M. Hamada

发表

Combination chemotherapy consisting of irinotecan, etoposide, and carboplatin for refractory or relapsed neuroblastoma

S. Kojima, H. Muramatsu, Yoshiyuki Takahashi, 2022, Cancer medicine.

Development of clinical paroxysmal nocturnal haemoglobinuria in children with aplastic anaemia

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

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

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

Recurrent MYB rearrangement in blastic plasmacytoid dendritic cell neoplasm

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

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

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

Trichothiodystrophy, complementation group A complicated with squamous cell carcinoma

M. Akiyama, Y. Okuno, T. Takeichi, 2018, Journal of the European Academy of Dermatology and Venereology : JEADV.

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.

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.

Whole-exome analysis of 177 pediatric patients with undiagnosed diseases

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

A progression to dermatofibrosarcoma protuberans with a fibrosarcomatous component: a special reference to the chromosomal aberrations.

M. Tsuneyoshi, T. Fukuda, M. Furue, 1999, Pathology, research and practice.

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

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

Integrated diagnosis based on transcriptome analysis in suspected pediatric sarcomas

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

Osteochondritis dissecans of the humeral head.

M. Hamada, S. Hamada, S. Nishiue, 1992, Arthroscopy : the journal of arthroscopic & related surgery : official publication of the Arthroscopy Association of North America and the International Arthroscopy Association.

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.

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.

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

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

Dexamethasone palmitate for patients with engraftment syndrome is associated with favorable outcome for children with hematological malignancy

K. Matsumoto, K. Narita, M. Hamada, 2016, 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.

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.

DOCK8 mutation diagnosed using whole-exome sequencing of the dried blood spot-derived DNA: a case report of an Iraqi girl diagnosed in Japan

Y. Okuno, Y. Nakazawa, K. Sano, 2019, BMC Medical Genetics.

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.

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.

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

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

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

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

Physicians – Poster Session

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

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.