Nakazawa Makoto | Pediatric And Lifelong Congenital Cardiology Institute Southern Tohoku General Hospital

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著作論文

OE-389 Clinical Phenotype of Japanese LQT1 Form of Congenital Long QT Syndrome by Location and Coding Type From Japanese Multicenter Registry(Arrhythmia, diagnosis/Pathophysiology/EPS(02)(A),Oral Presentation(English),The 72nd Annual Scientific Meeting of
ファロー四徴症児の無酸素発作予防のためのカテーテル前投薬におけるペチジンの有用性について : 後方視的検討および前方視的無作為検討の結果から
1 Molecular Basis for Low Penetrance in the Long QT Syndrome(Meet the Expert 7 (ME7) (A) : Issues on Sudden Cardiac Death)(Special Program)
CHARACTERISTICS OF CARDIAC FUNCTION DURING EXERCISE IN PATIENTS WITH TA AFTER FONTAN'S OPERATION : Doppler, RI : I : 48 Annual Scientific Meeting, Japanese Circulation Society
ELECTROPHYSIOLOGICAL STUDIES IN PATIENTS WITH ATRIOVENTRICULAR DISCORDANCE : PROCEEDINGS OF THE 47th ANNUAL SCIENTIFIC MEETING OF THE JAPANESE CIRCULATION SOCIETY : Electrophysiology (I)
OJ-009 A Common KCNE1 Polymorphism, D85N, is a Genetic Modifier of Long QT Syndrome(Arrhythmia, diagnosis/ Pathophysiology/ EPS(03)(A),Oral Presentation(Japanese),The 72nd Annual Scientific Meeting of the Japanese Circulation Society)
A single mutation of cardiac sodium channel gene confers phenotypes of both Brugada and long QT syndromes
Ion channel mutations and polymorphisms in Japanese patients with acquired long QT syndrome
PE-103 Clinical Phenotype of Japanese LQT3 Form of Congenital Long QT Syndrome by Location of Mutation from Japanese Multicenter Registry(PE018,Arrhythmia, Others (Clinical/Pathophysiology) (A),Poster Session (English),The 73rd Annual Scientific Meeting o
FRS-117 Clinical and Electrocardiographic Characteristics of Japanese Probands with Brugada Syndrome with an SCN5A Mutation from Japanese Multicenter Registry(FRS24,Novel Mechanisms of Ventricular Arrhythmia (A),Featured Research Session (English),The 73r
PJ-208 Impact of Frameshift Mutation and Nonsense-mediated mRNA Decay on Clinical Phenotype in LQT2 Form of Congenital Long QT Syndrome(Arrhythmia,diagnosis/Pathophysiology/EPS(13)(A),Poster Session(Japanese),The 72nd Annual Scientific Meeting of the Japa
Congenital atrial standstill associated with coinheritance of a novel SCN5A mutation and connexin 40 polymorphisms
Risk Factors for Mortality and Morbidity in Patients with Cyanotic Congenital Heart Disease (Congenital Heart Disease/Kawasaki's Disease 2 (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
Arrhythmias Late After Repair of Tetralogy of Fallot : A Japanese Multicenter Study
Effect of beraprost sodium on pulmonary vascular resistance in candidates for a Fontan procedure : A preliminary study
An SCN5A Mutation Associated With Idiopathic Ventricular Fibrillation Alters The Na^+ Channel Pore Structure And Responses To Antiarrhythmic Drugs
PJ-190 A KCNE1 Single Nucleotide Polymorphism, D85N, Serves as a Modifier in Forme-fruste Type of Long QT syndrome(Genetics/Genetically engineered models/Gene therapy-3 (M) PJ32,Poster Session (Japanese),The 70th Anniversary Annual Scientific Meeting of t
Double SCN5A mutation underlying asymptomatic Brugada syndrome
Single Nucleotide Polymorphisms of Cardiac Na^+ Channel Gene SCN5A : Allelic Prevalence in Brugada Syndrome and Their Biophysical Properties
High-risk for Bradyarrhythmic Complications in Patients with Brugada Syndrome Caused by SCN5A Gene Mutations(Arrhythmia, Basic (A), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
5 Overlap Between LQT3 and Brugada Syndrome : Clinical Features in a Common Mutation and Underlying Biophysical Mechanisms(Plenary Session 4 (PL-4) (A) New Scientific Approaches to QT Prolongation,Special Program,The 72nd Annual Scientific Meeting of the
Increased P-Selectin Expression on Platelets and Decreased Plasma Thrombomodulin in Fontan Patients
Aortic and Valvular Size in Patients with Aortic Regurgitation Long after Arterial Switch Operation in Transposition of the Great Arteries
PE-307 Left Ventricular Noncompaction Associated With Mutations in Cardiac Na Channel Gene SCN5A(Cardiomyopathy, basic/clinical-4, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
OE-085 Genetic Factors Conferring Congenital Sick Sinus Syndrome in SCN5A Mutation Carriers(Arrhythmia, basic-1, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
Sustained Ventricular Tachycardia and Late Potentials after Repair of Tetralogy of Fallot(Congenital Heart Disease/Kawasaki's Disease 1 (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
1 Genotype-Phenotypes Relations of SCN5A-Positive Brugada Syndrome(Brugada Syndrome:From Cell to Bedside,Plenary Session 2 (PL2) (A),The 70th Anniversary Annual Scientific Meeting of the Japanese Circulation Society)
EVALUATION OF LEFT VENTRICULAR FUNCTION IN PATIENTS AFTER JATENE PROCEDURE, A STUDY USING LEFT VENTRICULAR END-SYSTOLIC WALL STRESS-VELOCITY OF FIBER SHORTENING RELATION : Ventricular Function : 53 Annual Scientific Meeting, Japanese Circulation Society
Guidelines for Diagnosis and Management of Cardiovascular Sequelae in Kawasaki Disease (JCS 2008) : Digest Version
Immunonutritional effects during synbiotics therapy in pediatric patients with short bowel syndrome
HEMODYNAMIC EFFECTS OF ISOPROTERENOL DURING EARLY STAGES OF MORPHOGENESIS, DIFFERENCE BETWEEN CHICK AND RAT EMBRYOS : Cardiovascular Drugs : 53 Annual Scientific Meeting, Japanese Circulation Society
Afterload Mismatch, and Cerebral Intraventricular and Pulmonary Hemorrhage in Preterm Infants
OE-284 Oxygen Causes Contraction of the Ductus Arteriosus By Decreasing Intracellular H_2O_2 Generation(Congenital Heart Disease/Kawasaki's Disease 1 (M) : OE35)(Oral Presentation (English))
Arrhyhtmias in Postoperative Cyanotic Congenital Heart Disease : -Japanese Experience-(ALTAS-CHD Study)(Diagnosis and Management of Arrhythmias in Adults with Congenital Heart, The 69th Annual Scientific Meeting of the Japanese Circulation Society)
Guidelines for Risks and Prevention of Sudden Cardiac Death (JCS 2010) : Digest Version

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