Browsing byAuthorChung K.W.

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Showing results 23 to 52 of 69

Issue DateTitleAuthor(s)Type
2017Decreased S100B expression in chronic liver diseases문일환; 유권; 김태헌Article
2009Development of a Y-STR 12-plex PCR system and haplotype analysis in a Korean population최병옥Article
2008Different clinical and magnetic resonance imaging features between Charcot-Marie-Tooth disease type 1A and 2A최경규; 박기덕; 유정현; 최병옥Article
2021Diving below the Spin-down Limit: Constraints on Gravitational Waves from the Energetic Young Pulsar PSR J0537-6910전건상; 김정리Article
2006Early onset severe and late-onset mild Charcot-Marie-Tooth disease with mitofusin 2 (MFN2) mutations김원기; 서정수; 최경규; 박기덕; 이정희; 최병옥; 은효원Article
2010Early-onset Charcot-Marie-Tooth patients with mitofusin 2 mutations and brain involvement유정현; 최병옥; 황지영; 조선영Article
2008Early-onset stroke associated with a mutation in mitofusin 2유정현; 최병옥Article
2013Erratum: Mutations in the PLEKHG5 gene is relevant with autosomal recessive intermediate Charcot-Marie-Tooth disease (Nutrition and Metabolism)구혜수; 유정현; 최병옥Erratum
2012Exome sequencing is an efficient tool for genetic screening of Charcot-Marie-Tooth Disease최경규; 최병옥; 김한수; 정성철Article
2010Frequency of intrahepatic FoxP3+ regulatory T cells during the natural course of chronic hepatitis B: An immunohistochemical study using needle-biopsied liver tissue한운섭; 구혜수; 성순희; 조민선; 이정경; 김태헌; 송동은Article
2008Genetic characteristics of 207 microsatellite markers in the Korean population and in other Asian populations원용진Article
2020Gravitational-wave Constraints on the Equatorial Ellipticity of Millisecond Pulsars김정리Article
2004Hereditary neuropathy with liability to pressure palsies (HNPP) patients of Korean ancestry with chromosome 17p11.2-p12 deletion박기덕; 최병옥Article
2018Impairment of PPARα and the fatty acid oxidation pathway aggravates renal fibrosis during aging오구택Article
2009Infectious mononucleosis hepatitis in young adults: Two case reports유권; 정성애; 조민선; 심기남; 김태헌Article
2011Inheritance of Charcot-Marie-tooth disease 1A with rare nonrecurrent genomic rearrangement최병옥Article
2013Missense mutations of mitofusin 2 in axonal Charcot-Marie-Tooth neuropathy: Polymorphic or incomplete penetration?최병옥Article
2015Molecular genetic diagnosis of a bethlem myopathy family with an autosomal-dominant COL6A1 mutation, as evidenced by exome sequencing박형준Article
2011MPZ mutation in an early-onset Charcot-Marie-Tooth disease type 1B family by genome-wide linkage analysis최경규; 구혜수; 박기덕; 유정현; 최병옥Article
2004Mutational analysis of PMP22, MPZ, GJB1, EGR2 and NEFL in Korean Charcot-Marie-Tooth neuropathy patients.최경규; 최병옥Article
2010Mutational analysis of whole mitochondrial DNA in patients with MELAS and MERRF diseases최병옥Article
2013Mutations in the PLEKHG5 gene is relevant with autosomal recessive intermediate Charcot-Marie-Tooth disease구혜수; 유정현; 최병옥Article
2007Mutations of KCNJ2 gene associated with Andersen-Tawil syndrome in Korean families최병옥Article
2010Myotonic dystrophy type i combined with X-linked dominant Charcot-Marie-Tooth neuropathy구혜수; 최병옥; 최선영Article
2019Narrow-band search for gravitational waves from known pulsars using the second LIGO observing run김정리Article
2008NEFL Pro22Arg mutation in Charcot-Marie-Tooth disease type 1최병옥Article
2015Novel compound heterozygous nonsense prx mutations in a korean dejerine-sottas neuropathy family구혜수Article
2023Open Data from the Third Observing Run of LIGO, Virgo, KAGRA, and GEO김정리Article
2011Primary adenosquamous cell carcinoma of the pancreas: A case report with a review of the Korean literature성순희; 유권; 정성애; 조민선; 심기남Article
2013Proximal dominant hereditary motor and sensory neuropathy with proximal dominance association with mutation in the TRK-fused gene구혜수; 박기덕; 유정현; 최병옥; 정성철Article

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