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Comprehensive analyses of the clinicopathological features and genomic mutations of combined hepatocellular‐cholangiocarcinoma.
- Published in:
- Hepatology Research, 2024, v. 54, n. 1, p. 103, doi. 10.1111/hepr.13965
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- Article
The protective association of HLA‐C*12:02 and HLA‐DQB1*06:01 with severe acute hepatitis of unknown origin in the Japanese population.
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- HLA: Immune Response Genetics, 2024, v. 103, n. 1, p. 1, doi. 10.1111/tan.15215
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- Article
Integrated analyses of the genetic and clinicopathological features of cholangiolocarcinoma: cholangiolocarcinoma may be characterized by mismatch‐repair deficiency.
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- Journal of Pathology, 2024, v. 263, n. 1, p. 32, doi. 10.1002/path.6257
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- Article
Living donor liver transplantation for myocerebrohepatopathy spectrum due to POLG mutations.
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- Pediatric Transplantation, 2024, v. 28, n. 1, p. 1, doi. 10.1111/petr.14659
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- Article
The New Challenge in Pediatric Liver Transplantation: Chronic Antibody-Mediated Rejection.
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- Journal of Clinical Medicine, 2022, v. 11, n. 16, p. 4834, doi. 10.3390/jcm11164834
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- Article
Management of Epstein–Barr Virus Infection and Post-Transplant Lymphoproliferative Disorder in Pediatric Liver Transplantation.
- Published in:
- Journal of Clinical Medicine, 2022, v. 11, n. 8, p. 2166, doi. 10.3390/jcm11082166
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- Article