Genetic tests in children with steroid-resistant nephrotic syndrome

by Hae Il Cheong
Published 2020-03-01

Genetic diagnosis of Alport syndrome

by Hae Il Cheong
Published 2019-05-01

Nephrotic syndrome: what's new, what's hot?

by Hee Gyung Kang, Hae Il Cheong
Published 2015-08-01

Recurrence and Treatment after Renal Transplantation in Children with FSGS

by Hee Gyung Kang, Il-Soo Ha, Hae Il Cheong
Published 2016-01-01

Hypokalemic periodic paralysis; two different genes responsible for similar clinical manifestations

by Hunmin Kim, Hee Hwang, Hae Il Cheong, Hye Won Park
Published 2011-11-01

A novel mutation of in a Korean patient of mixed phenotype of Bartter-Gitelman syndrome

by Hee-Won Cho, Sang Taek Lee, Heeyeon Cho, Hae Il Cheong
Published 2016-11-01

Autosomal dominant hypocalcemia with Bartter syndrome due to a novel activating mutation of calcium sensing receptor, Y829C

by Keun Hee Choi, Choong Ho Shin, Sei Won Yang, Hae Il Cheong
Published 2015-04-01

Gitelman syndrome combined with complete growth hormone deficiency

by Se Ra Min, Hyun Seok Cho, Jeana Hong, Hae Il Cheong, Sung Yeon Ahn
Published 2013-03-01

Disseminated adenovirus infection in a 10-year-old renal allograft recipient

by Bora Lee, Eujin Park, Jongwon Ha, Il Soo Ha, Hae Il Cheong, Hee Gyung Kang
Published 2018-12-01

A nonsense mutation in a family with congenital aniridia

by Kyoung Hee Han, Hye Jin Lee, Il-Soo Ha, Hee Gyung Kang, Hae Il Cheong
Published 2016-11-01

Genotype and Phenotype Analysis in X-Linked Hypophosphatemia

by Peong Gang Park, Seon Hee Lim, HyunKyung Lee, Yo Han Ahn, Yo Han Ahn, Yo Han Ahn, Hae Il Cheong, Hae Il Cheong, Hee Gyung Kang, Hee Gyung Kang, Hee Gyung Kang, Hee Gyung Kang
Published 2021-08-01

Life-Threatening Extrarenal Manifestations in an Infant with Atypical Hemolytic Uremic Syndrome Caused by a Complement 3-Gene Mutation

by Sa Ra Han, Myung Hyun Cho, Jin Soo Moon, Il Soo Ha, Hae Il Cheong, Hee Gyung Kang
Published 2019-09-01

Bilateral iliac and popliteal arterial thrombosis in a child with focal segmental glomerulosclerosis

by Kyoung Hee Han, Ji Youn Park, Seung-Kee Min, Il-Soo Ha, Hae Il Cheong, Hee Gyung Kang
Published 2016-05-01

Identification and Functional Characterization of P159L Mutation in in a Family with Maturity-Onset Diabetes of the Young 5 (MODY5)

by Eun Ky Kim, Ji Seon Lee, Hae Il Cheong, Sung Soo Chung, Soo Heon Kwak, Kyong Soo Park
Published 2014-12-01

Long-term outcomes for Asian patients with X-linked hypophosphataemia: rationale and design of the SUNFLOWER longitudinal, observational cohort study

by Takuo Kubota, Seiji Fukumoto, Hae Il Cheong, Toshimi Michigami, Noriyuki Namba, Nobuaki Ito, Shin Tokunaga, Yoshimi Gibbs, Keiichi Ozono
Published 2020-06-01

Mechanism of Chronic Kidney Disease Progression and Novel Biomarkers: A Metabolomic Analysis of Experimental Glomerulonephritis

by Kyoung Hee Han, Bora Kim, Sang Chun Ji, Hee Gyung Kang, Hae Il Cheong, Joo-Youn Cho, Il-Soo Ha
Published 2020-04-01

Acute kidney injury associated with Yersinia pseudotuberculosis infection: Forgotten but not gone

by Ye Kyung Kim, Myung Hyun Cho, Hye Sun Hyun, Eujin Park, Il-Soo Ha, Hae Il Cheong, Hee Gyung Kang
Published 2019-09-01

Genotype and Phenotype Analyses in Pediatric Patients with <i>HNF1B</i> Mutations

by Seon Hee Lim, Ji Hyun Kim, Kyoung Hee Han, Yo Han Ahn, Hee Gyung Kang, Il-Soo Ha, Hae Il Cheong
Published 2020-07-01

Outcomes of chronic dialysis in Korean children with respect to survival rates and causes of death

by Hye Jin Chang, Kyoung Hee Han, Min Hyun Cho, Young Seo Park, Hee Gyung Kang, Hae Il Cheong, Il Soo Ha
Published 2014-03-01

A familial case of Blau syndrome caused by a novel genetic mutation

by Woojoong Kim, Eujin Park, Yo Han Ahn, Jiwon M. Lee, Hee Gyung Kang, Byung Joo Kim, Il-Soo Ha, Hae Il Cheong
Published 2016-11-01