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| 1 |
Wilson Disease Comorbid with Hereditary Sensory Autonomic Neuropathy Type IV and Gitelman Syndrome
Ju Young Kim, Sung Sup Park, Hye Ran Yang
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| 2 |
Multiplex Ligation-dependent Probe Amplification Analysis Subsequent to Direct DNA Full Sequencing for Identifying ATP7B Mutations and Phenotype Correlations in Children with Wilson Disease
Jung Ok Shim, Hye Ran Yang, Jin Soo Moon, Ju Young Chang, Jae Sung Ko, Sung Sup Park, Jeong Kee Seo
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| 3 |
MRI of the Brain in Wilson Disease
Dong Ho Youm, Myung Soon Kim, In Ku Kang, Sang Cheol Shin, Jung Ho Kim, In Soo Hong
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| 4 |
Wilson Disease Misdiagnosed as Bipolar Disorder
Woori Moon, Yong Min Ahn
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| 5 |
Presentation of Progressive Familial Intrahepatic Cholestasis Type 3 Mimicking Wilson Disease: Molecular Genetic Diagnosis and Response to Treatment
Salih Boga, Dhanpat Jain, Michael L. Schilsky
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| 6 |
Bilateral Hypertrophic Olivary Degeneration in Wilson Disease
Josephin Otto, Peter Guenther, Karl-Titus Hoffmann
Korean J Radiol.2013;14(2):316-320. Published online 2013 February 22
DOI: http://dx.doi.org/10.3348/kjr.2013.14.2.316
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| 7 |
Diagnosis of Wilson Disease in Young Children: Molecular Genetic Testing and a Paradigm Shift from the Laboratory Diagnosis
Jeong Kee Seo
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| 8 |
A Korean Family with Wilson Disease Occurred in Two Consecutive Generations
Ji-Seon Choi, Joon-Hyeok Lee, Chang-Seok Ki
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| 9 |
Living-Related Liver Transplantation with Heterozygote Carrier Graft in Children with Wilson Disease
Jin Taek Kim, Soo Hee Chang, Bo Hwa Choi, Kyung Mo Kim, Han Wook Yoo, Young Joo Lee, Sung Gyu Lee
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| 10 |
The Study of the Initial Presentations of Wilson Disease at Diagonosis
Tae Jin Yang, Geun Ha Ji, Min Seop Song, Tae Gyu Hwang
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| 11 |
Mutation Analysis of Wilson Disease Gene: Arg778Leu Mutation in Korean Children
Jeong Kee Seo, Jong Won Kim
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