Search Results1-20 of  38

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  • Makita Naomasa ID: 9000398638949

    Articles in CiNii:1

    • Clinical Manifestations and Long-Term Mortality in Lamin A/C Mutation Carriers From a Japanese Multicenter Registry （2018）
  • MAKITA NAOMASA ID: 9000398148490

    Department of Molecular Physiology, Nagasaki University Graduate School of Biomedical Sciences （2018 from CiNii）

    Articles in CiNii:1

    • CaMKII as a novel therapeutic target for lethal ventricular tachyarrhythmias （2018）
  • MAKITA Naomasa ID: 9000000703877

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

    Articles in CiNii:1

    • Enhanced sodium channel intermediate inactivation in Brugada syndrome （2000）
  • MAKITA Naomasa ID: 9000006429794

    Department of Cardiovascular Medicine, Hokkaido University Graduate School of Medicine （2007 from CiNii）

    Articles in CiNii:1

    • Genetic Polymorphisms and Arrhythmia Susceptibility （2007）
  • MAKITA Naomasa ID: 9000006724838

    Department of Cardiovascular Medicine, Hokkaido University Graduate School of Medicine （2008 from CiNii）

    Articles in CiNii:1

    • Absence of a Trafficking Defect in R1232W/T1620M, a Double SCN5A Mutant Responsible for Brugada Syndrome （2008）
  • MAKITA Naomasa ID: 9000017040493

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

    Articles in CiNii:1

    • Phenotypic Overlap of Cardiac Sodium Channelopathies : Individual-Specific or Mutation-Specific? （2009）
  • MAKITA Naomasa ID: 9000018192145

    Department of Physiology, Nagasaki University, Graduate School of Medicine （2009 from CiNii）

    Articles in CiNii:1

    • Aborted Sudden Cardiac Death Associated with Short QT Syndrome （2009）
  • MAKITA Naomasa ID: 9000248246368

    Department of Molecular Pathophysiology, Nagasaki University Graduate School of Biomedical Sciences （2013 from CiNii）

    Articles in CiNii:1

    • Novel SCN3B Mutation Associated Witt Brugada Syndrome Affects Intracellular Trafficking and Function of Nav1.5 （2013）
  • MAKITA Naomasa ID: 9000309576332

    Department of Molecular Physiology, Nagasaki University （2015 from CiNii）

    Articles in CiNii:1

    • Investigating Mechanisms of Ventricular Arrhythmias Induced in the Purkinje Fiber Network Using Computer Simulation （2015）
  • Makita Naomasa ID: 9000004011259

    Department of Cardiovascular Medicine, Hokkaido University School of Medicine （1989 from CiNii）

    Articles in CiNii:3

    • NORADRENALINE-INDUCED ALTERATIONS IN ADENYLATE CYCLASE SYSTEM OF RAT HEART MEMBRANES : Cardiovascular Drugs : 53 Annual Scientific Meeting, Japanese Circulation Society （1989）
    • ALTERATIONS OF PHOSPHOINOSITIDE-SPECIFIC PHOSPHOLIPASE C AND PROTEIN KINASE C ACTIVITIES IN THE MYOCARDIUM OF SPONTANEOUSLY HYPERTENSIVE RATS (SHR) : Cardiomyopathy, Myocarditis : 53 Annual Scientific Meeting, Japanese Circulation Society （1989）
    • -P163- PARTIAL PURIFICATION AND CHARACTERIZATION OF PHOSPHATIDYLINOSITOL-SPECIFIC PHOSPHOLIPASE C IN RAT MYOCARDIUM （1987）
  • Makita Naomasa ID: 9000004064514

    Department of Cardiovascular Medicine,Hokkaido University （1990 from CiNii）

    Articles in CiNii:1

    • -0229-ALTERATIONS OF PHOSPHOLIPASE C (PLC) ISOZYME PATTERN IN THE AORTA OF SPONTANEOUSLY HYPERTENSIVE RATS (SHR) （1990）
  • Makita Naomasa ID: 9000004066720

    Department of Cardiovascular Medicine, Hokkaido University （1990 from CiNii）

    Articles in CiNii:1

    • -0532-ALTERATIONS OF MEMBRANE PHOSPHOINOSITIDE METABOLISM IN THE HEART OF CARDIOMYOPATHIC SYRIAN HAMSTER BIO 14.6 (BIO) （1990）
  • Makita Naomasa ID: 9000004079018

    Department of Cardiovascular Medicine, Hokkaido University Graduate School of Medicine （2002 from CiNii）

    Articles in CiNii:1

    • Mutations in Cardiac Na Channel Gene Associated With Druginduced Acquired Long-QT Syndrome and Asymptomatic Brugada Syndrome （2002）
  • Makita Naomasa ID: 9000004278761

    Department of Cardiovascular Medicine, Hokkaido University Graduate School of Medicine （2004 from CiNii）

    Articles in CiNii:1

    • 3 Ion Channel Mutations in Patients with Brugada Syndrome(APSC/JCS Joint Symposium (APSC) (H) : Emerging Issue in Cardiology for Asian)(Special Program) （2004）
  • Makita Naomasa ID: 9000004282047

    Department of Cardiovascular Medichine, Hokkaido University School of Medicine （2004 from CiNii）

    Articles in CiNii:1

    • OE-133 Novel intrinsic mechanism of the enhanced rate-dependant QT Shortening in R1623Q mutant of the LQT3 syndrome(Arrhythmia, Basic 4 (A) : OE16)(Oral Presentation (English)) （2004）
  • Makita Naomasa ID: 9000004312948

    Department of Cardiovascular Medicine, Hokkaido University Graduate School of Medicine （2003 from CiNii）

    Articles in CiNii:1

    • Molecular and Biophysical Bases of Brugada Syndrome （2003）
  • Makita Naomasa ID: 9000005854779

    Department of Cardiovascular Medicine, Hokkaido University Graduate School of Medicine （2005 from CiNii）

    Articles in CiNii:1

    • Molecular Basis for the Phenotypic Variability of Cardiac Sodium Channelopathies(Ion Channels and Cardiac Arrhythmias : Current Understanding and Future, The 69th Annual Scientific Meeting of the Japanese Circulation Society) （2005）
  • Makita Naomasa ID: 9000014666803

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

    Articles in CiNii:1

    • FRS-119 Familial Isolated Cardiac Conduction Defect Associated with a Mutation in the Connexin40 Gene GJA5(FRS24,Novel Mechanisms of Ventricular Arrhythmia (A),Featured Research Session (English),The 73rd Annual Scientific Meeting of The Japanese Circulation Society) （2009）
  • Makita Naomasa ID: 9000021662194

    Japanese LQTS Multicenter Registry by the Minister of Health, Labour and Welfare （2011 from CiNii）

    Articles in CiNii:1

    • Clinical and Genetic Features of Japanese Patient with Congenital Long QT Syndrome （2011）
  • Makita Naomasa ID: 9000021675157

    Nagasaki University （2011 from CiNii）

    Articles in CiNii:1

    • Clinical Features and Genetic Basis of Progressive Cardiac Conduction Defect: Japanese PCCD Registry （2011）
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