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H I Cheong

Showing results (11-20 of 29) with videos related to

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Journal of Nephrology|August 17, 2001
Circulating VEGF and TGF-beta1 in children with idiopathic nephrotic syndromeH I Cheong, J H Lee, H Hahn, et al.
Nephron|September 6, 2000
Association of angiotensin I converting enzyme gene polymorphism with reflux nephropathy in childrenH W Park, J W Koo, J S Kim, et al.
Nephron. Experimental Nephrology|February 27, 2010
Transcriptome analysis of the response of cultured murine podocytes to puromycin aminonucleosideH G Kang, K H Paik, H Y Cho, et al.
Pediatric Nephrology (Berlin, Germany)|October 1, 1987
Childhood renal diseases in Korea. A clinicopathological study of 657 casesK W Ko, I S Ha, D K Jin, et al.
Nephron|January 1, 1997
Six novel mutations in the vasopressin V2 receptor gene causing nephrogenic diabetes insipidusH I Cheong, H W Park, I S Ha, et al.
The Journal of Pediatrics|August 1, 1997
Renovascular hypertension in children with moyamoya diseaseY Choi, B C Kang, K J Kim, et al.
Pediatric Transplantation|May 1, 2001
Recurrent focal segmental glomerulosclerosis following renal transplantation in Korean pediatric patientsS J Kim, J Ha, I M Jung, et al.
Transplantation Proceedings|March 20, 1999
Focal segmental glomerulosclerosis progression to end-stage renal disease within 48 months is a risk factor for recurrence after pediatric renal transplantationS J Kim, M Kim, J Ha, et al.
Journal of Korean Medical Science|August 1, 1997
Molecular analysis of hypoxanthine guanine phosphoribosyltransferase (HPRT) gene in five Korean families with Lesch-Nyhan syndromeK J Kim, Y Yamada, K Suzumori, et al.
Pediatric Nephrology (Berlin, Germany)|August 19, 1999
Hereditary glomerulopathy associated with a mitochondrial tRNA(Leu) gene mutationH I Cheong, J H Chae, J S Kim, et al.
Pageof 3

Showing results (11-20 of 29) with videos related to

Sort By:
Pageof 3
Journal of Nephrology|August 17, 2001
Circulating VEGF and TGF-beta1 in children with idiopathic nephrotic syndromeH I Cheong, J H Lee, H Hahn, et al.
Nephron|September 6, 2000
Association of angiotensin I converting enzyme gene polymorphism with reflux nephropathy in childrenH W Park, J W Koo, J S Kim, et al.
Nephron. Experimental Nephrology|February 27, 2010
Transcriptome analysis of the response of cultured murine podocytes to puromycin aminonucleosideH G Kang, K H Paik, H Y Cho, et al.
Pediatric Nephrology (Berlin, Germany)|October 1, 1987
Childhood renal diseases in Korea. A clinicopathological study of 657 casesK W Ko, I S Ha, D K Jin, et al.
Nephron|January 1, 1997
Six novel mutations in the vasopressin V2 receptor gene causing nephrogenic diabetes insipidusH I Cheong, H W Park, I S Ha, et al.
The Journal of Pediatrics|August 1, 1997
Renovascular hypertension in children with moyamoya diseaseY Choi, B C Kang, K J Kim, et al.
Pediatric Transplantation|May 1, 2001
Recurrent focal segmental glomerulosclerosis following renal transplantation in Korean pediatric patientsS J Kim, J Ha, I M Jung, et al.
Transplantation Proceedings|March 20, 1999
Focal segmental glomerulosclerosis progression to end-stage renal disease within 48 months is a risk factor for recurrence after pediatric renal transplantationS J Kim, M Kim, J Ha, et al.
Journal of Korean Medical Science|August 1, 1997
Molecular analysis of hypoxanthine guanine phosphoribosyltransferase (HPRT) gene in five Korean families with Lesch-Nyhan syndromeK J Kim, Y Yamada, K Suzumori, et al.
Pediatric Nephrology (Berlin, Germany)|August 19, 1999
Hereditary glomerulopathy associated with a mitochondrial tRNA(Leu) gene mutationH I Cheong, J H Chae, J S Kim, et al.
Pageof 3