H. Muramatsu

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

Functional characterization of a novel GFI1B mutation causing congenital macrothrombocytopenia

S. Miyano, Y. Shiraishi, S. Ogawa, 2015, Journal of thrombosis and haemostasis : JTH.

Development of clinical paroxysmal nocturnal haemoglobinuria in children with aplastic anaemia

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

A novel WTX mutation in a female patient with osteopathia striata with cranial sclerosis and hepatoblastoma

N. Matsumoto, N. Miyake, Y. Tsurusaki, 2014, American journal of medical genetics. Part A.

ACTN1 mutations cause congenital macrothrombocytopenia.

Satoru Miyano, Yuichi Shiraishi, Ryoji Kobayashi, 2013, American journal of human genetics.

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.

Genetic heterogeneity of uncharacterized childhood autoimmune diseases with lymphoproliferation

S. Miyano, Y. Shiraishi, K. Chiba, 2018, Pediatric blood & cancer.

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

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

Exome sequencing identified RPS15A as a novel causative gene for Diamond-Blackfan anemia

N. Kenmochi, S. Miyano, Y. Shiraishi, 2017, Haematologica.

Phosphatase and tensin homolog (PTEN) mutation can cause activated phosphatidylinositol 3-kinase δ syndrome-like immunodeficiency.

O. Ohara, S. Miyano, Y. Shiraishi, 2016, The Journal of allergy and clinical immunology.

Diagnostic challenge of Diamond–Blackfan anemia in mothers and children by whole-exome sequencing

S. Miyano, Y. Shiraishi, K. Chiba, 2017, 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.

Late-Onset Combined Immunodeficiency with a Novel IL2RG Mutation and Probable Revertant Somatic Mosaicism

S. Miyano, Y. Shiraishi, K. Chiba, 2015, Journal of Clinical Immunology.

Clinical and genetic features of dyskeratosis congenita, cryptic dyskeratosis congenita, and Hoyeraal-Hreidarsson syndrome in Japan

S. Miyano, Y. Shiraishi, K. Chiba, 2015, International Journal of Hematology.

A Female Patient with Incomplete Hemophagocytic Lymphohistiocytosis Caused by a Heterozygous XIAP Mutation Associated with Non-Random X-Chromosome Inactivation Skewed Towards the Wild-Type XIAP Allele

S. Miyano, S. Ogawa, H. Kanegane, 2015, Journal of Clinical Immunology.

Whole-exome sequence analysis of ataxia telangiectasia-like phenotype

S. Miyano, Y. Shiraishi, K. Chiba, 2014, Journal of the Neurological Sciences.

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.

CMML AND aCML: NOVEL PATHOGENETIC LESIONS

H. Makishima, H. Muramatsu, P. Jaroslaw, 2012 .

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.

Allogeneic stem cell transplantation with reduced intensity conditioning for patients with adrenoleukodystrophy

M. Kaga, N. Shimozawa, Kyogo Suzuki, 2018, Molecular genetics and metabolism reports.

Role of ABCG2 as a biomarker for predicting resistance to CPT‐11/SN‐38 in lung cancer

R. Ueda, T. Oguri, H. Muramatsu, 2006, Cancer science.

The determinants of sensitivity and acquired resistance to gemcitabine differ in non–small cell lung cancer: a role of ABCC5 in gemcitabine sensitivity

R. Ueda, T. Oguri, H. Muramatsu, 2006, Molecular Cancer Therapeutics.

The role of thymidylate synthase and dihydropyrimidine dehydrogenase in resistance to 5-fluorouracil in human lung cancer cells.

R. Ueda, T. Oguri, H. Muramatsu, 2005, Lung cancer.

A novel CUL4B splice site variant in a young male exhibiting less pronounced features

T. Kawai, S. Saitoh, Y. Okuno, 2019, Human Genome Variation.

Targetable driver mutations in multicentric reticulohistiocytosis

Y. Okuno, H. Muramatsu, Yoshiyuki Takahashi, 2020, Haematologica.

Prognostic Factors for Outcomes of Allogeneic HSCT for Children and Adolescents/Young Adults with CML in the TKI Era.

H. Shimada, K. Ohashi, H. Muramatsu, 2022, Transplantation and cellular therapy.

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.

Outcome of 125 children with chronic myelogenous leukemia who received transplants from unrelated donors: the Japan Marrow Donor Program.

K. Kawa, H. Shimada, A. Yoshimi, 2010, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

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

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

Leukostasis in Children and Adolescents with Chronic Myeloid Leukemia: Japanese Pediatric Leukemia/Lymphoma Study Group

H. Shimada, S. Mizutani, K. Horibe, 2016, Pediatric blood & cancer.

Flow cytometric analysis as an additional predictive tool of treatment response in children with chronic‐phase chronic myeloid leukemia treated with imatinib

H. Shimada, S. Mizutani, K. Horibe, 2017, Pediatric blood & cancer.

Concurrent Langerhans cell histiocytosis and nephroblastoma

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

Danaparoid as the prophylaxis for hepatic veno‐occlusive disease after allogeneic hematopoietic stem cell transplantation in childhood hematological malignancy

H. Muramatsu, Koji Kato, Kimikazu Matsumoto, 2010, Pediatric blood & cancer.

Immunonutritional status and pulmonary cavitation in patients with tuberculosis: A revisit with an assessment of neutrophil/lymphocyte ratio.

H. Muramatsu, K. Fujita, M. Nakao, 2019, Respiratory investigation.

The Evaluation of Three Cases of Large Cell Neuroendocrine Carcinoma Successfully Treated with Atezolizumab

H. Muramatsu, K. Fujita, M. Nakao, 2020, Haigan.

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 conditioning regimens for autologous stem cell transplantation in children with acute myeloid leukemia: A nationwide retrospective study in Japan

Y. Nakazawa, H. Muramatsu, N. Shiba, 2018, Pediatric blood & cancer.

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.

Mutational analysis of RNA splicing machinery components in 206 children with myeloid malignancies.

A. Jankowska, J. Maciejewski, A. Jerez, 2012, Leukemia research : a Forum for Studies on Leukemia and Normal Hemopoiesis.

Casitas B-cell lymphoma mutation in childhood T-cell acute lymphoblastic leukemia.

J. Maciejewski, Y. Matsubara, S. Kojima, 2012, Leukemia research.

Reduced-intensity conditioning is effective for hematopoietic stem cell transplantation in young pediatric patients with Diamond–Blackfan anemia

S. Miyano, S. Ogawa, Kenichi Yoshida, 2020, Bone Marrow Transplantation.

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.

Somatic mosaicism for oncogenic NRAS mutations in juvenile myelomonocytic leukemia.

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

A retrospective analysis of azacitidine treatment for juvenile myelomonocytic leukemia

T. Meguro, H. Moritake, Shuichi Ozono, 2021, International Journal of Hematology.

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.

De novo childhood myelodysplastic/myeloproliferative disease with unique molecular characteristics

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

A neonate diagnosed with Noonan syndrome with myeloproliferative change

H. Takada, H. Muramatsu, H. Fukushima, 2021, Pediatrics international : official journal of the Japan Pediatric Society.

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 course of juvenile myelomonocytic leukemia in the blast crisis phase treated by acute myeloid leukemia-oriented chemotherapy and allogeneic hematopoietic stem cell transplantation

S. Kojima, H. Muramatsu, H. Sakaguchi, 2014, International Journal of Hematology.

Central nervous system lesions due to juvenile myelomonocytic leukemia progressed in a boy undergoing first line chemotherapy

Y. Morishita, H. Muramatsu, Keisuke Kato, 2012, International Journal of Hematology.

Serial investigation of PTPN11 mutation in nonhematopoietic tissues in a patient with juvenile myelomonocytic leukemia who was treated with unrelated cord blood transplantation

T. Imamura, H. Hosoi, S. Kojima, 2015, International Journal of Hematology.

Germline Mutation of CBL Is Associated With Moyamoya Disease in a Child With Juvenile Myelomonocytic Leukemia and Noonan Syndrome‐Like Disorder

S. Kojima, H. Muramatsu, Y. Chinen, 2015, Pediatric blood & cancer.

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.

Risk factors for unplanned removal of central venous catheters in hospitalized children with hematological and oncological disorders

M. Nakatochi, S. Kojima, H. Muramatsu, 2020, International Journal of Hematology.

The Evaluation of Four Cases of Non-small Cell Lung Cancer Requiring Pericardial Drainage After Pembrolizumab Therapy

H. Muramatsu, K. Fujita, M. Nakao, 2019, Haigan.

Echocardiography Monitoring of Pulmonary Hypertension after Pediatric Hematopoietic Stem Cell Transplantation: Pediatric Pulmonary Arterial Hypertension and Pulmonary Veno-Occlusive Disease after Hematopoietic Stem Cell Transplantation

Y. Okuno, H. Ishibashi-Ueda, S. Kojima, 2022, Transplantation and Cellular Therapy.

Microsatellite instability-high is rare events in refractory pediatric solid tumors

H. Muramatsu, Yoshiyuki Takahashi, A. Natsume, 2020, Pediatric hematology and oncology.

Comparison of high-dose and low-dose corticosteroid therapy for refractory Mycoplasma pneumoniae pneumonia in children.

M. Nakatochi, H. Kidokoro, H. Muramatsu, 2019, Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy.

Sequential use of second‐generation tyrosine kinase inhibitors following imatinib therapy in pediatric chronic myeloid leukemia: A report from the Japanese Pediatric Leukemia/Lymphoma Study Group

H. Shimada, S. Mizutani, K. Horibe, 2018, Pediatric blood & cancer.

Biallelic mutations in SZT2 cause a discernible clinical entity with epilepsy, developmental delay, macrocephaly and a dysmorphic corpus callosum

S. Saitoh, Y. Okuno, S. Kojima, 2018, Brain and Development.

Evaluation of topotecan monotherapy for relapsed small-cell lung cancer after amrubicin monotherapy failure

H. Muramatsu, K. Fujita, M. Nakao, 2021, Journal of rural medicine : JRM.

Nab-paclitaxel Monotherapy for Relapsed Small Cell Lung Cancer: Retrospective Analysis and Review

H. Muramatsu, K. Fujita, M. Nakao, 2020, AntiCancer Research.

Tacrolimus/Methotrexate versus cyclosporine/methotrexate as graft-versus-host disease prophylaxis in patients with severe aplastic anemia who received bone marrow transplantation from unrelated donors: results of matched pair analysis.

Y. Kodera, S. Kojima, H. Sakamaki, 2009, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Diagnostic Efficacy of FeNO Testing in Patients With Cough

H. Muramatsu, M. Nakao, Masaya Higuchi, 2019, JOURNAL OF THE JAPANESE ASSOCIATION OF RURAL MEDICINE.

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.

Somatic Mutations in Schinzel-Giedion Syndrome Gene SETBP1 Determine Progression in Myeloid Malignancies

S. Miyano, Y. Shiraishi, K. Chiba, 2012 .

First-line treatment for severe aplastic anemia in children: bone marrow transplantation from a matched family donor versus immunosuppressive therapy

R. Suzuki, S. Ohga, S. Kojima, 2014, Haematologica.

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.

Long-term outcome after immunosuppressive therapy with horse or rabbit antithymocyte globulin and cyclosporine for severe aplastic anemia in children

S. Kojima, H. Muramatsu, Yoshiyuki Takahashi, 2014, Haematologica.

Studies of α-gal dependent hyperacute xenotransplant rejection using double knockout embryonic stem cells

T. Muramatsu, H. Muramatsu, H. Ogawa, 1997 .

Correlation of CYP2C19 Phenotype With Voriconazole Plasma Concentration in Children

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

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.

Whole-exome analysis of 177 pediatric patients with undiagnosed diseases

Y. Okuno, T. Yonekawa, S. Kojima, 2022, Scientific Reports.

Comparison of clinical characteristics of human metapneumovirus and respiratory syncytial virus infection in hospitalized young children.

H. Kidokoro, H. Muramatsu, Yoshiyuki Takahashi, 2019, Japanese journal of infectious diseases.

C. O'keefe, J. Maciejewski, Y. Saunthararajah, 2012, Leukemia.

with resistance to intravenous immunoglobulin therapy in patients with Kawasaki disease

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

Acquired Molecular Defects in Spliceosome Machinery: Novel Pathogenetic Pathways in Myeloid Leukemogenesis

A. Jankowska, J. Maciejewski, A. Jerez, 2011 .

Usefulness of functional splicing analysis to confirm precise disease pathogenesis in Diamond-Blackfan anemia caused by intronic variants in RPS19

T. Toki, E. Ito, M. Matsuo, 2021, Pediatric hematology and oncology.

Prospective randomized trial comparing two doses of rabbit anti‐thymocyte globulin in patients with severe aplastic anaemia

Jingliao Zhang, S. Kojima, H. Muramatsu, 2019, British journal of haematology.

Azacitidine as a bridge to transplantation in juvenile myelomonocytic leukemia.

Y. Kawasaki, H. Muramatsu, Masaki Yamamoto, 2022, Pediatrics international : official journal of the Japan Pediatric Society.

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.

Danaparoid reduces transplant‐related mortality in stem cell transplantation for children

H. Muramatsu, Koji Kato, A. Narita, 2018, Pediatric transplantation.

Relationship between tacrolimus blood concentrations and clinical outcome during the first 4 weeks after SCT in children

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

Recurrent Cellulitis Caused by Helicobacter cinaedi in a Patient with X-linked Agammaglobulinaemia.

M. Akiyama, S. Kojima, H. Muramatsu, 2017, Acta dermato-venereologica.

Immunosuppressive therapy with horse anti-thymocyte globulin and cyclosporine as treatment for fulminant aplastic anemia in children

H. Shimada, S. Ohga, S. Kojima, 2014, Annals of Hematology.

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.

A case of GATA2‐related myelodysplastic syndrome with unbalanced translocation der(1;7)(q10;p10)

Y. Okuno, Y. Nakazawa, H. Muramatsu, 2017, Pediatric blood & cancer.

Outcome of hematopoietic cell transplantation for DNA double‐strand break repair disorders

A. Fischer, A. Schulz, B. Wolska-Kuśnierz, 2018, The Journal of allergy and clinical immunology.

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.

The phenotype and clinical course of Japanese Fanconi Anaemia infants is influenced by patient, but not maternal ALDH2 genotype

S. Ogawa, K. Matsuo, Y. Okuno, 2016, 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.

B-cell function after unrelated umbilical cord blood transplantation using a minimal-intensity conditioning regimen in patients with X-SCID

T. Morio, H. Takada, T. Hara, 2013, International Journal of Hematology.

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.

Recipient seropositivity for adenovirus type 11 (AdV11) is a highly predictive factor for the development of AdV11-induced hemorrhagic cystitis after allogeneic hematopoietic SCT

Y. Nakazawa, S. Adachi, T. Nakahata, 2013, Bone Marrow Transplantation.

Increased expression of cyclooxygenase 2 occurs frequently in human lung cancers, specifically in adenocarcinomas.

Y. Yatabe, T. Mitsudomi, Takashi Takahashi, 1998, Cancer research.

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

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

Treatment of Cryptococcus gattii Infection Using Voriconazole

H. Muramatsu, S. Tomita, K. Fujita, 2021, Internal medicine.

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.

Difficulties in diagnosing Malassezia furfur bloodstream infection and possibility of spontaneous resolution in a patient undergoing chemotherapy for neuroblastoma: A case report.

H. Muramatsu, Yoshiyuki Takahashi, H. Morioka, 2022, Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy.

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

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

Somatic SETBP1 mutations in myeloid malignancies

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

Primary infection of human herpesvirus-6 in an infant who received cord blood SCT

S. Kojima, H. Muramatsu, K. Matsumoto, 2009, Bone Marrow Transplantation.

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.

Simple diagnosis of STAT1 gain‐of‐function alleles in patients with chronic mucocutaneous candidiasis

J. Casanova, T. Morio, A. Puel, 2014, Journal of leukocyte biology.

International Meeting on Genetic Syndromes of the Ras / MapK Pathway “ Finding Our Way Back to the Bedside ”

Y. Matsubara, S. Kojima, A. Ohtake, 2011 .

alpha-Galactosyl oligosaccharides conjugated with polyethylene glycol as potential inhibitors of hyperacute rejection upon xenotransplantation.

T. Muramatsu, H. Muramatsu, T. Kobayashi, 1997, Biochemical and biophysical research communications.

Epidermal growth factor receptor-tyrosine kinase inhibitors for non-small-cell lung cancer patients aged 80 years or older: A retrospective analysis.

H. Muramatsu, M. Nakao, S. Aoki, 2015, Molecular and clinical oncology.

A nationwide survey of late effects in survivors of juvenile myelomonocytic leukemia in Japan

Shuichi Ozono, H. Muramatsu, A. Manabe, 2022, Pediatric blood & cancer.

KLF1 mutation E325K induces cell cycle arrest in erythroid cells differentiated from congenital dyserythropoietic anemia patient-specific induced pluripotent stem cells.

S. Ogawa, Y. Okuno, Kenichi Yoshida, 2019, Experimental hematology.

Neonatal intestinal obstruction in Hoyeraal–Hreidarsson syndrome with novel RTEL1 variants

J. Shibahara, S. Ohga, H. Muramatsu, 2023, Pediatric blood & cancer.

Pathogenic mutations identified by a multimodality approach in 117 Japanese Fanconi anemia patients

K. Kinoshita, S. Miyano, Y. Shiraishi, 2019, Haematologica.

Two Aldehyde Clearance Systems Are Essential to Prevent Lethal Formaldehyde Accumulation in Mice and Humans

Nicola K. Wilson, B. Göttgens, N. Wilson, 2020, Molecular cell.

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

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

Analysis of mutations and recombination activity in RAG-deficient patients.

O. Ohara, T. Morio, S. Nampoothiri, 2011, Clinical immunology.

Detection of subclonal SETBP1 and JAK3 mutations in juvenile myelomonocytic leukemia using droplet digital PCR

Y. Okuno, S. Kojima, Kyogo Suzuki, 2020, Leukemia.

Erratum: A randomized study of pomalidomide vs placebo in persons with myeloproliferative neoplasm-associated myelofibrosis and RBC-transfusion dependence

Y. Okuno, S. Kojima, T. Fukao, 2017, Leukemia.

International Consensus Definition of DNA Methylation Subgroups in Juvenile Myelomonocytic Leukemia

M. Loh, A. Olshen, C. Plass, 2020, Clinical Cancer Research.

Integrated diagnosis based on transcriptome analysis in suspected pediatric sarcomas

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

Cyclooxygenase-2 inhibitor induces apoptosis and enhances cytotoxicity of various anticancer agents in non-small cell lung cancer cell lines.

T. Mitsudomi, Takashi Takahashi, H. Muramatsu, 2000, Clinical cancer research : an official journal of the American Association for Cancer Research.

Integrated molecular profiling of juvenile myelomonocytic leukemia.

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

Loss of heterozygosity in 7q myeloid disorders: clinical associations and genomic pathogenesis.

A. Jankowska, M. McDevitt, G. Mufti, 2012, Blood.

Pneumocystis Pneumonia Secondary to Idiopathic CD4+ T-lymphocytopenia: A Comparison of AIDS and Non-AIDS Patients

A. Niimi, H. Muramatsu, M. Nakao, 2017, Internal medicine.

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.

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

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

Defective Epstein–Barr virus in chronic active infection and haematological malignancy

Masahiro Yoshida, S. Miyano, M. Seto, 2019, Nature Microbiology.

Next-Generation Sequencing to Detect Pathogens in Pediatric Febrile Neutropenia: A Single-Center Retrospective Study of 112 Cases

T. Ogi, H. Muramatsu, Yoshiyuki Takahashi, 2021, Open forum infectious diseases.

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.

MicroRNA-155-5p Plays a Critical Role in Transient Leukemia of Down Syndrome by Targeting Tumor Necrosis Factor Receptor Superfamily Members.

C. Blag, Alina-Andreea Zimta, S. Pașca, 2020, Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology.

PIEZO1 gene mutation in a Japanese family with hereditary high phosphatidylcholine hemolytic anemia and hemochromatosis-induced diabetes mellitus

S. Miyano, Y. Shiraishi, K. Chiba, 2016, International Journal of Hematology.

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

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

Minor PNH clones do not distinguish inherited bone marrow failure syndromes from immune-mediated aplastic anemia

Y. Okuno, H. Muramatsu, Yoshiyuki Takahashi, 2022, Blood advances.

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.

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

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

Distinct impact of imatinib on growth at prepubertal and pubertal ages of children with chronic myeloid leukemia.

H. Shimada, K. Horibe, H. Muramatsu, 2011, The Journal of pediatrics.

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.

Conditioning regimen for allogeneic bone marrow transplantation in children with acquired bone marrow failure: fludarabine/melphalan vs. fludarabine/cyclophosphamide

R. Suzuki, S. Kojima, H. Muramatsu, 2020, Bone Marrow Transplantation.

Digenic mutations in ALDH2 and ADH5 impair formaldehyde clearance and cause a multisystem disorder, AMeD syndrome

M. Nagasaki, K. Matsuo, F. Matsuda, 2020, Science advances.

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.

Bloodstream infection after stem cell transplantation in children with idiopathic aplastic anemia.

K. Kawa, R. Suzuki, S. Kojima, 2014, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

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

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

Clinical diagnostic value of telomere length measurement in inherited bone marrow failure syndromes

Y. Okuno, S. Kojima, Kyogo Suzuki, 2021, Haematologica.

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

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

S. Kojima, H. Muramatsu, A. Narita, 2017, Bone Marrow Transplantation.

Second allogeneic hematopoietic stem cell transplantation in children with severe aplastic anemia

K. Kawa, R. Suzuki, S. Kojima, 2015, Bone Marrow Transplantation.

Autoimmune lymphoproliferative syndrome-like disease with somatic KRAS mutation.

T. Morio, M. Nagasawa, M. Takagi, 2011, Blood.

Hematopoietic Cell Transplantation for Chronic Granulomatous Disease in Japan

T. Morio, Masao Kobayashi, K. Imai, 2020, Frontiers in Immunology.

Rabbit antithymocyte globulin and cyclosporine as first-line therapy for children with acquired aplastic anemia.

E. Ito, S. Ohga, S. Kojima, 2013, Blood.

Associations of complementation group, ALDH2 genotype, and clonal abnormalities with hematological outcome in Japanese patients with Fanconi anemia

S. Ogawa, K. Matsuo, Y. Okuno, 2018, Annals of Hematology.

Elucidation of the pathogenic mechanism and potential treatment strategy for a female patient with spastic paraplegia derived from a single-nucleotide deletion in PLP1

Y. Okuno, T. Kaname, Toshiyuki Yamamoto, 2019, Journal of Human Genetics.

Dyserythropoietic anaemia with an intronic GATA1 splicing mutation in patients suspected to have Diamond‐Blackfan anaemia

S. Miyano, S. Ogawa, Kenichi Yoshida, 2022, EJHaem.

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.

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 .

High Natural Killer Cell Count at Diagnosis Predicts a Good Response to Immunosuppressive Therapy in Aplastic Anemia

Y. Okuno, S. Kojima, H. Muramatsu, 2019, Blood.

Late-Onset Combined Immunodeficiency with a Novel IL2RG Mutation and Probable Revertant Somatic Mosaicism

S. Miyano, Y. Shiraishi, K. Chiba, 2015, Journal of Clinical Immunology.

Risk factors for early death in neonates with Down syndrome and transient leukaemia

Tomohiko Nakamura, S. Kojima, M. Hayakawa, 2008, British journal of haematology.

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

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

Prospective Study of 168 Infants with Transient Abnormal Myelopoiesis with Down Syndrome: Japan Pediatric Leukemia/Lymphoma Study Group, TAM-10 Study

Y. Hayashi, S. Mizutani, T. Toki, 2015 .

Mutations of e3 ubiquitin ligase cbl family members constitute a novel common pathogenic lesion in myeloid malignancies.

M. McDevitt, C. O'keefe, J. Maciejewski, 2009, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Defective Epstein–Barr virus in chronic active infection and haematological malignancy

Masahiro Yoshida, S. Miyano, M. Seto, 2019, Nature Microbiology.

Diagnostic delay of pulmonary tuberculosis in patients with acute respiratory distress syndrome associated with aspiration pneumonia: Two case reports and a mini-review from Japan.

H. Muramatsu, M. Nakao, Hidefumi Sato, 2016, Experimental and therapeutic medicine.

Publisher Correction: Defective Epstein–Barr virus in chronic active infection and haematological malignancy

Masahiro Yoshida, S. Miyano, M. Seto, 2019, Nature Microbiology.

Reduced intensity conditioning in allogeneic stem cell transplantation for AML with Down syndrome

K. Kawa, A. Suminoe, S. Adachi, 2014, Pediatric blood & cancer.

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.

Abnormal urinalysis on day 7 in patients with IgA vasculitis (Henoch–Schönlein purpura)

S. Kojima, H. Muramatsu, J. Natsume, 2016, Nagoya journal of medical science.

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.

Efficacy and safety of bevacizumab, irinotecan, and temozolomide combination for relapsed or refractory pediatric central nervous system embryonal tumor: a single-institution study.

H. Muramatsu, Yoshiyuki Takahashi, F. Ohka, 2023, Journal of neurosurgery. Pediatrics.

Two Cases of Juvenile Myelomonocytic Leukemia and Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease.

H. Kidokoro, H. Muramatsu, Yoshiyuki Takahashi, 2023, Pediatric neurology.

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.

Production and characterization of an active single-chain variable fragment antibody recognizing CD25.

Kazuhiro Yoshikawa, Ryuzo Ueda, S. Saga, 2005, Cancer letters.

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

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

Whole abdominopelvic intensity-modulated radiation therapy for peritoneal disseminated rhabdomyosarcoma with three-year follow-up: a case report

S. Naganawa, H. Muramatsu, Yoshiyuki Takahashi, 2019, Radiation oncology.

Utility of Newborn Screening for Severe Combined Immunodeficiency and X-Linked Agammaglobulinemia Using TREC and KREC Assays

Y. Okuno, S. Kojima, H. Muramatsu, 2019, Blood.

Hematopoietic stem cell transplantation for progressive combined immunodeficiency and lymphoproliferation in patients with activated phosphatidylinositol‐3‐OH kinase &dgr; syndrome type 1

O. Ohara, S. Ogawa, H. Kanegane, 2019, The Journal of allergy and clinical immunology.

Juvenile Hemochromatosis With Non-transfused Hemolytic Anemia Caused by a De Novo PIEZO1 Gene Mutation.

Y. Okuno, H. Muramatsu, K. Chonabayashi, 2023, Journal of pediatric hematology/oncology.

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.

Successful treatment of a novel type I interferonopathy due to a de novo PSMB9 gene mutation with a Janus kinase inhibitor.

T. Taketani, I. Nishino, Y. Okuno, 2021, The Journal of allergy and clinical immunology.

Gas-modified solid chromatography using organic vapours as carrier gas : II. Mechanism and application for aromatic amines☆

T. Tsuda, H. Muramatsu, D. Ishii, 1977 .

A case of wild-type transthyretin amyloidosis associated with organizing pneumonia

H. Muramatsu, Kouhei Fujita, M. Nakao, 2017, Journal of rural medicine : JRM.

An infant with generalized pustular psoriasis and geographic tongue had a heterozygous IL36RN mutation and IgG2 deficiency.

M. Akiyama, Y. Okuno, H. Muramatsu, 2018, Journal of dermatological science (Amsterdam).

CYFRA 21-1 as a Predictive Marker for Non-small Cell Lung Cancer Treated with Pemetrexed-based Chemotherapy.

T. Oguri, A. Niimi, M. Takemura, 2017, Anticancer research.

TREC/KREC Newborn Screening followed by Next-Generation Sequencing for Severe Combined Immunodeficiency in Japan

Y. Okuno, S. Kojima, H. Muramatsu, 2022, Journal of Clinical Immunology.

Design of a prospective multicenter randomized controlled trial evaluating the effects of gastric lavage on coffee-ground emesis in neonates: study protocol

M. Nakatochi, Ryoichi Ito, H. Kidokoro, 2019, Nagoya journal of medical science.

Physicians – Poster Session

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

Chronic myelomonocytic leukemia and atypical chronic myeloid leukemia: novel pathogenetic lesions.

J. Maciejewski, H. Makishima, H. Muramatsu, 2012, Seminars in oncology.

Immunological Status May Predict Response to Nivolumab in Non-small Cell Lung Cancer without Driver Mutations.

H. Muramatsu, K. Fujita, M. Nakao, 2017, Anticancer research.

Treatment with silver nitrate versus topical steroid treatment for umbilical granuloma: A non-inferiority randomized control trial

M. Ando, S. Kojima, H. Kidokoro, 2018, PloS one.

Nosocomial infection with rotavirus vaccine strain in paediatric patients with immunodeficiency.

T. Yoshikawa, H. Muramatsu, Yoshiyuki Takahashi, 2021, The Journal of hospital infection.

Combination of TREC Measurement and Next-Generation Sequencing in Newborn Screening for Severe Combined Immunodeficiency: A Pilot Program in Japan

Y. Okuno, S. Kojima, H. Muramatsu, 2018, Blood.

Compound heterozygous TYK2 mutations underlie primary immunodeficiency with T-cell lymphopenia

W. Sugiura, K. Horibe, T. Kawasaki, 2018, Scientific Reports.

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

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

Vedolizumab for children with intestinal graft-versus-host disease: a case report and literature review

H. Muramatsu, Yoshiyuki Takahashi, Masayuki Imaya, 2023, International Journal of Hematology.

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

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

Human leukocyte antigen 7/8-matched unrelated bone marrow transplantation using anti-thymocyte globulin in children

S. Kojima, Kyogo Suzuki, H. Muramatsu, 2023, International Journal of Hematology.

Successful treatment of DOCK8 deficiency by allogeneic hematopoietic cell transplantation from alternative donors

H. Kanegane, H. Takada, H. Muramatsu, 2023, International Journal of Hematology.

Suppression of antigen-antibody reaction in xenotransplantation.

T. Kato, D. Liu, T. Muramatsu, 2000, Transplantation proceedings.

Common Variable Immunodeficiency Caused by FANC Mutations

O. Ohara, S. Miyano, Y. Shiraishi, 2017, Journal of Clinical Immunology.

Study of pathophysiology and molecular characterization of congenital anemia in India using targeted next-generation sequencing approach

Y. Okuno, E. Ito, S. Kojima, 2019, International Journal of Hematology.

Association between graft source and response to live-attenuated vaccination in pediatric hematopoietic stem cell transplantation recipients: a single-center retrospective study

H. Muramatsu, Yoshiyuki Takahashi, Suguru Takeuchi, 2020, Bone Marrow Transplantation.

Somatic Mosaicism for a NRAS Mutation Associates with Disparate Clinical Features in RAS-associated Leukoproliferative Disease: a Report of Two Cases

S. Miyano, S. Ogawa, H. Kanegane, 2015, Journal of Clinical Immunology.

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

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

Genetic Background of Chronic Active Epstein-Barr Virus Disease

S. Miyano, Y. Shiraishi, K. Chiba, 2017 .

A patient with a GNAO1 mutation with decreased spontaneous movements, hypotonia, and dystonic features

Mami Shibata, T. Kawai, Y. Okuno, 2018, Brain and Development.

Immunosuppressive therapy for patients with Down syndrome and idiopathic aplastic anemia

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

Efficacy of neutrophil non-muscle myosin heavy chain-IIA immunofluorescence analysis in determining the pathogenicity of MYH9 variants

S. Kojima, H. Muramatsu, Yoshiyuki Takahashi, 2017, Annals of Hematology.

S. Miyano, S. Ogawa, H. Kanegane, 2015, Journal of Clinical Immunology.

DNA Methylation Subgroups in Juvenile Myelomonocytic Leukemia: An International Collaborative Analysis and Development of a Common Diagnostic Platform

M. Loh, A. Olshen, C. Plass, 2018, Blood.

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 .

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.

Elucidation of the pathogenic mechanism and potential treatment strategy for a female patient with spastic paraplegia derived from a single-nucleotide deletion in PLP1

Y. Okuno, T. Kaname, Toshiyuki Yamamoto, 2019, Journal of Human Genetics.

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.

Japanese siblings with cartilage-hair hypoplasia exhibiting different severity.

H. Muramatsu, Manabu Wakamatsu, H. Mizuno, 2023, Pediatrics international : official journal of the Japan Pediatric Society.

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.

Case Report: Rotavirus Vaccination and Severe Combined Immunodeficiency in Japan

H. Kanegane, T. Morio, T. Yoshikawa, 2022, Frontiers in 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.

Autoantibodies against the plakin family proteins as a novel marker for chronic graft-versus-host disease of the lung

Y. Okuno, S. Kojima, T. Hashimoto, 2021, Bone Marrow Transplantation.

A patient with very early onset FH-deficient renal cell carcinoma diagnosed at age seven

T. Tsuzuki, Y. Okuno, Yukichi Tanaka, 2021, Familial Cancer.

Comprehensive genetic analysis of donor cell derived leukemia with KMT2A rearrangement

T. Shimamura, Y. Okuno, M. Nakatochi, 2018, Pediatric blood & cancer.

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

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

Change of White Matter Integrity in Children With Hematopoietic Stem Cell Transplantation.

H. Kawai, T. Taoka, S. Naganawa, 2020, Pediatric neurology.

Correction: Treatment with silver nitrate versus topical steroid treatment for umbilical granuloma: A non-inferiority randomized control trial

N. Hibino, H. Dietz, M. Ando, 2019, PLoS ONE.

Cryptococcus gattii Genotype VGIIa Infection in an Immunocompetent Japanese Patient: A Case Report and Mini-review

H. Koga, H. Muramatsu, K. Kamei, 2016, Internal medicine.

Somatic Mosaicism for a NRAS Mutation Associates with Disparate Clinical Features in RAS-associated Leukoproliferative Disease: a Report of Two Cases

S. Miyano, S. Ogawa, H. Kanegane, 2015, Journal of Clinical Immunology.

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.

Germline Mutation of CBL Is Associated With Moyamoya Disease in a Child With Juvenile Myelomonocytic Leukemia and Noonan Syndrome‐Like Disorder

S. Kojima, H. Muramatsu, Y. Chinen, 2015, Pediatric blood & cancer.

A novel WTX mutation in a female patient with osteopathia striata with cranial sclerosis and hepatoblastoma

N. Matsumoto, N. Miyake, Y. Tsurusaki, 2014, American journal of medical genetics. Part A.

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.

Updated guidelines for chronic active Epstein–Barr virus disease

S. Ohga, H. Muramatsu, H. Kimura, 2023, International journal of hematology.

Long-term outcome after immunosuppressive therapy with horse or rabbit antithymocyte globulin and cyclosporine for severe aplastic anemia in children

S. Kojima, H. Muramatsu, Yoshiyuki Takahashi, 2014, Haematologica.

Spectrum of molecular defects in juvenile myelomonocytic leukaemia includes ASXL1 mutations

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

Novel biallelic FA2H mutations in a Japanese boy with fatty acid hydroxylase-associated neurodegeneration

Y. Okuno, A. Kihara, T. Kaname, 2019, Brain and Development.

A patient with a GNAO1 mutation with decreased spontaneous movements, hypotonia, and dystonic features

Mami Shibata, T. Kawai, Y. Okuno, 2018, Brain and Development.

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

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

Echocardiography Monitoring of Pulmonary Hypertension after Pediatric Hematopoietic Stem Cell Transplantation: Pediatric PAH and PVOD after HSCT.

Y. Okuno, H. Ishibashi-Ueda, S. Kojima, 2021, Transplantation and cellular therapy.

Paroxysmal cold hemoglobinuria caused by an IgM‐class Donath–Landsteiner antibody

S. Kojima, H. Muramatsu, Y. Ohshima, 2013, Pediatrics international : official journal of the Japan Pediatric Society.

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.