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Kidney Research and Clinical Practice|March 11, 2020
Genetic tests in children with steroid-resistant nephrotic syndromeHae Il CheongKorean Journal of Pediatrics|September 22, 2015
Nephrotic syndrome: what's new, what's hot?Hee Gyung Kang, Hae Il CheongIndian Journal of Pediatrics|September 4, 2010
Differential diagnosis of hereditary nephrogenic diabetes insipidus with desmopressin infusion testZelal Bircan, Hatice Mutlu, Hae Il CheongJournal of Pediatric Endocrinology & Metabolism : JPEM|July 2, 2013
A case of SCNN1A splicing mutation presenting as mild systemic pseudohypoaldosteronism type 1Zelal Ekinci, Mehmet Baha Aytac, Hae Il CheongPediatric Nephrology (Berlin, Germany)|June 5, 2012
GLCCI1 single nucleotide polymorphisms in pediatric nephrotic syndromeHae Il Cheong, Hee Gyung Kang, Johannes SchlondorffJournal of Pediatric Endocrinology & Metabolism : JPEM|December 17, 2010
A case of antenatal Bartter syndrome with sensorineural deafnessHyun Seung Lee, Hae Il Cheong, Chang-Seok KiBiomed Research International|May 24, 2016
Recurrence and Treatment after Renal Transplantation in Children with FSGSHee Gyung Kang, Il-Soo Ha, Hae Il CheongJournal of Korean Medical Science|June 18, 2013
Translational read-through of a nonsense mutation causing Bartter syndromeHee Yeon Cho, Beom Hee Lee, Hae Il CheongKorean Journal of Pediatrics|January 19, 2012
Hypokalemic periodic paralysis; two different genes responsible for similar clinical manifestationsHunmin Kim, Hee Hwang, Hae Il Cheong, et al.Annals of Clinical and Laboratory Science|September 22, 2016
First Korean Patients with Craniofrontonasal Syndrome Confirmed by EFNB1 AnalysisHani Yoo, Jung Min Ko, Byung Chan Lim, et al.Pageof 20