- Predictive factors for progression of chronic kidney disease in children: Results from a national cohort study
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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
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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
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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
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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
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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
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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)
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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
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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
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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
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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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