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Predictive factors for progression of chronic kidney disease in children: Results from a national cohort study
Yo Han Ahn1, Hyun Jin Choi2, Seong Heon Kim3, Kyung Hee Han4, Min Hyun Cho5, Hee Yeon Cho6, Joo Hoon Lee7, Hee Gyung Kang2, Young Seo Park7, Il-Soo Ha2
2018 ; 2018(1):
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The effect of serum uric acid on renal function
Se Won Oh, Hyunseo Kim, Ki joon Lim, Jihyun Yang, Myung-gyu Kim, Sang-Kyung Jo, Won-Yong Cho
2018 ; 2018(1):
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Low dietary fat consumption is associated with increased CKD development risk in subjects with normal renal function: Community based prospective cohort study
Young Su Joo, Jong Hyun Jhee, Ki Heon Nam, Hae-Ryoung Yoon, Sangmi Lee, Seung Hyeok Han, Tae-Hyun Yoo, Shin-Wook Kang, Jung Tak Park
2018 ; 2018(1):
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Microscopic hematuria is a risk factor of incident chronic kidney disease in the general population: a community-based prospective cohort study
Hyoungnae Kim, Ki Heon Nam, Seohyun Park, Jong Hyun Jhee, Hae-Ryong Yun, Jung Tak Park, Tae-Hyun Yoo, Shin-Wook Kang, Seung Hyeok Han
2018 ; 2018(1):
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Urinary CXCL16 and endostatin as biomarkers of tubulointerstitial fibrosis and rapid renal progression in patients with biopsy-proven advanced diabetic kidney disease
Yu Ho Lee1, Su-Woong Jung4, Young Hee Kim4, Ki Pyo Kim4, Yang Gyun Kim4, Ju-Young Moon4, Kyung-Hwan Jeong4, Young-Il Jo2, Hoon-Young Choi3, Sang-Ho Lee4
2018 ; 2018(1):
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Acquired cystic kidney disease in children and young adults undergoing dialysis
Myung Hyun Cho, Ji Hyun Kim, Hee Gyung Kang, Hae Il Cheong, Il-Soo Ha
2018 ; 2018(1):
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A novel missense mutation identified in a Korean family with X-linked Alport syndrome (AS) using next generation sequencing (NGS)
Songhee Oh1, Mi Jung Kim1, Hyoungnae Kim1, Jin Seok Jeon1, Hyunjin Noh1, Dong Cheol Han1, Jieun Kim2, So-Young Jin3, Soon Hyo Kwon1
2018 ; 2018(1):
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Genetic diagnosis of Systemic Lupus Erythematosus complicating hyper IgE syndrome
Beom Hee Lee, Joo Hoon Lee, Young Seo Park
2018 ; 2018(1):
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COMPREHENSIVE ANALYSIS FOR MUTATIONS IN A PATIENT WITH RENAL CELL CARCINOMA AND ADPKD
Kwang Eon Shim1, Jung hun Lee1, Bom Lee1, Yun kyu Oh3, Curie Ahn2, Jong woo Yoon1, Hyun suk Kim1
2018 ; 2018(1):
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The functional consequence of S148L HNF1B mutation as a cause of bilateral renal hypodysplasia with MODY5
Kyoug Hee Han1, Hee Gyung Kang2, Joo Hoon Lee3, Il-Soo Ha2, Young Seo Park3, Hae Il Cheong2
2018 ; 2018(1):
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