News

Notice more

About S-Space

SHERP

go

search

Browsing by Author Cheong, Hae Il

Jump to a point in the index
Or type in a year
Go
Or enter first few letters:

Search
  • Sort by
  • In order
  • Results/Page
  • Authors/record

Showing results 1 to 38 of 38

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

Cheong, Hae Il

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

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

link
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.

link
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.

link
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.

view filelink
2006
Nutcracker syndrome in children with gross haematuria: Doppler sonographic evaluation of the left renal vein
link
2006
Nephrotic syndrome in a child after umbilical-cord-blood transplantation
link
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.

link
2006
Idiopathic membranous nephropathy in children
link
2006
Genetics and clinical features of 15 Asian families with steroid-resistant nephrotic syndrome
link
2006
Primary focal segmental glomerular sclerosis in children:clinical course and prognosis
link
2006
Pattern of double glomerulopathy in children
link
2006
Clinical outcomes of childhood lupus nephritis: a single center's experience
link
2007
Complete factor H deficiency-associated atypical hemolytic uremic syndrome in a neonate
link
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.

link
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.

link
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.

view filelink
2008
Two Korean Infants with Genetically Confirmed Congenital Nephrotic Syndrome of Finnish Type
view filelink
2008
Renal manifestations of Dent disease and Lowe syndrome
link
2008
WT1 and NPHS2 mutations in Korean children with steroid-resistant nephrotic syndrome
link
2008
Variable phenotype of Pierson syndrome
link
2008
Atypical presentation of distal renal tubular acidosis in two siblings
link
2008
Familial focal segmental glomerulosclerosis associated with an ACTN4 mutation and paternal germline mosaicism
link
2008
Congenital thrombotic thrombocytopenic purpura associated with unilateral moyamoya disease
link
2008
Prevalence of hypouricaemia and SLC22A12 mutations in healthy Korean subjects
link
2009
Clinico-genetic study of nail-patella syndrome
view filelink
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

link
2012
Validity and reliability of the Korean version of the pediatric quality of life ESRD module
view filelink
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
view filelink
2015
Increased urinary Angiotensinogen/Creatinine (AGT/Cr) ratio may be associated with reduced renal function in autosomal dominant polycystic kidney disease patients
view filelink
2016
KNOW-Ped CKD (KoreaN cohort study for outcomes in patients with pediatric CKD): Design and methods
view filelink
2018
A familial case of Galloway-Mowat syndrome due to a novel TP53RK mutation: a case report
view filelink
2018
Three cases of multicentric carpotarsal osteolysis syndrome: a case series
view filelink
1
RSS 1.0 RSS 2.0

SNU Open Repository and Archive

Seoul National University Library, 1 Gwanak-ro, Gwanak-gu, Seoul 08826, Korea

TEL 02-880-8784 Email:s-space@snu.ac.kr

Browse

NEWS About S-Space Seoul National University Library LOGIN