Search Results1-20 of  27

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  • Minamikawa Shogo ID: 9000342448515

    Articles in CiNii:1

    • Cryptic exon activation in SLC12A3 in Gitelman syndrome (2017)
  • Minamikawa Shogo ID: 9000347661932

    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)
  • Minamikawa Shogo ID: 9000378104867

    Articles in CiNii:1

    • A birth of bipartite exon by intragenic deletion (2017)
  • Minamikawa Shogo ID: 9000378105381

    Articles in CiNii:1

    • Natural History and Genotype-Phenotype Correlation in Female X-Linked Alport Syndrome (2017)
  • Minamikawa Shogo ID: 9000380123315

    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)
  • Minamikawa Shogo ID: 9000380123483

    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)
  • Minamikawa Shogo ID: 9000399182727

    Articles in CiNii:1

    • The utility of urinary CD80 as a diagnostic marker in patients with renal diseases (2018)
  • Minamikawa Shogo ID: 9000399532548

    Articles in CiNii:1

    • Clinical and Genetic Characteristics in Patients With Gitelman Syndrome (2019)
  • Minamikawa Shogo ID: 9000399545229

    Articles in CiNii:1

    • Three Severe Cases of Viral Infections with Post-Kidney Transplantation Successfully Confirmed by Polymerase Chain Reaction and Flow Cytometry (2018)
  • Minamikawa Shogo ID: 9000399804308

    Articles in CiNii:1

    • A review of clinical characteristics and genetic backgrounds in Alport syndrome (2019)
  • Minamikawa Shogo ID: 9000401954561

    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)
  • Minamikawa Shogo ID: 9000402502244

    Articles in CiNii:1

    • Detection of copy number variations by pair analysis using next-generation sequencing data in inherited kidney diseases (2018)
  • Minamikawa Shogo ID: 9000402942263

    Articles in CiNii:1

    • Pair analysis and custom array CGH can detect a small copy number variation in COQ6 gene (2019)
  • Minamikawa Shogo ID: 9000402944192

    Pediatric Emergency and Trauma Care Center, Kitakyushu Municipal Yahata Hospital (2019 from CiNii)

    Articles in CiNii:1

    • Biliary Peritonitis Due to Bile Leakage Without Perforation, Associated With Infection of <i>Diphyllobothrium nihonkaiense</i>: A Report of a Pediatric Case (2019)
  • Minamikawa Shogo ID: 9000403324095

    Articles in CiNii:1

    • Molecular assay for an intronic variant in NUP93 that causes steroid resistant nephrotic syndrome (2019)
  • Minamikawa Shogo ID: 9000404481321

    Articles in CiNii:1

    • Determination of the pathogenicity of known COL4A5 intronic variants by in vitro splicing assay (2019)
  • Minamikawa Shogo ID: 9000404821349

    Articles in CiNii:1

    • Comparison between conventional and comprehensive sequencing approaches for genetic diagnosis of Alport syndrome (2019)
  • Minamikawa Shogo ID: 9000408475285

    Articles in CiNii:1

    • Molecular mechanisms determining severity in patients with Pierson syndrome (2020)
  • Minamikawa Shogo ID: 9000408805744

    Articles in CiNii:1

    • Determination of the pathogenicity of known COL4A5 intronic variants by in vitro splicing assay (2019)
  • Minamikawa Shogo ID: 9000408923300

    Articles in CiNii:1

    • Clinical and genetic variability of PAX2-related disorder in the Japanese population (2020)
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