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Clinical features of autosomal recessive polycystic kidney disease in the Japanese population and analysis of splicing in PKHD1 gene for determination of phenotypes.
Ishiko S, Morisada N, Kondo A, Nagai S, Aoto Y, Okada E, Rossanti R, Sakakibara N, Nagano C, Horinouchi T, Yamamura T, Ninchoji T, Kaito H, Hamada R, Shima Y, Nakanishi K, Matsuo M, Iijima K, Nozu K. Ishiko S, et al. Among authors: kondo a. Clin Exp Nephrol. 2022 Feb;26(2):140-153. doi: 10.1007/s10157-021-02135-3. Epub 2021 Sep 18. Clin Exp Nephrol. 2022. PMID: 34536170 Free PMC article.
Glomerular galactose-deficient IgA1 expression analysis in pediatric patients with glomerular diseases.
Ishiko S, Horinouchi T, Fujimaru R, Shima Y, Kaito H, Tanaka R, Ishimori S, Kondo A, Nagai S, Aoto Y, Sakakibara N, Nagano C, Yamamura T, Yoshimura M, Nakanishi K, Fujimura J, Kamiyoshi N, Nagase H, Yoshikawa N, Iijima K, Nozu K. Ishiko S, et al. Among authors: kondo a. Sci Rep. 2020 Aug 20;10(1):14026. doi: 10.1038/s41598-020-71101-y. Sci Rep. 2020. PMID: 32820208 Free PMC article.
Use of renin-angiotensin system inhibitors as initial therapy in children with Henoch-Schönlein purpura nephritis of moderate severity.
Nagai S, Horinouchi T, Ninchoji T, Kondo A, Aoto Y, Ishiko S, Sakakibara N, Nagano C, Yamamura T, Kaito H, Tanaka R, Shima Y, Fujimura J, Kamiyoshi N, Ishimori S, Nakanishi K, Yoshikawa N, Iijima K, Nozu K. Nagai S, et al. Among authors: kondo a. Pediatr Nephrol. 2022 Aug;37(8):1845-1853. doi: 10.1007/s00467-021-05395-z. Epub 2022 Jan 11. Pediatr Nephrol. 2022. PMID: 35015121
2,106 results