2006 | A complex peripheral neuropathy family harboring CMT1A duplication and HNPP deletion | 최병옥 | Meeting Abstract |
2011 | A complex phenotype of peripheral neuropathy, myopathy, hoarseness, and hearing loss is linked to an autosomal dominant mutation in MYH14 | 최경규; 구혜수; 박기덕; 유정현; 최병옥 | Article |
2007 | A family harboring CMT1A duplication and HNPP deletion | 최병옥 | Article |
2008 | A MELAS syndrome family harboring two mutations in mitochondrial genome | 최병옥; 이향운 | Article |
2008 | A novel GDAP1 Q218E mutation in autosomal dominant Charcot-Marie-Tooth disease | 최경규; 박기덕; 최병옥 | Article |
2011 | A novel Gly137Asp MPZ mutation in a Charcot-Marie-Tooth disease type 1B family | 최병옥 | Article |
2013 | A novel Lys141Thr mutation in small heat shock protein 22 (HSPB8) gene in Charcot-Marie-Tooth disease type 2L | 구혜수; 유정현; 최병옥 | Article |
2013 | A novel MYH7 mutation with prominent paraspinal and proximal muscle involvement | 구혜수; 유정현; 최병옥; 홍영빈 | Article |
2012 | A novel PSEN1 H163P mutation in a patient with early-onset Alzheimer's disease: Clinical, neuroimaging, and neuropathological findings | 최병옥 | Article |
2016 | ABERRANT NEUROPILIN 1 INTERACTION AS A BIOMARKER IN DIAGNOSING TRNA SYNTHETASE-LINKED CHARCOT-MARIE-TOOTH DISEASE | 최병옥 | Meeting Abstract |
2009 | Aging exacerbates intracerebral hemorrhage-induced brain injury | 최병옥 | Article |
2006 | Analysis of androgen receptor gene by capillary gel eelectrophoresis | 최병옥 | Article |
2006 | Analysis of Korean infertile males by PDMS microchip gel electrophoresis | 최병옥 | Article |
2011 | Cell-based quantification of homocysteine utilizing bioluminescent Escherichia coli auxotrophs | 최병옥 | Article |
2017 | Cerebral white matter abnormalities in patients with charcot-marie-tooth disease | 유정현; 최병옥; 이향운; 홍영빈; 박창현 | Article |
2009 | Charcot-Marie-Tooth 1A concurrent with schwannomas of the spinal cord and median nerve | 최병옥 | Article |
2013 | Clinical and histopathological study of Charcot-Marie-Tooth neuropathy with a novel S90W mutation in BSCL2 | 최경규; 구혜수; 박기덕; 최병옥 | Article |
2010 | Common CYP7A1 promoter polymorphism associated with risk of neuromyelitis optica | 최병옥; 조인호 | Article |
2012 | Comparison between clinical disabilities and electrophysiological values in Charcot-Marie-Tooth 1A patients with PMP22 duplication | 최경규; 박기덕; 최병옥 | Article |
2012 | Comparison between Clinical Disabilities and Electrophysiological Values in Charcot-Marie-Tooth 1A Patients with PMP22 Duplication (vol 8, pg 139, 2012) | 최경규; 박기덕; 최병옥; 김영화 | Correction |
2013 | Compound heterozygous mutations of TYMP as underlying causes of mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) | 최병옥 | Article |
2011 | Compound mutations of PEO1 and TYMP in a progressive external ophthalmoplegia patient with incomplete mitochondrial neurogastrointestinal encephalomyopathy phenotype | 최병옥 | Article |
2011 | Congestive heart failure after physical exercise in a young patient with myotonic dystrophy type 1 | 최병옥 | Article |
2009 | Development of a Y-STR 12-plex PCR system and haplotype analysis in a Korean population | 최병옥 | Article |
2008 | Different clinical and magnetic resonance imaging features between Charcot-Marie-Tooth disease type 1A and 2A | 최경규; 박기덕; 유정현; 최병옥 | Article |
2008 | Distal hereditary motor neuropathy in Korean patients with a small heat shock protein 27 mutation | 유정현; 최병옥 | Article |
2006 | DNA separation using cellulose derivatives and PEO by PDMS microchip | 최병옥 | Article |
2006 | Early onset severe and late onset mild Charcot-Marie-Tooth disease with mitofusin 2 (MFN2) mutations | 최경규; 박기덕; 최병옥 | Meeting Abstract |
2010 | Early-onset Charcot-Marie-Tooth patients with mitofusin 2 mutations and brain involvement | 유정현; 최병옥; 황지영; 조선영 | Article |
2008 | Early-onset stroke associated with a mutation in mitofusin 2 | 유정현; 최병옥 | Article |