Search Results1-7 of  7

  • YOSHIDA Hidetada ID: 9000003867937

    京都大学医学部附属病院循環器科 (2001 from CiNii)

    Articles in CiNii:18

    • Altered expresion of ATP-sensitive K channel subunit after myocardial infarction and its physiological implication. (1999)
    • 心筋虚血に伴うATP感受性カリウムチャネル遺伝子の調節 (1998)
    • ジギタリスによる虚血プレコンディショニング修飾の機序 -細胞膜ATP感受性カリウム・チャネルの機能的連関- (1999)
  • YOSHIDA Hidetada ID: 9000003883152

    Department of Cardiovascular Medicine, Kyoto University Graduate School of Medicine (2009 from CiNii)

    Articles in CiNii:23

    • Role of KCNQ1 in the Cell Swelling-Induced Enhancement of the Slowly Activating Delayed Rectifier K^+ Current (2002)
    • IS086 Novel missense mutation in the Pore region of HERG gene in Long QT syndrome Patient (1998)
    • IS092 Ion channel gene mutations in acquired long QT syndrome (1998)
  • Yoshida Hidetada ID: 9000003890664

    Devision of Cardiology, Shimada Municipal Hospital (1997 from CiNii)

    Articles in CiNii:2

    • 0465 The severity of reduction of microvasclar reflow after recanalization of an occluded coronary artery is an indicator of myocardial damage in acute myocardial infarction (1997)
    • 0977 Comparison of Thallium-201(T1)/GIucose/Insulin SPECT, T1 Stress-Reinjection SPECT and Dobutamine Echocardiography for Assessment of Myocardial Viability (1997)
  • Yoshida Hidetada ID: 9000256307868

    京都大学医学部医学研究科循環病態学 (1999 from CiNii)

    Articles in CiNii:1

    • Altered expression of ATP-sensitive K channel subunit after myocardial infarction and its physiological implication. (1999)
  • Yoshida Hidetada ID: 9000256872206

    Department of Cardiovascular Medicine, Kyoto University Graduate School of Medicine (1998 from CiNii)

    Articles in CiNii:1

    • Mutational analyses in patients of long QT syndrome:A missense mutation of KvLQT 1 in asymptomatic sisters (1998)
  • Yoshida Hidetada ID: 9000256874462

    Department of Cardiovascular Medicine, Kyoto University, Graduate School of Medicine (2000 from CiNii)

    Articles in CiNii:1

    • Long QT syndrome with a mutation in the Carboxyl Terminus of KCNQ1:genotypephenotype analysis (2000)
  • Yoshida Hidetada ID: 9000257770826

    Articles in CiNii:1

    • Role of KCNQ1 in the Cell Swelling-Induced Enhancement of the Slowly Activating Delayed Rectifier K+ Current. (2002)
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