A novel method for indexing echocardiographic left ventricular mass in infants, children and adolescents : Evaluation of obesity-induced left ventricular hypertrophy
スポンサーリンク
概要
- 論文の詳細を見る
- 1999-04-01
著者
-
橋本 郁夫
Department Of Pediatrics School Of Medicine University Of Toyama
-
Tsubata Shinichi
Toyama Medical And Pharmaceutical University
-
Hamamichi Yuuji
Department Of Pediatrics Toyama Medical And Pharmaceutical University
-
Hamamichi Yuji
Department Of Pediatric Cardiology Osaka Medical Center And Research Institute For Maternal And Chil
-
Hashimoto Ikuo
Department Of Pediatrics Toyama Medical And Pharmaceutical University
-
Uese Kei-ichiro
Department Of Pediatrics School Of Medicine University Of Toyama
-
Ichida Fukiko
Department Of Department Of Pediatrics Graduate School Of Medicine University Of Toyama
-
Miyazaki Ayumi
Department Of Pediatrics Toyama Medical And Pharmaceutical University
-
Tsubata Shin-ichi
Department Of Pediatrics National Cardiovascular Center
-
Tsukano Shinya
Department Of Pediatrics National Cardiovascular Center Osaka University Medical School
-
Hamamichi Yuji
Department Of Pediatrics Toyama Medical And Pharmaceutical University
-
Ichida Fukiko
Department Of Pediatrics Faculty Of Medicine University Of Toyama
-
Miyawaki Toshio
Department Of Dermatology Graduate School Of Medicine University Of Toyama
-
Miyawaki Toshio
Department Of Department Of Pediatrics Graduate School Of Medicine University Of Toyama
-
Ichida Fukiko
The Gene Cardiovascular Disease Epidemiology Committee Of Japanese Pediatric Cardiology And Cardiac
関連論文
- ブルトン・チロシン・キナーゼの第1イントロンにおける転写調節異常
- Novel Fas (CD95/APO-1) mutations in infants with a lymphopro liferative disorder
- lnhibitory action of sulfatide a putative ligand for L-selectiv on B cell proliferation and lg prodrction
- Characterization of Ventricular Myocardial Performance in the Fetus by Tissue Doppler Imaging
- 正常健常児において左室内血流伝搬速度に影響を与える要因の検討
- Open Heart Operation in a Child With Congenital Heart Disease and Hereditary Spherocytosis
- Genetic Analysis in Patients with Left Ventricular Noncompaction and Evidence for Genetic Heterogeneity(Myocardial Disease, Cardiomyopathy and Myocarditis (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- OJ-273 Validation of Myocardial Acceleration during Isovolumic Contraction as a Noninvasive Index of Left Ventricular Contractility(Echo/Doppler 10 (I) : OJ32)(Oral Presentation (Japanese))
- OE-283 Profound S100A12 Expression in Neutrophils in Early Stage of Acute Kawasaki Disease(Congenital Heart Disease/Kawasaki's Disease 1 (M) : OE35)(Oral Presentation (English))
- Transannular Patching for Tetralogy of Fallot With an Anomalous Right Coronary Artery
- Clinical features of isolated left ventricular noncompaction : infantile type and juvenile type
- Propagation velocity of transmitral flow is useful for the assessment of left ventricular diastolic function in children with cardiomyopathy
- Novel Gene Mutation in Isolated Left Ventricular Noncompaction
- Dobutamine Stress Radionuclide Ventriculography Reveals Silent Myocardial Dysfunction in Kawasaki Disease
- 0291 ISOLATED NONCOMPACTION OF THE VENTRICULAL MYOCARDIUM (INVM) : CONSIDERATION OF THE DISTINCTIVE CLINICAL ENTITY
- 1049 Dipyridamole Stress Cine MRI of Coronary Arteries in Kawasaki Disease
- Bronchial hyper-responsiveness to inhaled histamine in children with congenital heart disease
- Evaluation of pulmonary blood supply by multiplanar cine magnetic resonance imaging in patients with pulmonary atresia and severe pulmonary stenosis
- OE-283 Profound S100A12 Expression in Neutrophils in Early Stage of Acute Kawasaki Disease(Congenital Heart Disease/Kawasaki's Disease 1 (M) : OE35)(Oral Presentation (English))
- Evaluation of Cardiac Tumors in Children by Electron-Beam Computed Tomography : Rhabdomyoma and Fibroma
- 川崎病冠動脈局所性狭窄における虚血の定量的評価に対する電子ビームCT(EBT)の有用性
- Evaluation by Contrast-Enhanced Electron Beam Computed Tomography of Myocardial Perfusion and Tissue Characteristics in Congenital Aortic Stenosis
- Hepatocyte growth factor in transient myeloproliferative disorder of Down syndrome
- Distinct Clones Are Associated with the Development of Transient Myeloproliferative Disorder and Acute Megakaryocytic Leukemia in a Patient with Down Syndrome
- OE-269 Evidence of Genetic Heterogeneity in Left Ventricular Noncompaction(Cardiomyopathy, basic/clinical-1 (M) OE45,Oral Presentation (English),The 70th Anniversary Annual Scientific Meeting of the Japanese Circulation Society)
- FRS-092 Infective Endocarditis in Pediatric Patients and Adults with Congenital Heart Disease : Japanese Nationwide Survey(Preventive Medicine in Cardiovascular Disease (H) : FRS11)(Featured Research Session (English))
- Activation-dependent T cell expression of the X-linked lymphoproliferative disease gene product SLAM-associated protein and its assessment for patient detection
- Clinical and Genetic Analyses of Presumed Shwachman-Diamond Syndrome in Japan
- Three brothers of X-linked agammaglobulinemia : the relation between phenotype and neutropenia
- Peripheral blood lymphocyte subpopulations in three infants with hepatosplenomegaly caused by cytomegalovirus infection
- Mononucleosis-like illness in an infant associated with human herpesvirus 6 infection
- X-Linked Agammaglobulinemia Diagnosed in Adulthood : A Case Report
- X-Linked Lymphoproliferative Disease in an Adult
- PE-413 Association Between the Accumulation of Cardiovascular Risk Factors and Adipokine or Individual Risk Factor Levels in Adolescent Volunteers(PE069,Preventive Medicine/Epidemiology/Education 2 (H),Poster Session (English),The 73rd Annual Scientific M
- Early lineage switch in an infant acute lymphoblastic leukemia
- Successful Cardiac Resynchronization Therapy in a 3-Year-Old Girl With Isolated Left Ventricular Non-Compaction and Narrow QRS Complex : A Case Report
- Pneumocystis jiroveci pneumonia as an atypical presentation of X-linked agammaglobulinemia
- Spontaneous regression of aleukemic leukemia cutis harboring a NPM/RARA fusion gene in an infant with cutaneous mastosytosis
- Molecular characterization of two novel VEGFR3 mutations in Japanese families with Milroy's disease
- PE-306 SCN5A Variant in Japanese Patients with Left Ventricular Noncompaction and Arrhythmia(Cardiomyopathy, basic/clinical-4, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
- Acute lymphoblastic leukemia after living donor liver transplantation
- Mutational Analysis of the WASP Gene in 2 Korean Families with Wiskott-Aldrich Syndrome
- Identification of mutations in the Bruton's tyrosine kinase gene, including a novel genomic rearrangements resulting in large deletion, in Korean X-linked agammaglobulinemia patients
- The Relationship Between Serum Levels of Interleukin-6 and Thyroid Hormone During the Follow-up Study in Children with Nonthyroidal Illness: Marked Inverse Correlation in Kawasaki and Infectious Disease
- Effective use of corticosteroid in a child with life-threatening plastic bronchitis after Fontan operation
- Evaluation of Phenytoin Dosage Regimens Based on Genotyping of CYP2C Subfamily in Routinely Treated Japanese Patients
- Immunoblot analysis of cellular expression of Bcl-2 family proteins,Bcl-2,Bax,Bcl-X and Mcl-1,in human perpheral bolld and lymphoid tissues
- Phenotypic variations between affected siblings with ataxia-telangiectasia : ataxia-telangiectasia in Japan
- Safety and Usefulness of a Novel eMotion^【○!R】 Electric Mesh Nebulizer in Children with Asthma
- Ability of preschool children to use dry powder inhalers as evaluated by In-Check Meter
- Theophylline metabolism in acute asthma with MxA-indicated viral infection
- Novel LAMP-2 Mutation in a Family With Danon Disease Presenting With Hypertrophic Cardiomyopathy
- Evaluation of left ventricular volume using automatic border detection in children : A comparison with conventional off-line echocardiographic quantification
- Strong Association of the Intrauterine Environment and the Frequency of Congenital Cardiovascular Diseases (CCVDs) Based on Epidemiological Survey Data(Congenital Heart Disease/Kawasaki's Disease 1 (M), The 69th Annual Scientific Meeting of the Japanese C
- Point mutation in intron 11 of Bruton's tyrosine kinase in atypical X-linked agammaglobulinemia
- Non-progressive viral myelitis in X-linked agammaglobulinemia
- identification of an SH2D1A Mutation in a Hypogammaglobulinemic Male Patient with a Diagnosis of Common Variable Immunodeficiency
- PJ-007 Dynamic Changes of Myeloid-related Protein (MRP) 8/MRP14 Positive Circulating Endothelial Cells in Patients with Acute Kawasaki Disease(Coronary circulation, basic/clinical-4 (IHD) PJ2,Poster Session (Japanese),The 70th Anniversary Annual Scientifi
- Total Anomalous Pulmonary Venous Connection With Bronchogenic Cyst in Neonatal Period
- A novel immunoregulatory protein in human colostrum, syntenin-1, for promoting the development of IgA-producing cells from cord blood B cells
- Changes in T-Cell Receptor Subsets After Cardiac Surgery in Children
- 先天性心疾患をもつ乳児の発達とその関連要因
- Left Ventricular Noncompaction
- PJ-775 Maternal Smoking and Congenital Heart Disease in Fetus(PJ130,Congenital Heart Disease/Kawasaki's Disease (M),Poster Session (Japanese),The 73rd Annual Scientific Meeting of The Japanese Circulation Society)
- 術後先天性心疾患児の12ヵ月時点での精神運動発達
- Possible New Role of Vascular Endothelial Growth Factor-D During the Acute Phase of Kawasaki Disease
- 我が国における学童・生徒における肥満と喘息症状との関連
- Autoimmune lymphoproliferative syndrome mimicking chronic active Epstein-Barr virus infection
- Atypical case of X-linked agammaglobulinemia diagnosed at 45 years of age
- A novel method for indexing echocardiographic left ventricular mass in infants, children and adolescents : Evaluation of obesity-induced left ventricular hypertrophy
- Prevalence and Distribution of Sarcomeric Gene Mutations in Japanese Patients With Familial Hypertrophic Cardiomyopathy
- Cardiac papillary fibroelastoma originated from atrial side of mitral valve leaflet
- Genetic analysis of contiguous X-chromosome deletion syndrome encompassing the BTK and TIMM8A genes
- Delayed onset adenosine deaminase deficiency associated with acute disseminated encephalomyelitis
- N-terminal pro-Brain Natriuretic Peptide as a Predictor of Reoperation in Children With Surgically Corrected Tetralogy of Fallot
- Surgical Repair of Left Ventricular Noncompaction in a Patient with a Novel Mutation of the Myosin Heavy Chain 7 Gene
- Relapsing Campylobacter Coli Bacteremia with Reactive Arthritis in a Patient with X-linked Agammaglobulinemia
- Modification of KCNH2-Encoded Cardiac Potassium Channels by KCNE1 Polymorphism:– Reply –