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Department Of Pediatrics Faculty Of Medicine Toyama Medical And Pharmaceutical University | 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
- lnhibitory action of sulfatide a putative ligand for L-selectiv on B cell proliferation and lg prodrction
- 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)
- 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)
- M-protein-positive chronic active Epstein-Barr virus infection: features mimicking HIV-1 infection
- 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
- Evans syndrome in a patient with Langerhans cell histiocytosis : possible pathogenesis of autoimmunity in LCH
- Early lineage switch in an infant acute lymphoblastic leukemia
- 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