Hiroshi Kaito


Ontology type: schema:Person     


Person Info

NAME

Hiroshi

SURNAME

Kaito

Publications in SciGraph latest 50 shown

  • 2022-02-09 Efficacy of combination therapy for childhood complicated focal IgA nephropathy in CLINICAL AND EXPERIMENTAL NEPHROLOGY
  • 2022-01-11 Use of renin-angiotensin system inhibitors as initial therapy in children with Henoch–Schönlein purpura nephritis of moderate severity in PEDIATRIC NEPHROLOGY
  • 2021-09-18 Clinical features of autosomal recessive polycystic kidney disease in the Japanese population and analysis of splicing in PKHD1 gene for determination of phenotypes in CLINICAL AND EXPERIMENTAL NEPHROLOGY
  • 2021-08-09 Examination of the predicted prevalence of Gitelman syndrome by ethnicity based on genome databases in SCIENTIFIC REPORTS
  • 2021-04-07 Moyamoya disease with refractory hypertension associated with peripheral arterial stenosis in the renal parenchyma in CEN CASE REPORTS
  • 2020-10-14 An “old and new” complication in a child with nephrotic syndrome: Questions in PEDIATRIC NEPHROLOGY
  • 2020-10-14 An “old and new” complication in a child with nephrotic syndrome: Answers in PEDIATRIC NEPHROLOGY
  • 2020-10-04 Clinicopathological significance of glomerular capillary IgA deposition in childhood IgA nephropathy in PEDIATRIC NEPHROLOGY
  • 2020-08-20 Glomerular galactose-deficient IgA1 expression analysis in pediatric patients with glomerular diseases in SCIENTIFIC REPORTS
  • 2020-06-24 A rare case of peritonitis in a young woman on peritoneal dialysis in CEN CASE REPORTS
  • 2020-03-16 Clinical and genetic variability of PAX2-related disorder in the Japanese population in JOURNAL OF HUMAN GENETICS
  • 2020-01-28 Crescentic IgA nephropathy in children in PEDIATRIC NEPHROLOGY
  • 2020-01-21 Molecular mechanisms determining severity in patients with Pierson syndrome in JOURNAL OF HUMAN GENETICS
  • 2019-09-03 Determination of the pathogenicity of known COL4A5 intronic variants by in vitro splicing assay in SCIENTIFIC REPORTS
  • 2019-04-23 Molecular assay for an intronic variant in NUP93 that causes steroid resistant nephrotic syndrome in JOURNAL OF HUMAN GENETICS
  • 2018-12-24 Pair analysis and custom array CGH can detect a small copy number variation in COQ6 gene in CLINICAL AND EXPERIMENTAL NEPHROLOGY
  • 2018-11-23 The utility of urinary CD80 as a diagnostic marker in patients with renal diseases in SCIENTIFIC REPORTS
  • 2018-10-03 Lisinopril versus lisinopril and losartan for mild childhood IgA nephropathy: a randomized controlled trial (JSKDC01 study) in PEDIATRIC NEPHROLOGY
  • 2018-08-20 A review of clinical characteristics and genetic backgrounds in Alport syndrome in CLINICAL AND EXPERIMENTAL NEPHROLOGY
  • 2018-05-30 Congenital chloride diarrhea needs to be distinguished from Bartter and Gitelman syndrome in JOURNAL OF HUMAN GENETICS
  • 2018-05-17 Mutations in six nephrosis genes delineate a pathogenic pathway amenable to treatment in NATURE COMMUNICATIONS
  • 2018-03-19 Functional splicing analysis in an infantile case of atypical hemolytic uremic syndrome caused by digenic mutations in C3 and MCP genes in JOURNAL OF HUMAN GENETICS
  • 2018-02-19 Development of ultra-deep targeted RNA sequencing for analyzing X-chromosome inactivation in female Dent disease in JOURNAL OF HUMAN GENETICS
  • 2018-01-25 Detection of copy number variations by pair analysis using next-generation sequencing data in inherited kidney diseases in CLINICAL AND EXPERIMENTAL NEPHROLOGY
  • 2017-12-04 An in vitro splicing assay reveals the pathogenicity of a novel intronic variant in ATP6V0A4 for autosomal recessive distal renal tubular acidosis in BMC NEPHROLOGY
  • 2017-08-30 A case of mild phenotype Alport syndrome caused by COL4A3 mutations in CEN CASE REPORTS
  • 2017-06-29 Long-term outcome of childhood-onset complicated nephrotic syndrome after a multicenter, double-blind, randomized, placebo-controlled trial of rituximab in PEDIATRIC NEPHROLOGY
  • 2017-03-09 Characterization of contiguous gene deletions in COL4A6 and COL4A5 in Alport syndrome-diffuse leiomyomatosis in JOURNAL OF HUMAN GENETICS
  • 2017-03-01 Diagnostic strategy for inherited hypomagnesemia in CLINICAL AND EXPERIMENTAL NEPHROLOGY
  • 2017-01-10 Clinical characteristics and long-term outcome of diarrhea-associated hemolytic uremic syndrome: a single center experience in CLINICAL AND EXPERIMENTAL NEPHROLOGY
  • 2016-10-31 Female X-linked Alport syndrome with somatic mosaicism in CLINICAL AND EXPERIMENTAL NEPHROLOGY
  • 2016-10-27 Cryptic exon activation in SLC12A3 in Gitelman syndrome in JOURNAL OF HUMAN GENETICS
  • 2016-04-07 Identification of mutations in FN1 leading to glomerulopathy with fibronectin deposits in PEDIATRIC NEPHROLOGY
  • 2015-09-01 Pathogenesis of hypokalemia in autosomal dominant hypocalcemia type 1 in CLINICAL AND EXPERIMENTAL NEPHROLOGY
  • 2015-05-27 Somatic mosaicism and variant frequency detected by next-generation sequencing in X-linked Alport syndrome in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2015-04-16 Differential diagnosis of Bartter syndrome, Gitelman syndrome, and pseudo–Bartter/Gitelman syndrome based on clinical characteristics in GENETICS IN MEDICINE
  • 2015-02-06 Clinical practice guideline for pediatric idiopathic nephrotic syndrome 2013: medical therapy in CLINICAL AND EXPERIMENTAL NEPHROLOGY
  • 2015-02-06 Clinical practice guideline for pediatric idiopathic nephrotic syndrome 2013: general therapy in CLINICAL AND EXPERIMENTAL NEPHROLOGY
  • 2014-08-27 Renal biopsy criterion in idiopathic nephrotic syndrome with microscopic hematuria at onset in PEDIATRIC NEPHROLOGY
  • 2014-08-07 A patient with autosomal recessive Alport syndrome due to segmental maternal isodisomy in HUMAN GENOME VARIATION
  • 2014-06-07 Biopsy timing and Oxford classification variables in Childhood/Adolescent IgA nephropathy in PEDIATRIC NEPHROLOGY
  • 2014-03-15 Natural history of genetically proven autosomal recessive Alport syndrome in PEDIATRIC NEPHROLOGY
  • 2014-02-06 Rituximab treatment combined with methylprednisolone pulse therapy and immunosuppressants for childhood steroid-resistant nephrotic syndrome in PEDIATRIC NEPHROLOGY
  • 2013-05-08 Acute kidney injury after acute gastroenteritis in an infant with hereditary hypouricemia in EUROPEAN JOURNAL OF PEDIATRICS
  • 2013-02-16 Nephrotic-range proteinuria in an infant with thin basement membrane nephropathy in CEN CASE REPORTS
  • 2012-12-09 Renal transplantations from parents to siblings with autosomal recessive Alport syndrome caused by a rearrangement in an intronic antisense Alu element in the COL4A3 gene led to different outcomes in CEN CASE REPORTS
  • 2012-09-02 Spontaneous remission in children with IgA nephropathy in PEDIATRIC NEPHROLOGY
  • 2012-04-10 Two cases of atypical membranoproliferative glomerulonephritis showing opposite clinical course in CEN CASE REPORTS
  • 2012-02-21 Alport-like glomerular basement membrane changes with renal-coloboma syndrome in PEDIATRIC NEPHROLOGY
  • 2011-12-02 Validity of the Oxford classification of IgA nephropathy in children in PEDIATRIC NEPHROLOGY
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