A. Hama

发表

Clinical and genetic analyses of presumed shwachman-diamond syndrome in Japan

H. Kanegane, H. Yoneyama, J. Kamizono, 2006, International journal of hematology.

Congenital erythroid and myeloid hypoplasia terminating myelodysplastic syndrome.

S. Kojima, H. Muramatsu, Yoshiyuki Takahashi, 2008, Journal of pediatric hematology/oncology.

Downregulation of GATA-2 and overexpression of adipogenic gene-PPARgamma in mesenchymal stem cells from patients with aplastic anemia.

S. Kojima, H. Muramatsu, Yoshiyuki Takahashi, 2009, Experimental hematology.

Wiskott–Aldrich syndrome presenting with a clinical picture mimicking juvenile myelomonocytic leukaemia

T. Morio, S. Ehl, A. Yoshimi, 2013, Pediatric blood & cancer.

Prognostic factors for outcomes of pediatric patients with refractory or relapsed acute leukemia undergoing allogeneic progenitor cell transplantation.

K. Horibe, S. Kojima, H. Muramatsu, 2011, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Development of clinical paroxysmal nocturnal haemoglobinuria in children with aplastic anaemia

Y. Okuno, S. Kojima, Kyogo Suzuki, 2017, British journal of haematology.

Prognostic value of the revised International Prognostic Scoring System five-group cytogenetic abnormality classification for the outcome prediction of hematopoietic stem cell transplantation in pediatric myelodysplastic syndrome

Motohiro Kato, Yoshiyuki Takahashi, Y. Atsuta, 2021, Bone Marrow Transplantation.

Myelodysplastic syndromes in a pediatric patient with Cri du Chat syndrome with a ring chromosome 5

S. Kojima, T. Fukao, H. Ohnishi, 2020, International Journal of Hematology.

Whole-exome analysis to detect congenital hemolytic anemia mimicking congenital dyserythropoietic anemia

S. Miyano, S. Ogawa, Y. Okuno, 2018, International Journal of Hematology.

Paroxysmal nocturnal hemoglobinuria and telomere length predicts response to immunosuppressive therapy in pediatric aplastic anemia

Y. Okuno, E. Ito, H. Moritake, 2015, Haematologica.

Recurrent MYB rearrangement in blastic plasmacytoid dendritic cell neoplasm

Y. Okuno, M. Nakatochi, Y. Nakazawa, 2017, Leukemia.

Mutations profile of polycythemia vera and essential thrombocythemia among Japanese children

S. Kojima, H. Muramatsu, Yoshiyuki Takahashi, 2012, Pediatric blood & cancer.

Mutations of an E3 ubiquitin ligase c-Cbl but not TET2 mutations are pathogenic in juvenile myelomonocytic leukemia.

A. Jankowska, C. O'keefe, J. Maciejewski, 2010, Blood.

Response: Mutations of JAK2, JAK3 and GATA1 in acute megakaryoblastic leukemia of Down syndrome

S. Kojima, Yoshiyuki Takahashi, H. Kiyoi, 2008 .

Excellent outcomes of children with CML treated with imatinib mesylate compared to that in pre-imatinib era

S. Kojima, H. Muramatsu, Yoshiyuki Takahashi, 2011, International journal of hematology.

Late-onset non-infectious pulmonary complications following allogeneic hematopoietic stem cell transplantation in children

S. Kojima, H. Muramatsu, N. Nishio, 2009, Bone Marrow Transplantation.

Mosaic Down syndrome-associated acute myeloid leukemia does not require high-dose cytarabine treatment for induction and consolidation therapy

F. Bessho, Ryouhei Ishii, S. Kojima, 2010, International journal of hematology.

Concurrent Langerhans cell histiocytosis and nephroblastoma

S. Kojima, H. Muramatsu, Yoshiyuki Takahashi, 2009, Pediatric blood & cancer.

Integrated Molecular Characterization of the Lethal Pediatric Cancer Pancreatoblastoma.

S. Miyano, T. Shimamura, Y. Shiraishi, 2018, Cancer research.

Relapse of leukemia with loss of mismatched HLA resulting from uniparental disomy after haploidentical hematopoietic stem cell transplantation.

S. Ogawa, Motohiro Kato, S. Kojima, 2010, Blood.

Comparison of long-term outcomes between children with aplastic anemia and refractory cytopenia of childhood who received immunosuppressive therapy with antithymocyte globulin and cyclosporine

E. Ito, S. Ohga, S. Kojima, 2015, Haematologica.

Mutations in the ribosomal protein genes in Japanese patients with Diamond-Blackfan anemia

T. Hara, T. Toki, Gang Xu, 2010, Haematologica.

A case of congenital dyserythropoietic anemia type 1 in a Japanese adult with a CDAN1 gene mutation and an inappropriately low serum hepcidin-25 level.

K. Nakao, K. Hosoda, S. Kojima, 2012, Internal medicine.

Clinical parameter-based prediction of DNA methylation classification generates a prediction model of prognosis in patients with juvenile myelomonocytic leukemia

M. Loh, Y. Okuno, S. Kojima, 2022, Scientific Reports.

Clinical outcomes after allogeneic hematopoietic stem cell transplantation in children with juvenile myelomonocytic leukemia: A report from the Japan Society for Hematopoietic Cell Transplantation.

Motohiro Kato, H. Shimada, Yoshiyuki Takahashi, 2019, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Somatic mosaicism for oncogenic NRAS mutations in juvenile myelomonocytic leukemia.

Y. Hayashi, H. Kawaguchi, Yoko Furukawa-Hibi, 2012, Blood.

Correlation of Clinical Features With the Mutational Status of GM-CSF Signaling Pathway-Related Genes in Juvenile Myelomonocytic Leukemia

A. Yoshimi, K. Koike, S. Kojima, 2009, Pediatric Research.

Quantification of granulocyte-macrophage colony-stimulating factor hypersensitivity in juvenile myelomonocytic leukemia by 3H-thymidine assay.

A. Yoshimi, S. Kojima, Yoshiyuki Takahashi, 2008, Leukemia research.

De novo childhood myelodysplastic/myeloproliferative disease with unique molecular characteristics

R. Hanada, K. Horibe, S. Kojima, 2012, British journal of haematology.

Successful hematopoietic stem cell transplantation from an HLA‐mismatched parent for engraftment failure after unrelated cord blood transplantation in patients with juvenile myelomonocytic leukemia: Report of two cases

K. Goi, K. Koike, S. Kojima, 2019, Pediatric transplantation.

Clinical characteristics and treatment outcome in 65 cases with refractory cytopenia of childhood defined according to the WHO 2008 classification

A. Yoshimi, T. Nakahata, S. Kojima, 2014, British journal of haematology.

Lack of CD4+CD25+FOXP3+ regulatory T cells is associated with resistance to intravenous immunoglobulin therapy in patients with Kawasaki disease

Y. Okuno, S. Kojima, H. Muramatsu, 2013, European Journal of Pediatrics.

Plasmacytoid Dendritic Cell Leukemia in Children

S. Kojima, H. Muramatsu, Yoshiyuki Takahashi, 2009, Journal of pediatric hematology/oncology.

Spectrum of molecular defects in juvenile myelomonocytic leukaemia includes ASXL1 mutations

A. Jankowska, J. Maciejewski, Y. Sugimoto, 2010, British journal of haematology.

Atypical erythroblastosis in a patient with Diamond–Blackfan anemia who developed del(20q) myelodysplasia

H. Takada, T. Toki, E. Ito, 2018, International Journal of Hematology.

Aplastic anemia successfully treated with rituximab: the possible role of aplastic anemia‐associated autoantibodies as a marker for response

S. Kojima, Yoshiyuki Takahashi, S. Nakao, 2011, European journal of haematology.

Increased midkine gene expression in childhood B-precursor acute lymphoblastic leukemia.

K. Horibe, S. Kojima, Yoshiyuki Takahashi, 2007, Leukemia research.

Total body irradiation and melphalan as a conditioning regimen for children with hematological malignancies undergoing transplantation with stem cells from HLA‐identical related donors

K. Horibe, S. Kojima, H. Muramatsu, 2011, Pediatric transplantation.

Mutation in the THPO gene is not associated with aplastic anaemia in Japanese children

S. Kojima, H. Muramatsu, Yoshiyuki Takahashi, 2012, British journal of haematology.

Mutations in telomerase catalytic protein in Japanese children with aplastic anemia.

S. Kojima, Kimikazu Matsumoto, H. Yagasaki, 2006, Haematologica.

Clinical impact of HLA‐DR15, a minor population of paroxysmal nocturnal haemoglobinuria‐type cells, and an aplastic anaemia‐associated autoantibody in children with acquired aplastic anaemia

S. Kojima, Yoshiyuki Takahashi, N. Hirano, 2008, British journal of haematology.

Correlation of CYP2C19 Phenotype With Voriconazole Plasma Concentration in Children

Yoko Furukawa-Hibi, S. Kojima, H. Muramatsu, 2013, Journal of pediatric hematology/oncology.

Myelodysplastic syndrome in a child with 15q24 deletion syndrome

Y. Fukushima, S. Kojima, K. Wakui, 2012, American journal of medical genetics. Part A.

Aberrant phosphorylation of STAT5 by granulocyte-macrophage colony-stimulating factor in infant cytomegalovirus infection mimicking juvenile myelomonocytic leukemia.

S. Kojima, H. Muramatsu, Yoshiyuki Takahashi, 2011, Leukemia research.

Incidence, clinical features, and risk factors of idiopathic pneumonia syndrome following hematopoietic stem cell transplantation in children

S. Kojima, H. Muramatsu, Yoshiyuki Takahashi, 2012, Pediatric blood & cancer.

High probability of follow-up termination among AYA survivors after allogeneic hematopoietic cell transplantation.

H. Ogawa, K. Ohashi, K. Miyamura, 2019, Blood advances.

The effectiveness of busulfan‐based conditioning regimens for stem cell transplantation against lymphomas in children, adolescents, and young adults in Japan

R. Suzuki, Y. Atsuta, Koji Kato, 2019, Pediatric blood & cancer.

with resistance to intravenous immunoglobulin therapy in patients with Kawasaki disease

Y. Okuno, S. Kojima, H. Muramatsu, 2013 .

Characteristics and outcomes of children with acute myeloid leukemia and Down syndrome who are ineligible for clinical trials due to severe comorbidities

S. Adachi, D. Hasegawa, T. Taga, 2019, Pediatric blood & cancer.

Aldehyde dehydrogenase‐2 polymorphism contributes to the progression of bone marrow failure in children with idiopathic aplastic anaemia

S. Kojima, H. Muramatsu, Yoshiyuki Takahashi, 2015, British journal of haematology.

Comparison of matched-sibling donor BMT and unrelated donor BMT in children and adolescent with acquired severe aplastic anemia

K. Horibe, S. Kojima, H. Muramatsu, 2010, Bone Marrow Transplantation.

Engraftment syndrome following allogeneic hematopoietic stem cell transplantation in children

A. Yoshimi, S. Kojima, H. Muramatsu, 2009, Pediatric transplantation.

Autoimmune-like hepatitis following unrelated BMT successfully treated with rituximab

S. Kojima, H. Muramatsu, A. Narita, 2012, Bone Marrow Transplantation.

Acute megakaryoblastic leukaemia (AMKL) in children: a comparison of AMKL with and without Down syndrome

A. Yoshimi, K. Horibe, S. Kojima, 2008, British journal of haematology.

Excellent outcome of allogeneic bone marrow transplantation for Fanconi anemia using fludarabine-based reduced-intensity conditioning regimen

S. Kojima, H. Muramatsu, Yoshiyuki Takahashi, 2012, International Journal of Hematology.

Fulminant adenovirus hepatitis after hematopoietic stem cell transplant: Retrospective real-time PCR analysis for adenovirus DNA in two cases.

N. Asai, Y. Okuno, S. Kojima, 2015, Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy.

RUNX1 mutation associated with clonal evolution in relapsed pediatric acute myeloid leukemia with t(16;21)(p11;q22)

S. Kojima, H. Muramatsu, Yoshiyuki Takahashi, 2014, International Journal of Hematology.

Reduced‐intensity conditioning for alternative donor hematopoietic stem cell transplantation in patients with dyskeratosis congenita

S. Kojima, H. Muramatsu, Yoshiyuki Takahashi, 2010, Pediatric transplantation.

Kampo patterns and radiology in children receiving choreito for hemorrhagic cystitis after hematopoietic stem cell transplantation

S. Kojima, H. Muramatsu, Yoshiyuki Takahashi, 2016 .

Choreito formula for BK virus-associated hemorrhagic cystitis after allogeneic hematopoietic stem cell transplantation.

Y. Okuno, S. Kojima, H. Muramatsu, 2015, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Exome sequencing identifies secondary mutations of SETBP1 and JAK3 in juvenile myelomonocytic leukemia

S. Miyano, Y. Shiraishi, K. Chiba, 2013, Nature Genetics.

Hypercalcemia in childhood acute lymphoblastic leukemia: frequent implication of parathyroid hormone-related peptide and E2A-HLF from translocation 17;19

T. Inaba, K. Goi, S. Nakazawa, 2007, Leukemia.

Human herpesvirus‐6B infection in pediatric allogenic hematopoietic stem cell transplant patients: Risk factors and encephalitis

H. Yatsuya, T. Yoshikawa, S. Kojima, 2020, Transplant infectious disease : an official journal of the Transplantation Society.

Predicting response to immunosuppressive therapy in childhood aplastic anemia

T. Nakahata, S. Kojima, Yoshiyuki Takahashi, 2011, Haematologica.

Relapse of aplastic anemia in children after immunosuppressive therapy: a report from the Japan Childhood Aplastic Anemia Study Group

M. Nagasawa, E. Ito, F. Bessho, 2011, Haematologica.

Acute pancreatitis following allogeneic hematopoietic stem cell transplantation in children

A. Hama, H. Sakaguchi, N. Yoshida, 2021, International Journal of Hematology.

Aberrant DNA Methylation Is Associated with a Poor Outcome in Juvenile Myelomonocytic Leukemia

S. Miyano, Y. Shiraishi, S. Ogawa, 2015, PloS one.

Mutation of SBDS and SH2D1A is not associated with aplastic anemia in Japanese children

S. Kojima, Yoshiyuki Takahashi, N. Nishio, 2007, Haematologica.

Integrated diagnosis based on transcriptome analysis in suspected pediatric sarcomas

Y. Okuno, S. Kojima, S. Mizuno, 2021, NPJ genomic medicine.

Integrated molecular profiling of juvenile myelomonocytic leukemia.

H. Aburatani, S. Miyano, Y. Shiraishi, 2018, Blood.

MEF2D-BCL9 Fusion Gene Is Associated With High-Risk Acute B-Cell Precursor Lymphoblastic Leukemia in Adolescents.

Y. Okuno, S. Kojima, Kyogo Suzuki, 2016, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Congenital pancreatoblastoma associated with β‐catenin mutation

H. Tsuchiya, S. Kojima, M. Hayakawa, 2012, Pediatric blood & cancer.

The landscape of somatic mutations in Down syndrome–related myeloid disorders

S. Miyano, Y. Shiraishi, K. Chiba, 2013, Nature Genetics.

Peripheral blood lymphocyte telomere length as a predictor of response to immunosuppressive therapy in childhood aplastic anemia

E. Ito, H. Moritake, S. Ohga, 2014, Haematologica.

Haematopoietic cell transplantation for children with acute megakaryoblastic leukaemia without Down syndrome

S. Adachi, H. Muramatsu, Yoshiyuki Takahashi, 2023, British journal of haematology.

Clinical utility of next‐generation sequencing‐based minimal residual disease in paediatric B‐cell acute lymphoblastic leukaemia

Y. Okuno, S. Kojima, Kyogo Suzuki, 2017, British journal of haematology.

to myeloid leukemia progression myeloproliferative disorder: mutation classes correlate with mutations in transient abnormal GATA1 Down syndrome and

H. Kanegane, R. Kanezaki, T. Toki, 2013 .

Down syndrome and GATA1 mutations in transient abnormal myeloproliferative disorder: mutation classes correlate with progression to myeloid leukemia.

Y. Hayashi, H. Kanegane, R. Kanezaki, 2010, Blood.

Predictive factors for the development of leukemia in patients with transient abnormal myelopoiesis and Down syndrome

Y. Hayashi, S. Mizutani, T. Toki, 2021, Leukemia.

Highly sensitive detection of GATA1 mutations in patients with myeloid leukemia associated with Down syndrome by combining Sanger and targeted next generation sequencing

R. Kanezaki, T. Toki, E. Ito, 2020, Genes, chromosomes & cancer.

Markedly High Plasma Thrombopoietin (TPO) Level is a Predictor of Poor Response to Immunosuppressive Therapy in Children With Acquired Severe Aplastic Anemia

Y. Okuno, S. Kojima, H. Muramatsu, 2016, Pediatric blood & cancer.

Risk factors for secondary poor graft function after bone marrow transplantation in children with acquired aplastic anemia

S. Kojima, H. Muramatsu, Yoshiyuki Takahashi, 2020, Pediatric transplantation.

Correlation of rabbit antithymocyte globulin serum levels and clinical outcomes in children who received hematopoietic stem cell transplantation from an alternative donor

Y. Okuno, S. Kojima, H. Muramatsu, 2016, Pediatric transplantation.

A Cytokine‐Based Diagnostic Program in Pediatric Aplastic Anemia and Hypocellular Refractory Cytopenia of Childhood

Y. Okuno, S. Kojima, H. Muramatsu, 2016, Pediatric blood & cancer.

Natural history of transfusion-independent non-severe aplastic anemia in children

S. Kojima, H. Muramatsu, Yoshiyuki Takahashi, 2009, International journal of hematology.

GATA2 and secondary mutations in familial myelodysplastic syndromes and pediatric myeloid malignancies

S. Miyano, Y. Shiraishi, K. Chiba, 2015, Haematologica.

Diagnosis of acquired bone marrow failure syndrome during childhood using the 2008 World Health Organization classification system

S. Kojima, Wenyu Yang, Xiaofan Zhu, 2012, International Journal of Hematology.

Pediatric Philadelphia chromosome‐positive B‐lymphoblastic lymphoma with testicular relapse: A case report

A. Hama, H. Sakaguchi, N. Yoshida, 2021, Pediatric blood & cancer.

Hepatoblastoma associated with trisomy 18

Kosuke Chiba, K. Kaneko, A. Hama, 2020 .

Graft-versus-host disease-free, relapse-free, second transplant-free survival in allogeneic hematopoietic cell transplantation for genetic disorders.

K. Imai, Yoshiyuki Takahashi, Satoshi Miyamoto, 2023, Bone marrow transplantation.

Relationship between plasma rabbit anti‐thymocyte globulin concentration and immunosuppressive therapy response in patients with severe aplastic anemia

Y. Okuno, S. Kojima, Kyogo Suzuki, 2021, European journal of haematology.

Decision analysis of allogeneic bone marrow transplantation versus immunosuppressive therapy for young adult patients with aplastic anemia

S. Kako, Y. Kanda, M. Kurokawa, 2023, International Journal of Hematology.

Risk Factors for Donor-Type Aplasia After Bone Marrow Transplant in Children with Acquired Bone Marrow Failure Syndrome

S. Kojima, H. Muramatsu, Yoshiyuki Takahashi, 2012 .

Progressive hearing loss following acquired cytomegalovirus infection in an immunocompromised child.

S. Naganawa, S. Kojima, H. Muramatsu, 2013, American journal of otolaryngology.

Congenital dyserythropoietic anemia type 1 with a novel mutation in the CDAN1 gene previously diagnosed as congenital hemolytic anemia

S. Kojima, H. Muramatsu, H. Fujino, 2013, International Journal of Hematology.

Molecular lesions in childhood and adult acute megakaryoblastic leukaemia

Hirotoshi Sakaguchi, Yuka Sugimoto, Nobuhiro Watanabe, 2012, British journal of haematology.

JAK mutations in Down syndrome-associated transient myeloproliferative disorder and acute megakaryocytic leukemia. Authors' reply

P. Vyas, S. Kojima, Yoshiyuki Takahashi, 2008 .

Successful treatment with rituximab of refractory idiopathic thrombocytopenic purpura in a patient with Kabuki syndrome

S. Kojima, S. Mizuno, H. Muramatsu, 2009, International journal of hematology.

Expansion of human CMV-specific cytotoxic T lymphocytes to a clinical scale: a simple culture system using tetrameric HLA-peptide complexes.

K. Kuzushima, M. Isomura, A. Hama, 2004, Cytotherapy.

feasibility and Results of Bone Marrow Transplantation from an HLA-Mismatched Unrelated Donor for Children and Young Adults with Acquired Severe Aplastic Anemia

S. Kojima, Yoshiyuki Takahashi, N. Nishio, 2007, International journal of hematology.

Genetic analysis of Shwachman-Diamond syndrome: phenotypic heterogeneity in patients carrying identical SBDS mutations.

E. Ito, E. Shirahata, K. Hayasaka, 2005, The Tohoku journal of experimental medicine.

Acquisition of a rare NUP98–BPTF fusion gene associated with recurrence of acute myeloid leukemia

Kyogo Suzuki, H. Muramatsu, Yoshiyuki Takahashi, 2021, Pediatric blood & cancer.

Clinical utility of next-generation sequencing for inherited bone marrow failure syndromes

S. Miyano, Y. Shiraishi, K. Chiba, 2017, Genetics in Medicine.

The incidence of symptomatic osteonecrosis is similar between Japanese children and children in Western countries with acute lymphoblastic leukaemia treated with a Berlin‐Frankfurt‐Münster (BFM)95‐based protocol

K. Horibe, T. Imamura, H. Hiramatsu, 2021, British journal of haematology.

Integration Mapping of piggyBac-Mediated CD19 Chimeric Antigen Receptor T Cells Analyzed by Novel Tagmentation-Assisted PCR

Y. Okuno, Y. Nakazawa, S. Kojima, 2018, EBioMedicine.

Physicians – Poster Session

S. Kojima, H. Muramatsu, F. Ipsevich, 2017, Bone Marrow Transplantation.

Neutropenia and myeloid dysplasia in a patient with delayed‐onset adenosine deaminase deficiency

H. Kanegane, T. Miyawaki, A. Hoshino, 2013, Pediatric blood & cancer.

Clinical Utility of Next-Generation Sequencing-Based Minimal Residual Disease in Childhood Acute Lymphoblastic Leukemia

Y. Okuno, S. Kojima, Kyogo Suzuki, 2015 .

JAK2, MPL, and CALR mutations in children with essential thrombocythemia

Y. Okuno, T. Imamura, S. Ohga, 2016, International Journal of Hematology.

Nationwide survey of bisphosphonate therapy for children with reactivated Langerhans cell histiocytosis in Japan

H. Kanegane, T. Imamura, J. Kamizono, 2011, Pediatric blood & cancer.

Simple and robust methylation test for risk stratification of patients with juvenile myelomonocytic leukemia

M. Loh, Y. Okuno, S. Kojima, 2021, Blood advances.

Immunosuppressive therapy for patients with Down syndrome and idiopathic aplastic anemia

Y. Okuno, S. Kojima, Kyogo Suzuki, 2016, International Journal of Hematology.

Long-Term Parvovirus B19 Infections With Genetic Drift After Cord Blood Transplantation Complicated by Persistent CD4+ Lymphocytopenia

S. Kojima, H. Muramatsu, Yoshiyuki Takahashi, 2014, Journal of pediatric hematology/oncology.

Diagnostic Whole Exome Sequencing for 166 Patients with Inherited Bone Marrow Failure Syndrome

Y. Okuno, S. Kojima, T. Ogi, 2020 .

Optimizing transplantation procedures through identification of prognostic factors in second remission for children with acute myeloid leukemia with no prior history of transplant.

J. Takita, Y. Atsuta, K. Koh, 2023, Haematologica.

Prospective validation of the provisional entity of refractory cytopenia of childhood, proposed by the World Health Organization

S. Kojima, H. Muramatsu, Yoshiyuki Takahashi, 2021, British journal of haematology.

Hematological abnormalities in Jacobsen syndrome: cytopenia of varying severities and morphological abnormalities in peripheral blood and bone marrow

Y. Okuno, S. Kojima, H. Muramatsu, 2023, Haematologica.

Acute myelopathy during chemotherapy for childhood acute lymphoblastic leukemia

A. Hama, H. Sakaguchi, N. Yoshida, 2021, Pediatrics International.

Successful T-cell reconstitution after unrelated cord blood transplantation in a patient with complete DiGeorge syndrome.

Y. Okuno, K. Imai, S. Kojima, 2016, The Journal of allergy and clinical immunology.

CD20-negative Epstein–Barr virus-associated post-transplant lymphoproliferative disease refractory to rituximab in a patient with severe aplastic anemia

S. Kojima, H. Muramatsu, Yoshiyuki Takahashi, 2011, International journal of hematology.

Extrapulmonary tuberculosis mimicking Mendelian susceptibility to mycobacterial disease in a patient with signal transducer and activator of transcription 1 (STAT1) gain-of-function mutation.

Y. Okuno, S. Okada, M. Tsumura, 2016, Journal of Allergy and Clinical Immunology.

Aberrant DNA Methylation Is Associated with a Poor Outcome in Juvenile Myelomonocytic Leukemia

S. Miyano, Y. Shiraishi, S. Ogawa, 2015, PloS one.

Myelodysplastic syndrome in a child with 15q24 deletion syndrome

Y. Fukushima, S. Kojima, K. Wakui, 2012, American journal of medical genetics. Part A.

Mutations in telomerase catalytic protein in Japanese children with aplastic anemia.

S. Kojima, Kimikazu Matsumoto, H. Yagasaki, 2006, Haematologica.

Relapse of leukemia with loss of mismatched HLA resulting from uniparental disomy after haploidentical hematopoietic stem cell transplantation.

S. Ogawa, S. Kojima, H. Saji, 2010, Blood.

Long‐term outcomes of 95 children with moderate aplastic anemia treated with horse antithymocyte globulin and cyclosporine

S. Ohga, S. Kojima, H. Muramatsu, 2017, Pediatric blood & cancer.

Single-Cell Transcriptomic Analysis of Epstein-Barr Virus-Associated Hemophagocytic Lymphohistiocytosis.

T. Yoshikawa, H. Kimura, Takako Suzuki, 2024, Journal of clinical immunology.

Application of extensively targeted next-generation sequencing for the diagnosis of primary immunodeficiencies.

Y. Okuno, S. Kojima, H. Muramatsu, 2016, The Journal of allergy and clinical immunology.