Emergent thoracic aortic angioplasty and stenting for middle aortic syndrome in non-specific aortitis
スポンサーリンク
概要
- 論文の詳細を見る
- 2010-07-01
著者
-
Shimizu Masami
Cardiovascular Checkup Committee For School Pupils Of Kanazawa Medical Association
-
Mizuno Sumio
福井心臓血圧センター
-
Mizuno Sumio
金沢大学 循環器内科
-
Yamaguchi Masato
Division Of Cardiovascular Medicine Kanazawa University Graduate School Of Medical Science
-
Shimizu Masami
金沢大学 循環器内科
-
Yamgishi Masakazu
Department Of Organ Transplantation National Cardiovascular Center
-
Miwa Yoshikazu
国立循環器病センター 高血圧腎臓内科
-
Mabuchi Tomohito
Department of Cardiology, Fukui Prefectural Hospital
-
Noji Yoshihiro
Department of Cardiology, Fukui Prefectural Hospital
-
Yanase Masanobu
Department Of Cardiology National Cardiovascular Center
-
Noji Yoshihiro
Department Of Cardiology Fukui Prefectural Hospital
-
Mabuchi Tomohito
Department Of Cardiology Fukui Prefectural Hospital
-
Fujino Susumu
Department Of Cardiology Fukui Prefectural Hospital
-
Aoyama Takahiko
Department Of Cardiac Surgery Aichi Medical University
-
Aoyama Takahiko
Department Of Cardiology Fukui Prefectural Hospital
-
Shimizu Masami
Second Department Of Internal Medicine School Of Medicine Kanazawa University
-
Shimizu Masami
The Second Department Of Internal Medicine School Of Medicine Kanazawa University
-
Yoshida Shohei
Department Of Molecular Biology Graduate School Of Biological Sciences Nara Institute Of Science And
-
Yamagishi Masakazu
Molecular Genetics Of Cardiovascular Disorders Graduate School Of Medical Science Kanazawa Universit
-
Yamaguchi Masato
Department Of Cardiology Fukui Prefectural Hospital
-
Shimizu Masami
The Second Department Of Internal Medicine School Of Medicine Kanazawa; University
-
Yamagishi Masakazu
Molecular Genetics Of Cardiovascular Disorders Graduate School Of Medical Science Kanazawa Universit
-
Yamagishi Masakazu
Molecular Genetics Of Cardiovascular Disorders Division Of Cardiovascular Medicine Graduate School O
-
Shimizu Masami
Molecular Genetics Of Cardiovascular Disorders Division Of Cardiovascular Medicine Graduate School O
-
SUZUKI Masatomo
Department of Cardiology, Fukui Prefectural Hospital
-
Yoshida Shohei
Department Of Cardiology Fukui Prefectural Hospital
-
Yamagishi Masakazu
Division Of Cardiology National Cardiovascular Center
-
Suzuki Masatomo
Department Of Cardiology Fukui Prefectural Hospital
-
Mizuno Sumio
Division Of Cardiology Fukui Cardiovascular Center Hospital
-
MABUCHI Tomohito
Department of Biological and Environmental Sciences, Faculty of Agriculture, Graduate School of Agricultural Science, Kobe University
関連論文
- Experience of appendicular thermal therapy applied to a patient with a left ventricular assist device awaiting heart transplantation
- Impact of Severe Earthquake on the Occurrence of Acute Coronary Syndrome and Stroke in a Rural Area of Japan : Experience From the Noto Peninsula Earthquake
- PJ-643 Prediction of Cardiac Events in Patients with Hypertrophic Cardiomyopathy : Usefulness of MIBG Myocardial Scintigraphy(Cardiomyopathy, basic/clinical-7 (M) PJ108,Poster Session (Japanese),The 70th Anniversary Annual Scientific Meeting of the Japane
- PE-067 Late Gadolinium Enhancement Cardiovascular Magnetic Resonance in Hypertrophic Cardiomyopathy Caused by Cardiac Troponinl Gene Mutation(Cardiomyopathy, basic/clinical-3 (M) PE12,Poster Session (English),The 70th Anniversary Annual Scientific Meeting
- OJ-223 A Novel Missense Mutation Met1107Thr in Cardiac Ryanodine Receptor Gene is Associated with Hypertrophic Cardiomyopathy(Cardiomyopathy, basic/clinical-2 (M) OJ38,Oral Presentation (Japanese),The 70th Anniversary Annual Scientific Meeting of the Japa
- OE-284 Usefulness of Late Gadolinium Enhancement Cardiovascular Magnetic Resonance in Patients with Hypertrophic Cardiomyopathy Associated with TNNI3 Gene Mutation(MRI/MRA-1 (I) OE48,Oral Presentation (English),The 70th Anniversary Annual Scientific Meeti
- OE-265 Genotype-Phenotype Variations in Cardiomyopathies Caused by a Cardiac Troponin I Gene Mutation(Cardiomyopathy, basic/clinical-1 (M) OE45,Oral Presentation (English),The 70th Anniversary Annual Scientific Meeting of the Japanese Circulation Society)
- OE-088 Differences in Diagnostic Value of Various Criteria of Negative T Waves for Hypertrophic Cardiomyopathy in a Genotyped Population(ECG/Body surface potential mapping/Holter-1 (A) OE15,Oral Presentation (English),The 70th Anniversary Annual Scientifi
- FRS-104 Association between Angiotensin II Receptor Gene Polymorphism and Left Ventricular Systolic Dysfunction in Sarcomere Gene Mutation-induced Hypertrophic Cardiomyopathy(Frontier of Cardiomyopathy Research-2 (M) FRS21,Featured Research Session (Engli
- Cardiac Sympathetic Nerve Activity and Left Ventricular Remodeling in Hypertrophic Cardiomyopathy(Cardiomyopathy, Clinical 3 (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Regional Cardiac Sympathetic Nerve Function in Cardiomyopathies : Dilated Cardiomyopathy Versus Dilated Phase of Hypertrophic Cardiomyopathy(Cardiomyopathy, Clinical 7 (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- PJ-424 Cardiac Sympathetic Nerve Activity in Patients with Hypertrophic Cardiomyopathy Caused by Thin Filament Gene Mutations(Cardiomyopathy, Clinical 5 (M) : PJ71)(Poster Session (Japanese))
- PJ-651 Predictors of the Improvement in Left Ventricular Ejection Fraction in Non-Ischemic Dilated Cardiomyopathy during Beta-Blocker Therapy(PJ109,Heart Failure (Treatment) 3 (M),Poster Session (Japanese),The 73rd Annual Scientific Meeting of The Japanes
- Three Cases of Iatrogenic Coronary Ostial Stenosis After Aortic Valve Replacement
- Abnormal sympathetic innervation of the heart in a patient with Emery-Dreifuss muscular dystrophy
- Risk Evaluation of Coronary Heart Disease and Cerebrovascular Disease by the Japan Atherosclerosis Society Guidelines 2002 Using the Cohort of the Holicos-PAT Study
- Differentiation between patients with takotsubo cardiomyopathy and those with anterior acute myocardial infarction
- PE-279 High Incidence of Sudden Cardiac Death with Conduction Disturbances and Atrial Cardiomyopathy Caused by a Mutation in the STA Gene(Cardiomyopathy, Clinical 3 (M) : PE48)(Poster Session (English))
- Reduction of hemolysis without reoperation following mitral valve repair
- PE-237 Cholesterol-years Score is Associated with Development of Senile Degenerative Aortic Stenosis in Heterozygous Familial Hypercholesterolemia(Atherosclerosis, clinical-9 (H) PE40,Poster Session (English),The 70th Anniversary Annual Scientific Meeting
- PE-285 J-LIT (Japan Lipid Intervention Trial) Score Predicts Recurrence of Coronary Event(Preventive medicine/Epidemiology/Education-4 (H) PE48,Poster Session (English),The 70th Anniversary Annual Scientific Meeting of the Japanese Circulation Society)
- OE-101 Relationship of lipoprotein lipase and hepatic triacylglycerol lipase activity to serum adiponectin levels in Japanese hyperlipidemic men(Cerebrovascular circulation/Stroke-1 (H) OE17,Oral Presentation (English),The 70th Anniversary Annual Scientif
- Type III hyperlipoproteinemia exaggerated by Sheehan's syndrome with advanced systemic atherosclerosis - A 28-year clinical course
- Enhanced Cholesterol Efflux from J774 Macrophages and Fu5AH Hepatoma Cells to Serum from CETP Deficiency(Atherosclerosis, Basic 6 (IHD), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Secreted Type II Phospholipase A_2 Decreases High-density-lipoprotein (HDL)-phospholipids and HDL_3-cholesterol in Human(Metabolism/Biochemistry/Energetics 1 (IHD), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Association Between ABCG5/G8 SNPs and Higher Cholesterol Absorption Marker in Hypercholesterolemia(Lipid Disorders 3 (H), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- RXRγ Gene Variant is Associated with Higher BMI, Lower HDL-C, Advanced Coronary Artery Disease, and Frequent in Familial Combined Hyperlipidemia(The Frontier of Atherosclerosis Research (IHD), The 69th Annual Scientific Meeting of the Japanese Circulation
- Japan Lipid Intervention Trial (J-LIT) Chart Predicts the Absence of Coronary Artery Disease More Accurately Than Symptom Limited Exercise Stress Electrocardiography
- Gene mutations in adult Japanese patients with dilated cardiomyopathy
- 1 Prevalence of Long QT Syndrome and Frequencies of Gene Mutation Carriers in Japanese Children : an Epidemiological and Genetic Study(Plenary Session 4 (PL-4) (A) New Scientific Approaches to QT Prolongation,Special Program,The 72nd Annual Scientific Mee
- Clinical Characteristics of Patients with Cardiopulmonary Arrest on Arrival in Acute Myocardial Infarction(Acute Myocardial Infarction, Clinical (Pathophysiology) 2 (IHD), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- OJ-297 Clinacal Characteristics of Patients with Cardiopulmonary Arrest on Arrival in Acute Myocardial Infarction(Acute Myocardial Infarction, Clinical (Pathophysiology) 5 (IHD) : OJ35)(Oral Presentation (Japanese))
- Effects of Reperfusion Therapy before Cardiac Rupture Following Acute Myocardial Infarction
- Effects of Immediate Sterling after Intravenous Coronary Thrombolysis for Acute Myocardial Infarction
- Coronary Embolism Associated with Atrial Fibrillation In the Patients with Acute Myocardial Infarction
- Clinacal Characteristics of Patients with Cardiopulmonary Arrest on Arrival in Acute Myocardial Infarction
- Improved Clinical Outcomes with Gradual Reperfusion Angioplasty Compared to Coronary Stenting for Acute Anterior Myocardial Infarction
- Improved Myocardial Salvage with Gradual Reperfusion Angioplasty Compared to Coronary Stenting for Acute Anterior Myocardial Infarction : Three-year Follow-Up Results
- Effect of immediate stenting after successful thrombolysis for acute myocardial infarction
- Distribution of QTc Values and Prevalence of Short QT Syndrome in the Japanese Population (ECG/Body Surface Potential Mapping/Holter 6 (A), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Gene Mutations in Patients with Hypertrophic Cardiomyopathy Showing Mild Left Ventricular Hypertrophy(Cardiomyopathy, Clinical 1 (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Differences in Diagnostic Value of Classic Electrocardiographic Voltage Criteria for Hypertrophic Cardiomyopathy in a Genotyped Population(Cardiomyopathy, Clinical 2 (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Ankyrin-B Gene Mutation is a Rare Cause of Long QT Syndrome in Japan(Arrhythmia, Basic 1 (A), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Long-Term Course of Patients with Cardiomyopathy Associated with Phospholamban Gene Mutations(Cardiomyopathy, Clinical 8 (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Early Development of Dilated Cardiomyopathy in Subjects with Hypertrophic Cardiomyopathy Caused by Mutations of the Thin Filament Genes(Cardiomyopathy, Clinical 7 (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Angiotensin II Type 1 Receptor A/C1166 Gene Polymorphism and Left Ventricular Systolic Dysfunction in Hypertrophic Cardiomyopathy with Sarcomere Gene Mutations(Cardiomyopathy, Clinical 7 (M), The 69th Annual Scientific Meeting of the Japanese Circulation
- Impact of Bundle-Branch Block on Clinical Manifestation in Patients with Hypertrophic Cardiomyopathy : Analyses Based on Molecular Genetic Diagnoses(Cardiomyopathy, Clinical 6 (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Cardiac Manifestations and Genotype-Phenotype Correlations in Carriers with the STA Gene Mutations(Myocardial Disease, Cardiomyopathy and Myocarditis (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Mutation of the β Myosin Heavy Chain Gene associated with Isolated Left Ventricular Noncompaction(Myocardial Disease, Cardiomyopathy and Myocarditis (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Clinical Features of Hypertrophic Cardiomyopathy Caused by a Novel Val85Leu Missense Mutation in the Cardiac Troponin T Gene(Cardiomyopathy, Clinical 1 (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Difference in the risk factors for coronary, renal and other peripheral arteriosclerosis in heterozygous familial hypercholesterolemia
- FRS-128 Mutations in Phospholamban Gene Cause Hypertrophic and Dilated Cardiomyopathy(Myocardial Disease (M) : FRS16)(Featured Research Session (English))
- Increased Circulating Matrix Metalloproteinase-2 in Patients with Hypertrophic Cardiomyopathy with Systolic Dysfunction
- Scintigraphic evaluation of regression of abnormal Q waves in myocardial infarction
- Prevalence and Onset of Hypertrophic Cardiomyopathy Caused by Thin Filament Gene Mutations(Cardiomyopathy, Clinical 6 (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- PJ-425 Early Development of Dilated Cardiomyopathy in Subjects with Mutations in the Cardiac Troponin Complex Genes(Cardiomyopathy, Clinical 5 (M) : PJ71)(Poster Session (Japanese))
- OJ-511 Missense Mutations in Cardiac Ryanodine Receptor Gene Cause Hypertrophic Cardiomyopathy Associated with Ventricular Arrhythmia or Massive Hypertrophy(Cardiomyopathy, Basic (M) : OJ62)(Oral Presentation (Japanese))
- OJ-229 Atrial Fibrillation in Patients with Hypertrophic Cardiomyopathy with Different Genotypes(Cardiomyopathy, Clinical 1 (M) : OJ26)(Oral Presentation (Japanese))
- OJ-078 Usefulness of Q-T Peak Dispersion for Diagnosis of KCNH2 Gene Mutations in Patients with Long QT Syndrome(Arrhythmia, Basic 1 (A) : OJ10)(Oral Presentation (Japanese))
- FRS-129 Mutations Responsible for Dilated Cardiomyopathy in Japan(Myocardial Disease (M) : FRS16)(Featured Research Session (English))
- PJ-596 Exercise-induced Systolic Dysfunction in Patients with Non-obstructive Hypertrophic Cardiomyopathy and Mutations in the Cardiac Troponin Genes(Cardiomyopathy, Clinical 7 (M) : PJ100)(Poster Session (Japanese))
- OJ-335 PRKAR1A Gene Mutation in Patients with Cardiac Myxoma(Valvular Heart Disease/Pericarditis/Cardiac Tumor 2 (M) : OJ40)(Oral Presentation (Japanese))
- Alterations in Echocardiographic Tissue Characterization in Patients with Cardiac Troponin I Gene Mutation a Possible Indicator of Preclinical Hypertrophic Cardiomyopathy
- Cardiac Actin and Alpha-Tropomyosin Genes Are Associated with Neither Hypertrophic Nor Dilated Cardiomyopathy in Patients from Hokuriku District in Japan
- The Correlation Between Coronary Stenosis Index and Flow-Mediated Dilation of the Brachial Artery
- 0347 THE CORRELATION BETWEEN CORONARY STENOSIS INDEX(CSI) AND FLOW-MEDIATED DILATION(FMD) IN THE BRACHIAL ARTERY
- Can LQT1 be Differentiated with ST-T Morphology from the Other Type of Long QT Syndrome?(Arrhythmia, Diagnosis/Pathophysiology/EPS 6 (A), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Prevalence of Gene Mutations in Patients with Congenital Long QT Syndrome(Arrhythmia, Basic 2 (A), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- PE-280 Missense Mutations in the MYBPC3 Gene are Responsible for Hypertrophic Cardiomyopathy with Left Ventricular Systolic Dysfunction and Dilatation(Cardiomyopathy, Clinical 3 (M) : PE48)(Poster Session (English))
- PE-278 Electrocardiography Shows Preferable Diagnostic Value Even in Carriers of Hypertrophic Cardiomyopathy who do not Manifest Ventricular Wall Hypertrophy on Echocardiography(Cardiomyopathy, Clinical 3 (M) : PE48)(Poster Session (English))
- OJ-237 KCNJ2 Gene Mutation is a Rare Cause of Long QT Syndrome(Arrhythmia, Diagnosis/Pathophysiology/EPS 9 (A) : OJ27)(Oral Presentation (Japanese))
- FRS-132 Phenotypic Discrepancies Between Electrocardiography and Echocardiography for Hypertrophic Cardiomyopathy in Genetically Affected Subjects(Myocardial Disease (M) : FRS16)(Featured Research Session (English))
- OE-057 Genetic Effects of Farnesoid-X-receptor on BMI, HDL-C, LDL-C and Development of Fatty Liver(Lipid disorders-1 (H) OE10,Oral Presentation (English),The 70th Anniversary Annual Scientific Meeting of the Japanese Circulation Society)
- Plasma Endothelin-1 Elevation Associated With Alcohol-Induced Variant Angina
- IS130 Dipylidamole induced stunning continues for at least one hour in patients with coronary artery disease : Evaluation with quantitative gated SPECT
- P244 PROGNOSES OF THE JAPANESE VASOSPASTIC ANGINA PECTORIS PATIENTS
- 1015 Comparison of the Effects of Prolonged Versus Standard Balloon Inflation for Acute Anterior Myocardial Infarction
- P699 Semiquantitative Analysis of Pathological Findings and serum concentration of collagen in Restenosis after Atherectomy
- 0624 Efficacy of Using Perfusion Balloon Catheter as Initial Balloon in Coronary Angioplasty for Acute Myocardial Infarction
- -P385- Semiquantitative Analysis of Pathological Findings in Restenosis after Atherectomy(PROCEEDINGS OF THE 59th ANNUAL SCIENTIFIC MEETING OF THE JAPANESE CIRCULATION SOCIETY)
- -1286- CLINICAL SIGNIFICANCE OF RECRUITABLE COLLATERAL VESSELS IN CORONARY ARTERY DISEASE(PROCEEDINGS OF THE 59th ANNUAL SCIENTIFIC MEETING OF THE JAPANESE CIRCULATION SOCIETY)
- -0374- MYOCARDIAL DAMAGE OF THE PATIENTS WITH VASOSPASTIC ANGINA PECTORIS : FOLLOW UP STUDY WITH I-123 BUMIPP SPECT(PROCEEDINGS OF THE 59th ANNUAL SCIENTIFIC MEETING OF THE JAPANESE CIRCULATION SOCIETY)
- OJ-415 Electrocardiographic Events and Cholesterol Reduction with Pravastatin in Patients with Hypercholesterolemia : Hokuriku Lipid Coronary Heart Disease Study-Pravastatin Atherosclerosis Trial(Preventive Medicine/Epidemiology/Education 3 (H) : OJ50)(Or
- Usefulness of Acoustic Densitometry Method for Detection of Myocardial Changes in Preclinical Patients with Hypertrophic Cardiomyopathy
- Prevalence of Long QT Syndrome in Japanese Children(ECG/Body Surface Potential Mapping/Holter 1 (A), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Q-T peak dispersion in congenital long QT syndrome: Possible marker of mutation of HERG
- Cardiac Manifestations and Long-Term Course in Emery-Dreifuss Muscular Dystrophy Caused by a Nonsense Mutation in the STA Gene
- Diagnostic Values of Abnormal Q Waves for Hypertrophic Cardiomyopathy Based on the Genetic Information
- QT Variables in Preclinical Patients with Hypertrophic Cardiomyopathy
- QT Variables in Various Genotyped Patients with Hypertrophic Cardiomyopathy
- Mitochondrial DNA Mutations in Hypertrophic Cardiomyopathy
- Frequency of Asymmetric Septal Hypertrophy in Patients with Hypertrophic Cardiomyopathy : Difference in Genotypes
- OE-038 Coronary Endothelial Dysfunction Pleiotropically Accelerates Atherothrombogenic Processes in Patients with Coronary Artery Disease(Angina Pectoris, Basic and Clinical (IHD) : OE5)(Oral Presentation (English))
- IS153 Heterogeneity in Contents From Intracoronary Aspiration Thorombectomy for Acute Myocardial Infarction
- 0239 A Comparison of New Device(DCA and STENT)With Balloon Angioplasty in Patients With Recurrent Restenosis
- Clinical and Electrophysiological Characteristics of Brugada Syndrome Caused by a Missense Mutation in the S5-pore site of SCN5A(Arrhythmia, Diagnosis/Pathophysiology/EPS 5 (A), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- FRS-144 A Novel Missense Mutation of SCN5A Gene Associated with Brugada Syndrome by Bidirectional Effects on Blocking Actions of Antiarrhythmic Drugs(Sudden Cardiac Death (A) : FRS18)(Featured Research Session (English))
- PE-138 Benidipine, a Long-Acting Calcium Channel Blocker, Improves Coronary Flow Reserve and Endothelial Function in Patients With Hypertension and Diabetes Mellitus(Coronary Circulation, Basic/Clinical 1 (IHD) : PE24)(Poster Session (English))
- Vasomotor impacts of glucose intolerance on resistance coronary arteries in hypertensives
- Emergent thoracic aortic angioplasty and stenting for middle aortic syndrome in non-specific aortitis