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Department Of Pediatrics Graduate School Of Medicine University Of Toyama | 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
- Open Heart Operation in a Child With Congenital Heart Disease and Hereditary Spherocytosis
- 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
- Outcome of Non-T-Cell-Depleted HLA-Haploidentical Hematopoietic Stem Cell Transplantation from Family Donors in Children and Adolescents
- A de novo KCNQ2 mutation detected in non-familial benign neonatal convulsions
- Mutations of Neuronal Voltage-gated Na^+ Channel α1 Subunit Gene SCN1A in Core Severe Myoclonic Epilepsy in Infancy (SMEI) and in Borderline SMEI (SMEB)
- Clinical and Genetic Analyses of Presumed Shwachman-Diamond Syndrome in Japan
- Three brothers of X-linked agammaglobulinemia : the relation between phenotype and neutropenia
- 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
- 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
- Non-Hodgkin's Lymphoma of the Ascending Colon in a Patient with Becker Muscular Dystrophy : Report of a Case
- A case of intractable epiepsy positive for the detection of measles virus genome in the cerebrospinal fluid and peripheral mononuclear cells using reverse tansecriptase-polymerase chain reaction
- A case of intractable epilepsy with mental deterioration : Detection of measles virus genome in cerebrospinal fluid and peripheral mononuclear cells using reverse transcriptase-polymerase chain reaction