Search Results1-15 of  15

  • Horinouchi Tomoko ID: 9000342448512

    Articles in CiNii:1

    • Cryptic exon activation in SLC12A3 in Gitelman syndrome (2017)
  • Horinouchi Tomoko ID: 9000258011708

    Department of Pediatrics, Himeji Red Cross Hospital (2014 from CiNii)

    Articles in CiNii:1

    • A case of rickets associated with Dent disease in a young Japanese boy (2014)
  • Horinouchi Tomoko ID: 9000258011800

    Department of Pediatrics, Himeji Red Cross Hospital (2014 from CiNii)

    Articles in CiNii:1

    • Renal blood flow with ultrasonography and vesicoureteral reflux in childhood upper urinary tract infection (2014)
  • Horinouchi Tomoko ID: 9000312731425

    Articles in CiNii:1

    • Yersinia pseudotuberculosis infection in Kawasaki disease and its clinical characteristics (2015)
  • Horinouchi Tomoko ID: 9000380123314

    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)
  • Horinouchi Tomoko ID: 9000398991539

    Articles in CiNii:1

    • Study protocol: mycophenolate mofetil as maintenance therapy after rituximab treatment for childhood-onset, complicated, frequently-relapsing nephrotic syndrome or steroid-dependent nephrotic syndrome: a multicenter double-blind, randomized, placebo-controlled trial (JSKDC07) (2018)
  • Horinouchi Tomoko ID: 9000399182733

    Articles in CiNii:1

    • The utility of urinary CD80 as a diagnostic marker in patients with renal diseases (2018)
  • Horinouchi Tomoko ID: 9000399532550

    Articles in CiNii:1

    • Clinical and Genetic Characteristics in Patients With Gitelman Syndrome (2019)
  • Horinouchi Tomoko ID: 9000399545227

    Articles in CiNii:1

    • Three Severe Cases of Viral Infections with Post-Kidney Transplantation Successfully Confirmed by Polymerase Chain Reaction and Flow Cytometry (2018)
  • Horinouchi Tomoko ID: 9000399804307

    Articles in CiNii:1

    • A review of clinical characteristics and genetic backgrounds in Alport syndrome (2019)
  • Horinouchi Tomoko ID: 9000402502245

    Articles in CiNii:1

    • Detection of copy number variations by pair analysis using next-generation sequencing data in inherited kidney diseases (2018)
  • Horinouchi Tomoko ID: 9000402942261

    Articles in CiNii:1

    • Pair analysis and custom array CGH can detect a small copy number variation in COQ6 gene (2019)
  • Horinouchi Tomoko ID: 9000403324097

    Articles in CiNii:1

    • Molecular assay for an intronic variant in NUP93 that causes steroid resistant nephrotic syndrome (2019)
  • Horinouchi Tomoko ID: 9000404481318

    Articles in CiNii:1

    • Determination of the pathogenicity of known COL4A5 intronic variants by in vitro splicing assay (2019)
  • Tomoko Horinouchi ID: 9000403955626

    Articles in CiNii:1

    • A review of clinical characteristics and genetic backgrounds in Alport syndrome (2018)
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