Inatomi J - Search Results

1

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. Among authors: inatomi j. Pediatr Nephrol. 2005 Sep;20(9):1245-8. doi: 10.1007/s00467-005-1905-x. Epub 2005 Jun 23. Pediatr Nephrol. 2005. PMID: 15973528

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. 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

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: inatomi j. Pediatr Nephrol. 2004 Jul;19(7):728-33. doi: 10.1007/s00467-004-1424-1. Epub 2004 Mar 31. Pediatr Nephrol. 2004. PMID: 15054642

4

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. Among authors: inatomi j. Pediatr Nephrol. 2007 Jul;22(7):975-80. doi: 10.1007/s00467-007-0454-x. Epub 2007 Mar 24. Pediatr Nephrol. 2007. PMID: 17384968

5

Unraveling the molecular pathogenesis of isolated proximal renal tubular acidosis.

Igarashi T, Sekine T, Inatomi J, Seki G. Igarashi T, et al. Among authors: inatomi j. J Am Soc Nephrol. 2002 Aug;13(8):2171-7. doi: 10.1097/01.asn.0000025281.70901.30. J Am Soc Nephrol. 2002. PMID: 12138151 Review.

6

Molecular and clinical studies of Dent's disease in Japan: biochemical examination and renal ultrasonography do not predict carrier state.

Matsuyama T, Awazu M, Oikawa T, Inatomi J, Sekine T, Igarashi T. Matsuyama T, et al. Among authors: inatomi j. Clin Nephrol. 2004 Apr;61(4):231-7. doi: 10.5414/cnp61231. Clin Nephrol. 2004. PMID: 15125028

7

Functional analysis of NBC1 mutants associated with proximal renal tubular acidosis and ocular abnormalities.

Horita S, Yamada H, Inatomi J, Moriyama N, Sekine T, Igarashi T, Endo Y, Dasouki M, Ekim M, Al-Gazali L, Shimadzu M, Seki G, Fujita T. Horita S, et al. Among authors: inatomi j. J Am Soc Nephrol. 2005 Aug;16(8):2270-8. doi: 10.1681/ASN.2004080667. Epub 2005 Jun 1. J Am Soc Nephrol. 2005. PMID: 15930088

8

Mutational and functional analysis of SLC4A4 in a patient with proximal renal tubular acidosis.

Inatomi J, Horita S, Braverman N, Sekine T, Yamada H, Suzuki Y, Kawahara K, Moriyama N, Kudo A, Kawakami H, Shimadzu M, Endou H, Fujita T, Seki G, Igarashi T. Inatomi J, et al. Pflugers Arch. 2004 Jul;448(4):438-44. doi: 10.1007/s00424-004-1278-1. Epub 2004 Apr 14. Pflugers Arch. 2004. PMID: 15085340

9

Weber-Christian disease with benign cytophagic histiocytes in the skin lesion.

Inatomi J, Watanabe K, Igarashi T, Hayakawa H. Inatomi J, et al. Acta Paediatr Jpn. 1995 Feb;37(1):105-7. doi: 10.1111/j.1442-200x.1995.tb03699.x. Acta Paediatr Jpn. 1995. PMID: 7754752

10

Functional characterization of renal chloride channel, CLCN5, mutations associated with Dent'sJapan disease.

Igarashi T, Günther W, Sekine T, Inatomi J, Shiraga H, Takahashi S, Suzuki J, Tsuru N, Yanagihara T, Shimazu M, Jentsch TJ, Thakker RV. Igarashi T, et al. Among authors: inatomi j. Kidney Int. 1998 Dec;54(6):1850-6. doi: 10.1046/j.1523-1755.1998.00203.x. Kidney Int. 1998. PMID: 9853249 Free article.

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