Sekine T - Search Results

1

Ischemic colitis as a complication in a patient with steroid-dependent nephrotic syndrome.

Yanagisawa A, Namai Y, Sekine T, Igarashi T. Yanagisawa A, et al. Among authors: sekine t. Pediatr Nephrol. 2008 Apr;23(4):655-7. doi: 10.1007/s00467-007-0665-1. Epub 2007 Nov 24. Pediatr Nephrol. 2008. PMID: 18038157

2

A case of cerebral salt-wasting syndrome associated with aseptic meningitis in an 8-year-old boy.

Inatomi J, Yokoyama Y, Sekine T, Igarashi T. Inatomi J, et al. Among authors: sekine t. Pediatr Nephrol. 2008 Apr;23(4):659-62. doi: 10.1007/s00467-007-0679-8. Epub 2008 Jan 9. Pediatr Nephrol. 2008. PMID: 18183426

3

A familial case of multicystic dysplastic kidney.

Sekine T, Namai Y, Yanagisawa A, Shirahama H, Tashiro Y, Terahara M, Nagata M, Harita Y, Fukuoka U, Inatomi J, Igarashi T. Sekine T, et al. Pediatr Nephrol. 2005 Sep;20(9):1245-8. doi: 10.1007/s00467-005-1905-x. Epub 2005 Jun 23. Pediatr Nephrol. 2005. PMID: 15973528

4

Salt-losing nephrogenic diabetes insipidus caused by fetal exposure to angiotensin receptor blocker.

Miura K, Sekine T, Iida A, Takahashi K, Igarashi T. Miura K, et al. Among authors: sekine t. Pediatr Nephrol. 2009 Jun;24(6):1235-8. doi: 10.1007/s00467-008-1091-8. Epub 2009 Jan 20. Pediatr Nephrol. 2009. PMID: 19153776

5

Morphological and functional analyses of two infants with obstructive renal dysplasia.

Miura K, Sekine T, Nishimura R, Kanamori Y, Yanagisawa A, Sakai K, Nagata M, Igarashi T. Miura K, et al. Among authors: sekine t. Clin Exp Nephrol. 2011 Aug;15(4):602-6. doi: 10.1007/s10157-011-0429-x. Epub 2011 Apr 1. Clin Exp Nephrol. 2011. PMID: 21455661

6

Early occurrence of nephrotic syndrome associated with cord blood stem cell transplantation.

Miura K, Sekine T, Takamizawa M, Terashima H, Furuya A, Koh K, Takita J, Ida K, Igarashi T. Miura K, et al. Among authors: sekine t. Clin Exp Nephrol. 2012 Feb;16(1):180-2. doi: 10.1007/s10157-011-0538-6. Epub 2011 Oct 12. Clin Exp Nephrol. 2012. PMID: 21986678

7

The W258X mutation in SLC22A12 is the predominant cause of Japanese renal hypouricemia.

Komoda F, Sekine T, Inatomi J, Enomoto A, Endou H, Ota T, Matsuyama T, Ogata T, Ikeda M, Awazu M, Muroya K, Kamimaki I, Igarashi T. Komoda F, et al. Among authors: sekine t. Pediatr Nephrol. 2004 Jul;19(7):728-33. doi: 10.1007/s00467-004-1424-1. Epub 2004 Mar 31. Pediatr Nephrol. 2004. PMID: 15054642

8

Functional characterization of LMX1B mutations associated with nail-patella syndrome.

Sato U, Kitanaka S, Sekine T, Takahashi S, Ashida A, Igarashi T. Sato U, et al. Among authors: sekine t. Pediatr Res. 2005 Jun;57(6):783-8. doi: 10.1203/01.PDR.0000157674.63621.2C. Epub 2005 Mar 17. Pediatr Res. 2005. PMID: 15774843

9

Mutational analysis of idiopathic renal hypouricemia in Korea.

Cheong HI, Kang JH, Lee JH, Ha IS, Kim S, Komoda F, Sekine T, Igarashi T, Choi Y. Cheong HI, et al. Among authors: sekine t. Pediatr Nephrol. 2005 Jul;20(7):886-90. doi: 10.1007/s00467-005-1863-3. Epub 2005 May 24. Pediatr Nephrol. 2005. PMID: 15912381

10

OCRL1 mutations in patients with Dent disease phenotype in Japan.

Sekine T, Nozu K, Iyengar R, Fu XJ, Matsuo M, Tanaka R, Iijima K, Matsui E, Harita Y, Inatomi J, Igarashi T. Sekine T, et al. Pediatr Nephrol. 2007 Jul;22(7):975-80. doi: 10.1007/s00467-007-0454-x. Epub 2007 Mar 24. Pediatr Nephrol. 2007. PMID: 17384968

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