ScholarWorks@Korea University College of Medicine: Yoo, Kee Hwan

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Yoo, Kee Hwan (유기환)

Guro Hospital (Department of Pediatrics, Guro Hospital)

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Urinary tract infection:15||Hypertension:6||Child:6||children:6||Apoptosis:5||Acute kidney injury:5||Pyelonephritis:5||Vesicoureteral reflux:4||Obesity:4||Acute pyelonephritis:4||Kidney:4||Reninangiotensin system:4||Angiotensin II:4||Vesicoureteral reflux:4||Indomethacin:3||Biomarkers:3||hypertension:3||Fibrosis:3||Lipocalin2:3||Urinary tract infections:3||Btype natriuretic peptide:3||Growth and development:3||Children:3||Overnutrition:3||Ultrasonography:2||hematuria:2||hydronephrosis:2||Infant:2||Renin angiotensin system:2||Angiotensin converting enzyme:2||PDA:2||Abscess:2||Risk factor:2||심장:2||kidney development:2||Risk factors:2||Data collection:2||Patent ductus arteriosus:2||HenochSchonlein purpura:2||Pediatrics:2||2:2||1:2||mutation:2||neonate:2||Adolescent:2||nephrotic syndrome:2||Hydronephrosis:2||angiotensin:2||patent ductus arteriosus:2||Kidney development:2||Focal segmental glomerulosclerosis:2||Nephritis:2||proteinuria:2||apoptosis:2||Dimercaptosuccinic acid renal scan:2||Nephrotic syndrome:2||Proteinuria:2||Hypoxia:2||reninangiotensin system:2||Purpura:2||Pyuria:2||Rat:2||Extracellular matrix:2||Growth and Development:2||tubulointerstitial nephritis:2||Collagen:1||Combination therapy:1||Common Variable Immunodeficiency:1||Congenital chloride diarrhea:1||Creatine kinase:1||Credibility:1||Cystatin C:1||Cysts:1||Cytokines:1||DMSA:1||DMSA scan:1||DMSA scintigraphy:1||DWI:1||Delta anion gap:1||Delta bicarbonate:1||Desmopressin:1||Diabetes mellitus:1||Diagnosis:1||Disposable diapers:1||Ductus Arteriosus:1||Early:1||Echocardiographic sign:1||Edema:1||Electrolyte imbalance:1||EndStage Renal Disease:1||Endoscopy:1||Endothelins:1||Environment:1||Eosinophilia:1||Eosinophilic enteropathy:1||Epilepsy:1||EpsteinBarr virus:1||Escherichia coli:1||Etiology:1||Extendedspectrum βlactamase:1||FGFR2 gene:1||Factor Ⅶ deficiency:1||Febrile UTI:1||Fetal development:1||Fever:1||Fever duration:1||Fibroblast:1||First year relapse:1||Fluorescence insitu hybridization:1||Foley Balloon Catheterization:1||Foreign bodies:1||Genetic Variation:1||Glomerulonephritis, IGA:1||Grampositive uropathogens:1||Graves disease:1||Guidelines:1||Haemorrhagic fever with renal syndrome:1||Heart:1||Hemarthroses:1||Hematuria:1||HenochSchonlein:1||Hospitalization:1||Hospitalizations:1||Human:1||Hydrothorax:1||Hypertrophy:1||Hyperuricemia:1||Hypokalemia:1||Hypoxiainducible factor:1||IGA:1||IVIM:1||Ibuprofen:1||IgA nephropathy:1||Imipramine:1||Immunoglobulins:1||Imperforate hymen:1||Inflammation:1||Influenza:1||Ingestion:1||Intestinal lymphangiectasia:1||Intestinal perforation:1||Intravoxel incoherent motion:1||Japan:1||Ketogenic diet:1||Kidney Diseases:1||Kidney Tubules:1||Kidney information:1||Klebsiella pneumoniae:1||Korean children:1||Kyphosis:1||LeschNyhan syndrome:1||Leukocytes:1||Lowbirthweight infant:1||MRI:1||Macrophages:1||Magnetic resonance imaging:1||Male:1||Male sex:1||Malnutrition:1||Mass media:1||Melanoma:1||Membranoproliferative glomerulonephritis:1||Membranous Glomerulonephritis:1||Membranous nephropathy:1||Messenger ribonucleic acid:1||Metabolic acidosis:1||Mitogen activated protein kinases:1||Monozygotic:1||Moyamoya disease:1||Muscles:1||Mutation:1||NR3C2 gene:1||NaK2Cl cotransporter:1||Neonatal cholestasis:1||Neonatal kidney:1||Neovascularization:1||Nephrocalcinosis:1||Neurofibromatosis:1||Neuroleptic malignant syndrome:1||Neutrophil gelatinaseassociated lipocalin:1||Nevus:1||Nitric Oxide:1||Nitrite:1||Nneurofibromatosis 1:1||Nutcracker syndrome:1||Oseltamivir:1||Osteopontin:1||Osteoporosis:1||PCNA:1||PD123319:1||PDGF:1||Partial hypoxanthineguanine phosphoribosyl transferase(HPRT) deficiency:1||Patent:1||Pathologic:1||Peritoneal Dialysis:1||Pigmented:1||Plasma NGAL:1||Plasma atrial natriuretic peptide:1||Pleural effusion:1||Polymicrobial Infection:1||Postnatal growth:1||Postobstructive diuresis (POD):1||Practice guideline:1||Premature:1||Preterm infant:1||Primary monosymptomatic nocternal enuresis:1||Prognosis:1||Pseudohypoaldosteronism:1||Radioligand binding:1||Recurrence:1||Recurrent urinary tract infection:1||Regeneration:1||Renal artery stenosis:1||Renal complication:1||Renal cortical defect:1||Renal damage:1||Renal dysplasia:1||Renal insufficiency:1||Renal scarring:1||Renal symptoms:1||Renin Angiotensin System:1||ReninAngiotensin System:1||Rhabdomyolysis:1||Risk assessment:1||SARSCoV2:1||Salmonella enteritidis:1||Scar:1||SchinzelGiedion syndrome:1||School urine screening program:1||Scrotal involvement:1||Scrotum:1||Sex:1||Small kidney:1||SmithMagenis syndrome:1||South Korea:1||Specific Gravity:1||Steroid responsive nephrotic syndrome:1||Steroidresistant focal segmental glomerulosclerosis (SRFSGS):1||Stones:1||Streptococcus agalactiae:1||Suprapubic bladder aspiration:1||TGFbeta receptors:1||Technetium Tc 99 m dimercaptosuccinic acid:1||Therapeutic delay time:1||Therapeutics:1||Thrombospondin1:1||Thymus:1||Transformation:1||Treatment:1||Tubular epithelial cell:1||Twins:1||Type 3:1||Typhoid fever:1||UTI:1||UUO:1||Unilateral renal aplasia:1||Unilateral ureteral obstruction:1||Ureteral peristalsis:1||Uric acid stone:1||Urinalysis:1||Urinary Retention:1||Urinary Tract Infections:1||Urinary retention:1||Urine alkalinization:1||Urine collection:1||Urinoma:1||Urologic diseases:1||VIPAR:1||VPS33B:1||VUR:1||Vascular remodeling:1||VesicoUreteral Reflux:1||Vitamin D Deficiency:1||Vitamin Ddependent rickets:1||Voiding cystourethrography:1||Young age:1||Young infant:1||albumin:1||aldosterone:1||angiotensin II type 1 receptor:1||angiotensin converting enzyme:1||angiotensin converting enzyme inhibitors transforming growth factor beta 1:1||anticomplement factor H autoantibody:1||antibiotics:1||atypical hemolytic uremic syndrome:1||cJun NH2terminal kinase:1||cardiovascular problem:1||case report:1||chronic renal disease:1||chronic renal failure:1||clusterin:1||coenzyme Q10 deficiency:1||complement factor H:1||craniosynostosis:1||cytotoxic agents:1||dehydration:1||endstage renal disease (ESRD):1||endstage renal failure:1||endothelin:1||epidermal growth factor:1||fibroblast:1||fibrosis:1||focal segmental glomerulosclerosis:1||genetic analysis:1||glomerulonephritis:1||hypertrophy:1||hyponatremia:1||hypoxia:1||hypoxiainducible factor:1||indomethacin:1||infant:1||intrauterine growth retardation:1||kidney:1||kidney biopsy:1||longterm outcome:1||losartan:1||macrophage:1||macrophages:1||metabolic acidosis:1||mineralocorticoid receptors:1||mitochondrial cytopathy:1||mitochondrial proliferation in podocytes:1||mouse:1||myofibroblast:1||neonates:1||newborn infant:1||osmolality:1||p38 mitogenactivated protein kinases:1||p53:1||pediatric:1||pediatrics:1||polymorphisms:1||preterm infants:1||procedural pain:1||rat:1||ratio:1||remission of proteinuria:1||renal development:1||renal dysfunction:1||renal replacement therapy:1||respiratory difficulty:1||risk assessment:1||school urine mass screening:1||sensorineural hearing loss:1||steroid resistance:1||steroidresistant nephrotic syndrome:1||symptomatic PDA:1||transforming growth factor beta receptor:1||transforming growth factorbeta 1:1||transforming growth factorbeta(1):1||vesicoureteral reflux:1||가족:1||급성 연쇄상구군 감염후 사구체신염:1||뇌실주위 초음파음영 증가:1||뇌초음파 및 뇌유발전위 검사소견과 신경학적 예후:1||동맥관:1||만성신부전:1||방광요관 역류:1||방광요관역류:1||범혈구감소증과 서맥:1||분유수유:1||비만:1||소뇌 충부의 무형성을 동반한 Joubert 증후군:1||소아:1||신동맥혈류:1||신생백서:1||신생아 홍반성 낭창:1||신생아제대정맥도관:1||신세뇨관 재흡수능의 발달에 따른 Aldosterone:1||안지오텐신∥:1||알포트 증후군:1||요관폐쇄:1||요로감염:1||요비중:1||위험인자와 신경학:1||종성신우신염:1||항이뇨호르몬:1||혈뇨:1||형제:1||120170:1||APN:1||AT(1) receptors:1||AT(2) receptors:1||Abdominal pain:1||Acute gastroenteritis:1||Acute renal failure:1||Acute renal faliure:1||Acute tubulointerstitial nephritis:1||Acute urinary retention:1||Adiponectin:1||Adiposity:1||Age:1||Airborne Particulate Matter:1||Aldosterone:1||Angiogenic Proteins:1||Angiopoietins:1||Angiotensin:1||Angiotensin Convertiy:1||Angiotensin ii:1||Animal model:1||Antidiuretic hormone (ADH):1||Aquaporin2:1||Aquaporin2:1||Asian:1||Atrial Natriuretic Peptide:1||Atypical Hemolytic Uremic Syndrome:1||Autoimmunity:1||Azygos vein:1||BNT162 vaccine:1||Bacterial infections:1||Bacteriuria:1||Bartter syndrome:1||Bax:1||Bcl2:1||BclXL:1||BeareStevenson syndrome:1||Bilateral ureteral obstruction (BUO):1||Bladder:1||Bladder diameters:1||Bladder volume:1||Blood pressure:1||Body weight:1||Button battery:1||Creactive protein:1||COQ6 mutation:1||Case report:1||Case reports:1||Cell Proliferation:1||Cell Transdifferentiation:1||Cellular senescence:1||Central venous catheterization:1||Child Obesity:1||Childhood obesity:1||Chlorella:1||Chloride channels:1||Chromosomal study:1||Chronic kidney failure:1||Chronic renal insufficiency:1||ChurgStrauss syndrome:1||Citrulline:1||Clinical sign:1||Clusterin:1||Cockayne Syndrome:1||

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