Hiroshi Kaito

Hiroshi Kaito

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Hiroshi Kaito

Hiroshi Kaito

Publications by authors named "Hiroshi Kaito"

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Clinical and genetic variability of PAX2-related disorder in the Japanese population.

J Hum Genet 2020 Mar 16. Epub 2020 Mar 16.

Department of Pediatrics, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo-ku, Kobe, Hyogo, 650-0017, Japan.

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http://dx.doi.org/10.1038/s10038-020-0741-yDOI Listing
March 2020

Crescentic IgA nephropathy in children.

Pediatr Nephrol 2020 Jan 28. Epub 2020 Jan 28.

Clinical Research Center, Wakayama Medical University, Wakayama City, Wakayama, Japan.

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http://dx.doi.org/10.1007/s00467-020-04483-wDOI Listing
January 2020

Renal-hepatic-pancreatic dysplasia-1 diagnosed on comprehensive gene analysis.

Pediatr Int 2019 Feb 7;61(2):210-212. Epub 2019 Feb 7.

Department of Nephrology, Hyogo Prefectural Kobe Children's Hospital, Kobe, Hyogo, Japan.

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http://dx.doi.org/10.1111/ped.13758DOI Listing
February 2019

Leukocyte Differentiation by Histidine-Rich Glycoprotein/Stanniocalcin-2 Complex Regulates Murine Glioma Growth through Modulation of Antitumor Immunity.

Mol Cancer Ther 2018 09 26;17(9):1961-1972. Epub 2018 Jun 26.

Uppsala University, Department of Immunology, Genetics and Pathology, Science for Life Laboratory, The Rudbeck Laboratory, Uppsala, Sweden.

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http://dx.doi.org/10.1158/1535-7163.MCT-18-0097DOI Listing
September 2018

Diagnostic strategy for inherited hypomagnesemia.

Clin Exp Nephrol 2017 Dec 1;21(6):1003-1010. Epub 2017 Mar 1.

Department of Pediatrics, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo-ku, Kobe, 6500017, Japan.

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http://dx.doi.org/10.1007/s10157-017-1396-7DOI Listing
December 2017

A case of mild phenotype Alport syndrome caused by COL4A3 mutations.

CEN Case Rep 2017 Nov 30;6(2):189-193. Epub 2017 Aug 30.

Department of Nephrology, Nagasaki University Hospital, 1-7-1 Sakamoto, Nagasaki, 852-8501, Japan.

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http://dx.doi.org/10.1007/s13730-017-0273-2DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5694410PMC
November 2017

Female X-linked Alport syndrome with somatic mosaicism.

Clin Exp Nephrol 2017 Oct 31;21(5):877-883. Epub 2016 Oct 31.

Department of Pediatrics, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo, Kobe, 6500017, Japan.

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http://dx.doi.org/10.1007/s10157-016-1352-yDOI Listing
October 2017

Identification of mutations in FN1 leading to glomerulopathy with fibronectin deposits.

Pediatr Nephrol 2016 09 7;31(9):1459-67. Epub 2016 Apr 7.

Department of Biochemistry and Molecular Biology, Kobe University Graduate School of Medicine, Kobe, 658-0072, Japan.

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http://dx.doi.org/10.1007/s00467-016-3368-7DOI Listing
September 2016

Pathogenesis of hypokalemia in autosomal dominant hypocalcemia type 1.

Clin Exp Nephrol 2016 Apr 1;20(2):253-7. Epub 2015 Sep 1.

Department of Pediatrics, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo, Kobe, Hyogo, 6500017, Japan.

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http://dx.doi.org/10.1007/s10157-015-1160-9DOI Listing
April 2016

Combined Alport syndrome and Klinefelter syndrome.

Pediatr Int 2016 Feb 10;58(2):152-5. Epub 2015 Nov 10.

Department of Pediatric Cardiology and Nephrology, Kyoto Prefectural University of Medicine, Graduate School of Medical Science, Kyoto, Japan.

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http://dx.doi.org/10.1111/ped.12743DOI Listing
February 2016

A novel technique of catheter placement with fibrin glue to prevent pericatheter leakage and to enable no break-in period in peritoneal dialysis.

J Pediatr Urol 2015 Oct 7;11(5):299-300. Epub 2015 Aug 7.

Division of Pediatric Surgery, Department of Surgery, Kobe University Graduate School of Medicine, Kobe, Japan.

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https://linkinghub.elsevier.com/retrieve/pii/S14775131150029
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http://dx.doi.org/10.1016/j.jpurol.2015.07.005DOI Listing
October 2015

Renal biopsy criterion in idiopathic nephrotic syndrome with microscopic hematuria at onset.

Pediatr Nephrol 2015 Mar 27;30(3):445-50. Epub 2014 Aug 27.

Department of Pediatrics, Wakayama Medical University, 811-1 Kimiidera, Wakayama, 641-8509, Japan.

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http://dx.doi.org/10.1007/s00467-014-2946-9DOI Listing
March 2015

Biopsy timing and Oxford classification variables in childhood/adolescent IgA nephropathy.

Pediatr Nephrol 2015 Feb 7;30(2):293-9. Epub 2014 Jun 7.

Department of Pediatrics, Wakayama Medical University, Wakayama, Japan.

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http://dx.doi.org/10.1007/s00467-014-2862-zDOI Listing
February 2015

Natural history of genetically proven autosomal recessive Alport syndrome.

Pediatr Nephrol 2014 Sep 15;29(9):1535-44. Epub 2014 Mar 15.

Department of Pediatrics, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo, Kobe, Hyogo, 6500017, Japan.

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http://dx.doi.org/10.1007/s00467-014-2797-4DOI Listing
September 2014

Alport syndrome caused by a COL4A5 deletion and exonization of an adjacent AluY.

Mol Genet Genomic Med 2014 Sep 28;2(5):451-3. Epub 2014 May 28.

Faculty of Medicine, University of Southampton Southampton, U.K.

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http://dx.doi.org/10.1002/mgg3.89DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4190880PMC
September 2014

Rituximab treatment combined with methylprednisolone pulse therapy and immunosuppressants for childhood steroid-resistant nephrotic syndrome.

Pediatr Nephrol 2014 Jul 6;29(7):1181-7. Epub 2014 Feb 6.

Department of Nephrology and Rheumatology, National Center for Child Health and Development, 2-10-1, Okura, Setagaya-ku, Tokyo, 157-8535, Japan,

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http://dx.doi.org/10.1007/s00467-014-2765-zDOI Listing
July 2014

Molecular background of urate transporter genes in patients with exercise-induced acute kidney injury.

Am J Nephrol 2013 4;38(4):316-20. Epub 2013 Oct 4.

Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.

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https://www.karger.com/Article/FullText/355430
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http://dx.doi.org/10.1159/000355430DOI Listing
June 2014

Acute kidney injury after acute gastroenteritis in an infant with hereditary hypouricemia.

Eur J Pediatr 2014 Feb 8;173(2):247-9. Epub 2013 May 8.

Department of Nephrology and Rheumatology, National Center for Child Health and Development, 2-10-1 Okura, Setagaya-ku, Tokyo, 157-8535, Japan,

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http://dx.doi.org/10.1007/s00431-013-2010-yDOI Listing
February 2014

Nephrotic-range proteinuria in an infant with thin basement membrane nephropathy.

CEN Case Rep 2013 Nov 16;2(2):194-196. Epub 2013 Feb 16.

Department of Pediatrics, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo, Kobe, Hyōgo, 6500017, Japan.

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http://dx.doi.org/10.1007/s13730-013-0063-4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5411551PMC
November 2013

SLC26A3 gene analysis in patients with Bartter and Gitelman syndromes and the clinical characteristics of patients with unidentified mutations.

Kobe J Med Sci 2013 Apr 18;59(2):E36-43. Epub 2013 Apr 18.

Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Hyogo, Japan.

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April 2013

Spontaneous remission in children with IgA nephropathy.

Pediatr Nephrol 2013 Jan 2;28(1):71-6. Epub 2012 Sep 2.

Department of Pediatrics, Wakayama Medical University, 811-1 Kimiidera, Wakayama City, Wakayama 641-8509, Japan.

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http://dx.doi.org/10.1007/s00467-012-2294-6DOI Listing
January 2013

Acute encephalopathy and tubulointerstitial nephritis associated with Yersinia pseudotuberculosis.

Pediatr Int 2012 Dec;54(6):926-8

Department of Nephrology, National Center for Child Health and Development, Tokyo, Japan.

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http://dx.doi.org/10.1111/j.1442-200X.2012.03615.xDOI Listing
December 2012

Renal biopsy criterion in children with asymptomatic constant isolated proteinuria.

Nephrol Dial Transplant 2012 Aug 9;27(8):3186-90. Epub 2012 Jan 9.

Department of Pediatrics, Wakayama Medical University, Wakayama, Japan.

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http://dx.doi.org/10.1093/ndt/gfr750DOI Listing
August 2012

Alport-like glomerular basement membrane changes with renal-coloboma syndrome.

Pediatr Nephrol 2012 Jul 21;27(7):1189-92. Epub 2012 Feb 21.

Department of Pediatrics, Kobe University Graduate School of Medicine, Japan.

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http://dx.doi.org/10.1007/s00467-012-2125-9DOI Listing
July 2012

Validity of the Oxford classification of IgA nephropathy in children.

Pediatr Nephrol 2012 May 2;27(5):783-92. Epub 2011 Dec 2.

Department of Pediatrics, Wakayama Medical University, 811-1, Kimiidera, Wakayama City, Wakayama 641-8509, Japan.

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http://dx.doi.org/10.1007/s00467-011-2061-0DOI Listing
May 2012

Recurrent EIARF and PRES with severe renal hypouricemia by compound heterozygous SLC2A9 mutation.

Pediatrics 2011 Jun 2;127(6):e1621-5. Epub 2011 May 2.

Department of Pediatrics, Wakayama Medical University, Wakayama City, Wakayama, 641-8509, Japan.

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http://dx.doi.org/10.1542/peds.2010-2592DOI Listing
June 2011

Treatment strategies for Henoch-Schönlein purpura nephritis by histological and clinical severity.

Pediatr Nephrol 2011 Apr 4;26(4):563-9. Epub 2011 Jan 4.

Department of Pediatrics, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo-ku, Kobe, 6500017, Japan.

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http://link.springer.com/10.1007/s00467-010-1741-5
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http://dx.doi.org/10.1007/s00467-010-1741-5DOI Listing
April 2011

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

J Clin Endocrinol Metab 2010 Dec 1;95(12):E511-8. Epub 2010 Sep 1.

Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe 650-0017, Kusunokicho 7-5-1, Chuo, Kobe, Hyogo, Japan.

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http://dx.doi.org/10.1210/jc.2010-0392DOI Listing
December 2010

Severe Alport syndrome in a young woman caused by a t(X;1)(q22.3;p36.32) balanced translocation.

Pediatr Nephrol 2010 Oct 13;25(10):2165-70. Epub 2010 Apr 13.

Department of Pediatrics, Division of Child Health and Development, Kobe University Graduate School of Medicine, 7-5-2 Kusunoki-Cho, Chuo-ku, Kobe, 650-0017, Japan.

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http://link.springer.com/10.1007/s00467-010-1514-1
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http://dx.doi.org/10.1007/s00467-010-1514-1DOI Listing
October 2010

ABO-incompatible renal transplantation in Epstein syndrome.

Clin Transplant 2010 Jul;24 Suppl 22:31-4

Department of Pediatric Nephrology, National Center for Child Health and Development, 2-10-1 Okura, Setagaya-ku, Tokyo, 157-8535, Japan.

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http://dx.doi.org/10.1111/j.1399-0012.2010.01274.xDOI Listing
July 2010

Successful treatment of collapsing focal segmental glomerulosclerosis with a combination of rituximab, steroids and ciclosporin.

Pediatr Nephrol 2010 May 22;25(5):957-9. Epub 2009 Dec 22.

Department of Nephrology, National Center for Child Health and Development, Setagaya, Tokyo, Japan.

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http://link.springer.com/10.1007/s00467-009-1410-8
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http://dx.doi.org/10.1007/s00467-009-1410-8DOI Listing
May 2010

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

BMC Nephrol 2009 Nov 14;10:37. Epub 2009 Nov 14.

Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Hyogo, Japan.

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http://dx.doi.org/10.1186/1471-2369-10-37DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2779785PMC
November 2009

In vivo and in vitro splicing assay of SLC12A1 in an antenatal salt-losing tubulopathy patient with an intronic mutation.

Hum Genet 2009 Oct 10;126(4):533-8. Epub 2009 Jun 10.

Department of Pediatrics, Kobe University Graduate School of Medicine, Kusunokicho 7-5-1, Chuo, Kobe, Hyogo 650-0017, Japan.

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http://dx.doi.org/10.1007/s00439-009-0697-7DOI Listing
October 2009

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

Pediatr Nephrol 2008 Nov 27;23(11):2085-90. Epub 2008 Jun 27.

Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Hyogo, Japan.

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http://dx.doi.org/10.1007/s00467-008-0878-yDOI Listing
November 2008

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

Nephrol Dial Transplant 2008 Aug 10;23(8):2525-30. Epub 2008 Mar 10.

Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe 650-0017, Hyogo, Japan.

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http://dx.doi.org/10.1093/ndt/gfn005DOI Listing
August 2008

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

Pediatr Nephrol 2007 Nov 3;22(11):1957-61. Epub 2007 Aug 3.

Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe 650-0017, Kusunokicho 7-5-1, Chuo, Kobe, Hyogo, Japan.

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http://link.springer.com/10.1007/s00467-007-0555-6
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http://dx.doi.org/10.1007/s00467-007-0555-6DOI Listing
November 2007

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

Pediatr Nephrol 2007 Aug 31;22(8):1219-23. Epub 2007 Mar 31.

Department of Pediatrics, Kobe University Graduate School of Medicine, and Shinko Hospital, Kobe 650-0017, Kusunokicho 7-5-1, Chuo, Kobe, Hyogo, Japan.

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http://dx.doi.org/10.1007/s00467-007-0468-4DOI Listing
August 2007

The effect of aldosterone blockade in patients with Alport syndrome.

Pediatr Nephrol 2006 Dec 13;21(12):1824-9. Epub 2006 Oct 13.

Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Hyogo 6500017, Japan.

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http://dx.doi.org/10.1007/s00467-006-0270-8DOI Listing
December 2006

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

Nephrol Dial Transplant 2006 Oct 24;21(10):2959-62. Epub 2006 Jun 24.

Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe 650-0017, Kusunokicho 7-5-1, Chuo, Kobe, Hyogo, Japan.

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http://dx.doi.org/10.1093/ndt/gfl328DOI Listing
October 2006