Portal hypertension in biliary atresia: a Japanese biliary atresia registry study
In native liver survivors without jaundice following KP, PH influenced prognosis, but successful treatment enabled long-term survival comparable to patients with mild or no PH.
Authors
- Tsuyoshi Sakurai (ORCID: https://orcid.org/0000-0001-9242-537X)
- Ryuji Okubo (ORCID: https://orcid.org/0000-0001-8405-1902)
- Taichi Fukuzawa (ORCID: https://orcid.org/0000-0002-6442-6815)
- Hironori Kudo (ORCID: https://orcid.org/0000-0003-2076-1168)
- Ryo Ando (ORCID: https://orcid.org/0000-0001-8649-7828)
- Masaki Nio (ORCID: https://orcid.org/0000-0002-5862-1067)
- Motoshi Wada (ORCID: https://orcid.org/0000-0003-0413-4017)
- Keisuke Tada (ORCID: https://orcid.org/0000-0003-1492-3888)
- H. Sasaki (ORCID: https://orcid.org/0000-0003-3208-1872)
- Masatoshi Hashimoto
Institutions
- Yamagata University (JP)
- Tohoku University (JP)
- Miyagi Children's Hospital (JP)
Publication Details
- Journal
- Pediatric Surgery International
- Published
- 2025-10-31
- DOI
- https://doi.org/10.1007/s00383-025-06222-4
- Citations
- 1
- Primary Topic
- Pediatric Hepatobiliary Diseases and Treatments
- Type
- article
- Field-Weighted Citation Impact
- 2.01
Funders
- Ministry of Health, Labour and Welfare