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Low-frequency mosaicism in cryopyrin-associated periodic fever syndrome: mosaicism in systemic autoinflammatory diseases

International immunology, 2019-09, Vol.31 (10), p.649-655

2019

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Rapid Flow Cytometry-Based Assay for the Functional Classification of MEFV Variants

Journal of clinical immunology, 2021-08, Vol.41 (6), p.1187-1197

2021

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Augmentation of Stimulator of Interferon Genes–Induced Type I Interferon Production in COPA Syndrome

Arthritis & rheumatology (Hoboken, N.J.), 2021-11, Vol.73 (11), p.2105-2115

2021

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Simple and Sensitive Analysis for Dried Blood Spot Proteins by Sodium Carbonate Precipitation for Clinical Proteomics

Journal of proteome research, 2020-07, Vol.19 (7), p.2821-2827

2020

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Functional evaluation of the pathological significance of MEFV variants using induced pluripotent stem cell–derived macrophages

Journal of allergy and clinical immunology, 2019-11, Vol.144 (5), p.1438-1441.e12

2019

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Correction to: Helicobacter cinaedi-Associated Refractory Cellulitis in Patients with X-Linked Agammaglobulinemia

Journal of clinical immunology, 2021-05, Vol.41 (4), p.847-847

2021

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Robust and highly-efficient differentiation of functional monocytic cells from human pluripotent stem cells under serum- and feeder cell-free conditions

PloS one, 2013-04, Vol.8 (4), p.e59243-e59243

2013

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Recurrent tandem duplication of UNC13D in familial hemophagocytic lymphohistiocytosis type 3

Clinical immunology (Orlando, Fla.), 2022-09, Vol.242, p.109104-109104, Article 109104

2022

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Rescue of recurrent deep intronic mutation underlying cell type-dependent quantitative NEMO deficiency

The Journal of clinical investigation, 2019-02, Vol.129 (2), p.583-597

2019

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Induced Pluripotent Stem Cell-Derived Monocytes/Macrophages in Autoinflammatory Diseases

Frontiers in immunology, 2022-05, Vol.13, p.870535-870535

2022

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A sporadic case of CTLA4 haploinsufficiency manifesting as Epstein–Barr virus-positive diffuse large B-cell lymphoma

Journal of Clinical and Experimental Hematopathology, 2022, Vol.62(1), pp.52-57

2022

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Outcomes in children with hemophagocytic lymphohistiocytosis treated using HLH-2004 protocol in Japan

International journal of hematology, 2019-02, Vol.109 (2), p.206-213

2019

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Influence of post-transplant mucosal-associated invariant T cell recovery on the development of acute graft-versus-host disease in allogeneic bone marrow transplantation

International journal of hematology, 2018-07, Vol.108 (1), p.66-75

2018

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Case Report: A Case of Epstein-Barr Virus-Associated Acute Liver Failure Requiring Hematopoietic Cell Transplantation After Emergent Liver Transplantation

Frontiers in immunology, 2022-01, Vol.13, p.825806

2022

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Real‐world results with IgPro20 for hypo‐ or agammaglobulinemia in Japan

Pediatrics international, 2022-01, Vol.64 (1), p.e15362-n/a

2022

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Tocilizumab modifies clinical and laboratory features of macrophage activation syndrome complicating systemic juvenile idiopathic arthritis

Pediatric rheumatology online journal, 2020-01, Vol.18 (1), p.2-2, Article 2

2020

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Human CTL-based functional analysis shows the reliability of a munc13-4 protein expression assay for FHL3 diagnosis

Blood, 2018-05, Vol.131 (18), p.2016-2025

2018

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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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Fruit intake reduces the onset of respiratory allergic symptoms in schoolchildren

Pediatric allergy and immunology, 2017-12, Vol.28 (8), p.793-800

2017

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GATA2 mutation underlies hemophagocytic lymphohistiocytosis in an adult with primary cytomegalovirus infection

Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy, 2020-02, Vol.26 (2), p.252-256

2020

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Case Report: A Pediatric Case of Familial Mediterranean Fever Concurrent With Autoimmune Hepatitis

Frontiers in immunology, 2022-06, Vol.13

2022

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Comprehensive molecular diagnosis of Epstein–Barr virus-associated lymphoproliferative diseases using next-generation sequencing

International journal of hematology, 2018-09, Vol.108 (3), p.319-328

2018

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Hereditary angioedema with a novel mutation, c.1481G>C, in the SERPING1 gene

Journal of cutaneous immunology and allergy, 2021-06, Vol.4 (3), p.73-74

2021

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Pyoderma gangrenosum associated with chronic recurrent multifocal osteomyelitis as a possible paradoxical reaction to anti‐tumor necrosis factor‐α therapy

Journal of dermatology, 2020-08, Vol.47 (8), p.e283-e284

2020

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Transitioning from paediatric to adult rheumatological healthcare: English summary of the Japanese Transition Support Guide

Modern rheumatology, 2022-02, Vol.32 (2), p.248-255

2022

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Low-frequency mosaicism in cryopyrin-associated periodic fever syndrome: mosaicism in systemic autoinflammatory diseases

Rapid Flow Cytometry-Based Assay for the Functional Classification of MEFV Variants

Augmentation of Stimulator of Interferon Genes–Induced Type I Interferon Production in COPA Syndrome

Simple and Sensitive Analysis for Dried Blood Spot Proteins by Sodium Carbonate Precipitation for Clinical Proteomics

Functional evaluation of the pathological significance of MEFV variants using induced pluripotent stem cell–derived macrophages

Correction to: Helicobacter cinaedi-Associated Refractory Cellulitis in Patients with X-Linked Agammaglobulinemia

Robust and highly-efficient differentiation of functional monocytic cells from human pluripotent stem cells under serum- and feeder cell-free conditions

Recurrent tandem duplication of UNC13D in familial hemophagocytic lymphohistiocytosis type 3

Rescue of recurrent deep intronic mutation underlying cell type-dependent quantitative NEMO deficiency

Induced Pluripotent Stem Cell-Derived Monocytes/Macrophages in Autoinflammatory Diseases

A sporadic case of CTLA4 haploinsufficiency manifesting as Epstein–Barr virus-positive diffuse large B-cell lymphoma

Outcomes in children with hemophagocytic lymphohistiocytosis treated using HLH-2004 protocol in Japan

Influence of post-transplant mucosal-associated invariant T cell recovery on the development of acute graft-versus-host disease in allogeneic bone marrow transplantation

Case Report: A Case of Epstein-Barr Virus-Associated Acute Liver Failure Requiring Hematopoietic Cell Transplantation After Emergent Liver Transplantation

Real‐world results with IgPro20 for hypo‐ or agammaglobulinemia in Japan

Tocilizumab modifies clinical and laboratory features of macrophage activation syndrome complicating systemic juvenile idiopathic arthritis

Human CTL-based functional analysis shows the reliability of a munc13-4 protein expression assay for FHL3 diagnosis

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

Fruit intake reduces the onset of respiratory allergic symptoms in schoolchildren

GATA2 mutation underlies hemophagocytic lymphohistiocytosis in an adult with primary cytomegalovirus infection

Case Report: A Pediatric Case of Familial Mediterranean Fever Concurrent With Autoimmune Hepatitis

Comprehensive molecular diagnosis of Epstein–Barr virus-associated lymphoproliferative diseases using next-generation sequencing

Hereditary angioedema with a novel mutation, c.1481G>C, in the SERPING1 gene

Pyoderma gangrenosum associated with chronic recurrent multifocal osteomyelitis as a possible paradoxical reaction to anti‐tumor necrosis factor‐α therapy

Transitioning from paediatric to adult rheumatological healthcare: English summary of the Japanese Transition Support Guide

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