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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