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Showing results 1 to 41 of 41

Issue Date Title / Author(s) / CitationFileAltmetrics
1994-06
The Pathogenetic Role of Reactive Oxygen Species in Aminonucleoside Nephrosis

Cheong, Hae Il; Choi, Yong; Ko, Kwang Wook; Shin, Mi Ja; Kim, Myung-suk

Seoul J Med, Vol.35 No.2, pp. 105-111

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1994-06
A Molecular Genetic Study of X-Linked Nephrogenic Diabetes lnspidus

Cheong, Hae Il

Seoul J Med, Vol.35 No.2, pp. 99-103

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2002
Reduction of plasma homocysteine by folic acid in children with chronic renal failure
link
2005-02
Phenotype and genotype of Dent's disease in three Korean boys
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2005-05
Mutational analysis of idiopathic renal hypouricemia in Korea
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2005-07
Familial hypomagnesemia with hypercalciuria and nephrocalcinosis associated with CLDN16 mutations

Kang, Ju Hyung; Choi, Hyun Jin; Cho, Hee Yeon; Lee, Joo Hoon; Ha, Il Soo; Cheong, Hae Il; Choi, Yong

Pediatr Nephrol. 2005 Oct;20(10):1490-3. Epub 2005 Jul 27.

link
2005-10
Unilateral renal angiodysplasia in a girl with hypertension

Choi, Yong; Nagata, Michio; Kang, Ju Hyung; Lee, In Sil; Ha, Il Soo; Kim, In One; Cheong, Hae Il

Pediatr Nephrol. 2006 Feb;21(2):292-4. Epub 2005 Oct 27.

link
2005-12
A case of atypical hemolytic uremic syndrome with a transient decrease in complement factor H

Hahn, Hyewon; Um, Eun Young; Park, Young Seo; Cheong, Hae Il

Pediatr Nephrol. 2006 Feb;21(2):295-8. Epub 2005 Dec 17.

link
2006-02
Two cases of isolated diffuse mesangial sclerosis with WT1 mutations

Hahn, Hyewon; Cho, Young Mi; Park, Young Seo; You, Han Wook; Cheong, Hae Il

J Korean Med Sci. 2006 Feb;21(1):160-4.

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2006-04
Nutcracker syndrome in children with gross haematuria: Doppler sonographic evaluation of the left renal vein
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2006-06
Nephrotic syndrome in a child after umbilical-cord-blood transplantation
DOI
2006-08
Hydrothorax in a patient with Denys-Drash syndrome associated with a diaphragmatic defect

Cho, Hee Yeon; Lee, Byong Sop; Kang, Chang Hyun; Kim, Woong-Han; Ha, Il Soo; Cheong, Hae Il; Choi, Young

Pediatr Nephrol. 2006 Dec;21(12):1909-12. Epub 2006 Aug 25.

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2006-09
Idiopathic membranous nephropathy in children
DOI
2006-09
Genetics and clinical features of 15 Asian families with steroid-resistant nephrotic syndrome
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2006-10
Primary focal segmental glomerular sclerosis in children:clinical course and prognosis
DOI
2006-11
Pattern of double glomerulopathy in children
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2006-11
Clinical outcomes of childhood lupus nephritis: a single center's experience
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2007-02
Complete factor H deficiency-associated atypical hemolytic uremic syndrome in a neonate
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2007-03
Molecular genetic study of congenital nephrogenic diabetes insipidus and rescue of mutant vasopressin V2 receptor by chemical chaperones

Cheong, Hae Il; Cho, Hee Yeon; Park, Hye Won; Ha, Il Soo; Choi, Yong

Nephrology (Carlton). 2007 Apr;12(2):113-7.

link
2007-06
A clinico-genetic study of renal coloboma syndrome in children

Cheong, Hae Il; Cho, Hee Yeon; Kim, Jeong Hun; Yu, Young Suk; Ha, Il Soo; Choi, Yong

Pediatr Nephrol. 2007 Sep;22(9):1283-9. Epub 2007 May 31.

link
2007-11
Proteinuria in a boy with infectious mononucleosis, C1q nephropathy, and Dent's disease

Lim, In Seok; Yun, Ki Wook; Moon, Kyung Chul; Cheong, Hae Il

J Korean Med Sci. 2007 Oct;22(5):928-31.

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2008
Renal manifestations of Dent disease and Lowe syndrome
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2008
WT1 and NPHS2 mutations in Korean children with steroid-resistant nephrotic syndrome
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2008
Two Korean Infants with Genetically Confirmed Congenital Nephrotic Syndrome of Finnish Type
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2008-02
Variable phenotype of Pierson syndrome
DOI
2008-04
Atypical presentation of distal renal tubular acidosis in two siblings
link
2008-04
Familial focal segmental glomerulosclerosis associated with an ACTN4 mutation and paternal germline mosaicism
DOI
2008-05
Congenital thrombotic thrombocytopenic purpura associated with unilateral moyamoya disease
DOI
2008-11
Prevalence of hypouricaemia and SLC22A12 mutations in healthy Korean subjects
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2009-02
Clinico-genetic study of nail-patella syndrome
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2009-09
Atypical Hemolytic Uremic Syndrome Associated With Complement Factor H Autoantibodies and CFHR1/CFHR3 Deficiency
2010-05
A single large-scale deletion of mtDNA in a child with recurrent encephalopathy and tubulopathy

Chae, Jong-Hee; Lim, Byung Chan; Cheong, Hae Il; Hwang, Yong Seung; Hwang, Hee; Kim, Ki Joong

JOURNAL OF THE NEUROLOGICAL SCIENCES; Vol.292 01월 02일; 104-106

DOI
2012-06
Validity and reliability of the Korean version of the pediatric quality of life ESRD module
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2012-08
Urinary N-acetyl-ß-D Glucosaminidase as a Surrogate Marker for Renal Function in Autosomal Dominant Polycystic Kidney Disease : 1 year Prospective Cohort Study
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2015-06
Increased urinary Angiotensinogen/Creatinine (AGT/Cr) ratio may be associated with reduced renal function in autosomal dominant polycystic kidney disease patients
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2016-03
KNOW-Ped CKD (KoreaN cohort study for outcomes in patients with pediatric CKD): Design and methods
view fileDOI
2018-07
A familial case of Galloway-Mowat syndrome due to a novel TP53RK mutation: a case report
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2018-09
Three cases of multicentric carpotarsal osteolysis syndrome: a case series
view fileDOI
2022
Burden of disease of X hiked hypophosphatemia in Japanese and Korean patients: a cross-sectional survey
DOI
2022-08
Effect of Burosumab Compared With Conventional Therapy on Younger vs Older Children With X-linked Hypophosphatemia
DOI
2022-10
Efficacy of Burosumab in Adults with X-linked Hypophosphatemia (XLH): A Post Hoc Subgroup Analysis of a Randomized Double-Blind Placebo-Controlled Phase 3 Study
DOI
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