Miyawaki Toshio | Department Of Dermatology Graduate School Of Medicine University Of Toyama

スポンサーリンク

概要

関連著者

もっと見る

著作論文

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
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))
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
0291 ISOLATED NONCOMPACTION OF THE VENTRICULAL MYOCARDIUM (INVM) : CONSIDERATION OF THE DISTINCTIVE CLINICAL ENTITY
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)
Clinical and Genetic Analyses of Presumed Shwachman-Diamond Syndrome in Japan
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
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
Evaluation of left ventricular volume using automatic border detection in children : A comparison with conventional off-line echocardiographic quantification
Point mutation in intron 11 of Bruton's tyrosine kinase in atypical X-linked agammaglobulinemia
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
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
Genetic analysis of contiguous X-chromosome deletion syndrome encompassing the BTK and TIMM8A genes
Delayed onset adenosine deaminase deficiency associated with acute disseminated encephalomyelitis

もっと見る

スポンサーリンク