- Efficacy and safety of sorafenib in patients with advanced hepatocellular carcinoma
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Heo J
- KMID: 1381445
- Korean J Hepatol.
- 2009 Jun;15(2):227-230.
- doi: 10.3350/kjhep.2009.15.2.227
No abstract available. -
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- Haplotype analysis at R778L mutation of ATP7B gene in Korean patients with Wilson disease
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Jin HS, Oh B
- KMID: 1374957
- Korean J Hepatol.
- 2009 Sep;15(3):295-298.
- doi: 10.3350/kjhep.2009.15.3.295
No abstract available. -
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- Haplotype analysis and possible founder effect at the R778L mutation of the ATP7B gene in Korean patients with Wilson's disease
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Bae SH, Kim JW, Seo JK
- KMID: 1374959
- Korean J Hepatol.
- 2009 Sep;15(3):309-319.
- doi: 10.3350/kjhep.2009.15.3.309
BACKGROUND/AIMS: Wilson's disease (WD) is an inherited disorder of copper metabolism caused by alteration of the P-type adenosine triphosphatase (ATP) 7B gene. In this study, we analyzed the frequency of... -
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- Identification of a Novel Mutation in the ATP7A Gene in a Korean Patient with Menkes Disease
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Kim YH, Lee R, Yoo HW, Yum MS, Bae SH, Chung SC, Park YM, Son JS
- KMID: 1094269
- J Korean Med Sci.
- 2011 Jul;26(7):951-953.
- doi: 10.3346/jkms.2011.26.7.951
Menkes disease is an infantile-onset X-linked recessive neurodegenerative disorder caused by diverse mutations in a copper-transport gene, ATP7A. Affected patients are characterized by progressive hypotonia, seizures, failure to thrive and... -
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- Wilson Disease: an Update
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Seo JK
- KMID: 760667
- Korean J Hepatol.
- 2006 Sep;12(3):333-363.
Wilson disease (WD) is an autosomal recessive disorder of copper transport that results in accumulation of copper primarily in the liver, the brain and the cornea. WD is the most... -
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