Kanegane Hirokazu | Department Of Pediatrics Faculty Of Medicine Toyama Medical And Pharmaceutical University

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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
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
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
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
Outcome of pediatric patients with Langerhans cell histiocytosis treated with 2 chlorodeoxyadenosine : a nationwide survey in Japan
A case of severe recurrent hepatitis with common variable immunodeficiency
Non-Hodgkin's Lymphoma of the Ascending Colon in a Patient with Becker Muscular Dystrophy : Report of a Case
Characterization of a Novel Nonsense Mutation in the Interleukin-7 Receptor α Gene in a Korean Patient with Severe Combined Immunodeficiency
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
A novel immunoregulatory protein in human colostrum, syntenin-1, for promoting the development of IgA-producing cells from cord blood B cells
Autoimmune lymphoproliferative syndrome mimicking chronic active Epstein-Barr virus infection
Atypical case of X-linked agammaglobulinemia diagnosed at 45 years of age
Mislocalization or low expression of mutated Shwachman-Bodian-Diamond syndrome protein
Hematopoietic stem cell transplantation with reduced intensity conditioning from a family haploidentical donor in an infant with familial hemophagocytic lymphohistocytosis
Genetic analysis of contiguous X-chromosome deletion syndrome encompassing the BTK and TIMM8A genes
Delayed onset adenosine deaminase deficiency associated with acute disseminated encephalomyelitis
Relapsing Campylobacter Coli Bacteremia with Reactive Arthritis in a Patient with X-linked Agammaglobulinemia
Therapeutic outcome of multifocal Langerhans cell histiocytosis in adults treated with the Special C regimen formulated by the Japan LCH Study Group

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