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Diversity of renal phenotypes in patients with <i>WDR19</i> mutations: Two case reportsTakahisa Yoshikawa, Kenji Ishikura, Seiichiro Shishido et al.|Nephrology|2017Cited by 16
Renal complications in 6p duplication syndrome: Microarray‐based investigation of the candidate gene(s) for the development of congenital anomalies of the kidney and urinary tract (CAKUT) and focal segmental glomerular sclerosis (FSGS)Megumi Yoshimura‐Furuhata, Tomoki Kosho, Akira Nishimura‐Tadaki et al.|American Journal of Medical Genetics Part A|2015Cited by 15
Long-term outcome of congenital nephrotic syndrome after kidney transplantation in JapanYuko Hamasaki, Seiichiro Shishido, Masaki Muramatsu et al.|Clinical and Experimental Nephrology|2017Cited by 12
Long‐term outcomes of pediatric kidney transplantation: A single‐center experience over the past 34 years in JapanYujiro Aoki, Seiichiro Shishido, Yuko Hamasaki et al.|International Journal of Urology|2019Cited by 12