Kyoko Kanda

Summary

Affiliation: Graduate School
Country: Japan

Publications

  1. pmc Autosomal dominant pseudohypoaldosteronism type 1 with a novel splice site mutation in MR gene
    Kyoko Kanda
    Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Hyogo, Japan
    BMC Nephrol 10:37. 2009
  2. doi request reprint Somatic mosaicism for a mutation of the COL4A5 gene is a cause of mild phenotype male Alport syndrome
    Rafal Przybyslaw Krol
    Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe 650 0017, Hyogo, Japan
    Nephrol Dial Transplant 23:2525-30. 2008
  3. doi request reprint The pharmacological characteristics of molecular-based inherited salt-losing tubulopathies
    Kandai Nozu
    Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe 650 0017, Kusunokicho 7 5 1, Chuo, Kobe, Hyogo, Japan
    J Clin Endocrinol Metab 95:E511-8. 2010
  4. doi request reprint The relationship between arginine vasopressin levels and hyponatremia following a percutaneous renal biopsy in children receiving hypotonic or isotonic intravenous fluids
    Kyoko Kanda
    Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan
    Pediatr Nephrol 26:99-104. 2011
  5. doi request reprint Detection of large deletion mutations in the COL4A5 gene of female Alport syndrome patients
    Kandai Nozu
    Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Hyogo, Japan
    Pediatr Nephrol 23:2085-90. 2008
  6. ncbi request reprint A novel mutation in KCNJ1 in a Bartter syndrome case diagnosed as pseudohypoaldosteronism
    Kandai Nozu
    Department of Pediatrics, Kobe University Graduate School of Medicine, and Shinko Hospital, Kobe 650 0017, Kusunokicho 7 5 1, Chuo, Kobe, Hyogo, Japan
    Pediatr Nephrol 22:1219-23. 2007
  7. doi request reprint Treatment strategies for Henoch-Schönlein purpura nephritis by histological and clinical severity
    Takeshi Ninchoji
    Department of Pediatrics, Kobe University Graduate School of Medicine, 7 5 1 Kusunoki cho, Chuo Ku, Kobe, 6500017, Japan
    Pediatr Nephrol 26:563-9. 2011
  8. ncbi request reprint Molecular analysis of patients with type III Bartter syndrome: picking up large heterozygous deletions with semiquantitative PCR
    Kandai Nozu
    Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Hyogo, 6500017, Japan
    Pediatr Res 62:364-9. 2007
  9. ncbi request reprint Detection of a transcript abnormality in mRNA of the SLC12A3 gene extracted from urinary sediment cells of a patient with Gitelman's syndrome
    Hiroshi Kaito
    Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Hyogo, Japan
    Pediatr Res 61:502-5. 2007
  10. ncbi request reprint The effect of aldosterone blockade in patients with Alport syndrome
    Hiroshi Kaito
    Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Hyogo 6500017, Japan
    Pediatr Nephrol 21:1824-9. 2006

Collaborators

Detail Information

Publications10

  1. pmc Autosomal dominant pseudohypoaldosteronism type 1 with a novel splice site mutation in MR gene
    Kyoko Kanda
    Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Hyogo, Japan
    BMC Nephrol 10:37. 2009
    ....
  2. doi request reprint Somatic mosaicism for a mutation of the COL4A5 gene is a cause of mild phenotype male Alport syndrome
    Rafal Przybyslaw Krol
    Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe 650 0017, Hyogo, Japan
    Nephrol Dial Transplant 23:2525-30. 2008
    ..mRNA extracted from the urinary sediments was analysed by RT-PCR and two PCR fragments were amplified, one consisting of a normal sequence and one with skipping of exon 44...
  3. doi request reprint The pharmacological characteristics of molecular-based inherited salt-losing tubulopathies
    Kandai Nozu
    Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe 650 0017, Kusunokicho 7 5 1, Chuo, Kobe, Hyogo, Japan
    J Clin Endocrinol Metab 95:E511-8. 2010
    ..However, the terminology of Bartter syndrome and Gitelman syndrome does not always accurately reflect their pathophysiological basis or clinical presentation, and some patients are difficult to diagnose from their clinical presentations...
  4. doi request reprint The relationship between arginine vasopressin levels and hyponatremia following a percutaneous renal biopsy in children receiving hypotonic or isotonic intravenous fluids
    Kyoko Kanda
    Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan
    Pediatr Nephrol 26:99-104. 2011
    ..In conclusion, elevated AVP levels were common among our patients following a percutaneous renal biopsy. Isotonic fluids prevented a fall in serum sodium and hyponatremia, while hypotonic fluids did not...
  5. doi request reprint Detection of large deletion mutations in the COL4A5 gene of female Alport syndrome patients
    Kandai Nozu
    Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Hyogo, Japan
    Pediatr Nephrol 23:2085-90. 2008
    ..Our findings indicate that this difference may, in part, be due to failure to detect this type of mutation with conventional analytical methods...
  6. ncbi request reprint A novel mutation in KCNJ1 in a Bartter syndrome case diagnosed as pseudohypoaldosteronism
    Kandai Nozu
    Department of Pediatrics, Kobe University Graduate School of Medicine, and Shinko Hospital, Kobe 650 0017, Kusunokicho 7 5 1, Chuo, Kobe, Hyogo, Japan
    Pediatr Nephrol 22:1219-23. 2007
    ..In such cases, KCNJ1 mutations should be suspected. In our case, genetic analysis of the KCNJ1 gene identified a novel homozygous 1-bp deletion mutation (c.607 del. C in exon 5)...
  7. doi request reprint Treatment strategies for Henoch-Schönlein purpura nephritis by histological and clinical severity
    Takeshi Ninchoji
    Department of Pediatrics, Kobe University Graduate School of Medicine, 7 5 1 Kusunoki cho, Chuo Ku, Kobe, 6500017, Japan
    Pediatr Nephrol 26:563-9. 2011
    ..Furthermore, aggressive therapies, particularly combination therapies, are unnecessary for moderate-severe HSPN...
  8. ncbi request reprint Molecular analysis of patients with type III Bartter syndrome: picking up large heterozygous deletions with semiquantitative PCR
    Kandai Nozu
    Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Hyogo, 6500017, Japan
    Pediatr Res 62:364-9. 2007
    ..This is the first report to identify large heterozygous deletion mutations in the CLCNKB gene in patients with type III BS...
  9. ncbi request reprint Detection of a transcript abnormality in mRNA of the SLC12A3 gene extracted from urinary sediment cells of a patient with Gitelman's syndrome
    Hiroshi Kaito
    Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Hyogo, Japan
    Pediatr Res 61:502-5. 2007
    ..Our investigation was the first to demonstrate exon 14 skipping in an NCCT transcript in renal cells. This methodology thus constitutes a potential noninvasive analytical tool for every inherited kidney disease...
  10. ncbi request reprint The effect of aldosterone blockade in patients with Alport syndrome
    Hiroshi Kaito
    Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Hyogo 6500017, Japan
    Pediatr Nephrol 21:1824-9. 2006
    ..SP can thus be expected to constitute a good renoprotective agent for Alport syndrome. These preliminary data indicate that large-scale trials of this therapy should be done...