Lee BH - Search Results

1

Diagnostic yield and clinical utility of whole exome sequencing using an automated variant prioritization system, EVIDENCE.

Seo GH, Kim T, Choi IH, Park JY, Lee J, Kim S, Won DG, Oh A, Lee Y, Choi J, Lee H, Kang HG, Cho HY, Cho MH, Kim YJ, Yoon YH, Eun BL, Desnick RJ, Keum C, Lee BH. Seo GH, et al. Among authors: lee bh, lee y, lee h, lee j. Clin Genet. 2020 Dec;98(6):562-570. doi: 10.1111/cge.13848. Epub 2020 Sep 17. Clin Genet. 2020. PMID: 32901917 Free PMC article.

2

Idiopathic membranous nephropathy in children.

Lee BH, Cho HY, Kang HG, Ha IS, Cheong HI, Moon KC, Lim IS, Choi Y. Lee BH, et al. Pediatr Nephrol. 2006 Nov;21(11):1707-15. doi: 10.1007/s00467-006-0246-8. Epub 2006 Sep 2. Pediatr Nephrol. 2006. PMID: 16951933

3

Familial focal segmental glomerulosclerosis associated with an ACTN4 mutation and paternal germline mosaicism.

Choi HJ, Lee BH, Cho HY, Moon KC, Ha IS, Nagata M, Choi Y, Cheong HI. Choi HJ, et al. Among authors: lee bh. Am J Kidney Dis. 2008 May;51(5):834-8. doi: 10.1053/j.ajkd.2008.01.018. Am J Kidney Dis. 2008. PMID: 18436095

4

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

Lee BH, Kang HG, Choi Y. Lee BH, et al. Pediatr Nephrol. 2009 Sep;24(9):1771-2. doi: 10.1007/s00467-009-1121-1. Epub 2009 Feb 3. Pediatr Nephrol. 2009. PMID: 19189133 No abstract available.

5

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

Kang HG, Lee BH, Choi Y. Kang HG, et al. Among authors: lee bh. Pediatr Nephrol. 2009 Aug;24(8):1599-601. doi: 10.1007/s00467-009-1131-z. Epub 2009 Feb 10. Pediatr Nephrol. 2009. PMID: 19205750 No abstract available.

6

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

Lee BH, Kwak SH, Shin JI, Lee SH, Choi HJ, Kang HG, Ha IS, Lee JS, Dragon-Durey MA, Choi Y, Cheong HI. Lee BH, et al. Among authors: lee sh, lee js. Pediatr Res. 2009 Sep;66(3):336-40. doi: 10.1203/PDR.0b013e3181b1bd4a. Pediatr Res. 2009. PMID: 19531976

7

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

Lee BH, Lee SH, Choi HJ, Kang HG, Oh SW, Lee DS, Ha IS, Choi Y, Cheong HI. Lee BH, et al. Among authors: lee sh, lee ds. Pediatr Nephrol. 2009 Nov;24(11):2211-6. doi: 10.1007/s00467-009-1238-2. Epub 2009 Jul 5. Pediatr Nephrol. 2009. PMID: 19579036

8

Mutations of the GLA gene in Korean patients with Fabry disease and frequency of the E66Q allele as a functional variant in Korean newborns.

Lee BH, Heo SH, Kim GH, Park JY, Kim WS, Kang DH, Choe KH, Kim WH, Yang SH, Yoo HW. Lee BH, et al. J Hum Genet. 2010 Aug;55(8):512-7. doi: 10.1038/jhg.2010.58. Epub 2010 May 27. J Hum Genet. 2010. PMID: 20505683

9

Proteomic analysis of sera of asymptomatic, early-stage patients with Wilson's disease.

Park JY, Mun JH, Lee BH, Heo SH, Kim GH, Yoo HW. Park JY, et al. Among authors: lee bh. Proteomics Clin Appl. 2009 Oct;3(10):1185-1190. doi: 10.1002/prca.200800057. Proteomics Clin Appl. 2009. PMID: 20556197 Free PMC article.

10

Clinical and functional characteristics of a novel heterozygous mutation of the IGF1R gene and IGF1R haploinsufficiency due to terminal 15q26.2->qter deletion in patients with intrauterine growth retardation and postnatal catch-up growth failure.

Choi JH, Kang M, Kim GH, Hong M, Jin HY, Lee BH, Park JY, Lee SM, Seo EJ, Yoo HW. Choi JH, et al. Among authors: lee bh, lee sm. J Clin Endocrinol Metab. 2011 Jan;96(1):E130-4. doi: 10.1210/jc.2010-1789. Epub 2010 Oct 20. J Clin Endocrinol Metab. 2011. PMID: 20962017

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