Search

  • HOME
  • Search
Original Article
721
Expression of Phospholipase A2 Receptor in Pediatric Hepatitis B Virus-Related Membranous Nephropathy
Sung-Eun Choi, Yoon Sung Bae, Keum Hwa Lee, Jae Il Shin, Hyeon Joo Jeong, Beom Jin Lim
Child Kidney Dis. 2020;24(1):36-41.   Published online April 30, 2020
View: 4631   Download: 64
681
Interleukin-13 Increases Podocyte Apoptosis in Cultured Human Podocytes
Keum Hwa Lee, Ji Young Oh, Su-Bin Seong, Tae-Sun Ha, Jae Il Shin
Child Kidney Dis. 2018;22(1):22-27.   Published online April 27, 2018
View: 5916   Download: 50  Citation: 1
Review Article
The Role of Thymic Stromal Lymphopoietin (TSLP) in Glomerulonephritis
Keum Hwa Lee, Jae Won Yang, Jin Young Cho, Joo Yup Lee, Eun Kyung Lim, Michael Eisenhut, Dong Yeon Jeong, Johanna Steingroever, Jae Il Shin
Child Kidney Dis. 2018;22(1):17-21.   Published online April 27, 2018
View: 6419   Download: 102
Case Report
A Successfully Treated Case of Recurrent Focal Segmental Glomerulosclerosis (FSGS) with Plasmapheresis and High dose Methylprednisolone Pulse Therapy
Sun Mi Her, Keum Hwa Lee, Jae Il Shin
Child Kidney Dis. 2017;21(2):165-168.   Published online October 30, 2017
View: 6593   Download: 120
Original Article
Therapeutic Plasma Exchange in Pediatric Kidney Disease: 23-year Experience at the Severance Children’s Hospital in Korea
Sun Mi Her, Keum Hwa Lee, Ji Hong Kim, Jae Seung Lee, Pyung Kil Kim, Jae Il Shin
Child Kidney Dis. 2017;21(2):81-88.   Published online October 30, 2017
View: 6509   Download: 153  Citation: 1
1 |

Childhood
Kidney Diseases

Print ISSN: 2384-0242
Online ISSN: 2384-0250

  • Instructions for Authors
  • MOST READ (Last two years)
    Viewed By
    3309
    Risk Factors for the Progression of Chronic Kidney Disease in Children
    Viewed By
    3030
    Clinical Genetic Testing in Children with Kidney Disease
    Viewed By
    2684
    A Case of Idiopathic Renal Hypouricemia with SLC22A12 Gene Mutation Showing General Weakness and Incidental Renal Stone
    Viewed By
    2597
    Pediatric Kidney Transplantation
    Viewed By
    2482
    A Novel Homozygous CLCNKB Mutation of Classic Bartter Syndrome Presenting with Renal Cysts in 6-year-Old Identical Twin Boys : A Case Report

    +more

    MOST CITED (2021-2023)

    +more

  • Manuscript Submission
    To submit a manuscript, please visit the Child Kidney Dis e-submission management system at esubmit, read the Instructions for Authors, and log into the Child Kidney Dis e-submission system. For assistance with manuscript submission, please contact: chikd@chikd.org.
  • Free archive
    Anyone may access any past or current articles without logging in.

Editorial Office
240, Gimpohangang 1-ro, Gimpo-si, Gyeonggi-do, 10078, Republic of Korea
TEL: +82-10-4391-0788   E-mail: chikd@chikd.org
Copyright© Korean Society of Pediatric Nephrology.         
Close layer