

PDF

630

WORD

226

HTML

3796

Figures (1-2)

172

Sum=4824

Publishing Process of This Article

The chart showing Browse series, Download series.

Item

Count

Browse

1059

Download

903

Sum=1962

Aug 28, 2014 (publication date) through Apr 25, 2024

Times Cited of This Article

Times Cited (17)

Journal Information of This Article

Publication Name

World Journal of Gastroenterology

ISSN

1007-9327

Publisher of This Article

Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

Topic Highlight

World J Gastroenterol. Aug 28, 2014; 20(32): 11062-11068
Published online Aug 28, 2014. doi: 10.3748/wjg.v20.i32.11062

Open in New Tab Full Size Figure Download Figure

Figure 1 Diagram of split liver transplant. The left lateral segment is donated to a child and the right trisegmental graft is designated for an adult.

Open in New Tab Full Size Figure Download Figure

Figure 2 Outcomes in the current era of biliary atresia and ways to improve patient outcomes. KP: Kasai portoenterostomy; NLS: Native liver survival; LT: Liver transplant; LRD: Living related donor; ILT: Incompatible donor liver transplant.

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: https://www.wjgnet.com/1007-9327/full/v20/i32/11062.htm
DOI: https://dx.doi.org/10.3748/wjg.v20.i32.11062