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Browsing by Author Cheong, Hae Il

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Showing results 1 to 38 of 38

Issue Date Title / Author(s) / CitationFile
1994
The Pathogenetic Role of Reactive Oxygen Species in Aminonucleoside Nephrosis
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1994
A Molecular Genetic Study of X-Linked Nephrogenic Diabetes lnspidus

Cheong, Hae Il

Seoul J Med 1994;35(2):99-103

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2002
Reduction of plasma homocysteine by folic acid in children with chronic renal failure
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2005
Phenotype and genotype of Dent's disease in three Korean boys
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2005
Mutational analysis of idiopathic renal hypouricemia in Korea
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2005
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.

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2005
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.

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2005
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.

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2006
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
Nutcracker syndrome in children with gross haematuria: Doppler sonographic evaluation of the left renal vein
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2006
Nephrotic syndrome in a child after umbilical-cord-blood transplantation
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2006
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
Idiopathic membranous nephropathy in children
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2006
Genetics and clinical features of 15 Asian families with steroid-resistant nephrotic syndrome
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2006
Primary focal segmental glomerular sclerosis in children:clinical course and prognosis
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2006
Pattern of double glomerulopathy in children
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2006
Clinical outcomes of childhood lupus nephritis: a single center's experience
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2007
Complete factor H deficiency-associated atypical hemolytic uremic syndrome in a neonate
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2007
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.

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2007
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.

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2007
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
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
Renal manifestations of Dent disease and Lowe syndrome
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2008
Variable phenotype of Pierson syndrome
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2008
Atypical presentation of distal renal tubular acidosis in two siblings
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2008
Familial focal segmental glomerulosclerosis associated with an ACTN4 mutation and paternal germline mosaicism
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2008
Congenital thrombotic thrombocytopenic purpura associated with unilateral moyamoya disease
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2008
Prevalence of hypouricaemia and SLC22A12 mutations in healthy Korean subjects
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2009
Clinico-genetic study of nail-patella syndrome
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2009
Atypical Hemolytic Uremic Syndrome Associated With Complement Factor H Autoantibodies and CFHR1/CFHR3 Deficiency
2010
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

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2012
Validity and reliability of the Korean version of the pediatric quality of life ESRD module
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2012
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
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
KNOW-Ped CKD (KoreaN cohort study for outcomes in patients with pediatric CKD): Design and methods
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2018
A familial case of Galloway-Mowat syndrome due to a novel TP53RK mutation: a case report
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2018
Three cases of multicentric carpotarsal osteolysis syndrome: a case series
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