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Page 1
An infantile case of Hinman syndrome with severe acute renal failure.
Chaichanamongkol V, Ikeda M, Ishikura K, Hamasaki Y, Hataya H, Satoh H, Asanuma H, Shishido S, Honda M. Chaichanamongkol V, et al. Among authors: hamasaki y. Clin Exp Nephrol. 2008 Aug;12(4):309-311. doi: 10.1007/s10157-008-0048-3. Epub 2008 Apr 15. Clin Exp Nephrol. 2008. PMID: 18409063
Combination of pulse methylprednisolone infusions with cyclosporine-based immunosuppression is safe and effective to treat recurrent focal segmental glomerulosclerosis after pediatric kidney transplantation.
Shishido S, Satou H, Muramatsu M, Hamasaki Y, Ishikura K, Hataya H, Honda M, Asanuma H, Aikawa A. Shishido S, et al. Among authors: hamasaki y. Clin Transplant. 2013 Mar-Apr;27(2):E143-50. doi: 10.1111/ctr.12079. Epub 2013 Feb 6. Clin Transplant. 2013. PMID: 23383697 Clinical Trial.
Pre-dialysis chronic kidney disease in children: results of a nationwide survey in Japan.
Ishikura K, Uemura O, Ito S, Wada N, Hattori M, Ohashi Y, Hamasaki Y, Tanaka R, Nakanishi K, Kaneko T, Honda M; Pediatric CKD Study Group; Japan Committee of Measures for Pediatric CKD of the Japanese Society of Pediatric Nephrology. Ishikura K, et al. Among authors: hamasaki y. Nephrol Dial Transplant. 2013 Sep;28(9):2345-55. doi: 10.1093/ndt/gfs611. Epub 2013 Jul 3. Nephrol Dial Transplant. 2013. PMID: 23825101
Progression to end-stage kidney disease in Japanese children with chronic kidney disease: results of a nationwide prospective cohort study.
Ishikura K, Uemura O, Hamasaki Y, Ito S, Wada N, Hattori M, Ohashi Y, Tanaka R, Nakanishi K, Kaneko T, Honda M; Pediatric CKD Study Group in Japan; Committee of Measures for Pediatric CKD of Japanese Society of Pediatric Nephrology. Ishikura K, et al. Among authors: hamasaki y. Nephrol Dial Transplant. 2014 Apr;29(4):878-84. doi: 10.1093/ndt/gfu012. Epub 2014 Feb 9. Nephrol Dial Transplant. 2014. PMID: 24516225
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).
Yoshimura-Furuhata M, Nishimura-Tadaki A, Amano Y, Ehara T, Hamasaki Y, Muramatsu M, Shishido S, Aikawa A, Hamada R, Ishikura K, Hataya H, Hidaka Y, Noda S, Koike K, Wakui K, Fukushima Y, Matsumoto N, Awazu M, Miyake N, Kosho T. Yoshimura-Furuhata M, et al. Among authors: hamasaki y. Am J Med Genet A. 2015 Mar;167A(3):592-601. doi: 10.1002/ajmg.a.36942. Am J Med Genet A. 2015. PMID: 25691411 Review.
449 results