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Issue DateTitleAuthor(s)Type
2016Recessive optic atrophy, sensorimotor neuropathy and cataract associated with novel compound heterozygous mutations in OPA1구혜수; 유정현; 정성철Article
2013SET binding factor 1 (SBF1) mutation causes Charcot-Marie-Tooth disease type 4B3김형래; 최경규; 구혜수; 유정현; 최병옥; 정성철Article
2016DGAT2 Mutation in a Family with Autosomal-Dominant Early-Onset Axonal Charcot-Marie-Tooth Disease구혜수; 정성철Article
2013Proximal dominant hereditary motor and sensory neuropathy with proximal dominance association with mutation in the TRK-fused gene구혜수; 박기덕; 유정현; 최병옥; 정성철Article
2008Unusual intracranial parasagittal meningioma extending into the internal jugular vein through the sinuses구혜수; 임수미; 서의교; 조용재Article
2013A compound heterozygous mutation in HADHB gene causes an axonal Charcot-Marie-tooth disease구혜수; 유정현; 정성철Article
2015A novel homozygous MPV17 mutation in two families with axonal sensorimotor polyneuropathy구혜수; 우소연; 정성철; 박형준Article
2000Middle mediastinal lesions: Imaging findings and pathologic correlation이정식; 구혜수; 유정현; 김유경Article
1997Adult T-cell leukemia/lymphoma with features of CD30-positive anaplastic large cell lymphoma - A case report권성원; 이순남; 구혜수; 남은미Article
2006Prognostic value of p16INK4a and p14ARF gene hypermethylation in human colon cancer한운섭; 김옥경; 구혜수; 성순희; 조민선; 이시내Article

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