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Showing results 1 to 18 of 18

Issue Date	Title / Author(s) / Citation	File	Altmetrics
2002	Reduction of plasma homocysteine by folic acid in children with chronic renal failure Kang, Hee Gyung; Lee, Byong Sop; Hahn, Hyewon; Lee, Jun Ho; Ha, Il Soo; Cheong, Hae Il; Choi, Yong Pediatr Nephrol 17:511-514	link
2005-02	Phenotype and genotype of Dent's disease in three Korean boys Cheong, Hae Il; Lee, Jung Won; Zheng, Shou Huan; Lee, Joo Hoon; Kang, Ju Hyung; Kang, Hee Gyung; Ha, Il Soo; Lee, Seung Joo; Choi, Yong Pediatr Nephrol. 2005 Apr;20(4):455-9. Epub 2005 Feb 18.	link
2005-05	Mutational analysis of idiopathic renal hypouricemia in Korea Cheong, Hae Il; Kang, Ju Hyung; Lee, Joo Hoon; Ha, Il Soo; Kim, Suhnggwon; Komoda, Fusako; Sekine, Takashi; Igarashi, Takashi; Choi, Yong Pediatr Nephrol. 2005 Jul;20(7):886-90. Epub 2005 May 24.	link
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.	view file link
2006-09	Genetics and clinical features of 15 Asian families with steroid-resistant nephrotic syndrome Kitamura, Akiko; Tsukaguchi, Hiroyasu; Iijima, Kazumoto; Araki, Jungo; Hattori, Motoshi; Ikeda, Masahiro; Honda, Masataka; Nozu, Kandai; Nakazato, Hitoshi; Yoshikawa, Norishige; Kagami, Shoji; Muramatsu, Masaaki; Choi, Yong; Cheong, Hae Il; Doi, Toshio Nephrol Dial Transplant. 2006 Nov;21(11):3133-8. Epub 2006 Sep 12.	link
2006-11	Clinical outcomes of childhood lupus nephritis: a single center's experience Lee, Byong Sop; Cho, Hee Yeon; Kim, Eo Jin; Kang, Hee Gyung; Ha, Il Soo; Cheong, Hae Il; Kim, Joong Gon; Lee, Hyun Soon; Choi, Yong Pediatr Nephrol. 2007 Feb;22(2):222-31. Epub 2006 Nov 28.	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.	view file link
2008	Renal manifestations of Dent disease and Lowe syndrome Cho, Hee Yeon; Lee, Bum Hee; Choi, Hyun Jin; Ha, Il Soo; Choi, Yong; Cheong, Hae Il Pediatr Nephrol 23:243-249	link
2008	WT1 and NPHS2 mutations in Korean children with steroid-resistant nephrotic syndrome Cho, Hee Yeon; Lee, Joo Hoon; Choi, Hyun Jin; Lee, Bum Hee; Ha, Il Soo; Choi, Yong; Cheong, Hae Il Pediatr Nephrol 23:63-70	link
2008-04	Atypical presentation of distal renal tubular acidosis in two siblings Tasic, Velibor; Korneti, Petar; Gucev, Zoran; Hoppe, Bernd; Blau, Nenad; Cheong, Hae Il Pediatr Nephrol. 23(7):1177-1181	link
2008-11	Prevalence of hypouricaemia and SLC22A12 mutations in healthy Korean subjects Lee, Joo Hoon; Choi, Hyun Jin; Lee, Beom Hee; Kang, Hee Kyung; Chin, Ho Jun; Yoon, Hyung Jin; Ha, Il Soo; Kim, Suhnggwon; Choi, Yong; Cheong, Hae Il Nephrology (Carlton). 2008; 13(8): 661-666	link
2009-09	Atypical Hemolytic Uremic Syndrome Associated With Complement Factor H Autoantibodies and CFHR1/CFHR3 Deficiency Lee, Beom Hee; Kwak, Soo Heon; Shin, Jae Il; Lee, So Hee; Kang, Hee Gyung; Lee, Jae Seung; Choi, Yong; Cheong, Hae Il; Dragon-Durey, Marie-Agnes; Ha, Il Soo; Choi, Hyun Jin PEDIATRIC RESEARCH; Vol.66 3; 336-340
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
2018-07	A familial case of Galloway-Mowat syndrome due to a novel TP53RK mutation: a case report Hyun, Hye Sun; Kim, Seong Heon; Park, Eujin; Cho, Myung Hyun; Kang, Hee Gyung; Lee, Hyun Soon; Miyake, Noriko; Matsumoto, Naomichi; Tsukaguchi, Hiroyasu; Cheong, Hae Il BMC Medical Genetics, 19(1):131	view file DOI
2018-09	Three cases of multicentric carpotarsal osteolysis syndrome: a case series Park, Peong Gang; Kim, Kee Hyuck; Hyun, Hye Sun; Lee, Chan Hee; Park, Jin-Su; Kie, Jeong Hae; Choi, Young Hun; Moon, Kyung Chul; Cheong, Hae Il BMC Medical Genetics, 19(1):164	view file DOI

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