Search Results1-20 of  32

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  • Yamamura Tomohiko ID: 9000342448516

    Articles in CiNii:1

    • Cryptic exon activation in SLC12A3 in Gitelman syndrome (2017)
  • Tomohiko YAMAMURA ID: 9000002586709

    Graduate School of Education, Gifu University (1998 from CiNii)

    Articles in CiNii:1

    • The Viewpointand the Method for the Development of Teaching Materials in Art Education(3) (1998)
  • Tomohiko Yamamura ID: 9000403955624

    Articles in CiNii:1

    • A review of clinical characteristics and genetic backgrounds in Alport syndrome (2018)
  • Yamamura Tomohiko ID: 9000021705881

    Department of Pediatrics, Matsudo City Hospital (2012 from CiNii)

    Articles in CiNii:1

    • Study on 10 heavy proteinuria cases of HSPN with good susceptibility toward combination therapy (2012)
  • Yamamura Tomohiko ID: 9000308727932

    Department of Pediatrics, Matsudo City Hospital Children's Medical Centre (2015 from CiNii)

    Articles in CiNii:1

    • The safety and efficacy of combination therapy of cyclosporine A and mizoribine for children with frequently relapsing steroid-dependent nephrotic syndrome. (2015)
  • Yamamura Tomohiko ID: 9000347661931

    Department of Pediatrics, Kobe University Graduate School of Medicine, Japan (2016 from CiNii)

    Articles in CiNii:1

    • A Novel Mutation in a Japanese Family with X-linked Alport Syndrome (2016)
  • Yamamura Tomohiko ID: 9000378104866

    Articles in CiNii:1

    • A birth of bipartite exon by intragenic deletion (2017)
  • Yamamura Tomohiko ID: 9000378105374

    Articles in CiNii:1

    • Natural History and Genotype-Phenotype Correlation in Female X-Linked Alport Syndrome (2017)
  • Yamamura Tomohiko ID: 9000380123309

    Articles in CiNii:1

    • An in vitro splicing assay reveals the pathogenicity of a novel intronic variant in ATP6V0A4 for autosomal recessive distal renal tubular acidosis (2017)
  • Yamamura Tomohiko ID: 9000380123482

    Articles in CiNii:1

    • Changes in the numbers of patients with acute gastroenteritis after voluntary introduction of the rotavirus vaccine in a Japanese children's primary emergency medical center (2017)
  • Yamamura Tomohiko ID: 9000399182730

    Articles in CiNii:1

    • The utility of urinary CD80 as a diagnostic marker in patients with renal diseases (2018)
  • Yamamura Tomohiko ID: 9000399532547

    Articles in CiNii:1

    • Clinical and Genetic Characteristics in Patients With Gitelman Syndrome (2019)
  • Yamamura Tomohiko ID: 9000399545228

    Articles in CiNii:1

    • Three Severe Cases of Viral Infections with Post-Kidney Transplantation Successfully Confirmed by Polymerase Chain Reaction and Flow Cytometry (2018)
  • Yamamura Tomohiko ID: 9000399804305

    Articles in CiNii:1

    • A review of clinical characteristics and genetic backgrounds in Alport syndrome (2019)
  • Yamamura Tomohiko ID: 9000401954560

    Articles in CiNii:1

    • Changes in the numbers of patients with acute gastroenteritis after voluntary introduction of the rotavirus vaccine in a Japanese children's primary emergency medical center (2017)
  • Yamamura Tomohiko ID: 9000402264837

    Department of Pediatrics, Kobe University Graduate School of Medicine (2019 from CiNii)

    Articles in CiNii:1

    • A case of non-IgA mesangial proliferative glomerulonephritis diagnosed as Alport syndrome by type IV collagen immunohistochemical staining (2019)
  • Yamamura Tomohiko ID: 9000402502243

    Articles in CiNii:1

    • Detection of copy number variations by pair analysis using next-generation sequencing data in inherited kidney diseases (2018)
  • Yamamura Tomohiko ID: 9000402942264

    Articles in CiNii:1

    • Pair analysis and custom array CGH can detect a small copy number variation in COQ6 gene (2019)
  • Yamamura Tomohiko ID: 9000403324093

    Articles in CiNii:1

    • Molecular assay for an intronic variant in NUP93 that causes steroid resistant nephrotic syndrome (2019)
  • Yamamura Tomohiko ID: 9000404481320

    Articles in CiNii:1

    • Determination of the pathogenicity of known COL4A5 intronic variants by in vitro splicing assay (2019)
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