Search Results - Ha, Ii-Soo

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  1. 1
    Features of Autosomal Recessive Alport Syndrome: A Systematic Review

    Features of Autosomal Recessive Alport Syndrome: A Systematic Review by Lee, Jiwon M, Nozu, Kandai, Choi, Dae Eun, Kang, Hee Gyung, Ha, Ii-Soo, Cheong, Hae Ii

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  2. 2
    Acute Kidney Injury in Pediatric Cancer Patients

    Acute Kidney Injury in Pediatric Cancer Patients by Park, Peong Gang, Hong, Che Ry, Kang, Eunjeong, Park, Minsu, Lee, Hajeong, Kang, Hyoung Jin, Shin, Hee Young, Ha, Il-Soo, Cheong, Hae Il, Yoon, Hyung Jin, Kang, Hee Gyung

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  3. 3
    Hepatorenal fibrocystic diseases in children

    Hepatorenal fibrocystic diseases in children by Park, Eujin, Lee, Jiwon M., Ahn, Yo Han, Kang, Hee Gyung, Ha, II Soo, Lee, Joo Hoon, Park, Young Seo, Kim, Nayoung K. D., Park, Woong-Yang, Cheong, Hae II

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  4. 4
    Early recurrent nephrotic syndrome after renal transplantation in children with focal segmental glomerulosclerosis

    Early recurrent nephrotic syndrome after renal transplantation in children with focal segmental glomerulosclerosis by Cheong, Hae Ii, Han, Hye Won, Park, Hye Won, Ha, Ii Soo, Han, Kyu Sup, Lee, Hyun Soon, Kim, Sang Joon, Choi, Yong

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  5. 5
    Acute kidney injury in childhood-onset nephrotic syndrome: Incidence and risk factors in hospitalized patients

    Acute kidney injury in childhood-onset nephrotic syndrome: Incidence and risk factors in hospitalized patients by Kim, Mi Young, Cho, Myung Hyun, Kim, Ji Hyun, Ahn, Yo Han, Choi, Hyun Jin, Ha, Il Soo, Il Cheong, Hae, Kang, Hee Gyung

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  6. 6
    Higher Incidence of BK Virus Nephropathy in Pediatric Kidney Allograft Recipients with Alport Syndrome

    Higher Incidence of BK Virus Nephropathy in Pediatric Kidney Allograft Recipients with Alport Syndrome by Cho, Young Hoon, Hyun, Hye Sun, Park, Eujin, Moon, Kyung Chul, Min, Sang-Il, Ha, Jongwon, Ha, Il-Soo, Cheong, Hae Il, Ahn, Yo Han, Kang, Hee Gyung

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  7. 7
    Hereditary glomerulopathy associated with a mitochondrial tRNA(Leu) gene mutation

    Hereditary glomerulopathy associated with a mitochondrial tRNA(Leu) gene mutation by Cheong, H I, Chae, J H, Kim, J S, Park, H W, Ha, I S, Hwang, Y S, Lee, H S, Choi, Y

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  8. 8
    Nephronophthisis 13: implications of its association with Caroli disease and altered intracellular localization of WDR19 in the kidney

    Nephronophthisis 13: implications of its association with Caroli disease and altered intracellular localization of WDR19 in the kidney by Lee, Jiwon M., Ahn, Yo Han, Kang, Hee Gyung, Ha, II Soo, Lee, Kyoungbun, Moon, Kyung Chul, Lee, Joo Hoon, Park, Young Seo, Cho, Yong Mee, Bae, Jun-Seok, Kim, Nayoung K. D., Park, Woong-Yang, Cheong, Hae II

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  9. 9
    A familial case of Blau syndrome caused by a novel NOD2 genetic mutation

    A familial case of Blau syndrome caused by a novel NOD2 genetic mutation by Kim, Woojoong, Park, Eujin, Ahn, Yo Han, Lee, Jiwon M, Kang, Hee Gyung, Kim, Byung Joo, Ha, Il-Soo, Cheong, Hae Il

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  10. 10
    Shiga toxin-associated hemolytic uremic syndrome complicated by intestinal perforation in a child with typical hemolytic uremic syndrome

    Shiga toxin-associated hemolytic uremic syndrome complicated by intestinal perforation in a child with typical hemolytic uremic syndrome by Chang, Hye Jin, Kim, Hwa Young, Choi, Jae Hong, Choi, Hyun Jin, Ko, Jae Sung, Ha, Il Soo, Cheong, Hae Il, Choi, Yong, Kang, Hee Gyung

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