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Treatment outcome of children with acute lymphoblastic leukemia: the Tokyo Children’s Cancer Study Group (TCCSG) Study L04-16

International journal of hematology, 2018-07, Vol.108 (1), p.98-108

2018

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Erythematous Plaques in a Child with Sweet Syndrome

The Journal of pediatrics, 2016-09, Vol.176, p.210-210.e1

2016

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Streptococcus gallolyticus subsp. pasteurianus meningitis in an infant

Pediatrics international, 2014-04, Vol.56 (2), p.282-285

2014

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Risks and prevention of severe RS virus infection among children with immunodeficiency and Down's syndrome

Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy, 2014-08, Vol.20 (8), p.455-459

2014

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Treatment outcomes of adolescent acute lymphoblastic leukemia treated on Tokyo Children’s Cancer Study Group (TCCSG) clinical trials

International journal of hematology, 2014-08, Vol.100 (2), p.180-187

2014

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A splenial lesion with transiently reduced diffusion in clinically mild encephalitis is not always reversible: A case report

Brain & development (Tokyo. 1979), 2009-10, Vol.31 (9), p.710-712

2009

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Residual disease detected by multidimensional flow cytometry shows prognostic significance in childhood acute myeloid leukemia with intermediate cytogenetics and negative FLT3-ITD: a report from the Tokyo Children’s Cancer Study Group

International journal of hematology, 2016-04, Vol.103 (4), p.416-422

2016

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Multicenter prospective evaluation of a novel rapid immunochromatographic diagnostic kit specifically detecting influenza A H1N1 2009 virus

Journal of clinical virology, 2011-05, Vol.51 (1), p.68-72

2011

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Identification and Characterization of a Novel Related Adhesion Focal Tyrosine Kinase (RAFTK) from Megakaryocytes and Brain

The Journal of biological chemistry, 1995-11, Vol.270 (46), p.27742-27751

1995

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Macrothrombocytopenia With Congenital Bilateral Cataracts: A Phenotype of MYH9 Disorder With Exon 24 Indel Mutations

Journal of pediatric hematology/oncology, 2018-01, Vol.40 (1), p.76-78

2018

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A Report of Three Girls with Antithyroid Drug-Induced Agranulocytosis; Retrospective Analysis of 18 Cases Aged 15 Years or Younger Reported between 1995 and 2009

Clinical Pediatric Endocrinology, 2011, Vol.20(2), pp.39-46

2011

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Prominence of NUDT15 genetic variation associated with 6‐mercaptopurine tolerance in a genome‐wide association study of Japanese children with acute lymphoblastic leukaemia

British journal of haematology, 2022-10, Vol.199 (2), p.260-269

2022

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A Report of Three Girls with Antithyroid Drug-Induced Agranulocytosis; Retrospective Analysis of 18 Cases Aged 15 Years or Younger Reported between 1995 and 2009

Clinical Pediatric Endocrinology, 2011, Vol.20 (2), p.39-46

2011

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NUDT15 Genetic Variation Is the Strongest Predictive Marker of Tolerance to 6-Mercaptopurine in Japanese Childhood ALL Patients: A Genome-Wide Association Study

Blood, 2019-11, Vol.134 (Supplement_1), p.1347-1347

2019

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Genome-wide assessment of genetic risk loci for childhood acute lymphoblastic leukemia in Japanese patients

Haematologica (Roma), 2024-04, Vol.109 (4), p.1247

2024

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Rare TCF3 variants associated with pediatric B cell acute lymphoblastic leukemia

Pediatric hematology and oncology, 2024, Vol.41 (1), p.81-87

2024

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Activated microglia in acute encephalopathy with biphasic seizures and late reduced diffusion

Journal of the neurological sciences, 2016-07, Vol.366, p.91-93

2016

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Characteristic Height Growth Pattern in Patients with Pseudohypoparathyroidism: Comparison between Type 1a and Type 1b

Clinical Pediatric Endocrinology, 2007, Vol.16(1), pp.31-36

2007

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The Association Between L-Asparaginase Hypersensitivity and Genetic Variants in Japanese Childhood ALL Patients

Blood, 2016-12, Vol.128 (22), p.5141-5141

2016

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Expression of CD203c on basophils as a marker of immunoglobulin E-mediated l-asparaginase allergy

Leukemia & lymphoma, 2014-01, Vol.55 (1), p.92-96

2014

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Characteristic Height Growth Pattern in Patients with Pseudohypoparathyroidism: Comparison between Type 1a and Type 1b

Clinical Pediatric Endocrinology, 2007, Vol.16 (1), p.31-36

2007

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Structural and Functional Studies of the Intracellular Tyrosine Kinase MATK Gene and Its Translated Product (∗)

The Journal of biological chemistry, 1995-01, Vol.270 (4), p.1833-1842

1995

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Treatment outcome of children with acute lymphoblastic leukemia: the Tokyo Children’s Cancer Study Group (TCCSG) Study L04-16

Erythematous Plaques in a Child with Sweet Syndrome

Streptococcus gallolyticus subsp. pasteurianus meningitis in an infant

Risks and prevention of severe RS virus infection among children with immunodeficiency and Down's syndrome

Treatment outcomes of adolescent acute lymphoblastic leukemia treated on Tokyo Children’s Cancer Study Group (TCCSG) clinical trials

A splenial lesion with transiently reduced diffusion in clinically mild encephalitis is not always reversible: A case report

Residual disease detected by multidimensional flow cytometry shows prognostic significance in childhood acute myeloid leukemia with intermediate cytogenetics and negative FLT3-ITD: a report from the Tokyo Children’s Cancer Study Group

Multicenter prospective evaluation of a novel rapid immunochromatographic diagnostic kit specifically detecting influenza A H1N1 2009 virus

Identification and Characterization of a Novel Related Adhesion Focal Tyrosine Kinase (RAFTK) from Megakaryocytes and Brain

Macrothrombocytopenia With Congenital Bilateral Cataracts: A Phenotype of MYH9 Disorder With Exon 24 Indel Mutations

A Report of Three Girls with Antithyroid Drug-Induced Agranulocytosis; Retrospective Analysis of 18 Cases Aged 15 Years or Younger Reported between 1995 and 2009

Prominence of NUDT15 genetic variation associated with 6‐mercaptopurine tolerance in a genome‐wide association study of Japanese children with acute lymphoblastic leukaemia

A Report of Three Girls with Antithyroid Drug-Induced Agranulocytosis; Retrospective Analysis of 18 Cases Aged 15 Years or Younger Reported between 1995 and 2009

NUDT15 Genetic Variation Is the Strongest Predictive Marker of Tolerance to 6-Mercaptopurine in Japanese Childhood ALL Patients: A Genome-Wide Association Study

Genome-wide assessment of genetic risk loci for childhood acute lymphoblastic leukemia in Japanese patients

Rare TCF3 variants associated with pediatric B cell acute lymphoblastic leukemia

Activated microglia in acute encephalopathy with biphasic seizures and late reduced diffusion

Regional evaluation of childhood acute lymphoblastic leukemia genetic susceptibility loci among Japanese

Characteristic Height Growth Pattern in Patients with Pseudohypoparathyroidism: Comparison between Type 1a and Type 1b

The Association Between L-Asparaginase Hypersensitivity and Genetic Variants in Japanese Childhood ALL Patients

Genetic Susceptibility Loci for Childhood Acute Lymphoblastic Leukemia Among Japanese

Expression of CD203c on basophils as a marker of immunoglobulin E-mediated l-asparaginase allergy

Characteristic Height Growth Pattern in Patients with Pseudohypoparathyroidism: Comparison between Type 1a and Type 1b

Structural and Functional Studies of the Intracellular Tyrosine Kinase MATK Gene and Its Translated Product (∗)

Significance Of Minimal Residual Disease Detected By Multi-Color Flow Cytometry In Childhood Acute Myeloid Leukemia With The Intermideate-Risk Cytogenetics and Negative FMS-Like Tyrosine Kinase 3 Internal Tandem Duplication: A Report Of The Tokyo Children's Cancer Study Group

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