<저서> 

1. 대한신장학회 당뇨병콩팥병 진료지침 (2023)

2. 대한소아신장학회 진료지침위원회 소아청소년 혈뇨의 근거 기반 진료권고안 (2023)

<논문> 

1. Woo HA, Lee H, Choi YH, Min J, Kang HG, Ahn YH, Lee HK. Clinical outcomes of nephrocalcinosis in preschool-age children: association between nephrocalcinosis improvement and long-term kidney function. Front Pediatr. 2023;11:1214704. 

2. Lee HK. CUBN mutation: a benign genetic cause of proteinuria? Child Kidney Dis. 2023;27:19-25. 

3. Kim DH, Hyun YY, Cha JJ, Lee S, Lee HK, Choi JW, Kim SH, Han SY, Park CW, Lee EY, Cha DR, Kim SG, Lim CS, Park SH. Kidney Health Plan 2033 in Korea: bridging the gap between the present and the future Kidney Res Clin Pract. 2024;43:8-19.

4. Park PG, Lim SH, Lee HK, Ahn YH, Cheong HI, Kang HG. Genotype and Phenotype Analysis in X-Linked Hypophosphatemia. Front Pediatr. 2021;9:699767.

5. Kang HG, Lee HK, Ahn YH, Joung JG, Nam J, Kim NK, Ko JM, Cho MH, Shin JI, Kim J, Park HW, Park YS, Ha IS, Chung WY, Lee DY, Kim SY, Park WY, Cheong HI. Targeted exome sequencing resolves allelic and the genetic heterogeneity in the genetic diagnosis of nephronophthisis - related ciliopathy. Exp Mol Med. 2016;48:e251.

6. Lee SE, Jung YH, Han KH, Lee HK, Kang HG, Ha IS, Choi Y, Cheong HI. A case of pseudohypoaldosteronism type 1 with a mutation in the mineralocorticoid receptor gene. Korean J Pediatr. 2011;54:90-3.

7. Lee SE, Han KH, Jung YH, Lee HK, Kang HG, Moon KC, Ha IS, Choi Y, Cheong HI. Renal transplantation in a patient with Bartter syndrome and glomerulosclerosis. Korean J Pediatr. 2011;54:36-9.

8. Lee HK, Han KH, Jung YH, Kang HG, Moon KC, Ha IS, Choi Y, Cheong HI. Variable renal phenotype in a family with an INF2 mutation. Pediatr Nephrol. 2011;26:73-6.

9. Lee HK, Han KH, Park HW, Shin JI, Kim CJ, Namgung MK, Kim KH, Koo JW, Chung WY, Lee DY, Kim SY, Cheong HI. Familial renal glucosuria: a clinicogenetic study of 23 additional cases. Pediatr Nephrol. 2012;27:1091-5.

10. Lee HK, Han KH, Lee SE, Kim SH, Kang HG, Cheong HI. Urinary exosomal WT1 in childhood nephrotic syndrome. Pediatr Nephrol. 2012;27:317-20.

11. Lee BH, Cho HY, Lee HK, Han KH, Kang HG, Ha IS, Lee JH, Park YS, Shin JI, Lee DY, Kim SY, Choi Y, Cheong HI. Genetic basis of Bartter syndrome in Korea. Nephrol Dial Transplant. 2012r;27:1516-21.

12. Choi HJ, Cho HY, Ro H, Lee SH, Han KH, Lee HK, Kang HG, Ha IS, Choi Y, Cheong HI. Polymorphisms of the MDR1 and MIF genes in children with nephrotic syndrome. Pediatr Nephrol. 2011;26:1981-8.

13. Han KH, Lee HK, Kang HG, Moon KC, Lee JH, Park YS, Ha IS, Ahn HS, Choi Y, Cheong HI. Renal manifestations of patients with MYH9-related disorders. Han KH, Lee H et al. Pediatr Nephrol. 2011;26:549-55.

14. Lee HK, Han KH, Jung YH, Kang HG, Moon KC, Ha IS, Choi Y, Cheong HI. A case of systemic amyloidosis associated with cyclic neutropenia. Pediatr Nephrol. 2011;26:625-9.