A case of ferroportin disease B complicated with hepatocellular carcinoma-Reference-Cited by-同舟云学术

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A case of ferroportin disease B complicated with hepatocellular carcinoma

Published:2017 Issue:8 Volume:58 Page:441-447
ISSN:0451-4203
Container-title:Kanzo
language:en
Short-container-title:Acta hepatologica Japonica

Author:

Hibino Chihiro¹,Naito Masafumi¹,Kawasaki Yosuke¹,Tokuda Takaaki¹,Sato Yu¹,Matsushita Megumi¹,Kusakabe Akira¹,Sakai Ayako¹,Tatsumi Yasuaki²,Kato Koichi²,Kato Ayako²,Kasugai Tsutomu³,Ito Toshifumi¹

Affiliation:

1. Department of Gastroenterology and Hepatology, Japan Community Healthcare Organization (JCHO) Osaka Hospital

2. Department of Medicine, Aichi Gakuin University School of Pharmacy

3. Department of Pathology, Japan Community Healthcare Organization (JCHO) Osaka Hospital

Publisher

Japan Society of Hepatology

Subject

Hepatology

Link

https://www.jstage.jst.go.jp/article/kanzo/58/8/58_441/_pdf

Reference24 articles.

1. 1) Feder JN, Gnirke A, Thomas W, et al. A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis. Nat Genet 1996; 13: 399-408

2. 2) Kato J, Kobune M, Nakamura T, et al. Normalization of elevated hepatic 8-hydroxy-2'-deoxyguanosine levels in chronic hepatitis C patients by phlebotomy and low iron diet. Cancer Res 2001; 61: 8697-8702

3. 3) Pietrangelo A. Hereditary hemochromatosis: Pathogenesis, diagnosis, and treatment. Gastroenterology 2010; 136: 393-408

4. 4) Hattori A, Miyajima H, Tomosugi N, et al. Clinicopathological study of Japanese patients with genetic iron overload syndromes. Pathol Int 2012; 62: 612-618

5. 5) Deugnier Y, Turlin B. Iron and hepatocellular carcinoma. J Gastroenterol Hepatol 2001; 16: 491-494

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