Kanda K - Search Results

1

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: kanda s, kanda k. Pediatr Res. 2007 Sep;62(3):364-9. doi: 10.1203/PDR.0b013e318123fb90. Pediatr Res. 2007. PMID: 17622951

2

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: kanda k. J Med Genet. 2008 Mar;45(3):182-6. doi: 10.1136/jmg.2007.052944. J Med Genet. 2008. PMID: 18310267

3

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: kanda k. 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.

4

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. Among authors: kanda k. Pediatr Res. 2007 Apr;61(4):502-5. doi: 10.1203/pdr.0b013e318031935a. Pediatr Res. 2007. PMID: 17414160

5

Detection of large deletion mutations in the COL4A5 gene of female Alport syndrome patients.

Nozu K, Przybyslaw Krol R, Ohtsuka Y, Nakanishi K, Yoshikawa N, Nozu Y, Kaito H, Kanda K, Hashimura Y, Hamasaki Y, Iijima K, Matsuo M. Nozu K, et al. Among authors: kanda k. Pediatr Nephrol. 2008 Nov;23(11):2085-90. doi: 10.1007/s00467-008-0878-y. Epub 2008 Jun 27. Pediatr Nephrol. 2008. PMID: 18584212

6

The pharmacological characteristics of molecular-based inherited salt-losing tubulopathies.

Nozu K, Iijima K, Kanda K, Nakanishi K, Yoshikawa N, Satomura K, Kaito H, Hashimura Y, Ninchoji T, Komatsu H, Kamei K, Miyashita R, Kugo M, Ohashi H, Yamazaki H, Mabe H, Otsubo A, Igarashi T, Matsuo M. Nozu K, et al. Among authors: kanda k. J Clin Endocrinol Metab. 2010 Dec;95(12):E511-8. doi: 10.1210/jc.2010-0392. Epub 2010 Sep 1. J Clin Endocrinol Metab. 2010. PMID: 20810575

7

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. Among authors: kanda k. Pediatr Nephrol. 2006 Dec;21(12):1824-9. doi: 10.1007/s00467-006-0270-8. Epub 2006 Oct 13. Pediatr Nephrol. 2006. PMID: 17039334

8

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: kanda k. Nephrol Dial Transplant. 2008 Aug;23(8):2525-30. doi: 10.1093/ndt/gfn005. Epub 2008 Mar 10. Nephrol Dial Transplant. 2008. PMID: 18332068

9

Autosomal dominant pseudohypoaldosteronism type 1 with a novel splice site mutation in MR gene.

Kanda K, Nozu K, Yokoyama N, Morioka I, Miwa A, Hashimura Y, Kaito H, Iijima K, Matsuo M. Kanda K, et al. BMC Nephrol. 2009 Nov 14;10:37. doi: 10.1186/1471-2369-10-37. BMC Nephrol. 2009. PMID: 19912655 Free PMC article.

10

The relationship between arginine vasopressin levels and hyponatremia following a percutaneous renal biopsy in children receiving hypotonic or isotonic intravenous fluids.

Kanda K, Nozu K, Kaito H, Iijima K, Nakanishi K, Yoshikawa N, Ninchoji T, Hashimura Y, Matsuo M, Moritz ML. Kanda K, et al. Pediatr Nephrol. 2011 Jan;26(1):99-104. doi: 10.1007/s00467-010-1647-2. Epub 2010 Oct 16. Pediatr Nephrol. 2011. PMID: 20953635

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