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Showing results 14 to 43 of 75

Issue DateTitleAuthor(s)Type
2011Cell-based quantification of homocysteine utilizing bioluminescent Escherichia coli auxotrophs최병옥Article
2017Cerebral white matter abnormalities in patients with charcot-marie-tooth disease유정현; 최병옥; 이향운; 홍영빈; 박창현Article
2009Charcot-Marie-Tooth 1A concurrent with schwannomas of the spinal cord and median nerve최병옥Article
2004Charcot-Marie-Tooth 환자에서 GJB1, EGR2, NEFL 유전자 돌연변이 및 임상적, 전기생리학적, 병리학적 특성 분석趙賢智Master's Thesis
2005Ciclopirox protects mitochondria from hydrogen peroxide toxicity김원기; 김희선; 최병옥Article
2013Clinical and histopathological study of Charcot-Marie-Tooth neuropathy with a novel S90W mutation in BSCL2최경규; 구혜수; 박기덕; 최병옥Article
2009Clinical phenotypes and electrophysiological findings in Korean CMT1A patients with 17p11.2-p12 duplication황수진Master's Thesis
2010Common CYP7A1 promoter polymorphism associated with risk of neuromyelitis optica최병옥; 조인호Article
2012Comparison between clinical disabilities and electrophysiological values in Charcot-Marie-Tooth 1A patients with PMP22 duplication최경규; 박기덕; 최병옥Article
2012Comparison between Clinical Disabilities and Electrophysiological Values in Charcot-Marie-Tooth 1A Patients with PMP22 Duplication (vol 8, pg 139, 2012)최경규; 박기덕; 최병옥; 김영화Correction
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
2011Congestive heart failure after physical exercise in a young patient with myotonic dystrophy type 1최병옥Article
2009Connexin 32 유전자 돌연변이를 가진 샤르코-마리-투스 환자들의 임상적 특성 및 전기 생리학적 특성 분석유수연Master's Thesis
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
2008Distal hereditary motor neuropathy in Korean patients with a small heat shock protein 27 mutation유정현; 최병옥Article
2006DNA separation using cellulose derivatives and PEO by PDMS microchip최병옥Article
2006Early onset severe and late onset mild Charcot-Marie-Tooth disease with mitofusin 2 (MFN2) mutations최경규; 박기덕; 최병옥Meeting Abstract
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
2013Exome Sequencing Identifies a Novel PRPS1 Mutation and a Novel DNM2 Mutation최경규; 박기덕; 최병옥Meeting Abstract
2012Exome sequencing is an efficient tool for genetic screening of Charcot-Marie-Tooth Disease최경규; 최병옥; 김한수; 정성철Article
2005Familial amyloid polyneuropathy in Korea: The first case report with a proven ATTR Lys35Asn gene최병옥Article
2013Glysyl-tRNA Synthetase (GARS) Gene Mutations of Distal Hereditary Motor Neuropathy Type V Patients in Korea최경규; 박기덕; 김용재; 최병옥; 이향운Meeting Abstract
2004Hereditary neuropathy with liability to pressure palsies (HNPP) patients of Korean ancestry with chromosome 17p11.2-p12 deletion박기덕; 최병옥Article
2003Homozygous C677T mutation in the MTHFR gene as an independent risk factor for multiple small-artery occlusions최병옥Article
2003Hyperhomocysteinemia as an independent risk factor for silent brain infarction최경규; 최병옥Article

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