Ahn YH - Search Results

1

Corrigendum: Long-term outcome of Bartter syndrome in 54 patients: a multicenter study in Korea.

Choi N, Kim SH, Bae EH, Yang EM, Lee KH, Lee SH, Lee JH, Ahn YH, Cheong HI, Kang HG, Hyun HS, Kim JH. Choi N, et al. Among authors: ahn yh. Front Med (Lausanne). 2023 May 31;10:1225353. doi: 10.3389/fmed.2023.1225353. eCollection 2023. Front Med (Lausanne). 2023. PMID: 37324139 Free PMC article.

2

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

Lee BH, Ahn YH, Choi HJ, Kang HK, Kim SD, Cho BS, Moon KC, Ha IS, Cheong HI, Choi Y. Lee BH, et al. Among authors: ahn yh. J Korean Med Sci. 2009 Jan;24 Suppl(Suppl 1):S210-4. doi: 10.3346/jkms.2009.24.S1.S210. Epub 2009 Jan 28. J Korean Med Sci. 2009. PMID: 19194555 Free PMC article.

3

Tumour lysis syndrome in children: experience of last decade.

Ahn YH, Kang HJ, Shin HY, Ahn HS, Choi Y, Kang HG. Ahn YH, et al. Among authors: ahn hs. Hematol Oncol. 2011 Dec;29(4):196-201. doi: 10.1002/hon.995. Epub 2011 Jun 24. Hematol Oncol. 2011. PMID: 21710502

4

Development of antirituximab antibodies in children with nephrotic syndrome.

Ahn YH, Kang HG, Lee JM, Choi HJ, Ha IS, Cheong HI. Ahn YH, et al. Pediatr Nephrol. 2014 Aug;29(8):1461-4. doi: 10.1007/s00467-014-2794-7. Epub 2014 Mar 12. Pediatr Nephrol. 2014. PMID: 24619426

5

Muscle involvement in Dent disease 2.

Park E, Choi HJ, Lee JM, Ahn YH, Kang HG, Choi YM, Park SJ, Cho HY, Park YH, Lee SJ, Ha IS, Cheong HI. Park E, et al. Among authors: ahn yh. Pediatr Nephrol. 2014 Nov;29(11):2127-32. doi: 10.1007/s00467-014-2841-4. Epub 2014 Jun 7. Pediatr Nephrol. 2014. PMID: 24912603

6

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

Kang HG, Ahn YH, Kim JH, Ha IS, Yu YS, Park YH, Cheong HI. Kang HG, et al. Among authors: ahn yh. Clin Exp Ophthalmol. 2015 Jul;43(5):437-42. doi: 10.1111/ceo.12469. Epub 2015 Jan 14. Clin Exp Ophthalmol. 2015. PMID: 25401970

7

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

Lee JM, Ahn YH, Kang HG, Ha II, Lee K, Moon KC, Lee JH, Park YS, Cho YM, Bae JS, Kim NK, Park WY, Cheong HI. Lee JM, et al. Among authors: ahn yh. Pediatr Nephrol. 2015 Sep;30(9):1451-8. doi: 10.1007/s00467-015-3068-8. Epub 2015 Mar 1. Pediatr Nephrol. 2015. PMID: 25726036

8

Hepatorenal fibrocystic diseases in children.

Park E, Lee JM, Ahn YH, Kang HG, Ha II, Lee JH, Park YS, Kim NK, Park WY, Cheong HI. Park E, et al. Among authors: ahn yh. Pediatr Nephrol. 2016 Jan;31(1):113-9. doi: 10.1007/s00467-015-3185-4. Epub 2015 Aug 11. Pediatr Nephrol. 2016. PMID: 26260382

9

NUP107 mutations in children with steroid-resistant nephrotic syndrome.

Park E, Ahn YH, Kang HG, Miyake N, Tsukaguchi H, Cheong HI. Park E, et al. Among authors: ahn yh. Nephrol Dial Transplant. 2017 Jun 1;32(6):1013-1017. doi: 10.1093/ndt/gfw103. Nephrol Dial Transplant. 2017. PMID: 27190346

10

Genotype-phenotype analysis of pediatric patients with WT1 glomerulopathy.

Ahn YH, Park EJ, Kang HG, Kim SH, Cho HY, Shin JI, Lee JH, Park YS, Kim KS, Ha IS, Cheong HI. Ahn YH, et al. Pediatr Nephrol. 2017 Jan;32(1):81-89. doi: 10.1007/s00467-016-3395-4. Epub 2016 Jun 14. Pediatr Nephrol. 2017. PMID: 27300205

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