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WASP-WIP complex in the molecular pathogenesis of Wiskott-Aldrich syndrome

Pediatrics international, 2016-01, Vol.58 (1), p.4-7

Sasahara, Yoji

2016

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Primary Immunodeficiencies Associated With Early-Onset Inflammatory Bowel Disease in Southeast and East Asia

Frontiers in immunology, 2022-01, Vol.12, p.786538-786538

2022

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Clinical practice recommendations for the diagnosis and management of human herpesvirus-6B encephalitis after allogeneic hematopoietic stem cell transplantation: the Japan Society for Hematopoietic Cell Transplantation

Bone marrow transplantation (Basingstoke), 2020-06, Vol.55 (6), p.1004-1013

2020

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Hematopoietic Cell Transplantation for Severe Combined Immunodeficiency Patients: a Japanese Retrospective Study

Journal of clinical immunology, 2021-11, Vol.41 (8), p.1865-1877

2021

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Ruxolitinib treatment of a patient with steroid-dependent severe autoimmunity due to STAT1 gain-of-function mutation

International journal of hematology, 2020-08, Vol.112 (2), p.258-262

2020

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Refractory T-cell/histiocyte-rich large B-cell lymphoma in a patient with ataxia–telangiectasia caused by novel compound heterozygous variants in ATM

International journal of hematology, 2021-12, Vol.114 (6), p.735-741

2021

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Hematopoietic Cell Transplantation for Inborn Errors of Immunity Other than Severe Combined Immunodeficiency in Japan: Retrospective Analysis for 1985–2016

Journal of clinical immunology, 2022-04, Vol.42 (3), p.529-545

2022

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Favorable prognosis of vaccine-associated immune thrombocytopenia in children is correlated with young age at vaccination: Retrospective survey of a nationwide disease registry

International journal of hematology, 2022, Vol.115 (1), p.114-122

2022

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Chronological changes of skin eruptions toward cold abscess formation in hyper‐immunoglobulin E syndrome

Journal of dermatology, 2021-07, Vol.48 (7), p.e316-e317

2021

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Chemoradiotherapy of spinal extradural Ewing sarcoma after the Fontan procedure

Pediatrics international, 2020-10, Vol.62 (10), p.1197-1199

2020

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The IL1RN Mutation Creating the Most-Upstream Premature Stop Codon Is Hypomorphic Because of a Reinitiation of Translation

Journal of clinical immunology, 2020-05, Vol.40 (4), p.643-645

2020

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Outcome of children with relapsed high-risk neuroblastoma in Japan and analysis of the role of allogeneic hematopoietic stem cell transplantation

Japanese journal of clinical oncology, 2022-05, Vol.52 (5), p.486-492

2022

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Hematopoietic Stem Cell Transplantation for XIAP Deficiency in Japan

Journal of clinical immunology, 2017-01, Vol.37 (1), p.85-91

2017

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Case of atopic dermatitis concurrent with idiopathic thrombocytopenic purpura, whose serum thymus and activation‐regulated chemokine level remained undetectable

Journal of dermatology, 2018-05, Vol.45 (5), p.606-608

2018

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Efficacy of rituximab for the treatment and prevention of autoimmunity in patients with Wiskott-Aldrich syndrome and X-linked thrombocytopenia

Clinical immunology communications, 2024-06, Vol.5, p.34-40

2024

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Registry data analysis of hematopoietic stem cell transplantation on systemic chronic active Epstein–Barr virus infection patients in Japan

American journal of hematology, 2022-06, Vol.97 (6), p.780-790

2022

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

Bone marrow transplantation (Basingstoke), 2021-05, Vol.56 (5), p.1013-1020

2021

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Development of a multi-step leukemogenesis model of MLL-rearranged leukemia using humanized mice

PloS one, 2012-06, Vol.7 (6), p.e37892-e37892

2012

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Atopic dermatitis without serum immunoglobulin E elevation or loss‐of‐function filaggrin gene mutation in a patient with X‐linked agammaglobulinemia

Journal of dermatology, 2020-01, Vol.47 (1), p.58-60

2020

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Reduced-intensity conditioning is effective for allogeneic hematopoietic stem cell transplantation in infants with MECOM-associated syndrome

International journal of hematology, 2023-04, Vol.117 (4), p.598-606

2023

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Case Report: Infantile-Onset Fulminant Type 1 Diabetes Mellitus Caused by Novel Compound Heterozygous LRBA Variants

Frontiers in immunology, 2021-04, Vol.12, p.677572

2021

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Targeted Sequencing and Immunological Analysis Reveal the Involvement of Primary Immunodeficiency Genes in Pediatric IBD: a Japanese Multicenter Study

Journal of clinical immunology, 2017-01, Vol.37 (1), p.67-79

2017

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Pediatric psoriasis induced by HLA‐B46‐Cw1 haplotype: A retrospective study of psoriasis onset after hematopoietic stem cell transplantation

Journal of dermatology, 2021-09, Vol.48 (9), p.1381-1385

2021

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

Haematologica (Roma), 2017-03, Vol.102 (3), p.e93

2017

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Correction to: the IL1RN Mutation Creating the Most-Upstream Premature Stop Codon Is Hypomorphic because of a Reinitiation of Translation

Journal of clinical immunology, 2020-05, Vol.40 (4), p.646-646

2020

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WASP-WIP complex in the molecular pathogenesis of Wiskott-Aldrich syndrome

Primary Immunodeficiencies Associated With Early-Onset Inflammatory Bowel Disease in Southeast and East Asia

Clinical practice recommendations for the diagnosis and management of human herpesvirus-6B encephalitis after allogeneic hematopoietic stem cell transplantation: the Japan Society for Hematopoietic Cell Transplantation

Hematopoietic Cell Transplantation for Severe Combined Immunodeficiency Patients: a Japanese Retrospective Study

Ruxolitinib treatment of a patient with steroid-dependent severe autoimmunity due to STAT1 gain-of-function mutation

Refractory T-cell/histiocyte-rich large B-cell lymphoma in a patient with ataxia–telangiectasia caused by novel compound heterozygous variants in ATM

Hematopoietic Cell Transplantation for Inborn Errors of Immunity Other than Severe Combined Immunodeficiency in Japan: Retrospective Analysis for 1985–2016

Favorable prognosis of vaccine-associated immune thrombocytopenia in children is correlated with young age at vaccination: Retrospective survey of a nationwide disease registry

Chronological changes of skin eruptions toward cold abscess formation in hyper‐immunoglobulin E syndrome

Chemoradiotherapy of spinal extradural Ewing sarcoma after the Fontan procedure

The IL1RN Mutation Creating the Most-Upstream Premature Stop Codon Is Hypomorphic Because of a Reinitiation of Translation

Outcome of children with relapsed high-risk neuroblastoma in Japan and analysis of the role of allogeneic hematopoietic stem cell transplantation

Hematopoietic Stem Cell Transplantation for XIAP Deficiency in Japan

Case of atopic dermatitis concurrent with idiopathic thrombocytopenic purpura, whose serum thymus and activation‐regulated chemokine level remained undetectable

Efficacy of rituximab for the treatment and prevention of autoimmunity in patients with Wiskott-Aldrich syndrome and X-linked thrombocytopenia

Registry data analysis of hematopoietic stem cell transplantation on systemic chronic active Epstein–Barr virus infection patients in Japan

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

Development of a multi-step leukemogenesis model of MLL-rearranged leukemia using humanized mice

Atopic dermatitis without serum immunoglobulin E elevation or loss‐of‐function filaggrin gene mutation in a patient with X‐linked agammaglobulinemia

Reduced-intensity conditioning is effective for allogeneic hematopoietic stem cell transplantation in infants with MECOM-associated syndrome

Case Report: Infantile-Onset Fulminant Type 1 Diabetes Mellitus Caused by Novel Compound Heterozygous LRBA Variants

Targeted Sequencing and Immunological Analysis Reveal the Involvement of Primary Immunodeficiency Genes in Pediatric IBD: a Japanese Multicenter Study

Pediatric psoriasis induced by HLA‐B46‐Cw1 haplotype: A retrospective study of psoriasis onset after hematopoietic stem cell transplantation

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

Correction to: the IL1RN Mutation Creating the Most-Upstream Premature Stop Codon Is Hypomorphic because of a Reinitiation of Translation

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