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A case of pulmonary pleomorphic carcinoma with preexisting interstitial pneumonia successfully treated with pembrolizumab

Thoracic cancer, 2022-01, Vol.13 (1), p.129-132

2022

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Childhood pheochromocytoma in a survivor of central primitive neuroectodermal tumor

Pediatrics international, 2013-08, Vol.55 (4), p.e100-e102

2013

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AF5q31, a Newly Identified AF4-Related Gene, Is Fused to MLL in Infant Acute Lymphoblastic Leukemia with ins(5;11)(q31;q13q23)

Proceedings of the National Academy of Sciences - PNAS, 1999-12, Vol.96 (25), p.14535-14540

1999

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Aberrations of the hSNF5/INI1 gene are restricted to malignant rhabdoid tumors or atypical teratoid/rhabdoid tumors in pediatric solid tumors

Genes chromosomes & cancer, 2002-05, Vol.34 (1), p.33-41

2002

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A nationwide survey of newly diagnosed childhood idiopathic thrombocytopenic purpura in Japan

Journal of pediatric hematology/oncology, 2009-01, Vol.31 (1), p.27-32

2009

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Treatment with candesartan combined with angiotensin-converting enzyme inhibitor for immunosuppressive treatment-resistant nephrotic syndrome after allogeneic stem cell transplantation

International journal of hematology, 2006-06, Vol.83 (5), p.454-458

2006

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Improved outcome in the treatment of pediatric multifocal Langerhans cell histiocytosis

Cancer, 2006-08, Vol.107 (3), p.613-619

2006

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Blastic natural killer cell lymphoma/leukemia (CD56‐positive blastic tumor)

Cancer, 2005-09, Vol.104 (5), p.1022-1031

2005

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Long-term outcomes after splenectomy in children with immune thrombocytopenia: an update on the registry data from the Intercontinental Cooperative ITP Study Group

Haematologica (Roma), 2020-11, Vol.105 (11), p.2682-2685

2020

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SETBP 1 mutations in juvenile myelomonocytic leukaemia and myelodysplastic syndrome but not in paediatric acute myeloid leukaemia

British journal of haematology, 2014-01, Vol.164 (1), p.156-159

2014

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High incidence of human herpesvirus 6 infection with a high viral load in cord blood stem cell transplant recipients

Blood, 2002-09, Vol.100 (6), p.2005-2011

2002

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Molecular genetic analysis of a variant Bernard-Soulier syndrome due to compound heterozygosity for two novel glycoprotein Ibβ mutations

European journal of haematology, 2006-12, Vol.77 (6), p.501-512

2006

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Identification of Novel Type of ETV6-TTL Fusion Gene in Pediatric Myeloid/NK Cell Precursor Acute Leukemia Having t(12;13)(p13;q14)

Blood, 2005-11, Vol.106 (11), p.4520-4520

2005

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Molecular genetic analysis of a variant Bernard-Soulier syndrome due to compound heterozygosity for two novel glycoprotein Ibb mutations

European journal of haematology, 2006-12, Vol.77 (6), p.501-512

2006

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Molecular genetic analysis of a variant Bernard-Soulier syndrome due to compound heterozygosity for two novel glycoprotein Ibbeta mutations

European journal of haematology, 2006-12, Vol.77 (6), p.501-512

2006

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MNX1–ETV6 fusion gene in an acute megakaryoblastic leukemia and expression of the MNX1 gene in leukemia and normal B cell lines

Cancer genetics and cytogenetics, 2008-10, Vol.186 (2), p.115-119

2008

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An infant with severe atopic dermatitis and progressive hepatomegaly due to fatty liver

Pediatrics international, 1999-10, Vol.41 (5), p.575-580

1999

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AUTOANTI-ENaFS PRODUCTION IN A PATIENT WITH SCID AFTER CORD BLOOD TRANSPLANTATION

Nihon Yuketsu Gakkai zasshi = Journal of the Japan Society of Blood Transfusion, 2004, Vol.50 (3), p.444-452

2004

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Low Frequency of KIT Gene Mutation in Pediatric Acute Myeloid Leukemia with inv(16)(p13q22): A Study of the Japanese Childhood AML Cooperative Study Group

International journal of hematology, 2007-10, Vol.86 (3), p.289-290

2007

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short report: Allogeneic haematopoietic cell transplantation from alternative donors with a conditioning regimen of low-dose irradiation, fludarabine and cyclophosphamide in Fanconi anaemia

British journal of haematology, 2006-07, Vol.134 (2), p.208-212

2006

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Mutations of the PTPN11 Gene in Childhood Hematological Malignancies

Blood, 2004-11, Vol.104 (11), p.4335-4335

2004

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Classification of Familial Hemophagocytic Lymphohistiocytosis Based on Genetic and Immunologic Analyses

Blood, 2004-11, Vol.104 (11), p.1327-1327

2004

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Effect of chemotherapy and stem cell transplantation on T lymphocytes clones in familial haemophagocytic lymphohistiocytosis

British journal of haematology, 2001-06, Vol.113 (3), p.822

2001

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t(10;11)-Acute leukemias with MLL-AF10 and MLL-ABI1 chimeric transcripts: Specific expression patterns of ABI1 gene in leukemia and solid tumor cell lines

Genes chromosomes & cancer, 2001-09, Vol.32 (1), p.1-10

2001

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Intravenous immunoglobulin for hemophagocytic lymphohistiocytosis?

Journal of clinical oncology, 2002-01, Vol.20 (2), p.599-601

2002

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A case of pulmonary pleomorphic carcinoma with preexisting interstitial pneumonia successfully treated with pembrolizumab

Childhood pheochromocytoma in a survivor of central primitive neuroectodermal tumor

AF5q31, a Newly Identified AF4-Related Gene, Is Fused to MLL in Infant Acute Lymphoblastic Leukemia with ins(5;11)(q31;q13q23)

Aberrations of the hSNF5/INI1 gene are restricted to malignant rhabdoid tumors or atypical teratoid/rhabdoid tumors in pediatric solid tumors

A nationwide survey of newly diagnosed childhood idiopathic thrombocytopenic purpura in Japan

Treatment with candesartan combined with angiotensin-converting enzyme inhibitor for immunosuppressive treatment-resistant nephrotic syndrome after allogeneic stem cell transplantation

Improved outcome in the treatment of pediatric multifocal Langerhans cell histiocytosis

Blastic natural killer cell lymphoma/leukemia (CD56‐positive blastic tumor)

Long-term outcomes after splenectomy in children with immune thrombocytopenia: an update on the registry data from the Intercontinental Cooperative ITP Study Group

SETBP 1 mutations in juvenile myelomonocytic leukaemia and myelodysplastic syndrome but not in paediatric acute myeloid leukaemia

High incidence of human herpesvirus 6 infection with a high viral load in cord blood stem cell transplant recipients

Molecular genetic analysis of a variant Bernard-Soulier syndrome due to compound heterozygosity for two novel glycoprotein Ibβ mutations

Identification of Novel Type of ETV6-TTL Fusion Gene in Pediatric Myeloid/NK Cell Precursor Acute Leukemia Having t(12;13)(p13;q14)

Molecular genetic analysis of a variant Bernard-Soulier syndrome due to compound heterozygosity for two novel glycoprotein Ibb mutations

Molecular genetic analysis of a variant Bernard-Soulier syndrome due to compound heterozygosity for two novel glycoprotein Ibbeta mutations

MNX1–ETV6 fusion gene in an acute megakaryoblastic leukemia and expression of the MNX1 gene in leukemia and normal B cell lines

An infant with severe atopic dermatitis and progressive hepatomegaly due to fatty liver

AUTOANTI-ENaFS PRODUCTION IN A PATIENT WITH SCID AFTER CORD BLOOD TRANSPLANTATION

Low Frequency of KIT Gene Mutation in Pediatric Acute Myeloid Leukemia with inv(16)(p13q22): A Study of the Japanese Childhood AML Cooperative Study Group

short report: Allogeneic haematopoietic cell transplantation from alternative donors with a conditioning regimen of low-dose irradiation, fludarabine and cyclophosphamide in Fanconi anaemia

Mutations of the PTPN11 Gene in Childhood Hematological Malignancies

Classification of Familial Hemophagocytic Lymphohistiocytosis Based on Genetic and Immunologic Analyses

Effect of chemotherapy and stem cell transplantation on T lymphocytes clones in familial haemophagocytic lymphohistiocytosis

t(10;11)-Acute leukemias with MLL-AF10 and MLL-ABI1 chimeric transcripts: Specific expression patterns of ABI1 gene in leukemia and solid tumor cell lines

Intravenous immunoglobulin for hemophagocytic lymphohistiocytosis?

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