Browsing byAuthorChung K.W.

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Showing results 15 to 44 of 69

Issue DateTitleAuthor(s)Type
2009Charcot-Marie-Tooth 1A concurrent with schwannomas of the spinal cord and median nerve최병옥Article
2013Clinical and histopathological study of Charcot-Marie-Tooth neuropathy with a novel S90W mutation in BSCL2최경규; 구혜수; 박기덕; 최병옥Article
2017Clinical characterization and genetic analysis of Korean patients with X-linked Charcot-Marie-Tooth disease type 1박형준Article
2012Comparison between clinical disabilities and electrophysiological values in Charcot-Marie-Tooth 1A patients with PMP22 duplication최경규; 박기덕; 최병옥Article
2013Compound heterozygous mutations of TYMP as underlying causes of mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)최병옥Article
2011Compound mutations of PEO1 and TYMP in a progressive external ophthalmoplegia patient with incomplete mitochondrial neurogastrointestinal encephalomyopathy phenotype최병옥Article
2022Constraints on dark photon dark matter using data from LIGO's and Virgo's third observing run전건상Article
2023Constraints on the Cosmic Expansion History from GWTC-3김정리Article
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

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