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Development of a Novel Risk Prediction Model for Sudden Cardiac Death in Childhood Hypertrophic Cardiomyopathy (HCM Risk-Kids)

JAMA cardiology, 2019-09, Vol.4 (9), p.918

2019

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Clinical Features and Natural History of Preadolescent Nonsyndromic Hypertrophic Cardiomyopathy

Journal of the American College of Cardiology, 2022-05, Vol.79 (20), p.1986-1997

2022

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Cardiac Ankyrin Repeat Protein Gene ( ANKRD1 ) Mutations in Hypertrophic Cardiomyopathy

Journal of the American College of Cardiology, 2009-07, Vol.54 (4), p.334-342

2009

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Effect of Addition of a Statin to Warfarin on Thromboembolic Events in Japanese Patients With Nonvalvular Atrial Fibrillation and Diabetes Mellitus

The American journal of cardiology, 2017-07, Vol.120 (2), p.230-235

2017

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Prevalence, Clinical Significance, and Genetic Basis of Hypertrophic Cardiomyopathy With Restrictive Phenotype

Journal of the American College of Cardiology, 2007-06, Vol.49 (25), p.2419-2426

2007

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Idiopathic restrictive cardiomyopathy is part of the clinical expression of cardiac troponin I mutations

The Journal of clinical investigation, 2003-01, Vol.111 (2), p.209-216

2003

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Novel mutation in cardiac troponin I in recessive idiopathic dilated cardiomyopathy

The Lancet (British edition), 2004-01, Vol.363 (9406), p.371-372

2004

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Lifelong Left Ventricular Remodeling of Hypertrophic Cardiomyopathy Caused by a Founder Frameshift Deletion Mutation in the Cardiac Myosin-Binding Protein C Gene Among Japanese

Journal of the American College of Cardiology, 2005-11, Vol.46 (9), p.1737-1743

2005

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Whole immunofluorescence staining of podocytes in fabry disease

Nephrology (Carlton, Vic.), 2019-01, Vol.24 (1), p.135-135

2019

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Differential clinical benefits of 5-fluorouracil-based adjuvant chemotherapy for patients with stage III colorectal cancer according to CD133 expression status

Japanese journal of clinical oncology, 2014-01, Vol.44 (1), p.42-48

2014

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Identification of Kaposi's Sarcoma-Associated Herpesvirus (KSHV)-Specific Cytotoxic T-Lymphocyte Epitopes and Evaluation of Reconstitution of KSHV-Specific Responses in Human Immunodeficiency Virus Type 1-Infected Patients Receiving Highly Active Antiretroviral Therapy

Journal of Virology, 2002-03, Vol.76 (6), p.2634-2640

2002

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Long-Term Prognosis of Dilated Cardiomyopathy Revisited: An Improvement in Survival Over the Past 20 Years

Circulation Journal, 2006, Vol.70(4), pp.376-383

2006

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Functional analysis of ssaJ and the ssaK/U operon, 13 genes encoding components of the type III secretion apparatus of Salmonella Pathogenicity Island 2

Molecular microbiology, 1997-04, Vol.24 (1), p.155-167

1997

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Identification of Human Herpesvirus 8-Specific Cytotoxic T-Cell Responses

Journal of Virology, 1999-07, Vol.73 (7), p.6136-6140

1999

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The role of the electrocardiographic phenotype in risk stratification for sudden cardiac death in childhood hypertrophic cardiomyopathy

European journal of preventive cardiology, 2022-03, Vol.29 (4), p.645

2022

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Frequency and clinical expression of cardiac troponin I mutations in 748 consecutive families with hypertrophic cardiomyopathy

Journal of the American College of Cardiology, 2004-12, Vol.44 (12), p.2315-2325

2004

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Prevalence, clinical significance, and genetic basis of hypertrophic cardiomyopathy with restrictive phenotype. Commentary

Journal of the American College of Cardiology, 2007, Vol.49 (25), p.2419-2429

2007

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1032-125 Electrocardiographic pattern of giant negative T wave in hypertrophic cardiomyopathy: Is it a specific feature of “Apical” hypertrophic cardiomyopathy?

Journal of the American College of Cardiology, 2004-03, Vol.43 (5), p.A165-A166

2004

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Lifelong left ventricular remodeling of hypertrophic cardiomyopathy caused by a founder frameshift deletion mutation in the cardiac myosin-binding protein C gene among Japanese. Commentary

Journal of the American College of Cardiology, 2005, Vol.46 (9), p.1737-1746

2005

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Frequency and clinical expression of Cardiac troponin I mutations in 748 consecutive families with hypertrophic cardiomyopathy. Commentary

Journal of the American College of Cardiology, 2004, Vol.44 (12), p.2315-2328

2004

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Development of a Novel Risk Prediction Model for Sudden Cardiac Death in Childhood Hypertrophic Cardiomyopathy (HCM Risk-Kids)

Clinical Features and Natural History of Preadolescent Nonsyndromic Hypertrophic Cardiomyopathy

Cardiac Ankyrin Repeat Protein Gene ( ANKRD1 ) Mutations in Hypertrophic Cardiomyopathy

Effect of Addition of a Statin to Warfarin on Thromboembolic Events in Japanese Patients With Nonvalvular Atrial Fibrillation and Diabetes Mellitus

Prevalence, Clinical Significance, and Genetic Basis of Hypertrophic Cardiomyopathy With Restrictive Phenotype

Idiopathic restrictive cardiomyopathy is part of the clinical expression of cardiac troponin I mutations

Novel mutation in cardiac troponin I in recessive idiopathic dilated cardiomyopathy

Lifelong Left Ventricular Remodeling of Hypertrophic Cardiomyopathy Caused by a Founder Frameshift Deletion Mutation in the Cardiac Myosin-Binding Protein C Gene Among Japanese

Whole immunofluorescence staining of podocytes in fabry disease

Differential clinical benefits of 5-fluorouracil-based adjuvant chemotherapy for patients with stage III colorectal cancer according to CD133 expression status

Identification of Kaposi's Sarcoma-Associated Herpesvirus (KSHV)-Specific Cytotoxic T-Lymphocyte Epitopes and Evaluation of Reconstitution of KSHV-Specific Responses in Human Immunodeficiency Virus Type 1-Infected Patients Receiving Highly Active Antiretroviral Therapy

Long-Term Prognosis of Dilated Cardiomyopathy Revisited: An Improvement in Survival Over the Past 20 Years

Functional analysis of ssaJ and the ssaK/U operon, 13 genes encoding components of the type III secretion apparatus of Salmonella Pathogenicity Island 2

Identification of Human Herpesvirus 8-Specific Cytotoxic T-Cell Responses

The role of the electrocardiographic phenotype in risk stratification for sudden cardiac death in childhood hypertrophic cardiomyopathy

Frequency and clinical expression of cardiac troponin I mutations in 748 consecutive families with hypertrophic cardiomyopathy

Prevalence, clinical significance, and genetic basis of hypertrophic cardiomyopathy with restrictive phenotype. Commentary

1032-125 Electrocardiographic pattern of giant negative T wave in hypertrophic cardiomyopathy: Is it a specific feature of “Apical” hypertrophic cardiomyopathy?

Lifelong left ventricular remodeling of hypertrophic cardiomyopathy caused by a founder frameshift deletion mutation in the cardiac myosin-binding protein C gene among Japanese. Commentary

Frequency and clinical expression of Cardiac troponin I mutations in 748 consecutive families with hypertrophic cardiomyopathy. Commentary

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