CAU Scholar's Space: Lee, Hyun Kyung

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Lee, Hyun Kyung (이현경)

의과대학 (의학부(임상-서울))

Research Area: 소아청소년과학, 소아신장학, 소아신장유전학, pediatrics, pediatric nephrology, genetic nephrology

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Children:4||Bartter syndrome:3||Kidney transplantation:2||Nephrotic syndrome:2||Focal segmental glomerulosclerosis:2||Child:2||Peritoneal dialysis:2||Single nucleotide polymorphism:2||Hematuria:2||Childhood nephrotic syndrome:1||Chromosome walking:1||Chronic kidney disease:1||Chronic kidney failure:1||Chronic peritoneal dialysis:1||Chronic proteinuria:1||Continuous ambulatory peritoneal dialysis:1||Continuous cyclic peritoneal dialysis:1||Cubilin:1||Cyclic neutropenia:1||Diabetic nephropathies:1||Dialysis adequacy:1||ELA2 gene:1||Endstage renal disease:1||Endocytosis:1||Enterohemorrhagic Escherichia coli:1||Evaluation study:1||Evidencebased practice:1||Familial renal glucosuria:1||Family history:1||Formin:1||GRADE approach:1||Genetic polymorphism:1||Genetic testing:1||Glomerulopathy:1||Glucocorticoid receptor:1||Guideline:1||Hemolytic uremic syndrome:1||Hyperphosphatemia:1||Hypocalcemia:1||INF2 gene:1||Idiopathic nephrotic syndrome:1||Infant:1||Infrafamilial spread:1||Kidney:1||Kidney Health Plan 2033:1||Kidney disease:1||Kidney tubules, proximal:1||Korean Society of Nephrology:1||Location:1||Longterm follow up:1||MYH9 gene:1||MYH9related disorder:1||Macrophage migration inhibitory factor gene:1||Management:1||Mapbased cloning:1||Mineralocorticoid:1||Motor domain:1||Multiorgan involvement:1||Multicystic dysplastic kidney:1||Multiple drug resistance 1 gene:1||Mutation:1||NR3C1:1||NR3C2 gene:1||Nephrogenic diabetes insipidus:1||Nightly intermittent peritoneal dialysis:1||Nonmuscle myosin heavy chain IIA:1||Pediatrics:1||Perihilar variant:1||Peritonitis:1||Phenotype:1||Practice guideline:1||Presenting symptom:1||Protein loss:1||Pseudohypoaldosteronism:1||Receptor:1||Recombinant human granulocyte colonystimulating factor:1||Recurrence:1||Retrospective studies:1||SGLT2:1||SLC12A1 gene:1||SLC5A2 gene:1||SSLP marker:1||Serum amyloid A:1||Sodiumglucose cotransporter:1||Solitary kidney:1||Stone analysis:1||Tail domain:1||Underlying cause:1||Urinary exosome:1||Urinary lithiasis:1||Urinary tract:1||Urogenital abnormalities:1||WT1:1||Wegener's granulomatosis:1||Xlinked hypophosphatemic rickets:1||children:1||common mutation:1||eGFR:1||genotype:1||genotypephenotype analysis:1||genotypephenotype correlation:1||graft outcome:1||kidney failure:1||kidney function:1||kidney ultrasonography:1||nephrocalcinosis:1||persistent hyperparathyroidism:1||preterm:1||truncating mutation:1||AA amyloidosis:1||tubular disorders:1||Actin:1||Age:1||Albuminuria:1||Automated peritoneal dialysis:1||Biomaker:1||CLCNKB gene:1||CUBN variants:1||Childhood:1||

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84, Heukseok-ro, Dongjak-gu, Seoul, Republic of Korea (06974)02-820-6194

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