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Deletion in the Cobalamin Synthetase W Domain-Containing Protein 1 Gene Is associated with Congenital Anomalies of the Kidney and Urinary Tract.
Kanda S, Ohmuraya M, Akagawa H, Horita S, Yoshida Y, Kaneko N, Sugawara N, Ishizuka K, Miura K, Harita Y, Yamamoto T, Oka A, Araki K, Furukawa T, Hattori M. Kanda S, et al. Among authors: hattori m. J Am Soc Nephrol. 2020 Jan;31(1):139-147. doi: 10.1681/ASN.2019040398. Epub 2019 Dec 20. J Am Soc Nephrol. 2020. PMID: 31862704 Free PMC article.
Clinical features and mutational survey of NPHS2 (podocin) in Japanese children with focal segmental glomerulosclerosis who underwent renal transplantation.
Furue T, Hattori M, Tsukaguchi H, Kitamura A, Oomori T, Ogino D, Nakakura H, Ashida A, Miura K, Hisano M, Takahashi K, Chikamoto H, Akioka Y, Sakano T. Furue T, et al. Among authors: hattori m. Pediatr Transplant. 2008 May;12(3):341-6. doi: 10.1111/j.1399-3046.2007.00752.x. Epub 2008 Jan 16. Pediatr Transplant. 2008. PMID: 18208440
Screening of vesicoureteral reflux in pediatric patients with kidney transplantation showing non-specific interstitial fibrosis and tubular atrophy with interstitial Tamm-Horsfall protein deposits in protocol allograft biopsy.
Akioka Y, Chikamoto H, Horita S, Yago R, Tanabe K, Yamaguchi Y, Hattori M. Akioka Y, et al. Among authors: hattori m. Clin Transplant. 2009 Aug;23 Suppl 20:2-5. doi: 10.1111/j.1399-0012.2009.01000.x. Clin Transplant. 2009. PMID: 19594587
Patients with Epstein-Fechtner syndromes owing to MYH9 R702 mutations develop progressive proteinuric renal disease.
Sekine T, Konno M, Sasaki S, Moritani S, Miura T, Wong WS, Nishio H, Nishiguchi T, Ohuchi MY, Tsuchiya S, Matsuyama T, Kanegane H, Ida K, Miura K, Harita Y, Hattori M, Horita S, Igarashi T, Saito H, Kunishima S. Sekine T, et al. Among authors: hattori m. Kidney Int. 2010 Jul;78(2):207-14. doi: 10.1038/ki.2010.21. Epub 2010 Mar 3. Kidney Int. 2010. PMID: 20200500 Free article.
Pretransplantation combined therapy with plasmapheresis and rituximab in a second living-related kidney transplant pediatric recipient with a very high risk for focal segmental glomerulosclerosis recurrence.
Chikamoto H, Hattori M, Kuroda N, Kajiho Y, Matsumura H, Fujii H, Ishizuka K, Hisano M, Akioka Y, Nozu K, Kaito H, Shimizu M. Chikamoto H, et al. Among authors: hattori m. Pediatr Transplant. 2012 Nov;16(7):E286-90. doi: 10.1111/j.1399-3046.2011.01610.x. Epub 2011 Nov 30. Pediatr Transplant. 2012. PMID: 22129369
2,628 results