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Clinical and molecular characteristics of MEF2D fusion-positive B-cell precursor acute lymphoblastic leukemia in childhood, including a novel translocation resulting in MEF2D-HNRNPH1 gene fusion

Haematologica (Roma), 2019-01, Vol.104 (1), p.128

2019

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A novel BMPR1A mutation affects mRNA splicing in juvenile polyposis syndrome

Pediatrics international, 2022-01, Vol.64 (1), p.e15041-n/a

2022

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Cancer predisposition genes in Japanese children with rhabdomyosarcoma

Journal of human genetics, 2022-01, Vol.67 (1), p.35-41

2022

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Medical researchers’ perceptions regarding research evaluation: a web-based survey in Japan

BMJ open, 2024-05, Vol.14 (5), p.e079269-e079269

2024

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A neonate diagnosed with Noonan syndrome with myeloproliferative change

Pediatrics international, 2021-12, Vol.63 (12), p.1521-1523

2021

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Proton beam therapy for pediatric ependymoma

Pediatrics international, 2015-08, Vol.57 (4), p.567-571

2015

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Involvement of the optic pathway and outcome of visual function in patients with neurohypophyseal germ cell tumor

Acta neurochirurgica, 2021-11, Vol.163 (11), p.3191-3199

2021

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Pneumococcal Serotype-specific Opsonophagocytic Activity in Interleukin-1 Receptor-associated Kinase 4-deficient Patients

The Pediatric infectious disease journal, 2021-05, Vol.40 (5), p.460

2021

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Severe adenovirus type F enteritis in a young child with acute myeloid leukemia

Pediatrics international, 2021-05, Vol.63 (5), p.604-606

2021

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Proton therapy for newly diagnosed pediatric diffuse intrinsic pontine glioma

Child's nervous system, 2020-03, Vol.36 (3), p.507-512

2020

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Resistance of t(17;19)‐acute lymphoblastic leukemia cell lines to multiagents in induction therapy

Cancer medicine (Malden, MA), 2019-09, Vol.8 (11), p.5274-5288

2019

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A systematic review and meta-analysis of radiotherapy and particle beam therapy for skull base chondrosarcoma: TRP-chondrosarcoma 2024

Frontiers in oncology, 2024-03, Vol.14, p.1380716-1380716

2024

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Identification of a novel KLC1–ROS1 fusion in a case of pediatric low-grade localized glioma

Brain tumor pathology, 2019-01, Vol.36 (1), p.14-19

2019

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Cold Agglutinin Syndrome

The New England journal of medicine, 2023-08, Vol.389 (7), p.642-642

2023

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Recovery of lymphocyte subpopulations is incomplete in the long‐term setting in pediatric solid tumor survivors

Pediatrics international, 2022-01, Vol.64 (1), p.e15257-n/a

2022

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Malignant brain tumor in an infant showing histopathological features of yolk sac tumor but genetic and epigenetic features of AT/RT

Pediatric blood & cancer, 2021-09, Vol.68 (9), p.e29192-n/a

2021

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Analysis of person-hours required for proton beam therapy for pediatric tumors

Journal of radiation research, 2023-05, Vol.64 (3), p.599-601

2023

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A case of fetal‐onset type 3 familial hemophagocytic lymphohistiocytosis surviving without severe complications after early diagnosis and treatment

Pediatric blood & cancer, 2021-07, Vol.68 (7), p.e29016-n/a

2021

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A Retrospective Study of Renal Growth Changes after Proton Beam Therapy for Pediatric Malignant Tumor

Current oncology (Toronto), 2023-01, Vol.30 (2), p.1560-1570

2023

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Schuurs‐Hoeijmakers syndrome in two patients from Japan

American journal of medical genetics. Part A, 2019-03, Vol.179 (3), p.341-343

2019

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A case report of epithelioid inflammatory myofibroblastic sarcoma with RANBP2-ALK fusion gene treated with the ALK inhibitor, crizotinib

Japanese journal of clinical oncology, 2014-09, Vol.44 (9), p.868-871

2014

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Drug screening with a novel tumor-derived cell line identified alternative therapeutic options for patients with atypical teratoid/rhabdoid tumor

Human cell : official journal of Human Cell Research Society, 2021, Vol.34 (1), p.271-278

2021

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Genotyping NUDT15 can predict the dose reduction of 6-MP for children with acute lymphoblastic leukemia especially at a preschool age

Journal of human genetics, 2016-09, Vol.61 (9), p.797-801

2016

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Rhabdoid tumor predisposition syndrome with renal tumor 10 years after brain tumor

Pathology international, 2021-02, Vol.71 (2), p.155-160

2021

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Clinical and molecular characteristics of MEF2D fusion-positive B-cell precursor acute lymphoblastic leukemia in childhood, including a novel translocation resulting in MEF2D-HNRNPH1 gene fusion

A novel BMPR1A mutation affects mRNA splicing in juvenile polyposis syndrome

Cancer predisposition genes in Japanese children with rhabdomyosarcoma

Medical researchers’ perceptions regarding research evaluation: a web-based survey in Japan

A neonate diagnosed with Noonan syndrome with myeloproliferative change

Proton beam therapy for pediatric ependymoma

Involvement of the optic pathway and outcome of visual function in patients with neurohypophyseal germ cell tumor

Pneumococcal Serotype-specific Opsonophagocytic Activity in Interleukin-1 Receptor-associated Kinase 4-deficient Patients

Severe adenovirus type F enteritis in a young child with acute myeloid leukemia

Proton therapy for newly diagnosed pediatric diffuse intrinsic pontine glioma

Resistance of t(17;19)‐acute lymphoblastic leukemia cell lines to multiagents in induction therapy

A systematic review and meta-analysis of radiotherapy and particle beam therapy for skull base chondrosarcoma: TRP-chondrosarcoma 2024

Identification of a novel KLC1–ROS1 fusion in a case of pediatric low-grade localized glioma

Cold Agglutinin Syndrome

Recovery of lymphocyte subpopulations is incomplete in the long‐term setting in pediatric solid tumor survivors

Malignant brain tumor in an infant showing histopathological features of yolk sac tumor but genetic and epigenetic features of AT/RT

Analysis of person-hours required for proton beam therapy for pediatric tumors

A case of fetal‐onset type 3 familial hemophagocytic lymphohistiocytosis surviving without severe complications after early diagnosis and treatment

Late Changes in Renal Volume and Function after Proton Beam Therapy in Pediatric and Adult Patients: Children Show Significant Renal Atrophy but Deterioration of Renal Function Is Minimal in the Long-Term in Both Groups

A Retrospective Study of Renal Growth Changes after Proton Beam Therapy for Pediatric Malignant Tumor

Schuurs‐Hoeijmakers syndrome in two patients from Japan

A case report of epithelioid inflammatory myofibroblastic sarcoma with RANBP2-ALK fusion gene treated with the ALK inhibitor, crizotinib

Drug screening with a novel tumor-derived cell line identified alternative therapeutic options for patients with atypical teratoid/rhabdoid tumor

Genotyping NUDT15 can predict the dose reduction of 6-MP for children with acute lymphoblastic leukemia especially at a preschool age

Rhabdoid tumor predisposition syndrome with renal tumor 10 years after brain tumor

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