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Showing results 1 to 17 of 17

Issue DateTitleAuthor(s)Type
2017A novel pan-Nox inhibitor, APX-115, protects kidney injury in streptozotocin-induced diabetic mice: Possible role of peroxisomal and mitochondrial biogenesis배윤수; 하헌주Article
2023Are ‘cultural omnivores’ more accepting of outgroup members? Survey findings from a new immigrant destination김현수Article
2016Clinical applications of next-generation sequencing-based gene panel in patients with muscular dystrophy: Korean experience조안나Article
2020Deep Convolutional Neural Network Based Interictal-Preictal Electroencephalography Prediction: Application to Focal Cortical Dysplasia Type-II최선아Article
2023Dialysis specialist care and patient survival in hemodialysis facilities: a Korean nationwide cohort study류동열Article
2000Fast luminescence decay processes of photoexcited Eu3+ in CaS:Eu,La김성진; 이민영Article
2020Genomic profiling of 553 uncharacterized neurodevelopment patients reveals a high proportion of recessive pathogenic variant carriers in an outbred population조안나Article
2021Health promotion behavior among older korean family caregivers of people with dementia차지영Article
2023Hemodialysis facility star rating affects mortality in chronic hemodialysis patients: A longitudinal observational cohort study류동열Article
2021Impact of mobile health application on data collection and self-management of epilepsy최선아Article
2018Metabolic changes in urine and serum during progression of diabetic kidney disease in a mouse model하헌주; 황금숙Article
2022Nurse Caseload and Patient Survival in Hemodialysis Units: A Korean Nationwide Cohort Study류동열Article
2016Pitfalls of Multiple Ligation-Dependent Probe Amplifications in Detecting DMD Exon Deletions or Duplications조안나Article
2020Protein particles decorated with Pd nanoparticles for the catalytic reduction of p-nitrophenol to p-aminophenol김진흥Article
2017Severe hypotonia and postnatal growth impairment in a girl with a missense mutation in COL1A1: Implication of expanded phenotypic spectrum of type I collagenopathy조안나Article
2017Sialic acid deficiency is associated with oxidative stress leading to muscle atrophy and weakness in GNE myopathy조안나Article
2015Utility of next generation sequencing in genetic diagnosis of early onset neuromuscular disorders조안나Article

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