An Adult Case with Hunters Syndrome Presenting Prominent Hepatic Failure: Light and Electron Microscopic Features of the Liver-Reference-Cited by-同舟云学术

An Adult Case with Hunters Syndrome Presenting Prominent Hepatic Failure: Light and Electron Microscopic Features of the Liver

Published:2006 Issue:20 Volume:45 Page:1133-1135
ISSN:0918-2918
Container-title:Internal Medicine
language:en
Short-container-title:Intern. Med.

Author:

Yoshimoto Tsuyoshi¹,Nakamuta Makoto¹,Kotoh Kazuhiro¹,Kohjima Motoyuki¹,Morizono Shusuke¹,Miyagi Yuzuru¹,Sakai Hironori²,Enjoji Munechika¹

Affiliation:

1. Department of Medicine and Bioregulatory Science, Graduate School of Medical Sciences, Kyushu University

2. Liver Center, National Hospital Kyushu Medical Center

Publisher

Japanese Society of Internal Medicine

Subject

General Medicine,Internal Medicine

Link

http://www.jstage.jst.go.jp/article/internalmedicine/45/20/45_20_1133/_pdf

Reference10 articles.

1. The Defect in the Hunter Syndrome: Deficiency of Sulfoiduronate Sulfatase

2. 2. McKusik VANeufeld EF. The mucopolysaccharidoses storage diseases. in: The Metabolic Basis of Inherited Disease. Stanbury JBWyngaarden JBFredrickson DS, Eds. McGraw-Hill, New York, 751777, 1983.

3. Hepatic fibrosis in the mucopolysaccharidoses

4. Light and electron microscopic features of the liver in mucopolysaccharidosis

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