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Showing results 5041 to 5060 of 8014

Issue DateTitleAuthor(s)Type
2015Multiple primary cancers involving lung cancer at a single tertiary hospital: Clinical features and prognosis장중현; 이진화; 류연주; 공경애Article
2013MULTIPLE PRIMARY MALIGNANCIES IN PATIENTS WITH LUNG CANCER: CLINICAL FEATURES AND PROGNOSIS장중현; 이진화; 류연주; 이석정Meeting Abstract
2009Multiple sclerosis and peripheral multifocal demyelinating neuropathies박기덕Meeting Abstract
2008Multiple sclerosis and peripheral multifocal demyelinating neuropathies occurring in a same patient박기덕; 정지향Article
2008Multiplex analysis of cytokines in the serum and cerebrospinal fluid of patients with Alzheimer's disease by color-coded bead technology최경규; 강상원; 최철희; 권종범; 정지향Article
2010Multiplexed amino acid array utilizing bioluminescent escherichia coli auxotrophs최병옥Article
2018Multitarget effects of Korean Red Ginseng in animal model of Parkinson's disease: antiapoptosis, antioxidant, antiinflammation, and maintenance of blood–brain barrier integrity오세관Article
2016Musashi-2 (MSI2) supports TGF-beta signaling and inhibits claudins to promote non-small cell lung cancer (NSCLC) metastasis안영호Article
2014Muscle involvement in Dent disease 2이승주Article
2006Mutation analysis of BRCA1 and BRCA2 from 793 Korean patients with sporadic breast cancer정화순; 이경은Article
2015MUTATION ANALYSIS OF JAK2, MPL, CALR, ASXL1, TET2, IDH1, IDH2, DNMT3A, AND SF3B1 IN MYELOPROLIFERATIVE NEOPLASM문영철Meeting Abstract
2014Mutation profile of the GNE gene in Japanese patients with distal myopathy with rimmed vacuoles (GNE myopathy)조안나Article
2005Mutational analysis of myelin protein zero gene in Korean families with Charcot-Marie-Tooth disease최병옥Meeting Abstract
2005Mutational analysis of neurofilarnent light chain (NEFL) gene in Korean patients with Charcot-Marie-Tooth disease박기덕; 최병옥Meeting Abstract
2010Mutational analysis of whole mitochondrial DNA in patients with MELAS and MERRF diseases최병옥Article
2007Mutations in PRPS1, which encodes the phosphoribosyl pyrophosphate synthetase enzyme critical for nucleotide biosynthesis, cause hereditary peripheral neuropathy with hearing loss and optic neuropathy (CMTX5)최병옥Article
2013Mutations in the PLEKHG5 gene is relevant with autosomal recessive intermediate Charcot-Marie-Tooth disease구혜수; 유정현; 최병옥Article
2009Mutations of E3 Ubiquitin Ligase Cbl Family Members Constitute a Novel Common Pathogenic Lesion in Myeloid Malignancies허정원Article
2007Mutations of KCNJ2 gene associated with Andersen-Tawil syndrome in Korean families최병옥Article
2010Mutations of the GLA gene in Korean patients with Fabry disease and frequency of the E66Q allele as a functional variant in Korean newborns강덕희Article

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