강희경

  #신부전 #만성신부전 #만성콩팥병 #사구체신질환 #단백뇨 #혈뇨 #수분-전해질이상 #신증후군 #선천요도계기형 #알러지성자반증 #HS자반증 #방광염 #요로감염 #이식환자 #신장이식 #방광요관역류 #소아청소년신장-요로계질환 #고혈압 #신장질환

학력

2001. 3 ~ 2005. 8 서울대학교 의과대학원 / 의학박사
1999. 3 ~ 2001 .2 서울대학교 의과대학원 / 의학석사
1992. 3 ~ 1996. 2 서울대학교 의과대학 / 의학사

경력

2014.07 ~ 현재 / 서울대학교 어린이병원 소아청소년 콩팥센터장
2014.07 ~ 현재 / 서울대학교 어린이병원 소아청소년과 소아신장분과 분과장
2017.09 ~ 현재 / 서울대학교 의과대학 교수
2012.03 ~ 2017.08 / 서울대학교 어린이병원 소아청소년과 / 부교수
2008 ~ 2012. 2 / 서울대학교 어린이병원 소아청소년과 / 조교수
2006. 7 ~ 2007. 11 / 미국 미시간대학 신장내과/연구요원
2005. 5 ~ 2006. 2 / 서울대학교병원 장기이식연구소 / 연구교수
2003. 5 ~ 2005. 2 / 미국 하버드 의대 Beth Israel Deaconess 메디컬센터 이식연구소/연구전임의
2001. 3 ~ 2003. 4 / 서울대학교 어린이병원 소아과 소아신장분과/전임의
1997. 3 ~ 2001. 2 / 서울대학교 어린이 병원 소아과 / 전공의
1996 .3 ~ 1997. 3 / 서울대학교병원 / 인턴

논문

Targeted Exome Sequencing Provided Comprehensive Genetic Diagnosis of Congenital Anomalies of the Kidney and Urinary Tract

Consensus regarding diagnosis and management of atypical hemolytic uremic syndrome

Clinical Significance of Crescent Formation in IgA Nephropathy - a Multicenter Validation Study

Acute Kidney Injury in Pediatric Cancer Patients

Long-term safety and tolerability of valsartan in children aged 6 to 17 years with hypertension

Anemia and Iron Deficiency in Children with Chronic Kidney Disease (CKD): Data from the Know-Ped CKD Study

Features of Autosomal Recessive Alport Syndrome: A Systematic Review

Association between Serum Matrix Metalloproteinase- (MMP-) 3 Levels and Systemic Lupus Erythematosus: A Meta-analysis

High prevalence of systemic hypertension in pediatric patients with moyamoya disease years after surgical treatment

Acute kidney injury associated with Yersinia pseudotuberculosis infection: Forgotten but not gone

Urological Problems in Patients with Menkes Disease

Reninoma: a rare cause of curable hypertension

A Pediatric Case of a D-Penicillamine Induced ANCA-associated Vasculitis Manifesting a Pulmonary-Renal Syndrome

Mental health and psychosocial adjustment in pediatric chronic kidney disease derived from the KNOW-Ped CKD study

Mycophenolate mofetil for maintenance of remission in children with steroid- and calcineurin inhibitor- dependent nephrotic syndrome: A prospective, randomized multicenter trial

Acute kidney injury predicts all-cause mortality in patients with cancer

Low relapse rate of urinary tract infections from extended-spectrum beta-lactamase-producing bacteria in young children

Post-Transplant Lymphoproliferative Diseases in Pediatric Kidney Allograft Recipients with Epstein-Barr Virus Viremia

Life-Threatening Extrarenal Manifestations in an Infant with Atypical Hemolytic Uremic Syndrome Caused by a Complement 3-Gene Mutation

Primary Hyperoxaluria in Korean Pediatric Patients

Higher Incidence of BK Virus Nephropathy in Pediatric Kidney Allograft Recipients with Alport Syndrome

Vascular Access Choice, Complications, and Outcomes in Children on Maintenance Hemodialysis: Findings From the International Pediatric Hemodialysis Network (IPHN) Registry

Cutaneous Skeletal Hypophosphatemia Syndrome in Association with a Mosaic HRAS Mutation

Predicting acute kidney injury in cancer patients using heterogeneous and irregular data

Genotype-Phenotype Analysis in Pediatric Patients with Distal Renal Tubular Acidosis

Disseminated adenovirus infection in a 10-year-old renal allograft recipient

Factors affecting serum concentration of vancomycin in critically ill oliguric pediatric patients receiving continuous venovenous hemodiafiltration

Kidney Transplantation in Patients with Atypical Hemolytic Uremic Syndrome due to Complement Factor H Deficiency: Impact of Liver Transplantation

A Case of an Ureteropelvic Junction Obstruction Caused by a Crossing Vessel

Acute kidney injury in childhood-onset nephrotic syndrome: Incidence and risk factors in hospitalized patients

A familial case of Galloway-Mowat syndrome due to a novel TP53RK mutation: a case report

Acute kidney injury and continuous renal replacement therapy in children; what pediatricians need to know

Impact of end-stage renal disease in children on their parents

Efficacy and safety of rituximab in childhood-onset, difficult-to-treat nephrotic syndrome: A multicenter open-label trial in Korea

Measurement of Fluid Status Using Bioimpedance Methods in Korean Pediatric Patients on Hemodialysis

Three cases of Gordon syndrome with dominant KLHL3 mutations

Focal segmental glomerulosclerosis and medullary nephrocalcinosis in children with ADCK4 mutations

COQ6 Mutations in Children With Steroid-Resistant Focal Segmental Glomerulosclerosis and Sensorineural Hearing Loss

NUP107 mutations in children with steroid-resistant nephrotic syndrome

Delayed transplantation may affect intellectual ability in children

Genotype and Phenotype Analysis in Pediatric Patients with Cystinuria

Long-term repeated rituximab treatment for childhood steroid-dependent nephrotic syndrome

A Case of Azathioprine Induced Severe Myelosuppression and Alopecia Totalis in IgA Nephropathy

Markers of disease and steroid responsiveness in paediatric idiopathic nephrotic syndrome: Whole-transcriptome sequencing of peripheral blood mononuclear cells

Loss of podocalyxin causes a novel syndromic type of congenital nephrotic syndrome

Epidemiology of Acute Kidney Injury in Critically Ill Children and Young Adults

Posttransplantation lymphoproliferative disorder after pediatric solid organ transplantation: experiences of 20 years in a single center

A Case of Severe Hypercalcemia Causing Acute Kidney Injury: An Unusual Presentation of Acute Lymphoblastic Leukemia

Long-Term Outcomes of Pediatric Renovascular Hypertension

A 7-year-old girl presenting with a Bartter-like phenotype: Questions

A 7-year-old girl presenting with a Bartter-like phenotype: Answers

Influence of the Method of Definition on the Prevalence of Left-Ventricular Hypertrophy in Children with Chronic Kidney Disease: Data from the Know-Ped CKD Study

The impact of end-stage renal disease in children on their parents

Health-related quality of life of children with pre-dialysis chronic kidney disease

Genotype-phenotype analysis of pediatric patients with WT1 glomerulopathy

Tacrolimus for children with refractory nephrotic syndrome: a one-year prospective, multicenter, and open-label study of Tacrobell(R), a generic formula

The International Human Epigenome Consortium: A Blueprint for Scientific Collaboration and Discovery

X-Linked and Autosomal Recessive Alport Syndrome: Pathogenic Variant Features and Further Genotype-Phenotype Correlations

Hepatorenal fibrocystic diseases in children

A familial case of Blau syndrome caused by a novel NOD2 genetic mutation

Aliskiren Regulates Neonatal Fc Receptor and IgG Metabolism with Attenuation of Anti-GBM Glomerulonephritis in Mice

Targeted exome sequencing resolves allelic and the genetic heterogeneity in the genetic diagnosis of nephronophthisis-related ciliopathy

Recurrence and Treatment after Renal Transplantation in Children with FSGS

KNOW-Ped CKD (KoreaN cohort study for outcomes in patients with pediatric CKD): Design and methods

Bilateral iliac and popliteal arterial thrombosis in a child with focal segmental glomerulosclerosis

A nonsense PAX6 mutation in a family with congenital aniridia

소아 신장이식 환자에서의 면역억제요법

Familial IPEX syndrome: different glomerulopathy in two siblings

Atypical hemolytic uremic syndrome: Korean pediatric series

Nephronophthisis 13: implications of its association with Caroli disease and altered intracellular localization of WDR19 in the kidney

The diagnosis of febrile urinary tract infection in children may be facilitated by urinary biomarkers

Severe Anemia Due to Parvovirus Infection Following Treatment with Rituximab in a Pediatric Kidney Transplant Recipient : Anemia after Treatment of Rituximab in Kidney Recipient Patient

Nephrotic syndrome: what's new, what's hot?

Atypical retinopathy in patients with nephronophthisis type 1: an uncommon ophthalmological finding

Nephronophthisis

Assessment of Worldwide Acute Kidney Injury, Renal Angina and Epidemiology in critically ill children (AWARE): study protocol for a prospective observational study

Initial steroid regimen in idiopathic nephrotic syndrome can be shortened based on duration to first remission

Pharmacodynamic Monitoring of Calcineurin Inhibitor in Pediatric Kidney Transplantation

Different Recurrence Rates Between Pediatric and Adult Renal Transplant for Immunoglobulin A Nephropathy: Predictors of Posttransplant Recurrence

Two siblings with Bardet-Biedl syndrome caused by mutations in BBS10 : the first case identified in Korea

Muscle involvement in Dent disease 2

Recurrence of idiopathic focal segmental glomerulosclerosis after kidney transplantation: experience of a Korean tertiary center

Incidence, risk factors and clinical outcomes for acute kidney injury after aortic arch repair in paediatric patients

X-linked recessive nephrogenic diabetes insipidus: a clinico-genetic study

A case of Sotos syndrome presented with end-stage renal disease due to the posterior urethral valve

Shiga toxin-associated hemolytic uremic syndrome complicated by intestinal perforation in a child with typical hemolytic uremic syndrome

Outcomes of chronic dialysis in Korean children with respect to survival rates and causes of death

Development of antirituximab antibodies in children with nephrotic syndrome

Conversion of twice-daily tacrolimus to once-daily tacrolimus formulation in stable pediatric kidney transplant recipients: pharmacokinetics and efficacy

Intravenous fluid prescription practices among pediatric residents in Korea

Outcome of Antimicrobial Therapy of Pediatric Urinary Tract Infections Caused by Extended-Spectrum beta-Lactamase-Producing Enterobacteriaceae

Leflunomide therapy for BK virus allograft nephropathy after pediatric kidney transplantation

Factors affecting growth and final adult height after pediatric renal transplantation

Active proteases in nephrotic plasma lead to a podocin-dependent phosphorylation of VASP in podocytes via protease activated receptor-1

Prevalence of 25(OH) vitamin D insufficiency and deficiency in pediatric patients on chronic dialysis

Divergent functions of the Rho GTPases Rac1 and Cdc42 in podocyte injury

신증후군 환아에서 Rituximab 사용 후 발생한 기쿠치병 1례

야뇨증의 병인 기전 -항이뇨호르몬, 고칼슘뇨증, 용질성 이뇨

Development of korean rare disease knowledge base

Quality of life in children with end-stage renal disease based on a PedsQL ESRD module

Validity and reliability of the Korean version of the pediatric quality of life ESRD module

Urinary exosomal WT1 in childhood nephrotic syndrome

Genetic basis of Bartter syndrome in Korea

Survival over 2 years of autosomal-recessive renal tubular dysgenesis

GLCCI1 single nucleotide polymorphisms in pediatric nephrotic syndrome

A case of pseudohypoaldosteronism type 1 with a mutation in the mineralocorticoid receptor gene

Renal transplantation in a patient with Bartter syndrome and glomerulosclerosis

Genetic basis of congenital and infantile nephrotic syndromes

Variable renal phenotype in a family with an INF2 mutation

A case of systemic amyloidosis associated with cyclic neutropenia

Transcriptome Profiling of Kidney Tissue from FGS/kist Mice, the Korean Animal Model of Focal Segmental Glomerulosclerosis

Treatment of Recurrent Nephrotic Syndrome after Transplantation

Treatment of steroid-resistant pediatric nephrotic syndrome

Renal manifestations of patients with MYH9-related disorders

Polymorphisms of the MDR1 and MIF genes in children with nephrotic syndrome

Tumour lysis syndrome in children: experience of last decade

Peritonitis in Children Undergoing Peritoneal Dialysis: 10 Years' Experience in a Single Center

A case of Bartter syndrome type I with atypical presentations

Relapsing peritonitis in children who undergo chronic peritoneal dialysis: a prospective study of the international pediatric peritonitis registry

Clinical Characteristics and Associated Anomalies in Children with Solitary Kidney

Mesenchymal Stem Cells Ameliorate Adriamycin Induced Proteinuric Nephropathy

Transcriptome analysis of the response of cultured murine podocytes to puromycin aminonucleoside

Donor-strain-derived immature dendritic cell pre-treatment induced hyporesponsiveness against allogeneic antigens

The immunosuppressive effect of embryonic stem cells and mesenchymal stem cells on both primary and secondary alloimmune responses

Loss of collagen-receptor DDR1 delays renal fibrosis in hereditary type IV collagen disease

Influence of VEGF Genetic Polymorphism on Peritoneal Solute Transport in Pediatric Dialysis Patients

복막 투석 중인 신증후군 환자의 복막을 통한 단백 소실

Chronic Renal Failure in Russell-Silver Syndrome

Mini-review: 멜라민에 의한 신요로계 결석

Decreased renal uptake of (99m)Tc-DMSA in patients with tubular proteinuria

Atypical hemolytic uremic syndrome associated with complement factor H autoantibodies and CFHR1/CFHR3 deficiency

Hyporeninemic hypoaldosteronism in a child with chronic kidney disease--is this condition renoprotective?

Clinico-genetic study of nail-patella syndrome

Two Korean infants with genetically confirmed congenital nephrotic syndrome of Finnish type

Cardiac dysfunction after renal transplantation incomplete resolution in pediatric population

UTI in infancy: are voiding cystourethrography and prophylactic antibiotics necessary?

Polymorphisms of the NR3C1 gene in Korean children with nephrotic syndrome

신장 이식 후의 Post-transplant Lymphoproliferative Disorder

급성 신부전을 동반한 발작 야간 혈색소뇨증 2례

신이식 후 면역반응의 이해 - 1부. 이식 거부 반응의 기전

신이식 후 면역반응의 이해 2부. 이식면역검사와 면역억제제

Urinary Tract Infection Following Voiding Cystourethrography

Prevalence of hypouricaemia and SLC22A12 mutations in healthy Korean subjects

Primary focal segmental glomerular sclerosis in children: clinical course and prognosis

Hydrogen peroxide increases human leukocyte adhesion to porcine aortic endothelial cells via NFkappaB-dependent up-regulation of VCAM-1

Clinical outcomes of childhood lupus nephritis: a single center's experience

Effects of cyclosporine on transplant tolerance: the role of IL-2

Idiopathic membranous nephropathy in children

Distinctive role of donor strain immature dendritic cells in the creation of allograft tolerance

소아 Henoch-Schonlein 신염의 예후 인자

Hereditary amyloidosis in early childhood associated with a novel insertion-deletion (indel) in the fibrinogen Aalpha chain gene

Phenotype and genotype of Dent's disease in three Korean boys

6개월 미만 영아 요로 감염의 특성과 재발의 위험 인자

Attempted treatment of factor H deficiency by liver transplantation

ATP6B1 gene mutations associated with distal renal tubular acidosis and deafness in a child

어린이의 신증후군

특발성 Takayasu's Arteritis -활동기의 치료경험 1례

소아에서 발생한 전신성 모세혈관 누출 증후군(Systemic Capillary Leak Syndrome) 1례

Reduction of plasma homocysteine by folic acid in children with chronic renal failure

일측성 요로폐쇄에 의한 실험적 신 간질 섬유화에서 Phosphodiesterase (PDE) 억제제의 항 섬유화 작용

Ifosfamide nephrotoxicity in pediatric cancer patients

우리나라 어린이 요로 감염의 치료 행태

어린이 말기 신부전 환자에서의 혈중 Homocysteine 에 관한 연구

소아 신이식 후의 키 성장에 영향을 미치는 인자들에 대한 연구

저서

저서 내용이 없습니다.

보도자료

서울 의사, 부산 환자에 전화 처방… 코로나 끝나면 원격진료 물 건너가나
https://news.chosun.com/site/data/html_dir/2020/03/06/2020030602053.html?utm_source=naver&utm_medium=original&utm_campaign=news

촌각 다투는 희귀병…현장 의견 무시하는 심사평가원
http://news.jtbc.joins.com/article/article.aspx?news_id=NB11934056

심박동기·자동복막투석기 '원격 모니터링', 막을 이유가 없다
http://news.chosun.com/site/data/html_dir/2018/09/27/2018092703641.html?utm_source=naver&utm_medium=original&utm_campaign=news

포스팅

포스팅 내용이 없습니다.

영상자료

영상자료 내용이 없습니다.

발표자료

발표자료 내용이 없습니다.