Showing results (51-60 of 198) with videos related to
Sort By:
Pageof 20
Genomics & Informatics|February 24, 2015
Identification and Functional Characterization of P159L Mutation in HNF1B in a Family with Maturity-Onset Diabetes of the Young 5 (MODY5)Eun Ky Kim, Ji Seon Lee, Hae Il Cheong, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|September 4, 2021
Gordon syndrome caused by a <i>CUL3</i> mutation in a patient with short stature in Korea: a case reportJi Hong Park, Ji Hyun Kim, Yo Han Ahn, et al.Pediatric Nephrology (Berlin, Germany)|August 13, 2002
Reduction of plasma homocysteine by folic acid in children with chronic renal failureHee Gyung Kang, Byong Sop Lee, Hyewon Hahn, et al.Pediatric Nephrology (Berlin, Germany)|May 17, 2003
Acute leukemia: an association with atypical hemolytic uremic syndromeHyewon Hahn, Il Soo Ha, Hyoung Soo Choi, et al.Pediatric Nephrology (Berlin, Germany)|February 27, 2004
Attempted treatment of factor H deficiency by liver transplantationHae Il Cheong, Byong Sop Lee, Hee-Gyung Kang, et al.BMJ Open|July 1, 2020
Long-term outcomes for Asian patients with X-linked hypophosphataemia: rationale and design of the SUNFLOWER longitudinal, observational cohort studyTakuo Kubota, Seiji Fukumoto, Hae Il Cheong, et al.Healthcare Informatics Research|January 25, 2013
Development of korean rare disease knowledge baseHeewon Seo, Dokyoon Kim, Jong-Hee Chae, et al.Pediatric Nephrology (Berlin, Germany)|October 28, 2005
Unilateral renal angiodysplasia in a girl with hypertensionYong Choi, Michio Nagata, Ju Hyung Kang, et al.Pediatric Nephrology (Berlin, Germany)|August 26, 2006
Hydrothorax in a patient with Denys-Drash syndrome associated with a diaphragmatic defectHee Yeon Cho, Byong Sop Lee, Chang Hyun Kang, et al.Pediatric Nephrology (Berlin, Germany)|October 16, 2007
WT1 and NPHS2 mutations in Korean children with steroid-resistant nephrotic syndromeHee Yeon Cho, Joo Hoon Lee, Hyun Jin Choi, et al.Pageof 20