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Showing results 801 to 820 of 2442

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Issue DateTitleJournal Title
2004General supportive treatment for genetic/metabolic disorders장애아동연구소논문집
2019Generation of an Induced Pluripotent Stem Cell (iPSC) Line From a 42-year-old Adult Cerebral Type X-linked Adrenoleukodystrophy (X-ALD) Patient STEM CELL RESEARCH
2020Generation of induced pluripotent stem cells (KSCBi009-A) from a patient with Prader-Willi syndrome (PWS) featuring deletion of the paternal chromosome region 15q11.2-q13 STEM CELL RESEARCH
2022Generation of mutation-corrected induced pluripotent stem cell lines derived from adrenoleukodystrophy patient by using homology directed repair STEM CELL RESEARCH
2019Generation of patient-specific induced pluripotent stem cells (KSCBi007-A) derived from a patient with Prader-Willi syndrome retain maternal uniparental disomy (UPD) STEM CELL RESEARCH
2017Generation of two induced pluripotent stem cell (iPSC) lines from X-linked adrenoleukodystrophy (X-ALD) patients with adrenomyeloneuropathy (AMN) STEM CELL RESEARCH
2003Genetic analysis of the VP1 region of human enterovirus 71 strains isolated in Korea during 2000ARCHIVES OF VIROLOGY
2019Genetic and clinical features of SCN8A developmental and epileptic encephalopathyEPILEPSY RESEARCH
2012Genetic and epileptic features in Rett syndrome YONSEI MEDICAL JOURNAL
2012Genetic basis of Bartter syndrome in KoreaNEPHROLOGY DIALYSIS TRANSPLANTATION
2011Genetic basis of congenital and infantile nephrotic syndromesAMERICAN JOURNAL OF KIDNEY DISEASES
2021Genetic Confirmation and Identification of Novel Variants for Glanzmann Thrombasthenia and Other Inherited Platelet Function Disorders: A Study by the Korean Pediatric Hematology Oncology Group (KPHOG) GENES
2020Genetic diagnosis and clinical characteristics by etiological classification in early-onset epileptic encephalopathy with burst suppression patternEPILEPSY RESEARCH
2018Genetic structures of invasive Streptococcus pneumoniae isolates from Korean children obtained between 1995 and 2013 BMC INFECTIOUS DISEASES
2020Genetic Study in Korean Pediatric Patients with Steroid-Resistant Nephrotic Syndrome or Focal Segmental Glomerulosclerosis JOURNAL OF CLINICAL MEDICINE
2019Genetic Variants in Antineutrophil Cytoplasmic Antibody-Associated Vasculitis: A Bayesian Approach and Systematic Review Journal of Clinical Medicine
2020Genetic variation and autism: A field synopsis and systematic meta-analysis BRAIN SCIENCES
2018Genetic variation and systemic lupus erythematosus: A field synopsis and systematic meta-analysisAUTOIMMUNITY REVIEWS
2009Genetic variation in the promoter region of chitinase 3-like 1 is associated with atopy.AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE
2020Genetic variations in MicroRNA genes and cancer risk: A field synopsis and meta-analysisEUROPEAN JOURNAL OF CLINICAL INVESTIGATION

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