Hidenobu Terai

Summary

Country: Japan

Publications

  1. ncbi request reprint Cardiac sympathetic nerve activity in patients with hypertrophic cardiomyopathy with malignant ventricular tachyarrhythmias
    Hidenobu Terai
    Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School of Medical Science, Kanazawa University, Kanazawa, Japan
    J Nucl Cardiol 10:304-10. 2003
  2. ncbi request reprint Diagnostic value of abnormal Q waves for identification of preclinical carriers of hypertrophic cardiomyopathy based on a molecular genetic diagnosis
    Tetsuo Konno
    Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School of Medical Science, Kanazawa University, Kanazawa Japan
    Eur Heart J 25:246-51. 2004
  3. ncbi request reprint Compound heterozygosity for mutations Asp611-->Tyr in KCNQ1 and Asp609-->Gly in KCNH2 associated with severe long QT syndrome
    Masato Yamaguchi
    Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School of Medical Science, Kanazawa University, Kanazawa 920 8640, Japan
    Clin Sci (Lond) 108:143-50. 2005
  4. ncbi request reprint Changes in cardiac tissue characterization in carriers with gene mutations associated with hypertrophic cardiomyopathy
    Tomoya Kaneda
    Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School of Medical Science, Kanazawa University, Takara machi 13 1, Kanazawa 920 8640, Japan
    Int J Cardiol 104:170-5. 2005
  5. ncbi request reprint Scintigraphic evaluation of regression of abnormal Q waves in myocardial infarction
    Tetsuo Konno
    Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School of Medical Science, Kanazawa University, Takara machi 13 1, Kanazawa 920 8640, Japan
    Ann Nucl Med 19:407-9. 2005
  6. ncbi request reprint In-hospital outcome in octogenarians with acute coronary syndrome undergoing emergent coronary angiography
    Kotaro Oe
    Division of Cardiovascular Medicine, Graduate School of Medical Science, Kanazawa University, Kanazawa, Japan
    Jpn Heart J 44:11-20. 2003
  7. ncbi request reprint Probucol aggravates long QT syndrome associated with a novel missense mutation M124T in the N-terminus of HERG
    Kenshi Hayashi
    Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School of Medical Science, Kanazawa University, Kanazawa, Japan
    Clin Sci (Lond) 107:175-82. 2004
  8. ncbi request reprint Q-T peak dispersion in congenital long QT syndrome: possible marker of mutation of HERG
    Masaru Inoue
    Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School of Medical Science, Kanazawa University, Japan
    Circ J 67:495-8. 2003
  9. ncbi request reprint Images in cardiovascular medicine. Adult patient with isolated noncompaction of ventricular myocardium
    Tomoya Kaneda
    Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School of Medical Science, Kanazawa University, Kanazawa 920 8640, Japan
    Circulation 112:e96-7. 2005
  10. ncbi request reprint Changes in cardiac sympathetic nerve innervation and activity in pathophysiologic transition from typical to end-stage hypertrophic cardiomyopathy
    Hidenobu Terai
    Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Kanazawa University, Kanazawa, Japan
    J Nucl Med 44:1612-7. 2003

Collaborators

Detail Information

Publications23

  1. ncbi request reprint Cardiac sympathetic nerve activity in patients with hypertrophic cardiomyopathy with malignant ventricular tachyarrhythmias
    Hidenobu Terai
    Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School of Medical Science, Kanazawa University, Kanazawa, Japan
    J Nucl Cardiol 10:304-10. 2003
    ..4 +/- 5.7%, P <.0001), although other parameters including heterogeneity indices did not differ. The logistic multiple regression analysis also determined that washout rate was the most powerful predictor of VT in patients with HCM...
  2. ncbi request reprint Diagnostic value of abnormal Q waves for identification of preclinical carriers of hypertrophic cardiomyopathy based on a molecular genetic diagnosis
    Tetsuo Konno
    Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School of Medical Science, Kanazawa University, Kanazawa Japan
    Eur Heart J 25:246-51. 2004
    ..The aim of this study was to determine the most accurate diagnostic definition of abnormal Q waves for HCM based on a molecular genetic diagnosis, and also to apply abnormal Q waves to the identification of preclinical carriers...
  3. ncbi request reprint Compound heterozygosity for mutations Asp611-->Tyr in KCNQ1 and Asp609-->Gly in KCNH2 associated with severe long QT syndrome
    Masato Yamaguchi
    Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School of Medical Science, Kanazawa University, Kanazawa 920 8640, Japan
    Clin Sci (Lond) 108:143-50. 2005
    ..Our results suggest that the mild phenotype produced by the D611Y mutation in KCNQ1 became more serious by addition of the D609G mutation in KCNH2 in the proband...
  4. ncbi request reprint Changes in cardiac tissue characterization in carriers with gene mutations associated with hypertrophic cardiomyopathy
    Tomoya Kaneda
    Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School of Medical Science, Kanazawa University, Takara machi 13 1, Kanazawa 920 8640, Japan
    Int J Cardiol 104:170-5. 2005
    ..Early detection in patients with hypertrophic cardiomyopathy (HCM) is very important. Integrated backscatter (IB) provides a useful noninvasive measure of the acoustic properties of the myocardium, and may detect early myocardial changes...
  5. ncbi request reprint Scintigraphic evaluation of regression of abnormal Q waves in myocardial infarction
    Tetsuo Konno
    Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School of Medical Science, Kanazawa University, Takara machi 13 1, Kanazawa 920 8640, Japan
    Ann Nucl Med 19:407-9. 2005
    ..Scintigraphic findings in the present case here may contribute to an interpretation of regression of abnormal Q waves in myocardial infarction...
  6. ncbi request reprint In-hospital outcome in octogenarians with acute coronary syndrome undergoing emergent coronary angiography
    Kotaro Oe
    Division of Cardiovascular Medicine, Graduate School of Medical Science, Kanazawa University, Kanazawa, Japan
    Jpn Heart J 44:11-20. 2003
    ..Therefore, impaired myocardial reserve may contribute to a large portion of in-hospital deaths in octogenarians with ACS...
  7. ncbi request reprint Probucol aggravates long QT syndrome associated with a novel missense mutation M124T in the N-terminus of HERG
    Kenshi Hayashi
    Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School of Medical Science, Kanazawa University, Kanazawa, Japan
    Clin Sci (Lond) 107:175-82. 2004
    ....
  8. ncbi request reprint Q-T peak dispersion in congenital long QT syndrome: possible marker of mutation of HERG
    Masaru Inoue
    Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School of Medical Science, Kanazawa University, Japan
    Circ J 67:495-8. 2003
    ..These results suggest that increased lag of the peak of the T wave in each precordial lead (QTpc dispersion) may be a possible index to differentiate LQTS patients with HERG mutation from those with KCNQ1 mutation...
  9. ncbi request reprint Images in cardiovascular medicine. Adult patient with isolated noncompaction of ventricular myocardium
    Tomoya Kaneda
    Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School of Medical Science, Kanazawa University, Kanazawa 920 8640, Japan
    Circulation 112:e96-7. 2005
  10. ncbi request reprint Changes in cardiac sympathetic nerve innervation and activity in pathophysiologic transition from typical to end-stage hypertrophic cardiomyopathy
    Hidenobu Terai
    Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Kanazawa University, Kanazawa, Japan
    J Nucl Med 44:1612-7. 2003
    ..The objective of this study was to evaluate the relationship between abnormalities on (123)I-MIBG myocardial scintigraphy and pathophysiologic changes in patients with HCM...
  11. ncbi request reprint High incidence of sudden cardiac death with conduction disturbances and atrial cardiomyopathy caused by a nonsense mutation in the STA gene
    Kenji Sakata
    Department of Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School of Medical Science, Kanazawa University, Takara machi, Ishikawa, Japan
    Circulation 111:3352-8. 2005
    ..Although it has been reported that EDMD caused by the STA gene mutation is associated with X-linked recessive inheritance, the genotype-phenotype correlations, with special reference to cardiac manifestations, are not well defined...
  12. ncbi request reprint A novel missense mutation in the myosin binding protein-C gene is responsible for hypertrophic cardiomyopathy with left ventricular dysfunction and dilation in elderly patients
    Tetsuo Konno
    Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School of Medical Science, Kanazawa University, Kanazawa, Japan
    J Am Coll Cardiol 41:781-6. 2003
    ..We studied the clinical features of hypertrophic cardiomyopathy (HCM) caused by a novel mutation in the myosin binding protein-C (MyBP-C) gene in patients and family members of Japanese descent...
  13. ncbi request reprint Chronologic electrocardiographic changes in patients with hypertrophic cardiomyopathy associated with cardiac troponin 1 mutation
    Masami Shimizu
    Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School of Medical Science, Kanazawa University, Kanazawa, Japan
    Am Heart J 143:289-93. 2002
    ..Deletion of lysine 183 (K183del) in the cardiac troponin I (cTnI) gene is one of the mutations that causes hypertrophic cardiomyopathy (HCM). However, the phenotypic expression of this mutation has not been well established...
  14. ncbi request reprint Differentiation between patients with takotsubo cardiomyopathy and those with anterior acute myocardial infarction
    Masaru Inoue
    Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School of Medical Science, Kanazawa University, Kanazawa, Japan
    Circ J 69:89-94. 2005
    ....
  15. ncbi request reprint Heterogeneity of cardiac sympathetic nerve activity and systolic dysfunction in patients with hypertrophic cardiomyopathy
    Masami Shimizu
    Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School of Medical Science, Kanazawa University, Kanazawa, Japan
    J Nucl Med 43:15-20. 2002
    ....
  16. ncbi request reprint Autopsy findings in siblings with hypertrophic cardiomyopathy caused by Arg92Trp mutation in the cardiac troponin T gene showing dilated cardiomyopathy-like features
    Masami Shimizu
    Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School of Medical Science, Kanazawa University, Kanazawa, Japan
    Clin Cardiol 26:536-9. 2003
    ..Although some patients with HCM have shown dilated cardiomyopathy (DCM)-like features, the relationship between genotype and histologic findings is not well known...
  17. ncbi request reprint T wave peak-to-end interval and QT dispersion in acquired long QT syndrome: a new index for arrhythmogenicity
    Masato Yamaguchi
    Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School of Medical Science, Kanazawa University, Takara machi 13 1, Kanazawa 920 8640, Japan
    Clin Sci (Lond) 105:671-6. 2003
    ..28 is a good cut-off point for TdP. Tpe did not correlate with the corrected maximum QT interval, whereas the QTDc did correlate with this parameter. In conclusion, Tpe may be the best predictor for TdP in patients with acquired LQTS...
  18. ncbi request reprint Effects of gender on the number of diseased vessels and clinical outcome in Japanese patients with acute coronary syndrome
    Kotaro Oe
    Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School of Medical Science, Kanazawa University, Japan
    Circ J 66:435-40. 2002
    ..Our results suggest that older age may be a potential explanation for the higher in-hospital mortality in women with AMI, but female gender itself may be an important predictor for it among those with UAP...
  19. ncbi request reprint Serial changes in glucose-loaded 18F-fluoro-2-deoxyglucose positron emission tomography, 99mTc-tetrofosmin and 123I-beta-methyl-p-iodophenyl-penta-decanoic acid myocardial single-photon emission computed tomography images in patients with anterior acute m
    Ryota Fukuoka
    Department of Cardiology, Kanazawa Cardiovascular Hospital, Kanazawa, Japan
    Circ J 77:137-45. 2013
    ....
  20. ncbi request reprint Clinical and electrophysiological characterization of a novel mutation (F193L) in the KCNQ1 gene associated with long QT syndrome
    Masato Yamaguchi
    Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School of Medical Science, Kanazawa University, Takara machi 13 1, Kanazawa 920 8641, Japan
    Clin Sci (Lond) 104:377-82. 2003
    ..This electrophysiological study indicates that F193L causes less severe KCNQ1 current suppression, and thereby this mutation may result in a mildly affected phenotype...
  21. doi request reprint Serial cardiac influence of volume overload induced by interventional therapy for central venous stenosis or occlusion in chronic hemodialysis patients
    Yuki Horita
    Department of Cardiology, Kanazawa Cardiovascular Hospital, Kanazawa, Japan
    J Cardiol 57:316-24. 2011
    ..Percutaneous transluminal angioplasty (PTA) for central venous lesions is first-choice treatment. Cardiac function can be evaluated by measuring the acute increase in venous return volume after PTA...
  22. ncbi request reprint Oxidative stress correlates with left ventricular volume after acute myocardial infarction
    Hiroyuki Fujii
    Division of Cardiovascular Medicine, Graduate School of Medical Science, Kanazawa University, Ishikawa, Japan
    Jpn Heart J 43:203-9. 2002
    ..These findings suggest that oxidative stress may play an important role in the development and progression of left ventricular remodeling after AMI...
  23. doi request reprint Influence of antiplatelet medications on bleeding events in hemodialysis patients
    Shoichiro Daimon
    Department of Nephrology, Daimon Clinic for Internal Medicine, Nephrology and Dialysis, Ishikawa Department of Cardiology, Cardio Vascular Center Kanazawa Circulation Hospital, Kanazawa, Japan
    Ther Apher Dial 15:454-9. 2011
    ....