Kaito H - Search Results

1

Cryptic exon activation in SLC12A3 in Gitelman syndrome.

Nozu K, Nozu Y, Nakanishi K, Konomoto T, Horinouchi T, Shono A, Morisada N, Minamikawa S, Yamamura T, Fujimura J, Nakanishi K, Ninchoji T, Kaito H, Morioka I, Taniguchi-Ikeda M, Vorechovsky I, Iijima K. Nozu K, et al. Among authors: kaito h. J Hum Genet. 2017 Feb;62(2):335-337. doi: 10.1038/jhg.2016.129. Epub 2016 Oct 27. J Hum Genet. 2017. PMID: 27784896

2

Enamel-renal syndrome associated with hypokalaemic metabolic alkalosis and impaired renal concentration: a novel syndrome?

Fu XJ, Nozu K, Goji K, Ikeda K, Kamioka I, Fujita T, Kaito H, Nishio H, Iijima K, Matsuo M. Fu XJ, et al. Among authors: kaito h. Nephrol Dial Transplant. 2006 Oct;21(10):2959-62. doi: 10.1093/ndt/gfl328. Epub 2006 Jun 24. Nephrol Dial Transplant. 2006. PMID: 16799168 No abstract available.

3

The effect of aldosterone blockade in patients with Alport syndrome.

Kaito H, Nozu K, Iijima K, Nakanishi K, Yoshiya K, Kanda K, Przybyslaw Krol R, Yoshikawa N, Matsuo M. Kaito H, et al. Pediatr Nephrol. 2006 Dec;21(12):1824-9. doi: 10.1007/s00467-006-0270-8. Epub 2006 Oct 13. Pediatr Nephrol. 2006. PMID: 17039334

4

A novel mutation in KCNJ1 in a Bartter syndrome case diagnosed as pseudohypoaldosteronism.

Nozu K, Fu XJ, Kaito H, Kanda K, Yokoyama N, Przybyslaw Krol R, Nakajima T, Kajiyama M, Iijima K, Matsuo M. Nozu K, et al. Among authors: kaito h. Pediatr Nephrol. 2007 Aug;22(8):1219-23. doi: 10.1007/s00467-007-0468-4. Epub 2007 Mar 31. Pediatr Nephrol. 2007. PMID: 17401586 Free article.

5

Detection of a transcript abnormality in mRNA of the SLC12A3 gene extracted from urinary sediment cells of a patient with Gitelman's syndrome.

Kaito H, Nozu K, Fu XJ, Kamioka I, Fujita T, Kanda K, Krol RP, Suminaga R, Ishida A, Iijima K, Matsuo M. Kaito H, et al. Pediatr Res. 2007 Apr;61(4):502-5. doi: 10.1203/pdr.0b013e318031935a. Pediatr Res. 2007. PMID: 17414160

6

Prognosis and pathological characteristics of five children with non-Shiga toxin-mediated hemolytic uremic syndrome.

Kamioka I, Nozu K, Fujita T, Kaito H, Tanaka R, Yoshiya K, Iijima K, Nakanishi K, Yoshikawa N, Matsuo M. Kamioka I, et al. Among authors: kaito h. Pediatr Int. 2007 Apr;49(2):196-201. doi: 10.1111/j.1442-200X.2007.02352.x. Pediatr Int. 2007. PMID: 17445038

7

Molecular analysis of patients with type III Bartter syndrome: picking up large heterozygous deletions with semiquantitative PCR.

Nozu K, Fu XJ, Nakanishi K, Yoshikawa N, Kaito H, Kanda K, Krol RP, Miyashita R, Kamitsuji H, Kanda S, Hayashi Y, Satomura K, Shimizu N, Iijima K, Matsuo M. Nozu K, et al. Among authors: kaito h. Pediatr Res. 2007 Sep;62(3):364-9. doi: 10.1203/PDR.0b013e318123fb90. Pediatr Res. 2007. PMID: 17622951

8

Long-term follow-up of juvenile acute nonproliferative glomerulitis (JANG).

Fujita T, Nozu K, Iijima K, Kamioka I, Kaito H, Tanaka R, Nakanishi K, Matsuo M, Yoshikawa N. Fujita T, et al. Among authors: kaito h. Pediatr Nephrol. 2007 Nov;22(11):1957-61. doi: 10.1007/s00467-007-0555-6. Epub 2007 Aug 3. Pediatr Nephrol. 2007. PMID: 17674054

9

Molecular analysis of digenic inheritance in Bartter syndrome with sensorineural deafness.

Nozu K, Inagaki T, Fu XJ, Nozu Y, Kaito H, Kanda K, Sekine T, Igarashi T, Nakanishi K, Yoshikawa N, Iijima K, Matsuo M. Nozu K, et al. Among authors: kaito h. J Med Genet. 2008 Mar;45(3):182-6. doi: 10.1136/jmg.2007.052944. J Med Genet. 2008. PMID: 18310267

10

Somatic mosaicism for a mutation of the COL4A5 gene is a cause of mild phenotype male Alport syndrome.

Krol RP, Nozu K, Nakanishi K, Iijima K, Takeshima Y, Fu XJ, Nozu Y, Kaito H, Kanda K, Matsuo M, Yoshikawa N. Krol RP, et al. Among authors: kaito h. Nephrol Dial Transplant. 2008 Aug;23(8):2525-30. doi: 10.1093/ndt/gfn005. Epub 2008 Mar 10. Nephrol Dial Transplant. 2008. PMID: 18332068

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