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The Japan Society for Neuro-Oncology guideline on the diagnosis and treatment of central nervous system germ cell tumors

Neuro-oncology (Charlottesville, Va.), 2022-04, Vol.24 (4), p.503-515

2022

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TERT promoter mutation status is necessary and sufficient to diagnose IDH-wildtype diffuse astrocytic glioma with molecular features of glioblastoma

Acta neuropathologica, 2021-08, Vol.142 (2), p.323-338

2021

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Acute myeloid leukemia post RAS‐associated autoimmune leukoproliferative disease

Pediatrics international, 2023-01, Vol.65 (1), p.e15521-n/a

2023

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Perfusable System Using Porous Collagen Gel Scaffold Actively Provides Fresh Culture Media to a Cultured 3D Tissue

International journal of molecular sciences, 2021-06, Vol.22 (13), p.6780

2021

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Chemotherapy-induced autoimmune-mediated encephalitis during germinoma treatment

Brain & development (Tokyo. 1979), 2021-10, Vol.43 (9), p.967-971

2021

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Genome-wide methylation profiles in primary intracranial germ cell tumors indicate a primordial germ cell origin for germinomas

Acta neuropathologica, 2017-03, Vol.133 (3), p.445-462

2017

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Development of Molecular Targeted Therapy Depending on Genetic Alterations in Pediatric Brain Tumors

Gan to kagaku ryoho, 2024-06, Vol.51 (6), p.615

Yamasaki, Kai

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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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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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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Monitoring Ponatinib in a Child with Philadelphia Chromosome-Positive Acute Lymphoblastic Leukemia

Case reports in oncology, 2021-01, Vol.14 (1), p.24-28

2021

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Phase I study of bevacizumab plus irinotecan in pediatric patients with recurrent/refractory solid tumors

Japanese journal of clinical oncology, 2013-11, Vol.43 (11), p.1073-1079

2013

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Subtyping of Group 3/4 medulloblastoma as a potential prognostic biomarker among patients treated with reduced dose of craniospinal irradiation: a Japanese Pediatric Molecular Neuro-Oncology Group study

Acta neuropathologica communications, 2023-09, Vol.11 (1), p.1-153, Article 153

2023

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Histological and genetic analysis of anaplastic pleomorphic xanthoastrocytoma suspected of malignant progression over a 12‐year clinical course

Pathology international, 2019-10, Vol.69 (10), p.608-613

2019

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MBCL-22. EFFICACY OF DOUBLE-CONDITIONING REGIMEN COMPRISING THIOTEPA AND MELPHALAN FOR RELAPSED MEDULLOBLASTOMA – A SINGLE INSTITUTION EXPERIENCE

Neuro-oncology (Charlottesville, Va.), 2020-12, Vol.22 (Suppl 3), p.iii393-iii393

2020

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GCT-21. Long-term outcome and follow up of intracranial germ cell tumors: Reduced-dose radiotherapy and intensified chemotherapy improves clinical outcome and quality of life for long-term survivors

Neuro-oncology (Charlottesville, Va.), 2022-06, Vol.24 (Supplement_1), p.i59-i59

2022

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TCF3::BEND2 in paediatric supratentorial tumour with carcinoma‐like epithelial features classifying as MN1‐altered astroblastoma by DNA methylation profiling

Neuropathology and applied neurobiology, 2024-10, Vol.50 (5), p.e13011-n/a

2024

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EPN-01MOLECULAR CLASSIFICATION OF EPENDYMOMAS IN A JAPANESE PEDIATRIC MOLECULAR NEURO-ONCOLOGY GROUP (JPMNG) SERIES

Neuro-oncology (Charlottesville, Va.), 2016-06, Vol.18 (suppl 3), p.iii30.1-iii30

2016

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Presacral malignant teratoid neoplasm in association with pathogenic DICER1 variation

Modern pathology, 2019-12, Vol.32 (12), p.1744-1750

2019

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PATH-28. MOLECULAR DIAGNOSIS FOR CENTRAL DIAGNOSIS OF BRAIN TUMORS FROM 2016 TO 2019— A REPORT FROM THE JAPAN CHILDREN’S CANCER GROUP (JCCG)

Neuro-oncology (Charlottesville, Va.), 2020-12, Vol.22 (Supplement_3), p.iii430-iii430

2020

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MBCL-22. EFFICACY OF DOUBLE-CONDITIONING REGIMEN COMPRISING THIOTEPA AND MELPHALAN FOR RELAPSED MEDULLOBLASTOMA – A SINGLE INSTITUTION EXPERIENCE

Neuro-oncology (Charlottesville, Va.), 2020-12, Vol.22 (Supplement_3), p.iii393-iii393

2020

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LGG-12. INTEGRATED CLINICAL AND MOLECULAR CHARACTERIZATION OF 200 DISSEMINATED PEDIATRIC LOW-GRADE GLIOMAS

Neuro-oncology (Charlottesville, Va.), 2024-06, Vol.26 (Suppl 4), p.0-0

2024

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MEDB-30. Subclassification of Group 3/4 medulloblastoma as a potential prognostic biomarker to reduce the dose of craniospinal irradiation in patients with metastatic tumors: A Japanese Pediatric Molecular Neuro-Oncology Group study

Neuro-oncology (Charlottesville, Va.), 2022-06, Vol.24 (Supplement_1), p.i111-i111

2022

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10206-GGE-21 MOLECULAR LANDSCAPE AND TUMOR EVOLUTION IN ASTROBLASTOMA

Neuro-oncology advances, 2023-12, Vol.5 (Supplement_5), p.v20-v21

2023

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The Japan Society for Neuro-Oncology guideline on the diagnosis and treatment of central nervous system germ cell tumors

TERT promoter mutation status is necessary and sufficient to diagnose IDH-wildtype diffuse astrocytic glioma with molecular features of glioblastoma

Acute myeloid leukemia post RAS‐associated autoimmune leukoproliferative disease

Perfusable System Using Porous Collagen Gel Scaffold Actively Provides Fresh Culture Media to a Cultured 3D Tissue

Chemotherapy-induced autoimmune-mediated encephalitis during germinoma treatment

Genome-wide methylation profiles in primary intracranial germ cell tumors indicate a primordial germ cell origin for germinomas

Development of Molecular Targeted Therapy Depending on Genetic Alterations in Pediatric Brain Tumors

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

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

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

Monitoring Ponatinib in a Child with Philadelphia Chromosome-Positive Acute Lymphoblastic Leukemia

Phase I study of bevacizumab plus irinotecan in pediatric patients with recurrent/refractory solid tumors

Subtyping of Group 3/4 medulloblastoma as a potential prognostic biomarker among patients treated with reduced dose of craniospinal irradiation: a Japanese Pediatric Molecular Neuro-Oncology Group study

Histological and genetic analysis of anaplastic pleomorphic xanthoastrocytoma suspected of malignant progression over a 12‐year clinical course

Low tumor cell content predicts favorable prognosis in germinoma patients

MBCL-22. EFFICACY OF DOUBLE-CONDITIONING REGIMEN COMPRISING THIOTEPA AND MELPHALAN FOR RELAPSED MEDULLOBLASTOMA – A SINGLE INSTITUTION EXPERIENCE

GCT-21. Long-term outcome and follow up of intracranial germ cell tumors: Reduced-dose radiotherapy and intensified chemotherapy improves clinical outcome and quality of life for long-term survivors

TCF3::BEND2 in paediatric supratentorial tumour with carcinoma‐like epithelial features classifying as MN1‐altered astroblastoma by DNA methylation profiling

EPN-01MOLECULAR CLASSIFICATION OF EPENDYMOMAS IN A JAPANESE PEDIATRIC MOLECULAR NEURO-ONCOLOGY GROUP (JPMNG) SERIES

Presacral malignant teratoid neoplasm in association with pathogenic DICER1 variation

PATH-28. MOLECULAR DIAGNOSIS FOR CENTRAL DIAGNOSIS OF BRAIN TUMORS FROM 2016 TO 2019— A REPORT FROM THE JAPAN CHILDREN’S CANCER GROUP (JCCG)

MBCL-22. EFFICACY OF DOUBLE-CONDITIONING REGIMEN COMPRISING THIOTEPA AND MELPHALAN FOR RELAPSED MEDULLOBLASTOMA – A SINGLE INSTITUTION EXPERIENCE

LGG-12. INTEGRATED CLINICAL AND MOLECULAR CHARACTERIZATION OF 200 DISSEMINATED PEDIATRIC LOW-GRADE GLIOMAS

MEDB-30. Subclassification of Group 3/4 medulloblastoma as a potential prognostic biomarker to reduce the dose of craniospinal irradiation in patients with metastatic tumors: A Japanese Pediatric Molecular Neuro-Oncology Group study

10206-GGE-21 MOLECULAR LANDSCAPE AND TUMOR EVOLUTION IN ASTROBLASTOMA

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