Search Results1-12 of  12

  • SHINOZAWA Keiko ID: 9000001979971

    Department of Laboratory Medicine, Tokyo Medical University (2007 from CiNii)

    Articles in CiNii:1

    • Molecular Characterization of 3 Factor V mutations, R2174L, V1813M, and a 5-bp Deletion, That Cause Factor V Deficiency (2007)
  • SHINOZAWA Keiko ID: 9000019059670

    Department of Molecular Genetics of Coagulation Disorders, Tokyo Medical University (2011 from CiNii)

    Articles in CiNii:1

    • Mutations to the probe of Cobas TaqMan HIV-1 ver. 1.0 assay causing undetectable viral load in a patient with acute HIV-1 infection (2011)
  • SHINOZAWA Keiko ID: 9000019147636

    Department of Molecular Genetics of Coagulation Disorders, Tokyo Medical University (2011 from CiNii)

    Articles in CiNii:1

    • Congenital factor XIII deficiency : A commentary on 'Homozygous intronic mutation leading to inefficient transcription combined with a novel frame-shift mutation in F13A1 gene causes FXIII deficiency' (2011)
  • SHINOZAWA Keiko ID: 9000021327803

    Department of Molecular Genetics of Coagulation Disorders, Tokyo Medical University (2012 from CiNii)

    Articles in CiNii:1

    • Causative mutation and single nucleotide polymorphisms associated with inhibitor development in patients with hemophilia (2012)
  • SHINOZAWA Keiko ID: 9000261655221

    東京医科大学血液凝固異常症遺伝子研究寄附講座 (2014 from CiNii)

    Articles in CiNii:1

    • Novel factor V mutation (W1920R, FV Nara) associated with serious deep vein thrombosis and APC resistance : The plot thickens (2014)
  • SHINOZAWA Keiko ID: 9000261674889

    Department of Molecular Genetics of Coagulation Disorders, Tokyo Medical University (2013 from CiNii)

    Articles in CiNii:1

    • Genotypic and phenotypic features of Japanese patients with mild to moderate hemophilia A (2013)
  • SHINOZAWA Keiko ID: 9000272997861

    Department of Molecular Genetics of Coagulation Disorders, Tokyo Medical University (2014 from CiNii)

    Articles in CiNii:1

    • Development of asymptomatic acquired factor V inhibitor after the administration of antibiotics (2014)
  • SHINOZAWA Keiko ID: 9000308728323

    Articles in CiNii:1

    • Genetic analysis is valuable for diagnostic testing for carrier status with hemophilia (2015)
  • SHINOZAWA Keiko ID: 9000364512883

    Articles in CiNii:21

    • The molecular basis for hemophilia A due to missense mutation (Asp116Asn) within the A1-domain of factor VIII (2006)
    • Congenital factor V deficiency and a mutation (2005)
    • Characterization of a Large Deletion that Leads to Congenital Factor XIII Deficiency (2008)
  • SHINOZAWA Keiko ID: 9000397800692

    Department of Molecular Genetics of Coagulation Disorders, Tokyo Medical University (2018 from CiNii)

    Articles in CiNii:1

    • Two cases of acquired factor V inhibitor which were initially diagnosed with congenital deficiency by cross mixing tests (2018)
  • SHINOZAWA Keiko ID: 9000402436316

    Department of Molecular Genetics of Coagulation Disorders, Tokyo Medical University (2019 from CiNii)

    Articles in CiNii:1

    • Exhaustive analysis of genetic mutations associated with protein S deficiency utilizing next-generation sequencing analysis (2019)
  • SHINOZAWA Keiko ID: 9000402922620

    Department of Molecular Genetics of Coagulation Disorders, Tokyo Medical University (2019 from CiNii)

    Articles in CiNii:1

    • The new approach of laboratory diagnosis for a patient with acquired factor XI deficiency with high titer auto-antibodies by combination use of synthetic chromogenic substrate assay for factor VIII and factor IX (2019)
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