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Elevated Soluble PD-L1 in Pregnant Women's Serum Suppresses the Immune Reaction

Frontiers in immunology, 2019-02, Vol.10, p.86

2019

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Hepcidin in Kawasaki disease: upregulation by acute inflammation in patients having resistance to intravenous immunoglobulin therapy

Clinical rheumatology, 2021-12, Vol.40 (12), p.5019-5024

2021

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STAT6 gain-of-function variant exacerbates multiple allergic symptoms

Journal of allergy and clinical immunology, 2023-05, Vol.151 (5), p.1402-1409.e6

2023

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Patient-reported outcomes in patients with primary immunodeficiency diseases in Japan: baseline results from a prospective observational study

Frontiers in immunology, 2023-09, Vol.14, p.1244250-1244250

2023

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Autoimmune hemolytic anemia associated with Takenouchi–Kosaki syndrome

Pediatrics international, 2021-12, Vol.63 (12), p.1528-1530

2021

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Vedolizumab therapy for pediatric steroid-refractory gastrointestinal acute graft-versus-host disease

International journal of hematology, 2022-04, Vol.115 (4), p.590-594

2022

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Haploinsufficiency of A20 caused by a novel nonsense variant or entire deletion of TNFAIP3 is clinically distinct from Behçet's disease

Arthritis research & therapy, 2019-06, Vol.21 (1), p.137-137, Article 137

2019

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A mycobacterium fortuitum infection in chronic mucocutaneous candidiasis

Pediatrics international, 2022-01, Vol.64 (1), p.e15166-n/a

2022

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Bronchial stenosis associated with non‐tuberculous mycobacterial infection

Pediatrics international, 2022-01, Vol.64 (1), p.e14947-n/a

2022

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Ecthyma gangrenosum in an infant with neutropenia

International journal of hematology, 2021, Vol.113 (1), p.3-4

2021

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Two novel gain-of-function mutations of STAT1 responsible for chronic mucocutaneous candidiasis disease: impaired production of IL-17A and IL-22, and the presence of anti-IL-17F autoantibody

The Journal of immunology (1950), 2014-11, Vol.193 (10), p.4880-4887

2014

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Live attenuated vaccines under immunosuppressive agents or biological agents: survey and clinical data from Japan

European journal of pediatrics, 2021-06, Vol.180 (6), p.1847-1854

2021

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A pregnant woman with thymoma-associated pure red cell aplasia

BMC pregnancy and childbirth, 2022-10, Vol.22 (1), p.1-795, Article 795

2022

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A novel STAT3 mutation associated with hyper immunoglobulin E syndrome with a paucity of connective tissue signs

Pediatrics international, 2021-05, Vol.63 (5), p.510-515

2021

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X‐linked agammaglobulinemia complicated with pulmonary aspergillosis

Pediatrics international, 2018-01, Vol.60 (1), p.90-92

2018

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Thymitis in chronic granulomatous disease

Pediatrics international, 2019-04, Vol.61 (4), p.429-431

2019

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Clinical features of very early-onset inflammatory bowel disease in Japan: a retrospective single-center study

Intestinal research, 2022-10, Vol.20 (4), p.475-481

2022

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Multiple osteolytic lesions on the skull of a girl with Mendelian susceptibility to mycobacterial disease

Pediatrics international, 2018-11, Vol.60 (11), p.1043-1044

2018

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Thalidomide attenuates excessive inflammation without interrupting lipopolysaccharide-driven inflammatory cytokine production in chronic granulomatous disease

Clinical immunology (Orlando, Fla.), 2013-05, Vol.147 (2), p.122-128

2013

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Effects of enzyme replacement therapy on immune function in ADA deficiency patient

Clinical immunology (Orlando, Fla.), 2015-12, Vol.161 (2), p.391-393

2015

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Single Cell-Based Vector Tracing in Patients with ADA-SCID Treated with Stem Cell Gene Therapy

Molecular therapy. Methods & clinical development, 2017-09, Vol.6 (C), p.8-16

2017

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Basiliximab treatment for steroid-resistant rejection in pediatric patients following liver transplantation for acute liver failure

Pediatric transplantation, 2014-12, Vol.18 (8), p.860-867

2014

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WHIM syndrome: congenital immune deficiency disease

Current opinion in hematology, 2009-01, Vol.16 (1), p.20-26

2009

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WHIM syndrome: congenital immune deficiency disease

Current opinion in hematology, 2009-01, Vol.16 (1), p.20

2009

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Obturator internus muscle abscess in a case of X-linked agammaglobulinemia

Pediatrics international, 2024-01, Vol.66 (1), p.e15775

2024

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Elevated Soluble PD-L1 in Pregnant Women's Serum Suppresses the Immune Reaction

Hepcidin in Kawasaki disease: upregulation by acute inflammation in patients having resistance to intravenous immunoglobulin therapy

STAT6 gain-of-function variant exacerbates multiple allergic symptoms

Patient-reported outcomes in patients with primary immunodeficiency diseases in Japan: baseline results from a prospective observational study

Autoimmune hemolytic anemia associated with Takenouchi–Kosaki syndrome

Vedolizumab therapy for pediatric steroid-refractory gastrointestinal acute graft-versus-host disease

Haploinsufficiency of A20 caused by a novel nonsense variant or entire deletion of TNFAIP3 is clinically distinct from Behçet's disease

A mycobacterium fortuitum infection in chronic mucocutaneous candidiasis

Bronchial stenosis associated with non‐tuberculous mycobacterial infection

Ecthyma gangrenosum in an infant with neutropenia

Two novel gain-of-function mutations of STAT1 responsible for chronic mucocutaneous candidiasis disease: impaired production of IL-17A and IL-22, and the presence of anti-IL-17F autoantibody

Live attenuated vaccines under immunosuppressive agents or biological agents: survey and clinical data from Japan

A pregnant woman with thymoma-associated pure red cell aplasia

A novel STAT3 mutation associated with hyper immunoglobulin E syndrome with a paucity of connective tissue signs

X‐linked agammaglobulinemia complicated with pulmonary aspergillosis

Thymitis in chronic granulomatous disease

Clinical features of very early-onset inflammatory bowel disease in Japan: a retrospective single-center study

Multiple osteolytic lesions on the skull of a girl with Mendelian susceptibility to mycobacterial disease

Thalidomide attenuates excessive inflammation without interrupting lipopolysaccharide-driven inflammatory cytokine production in chronic granulomatous disease

Effects of enzyme replacement therapy on immune function in ADA deficiency patient

Single Cell-Based Vector Tracing in Patients with ADA-SCID Treated with Stem Cell Gene Therapy

Basiliximab treatment for steroid-resistant rejection in pediatric patients following liver transplantation for acute liver failure

WHIM syndrome: congenital immune deficiency disease

WHIM syndrome: congenital immune deficiency disease

Obturator internus muscle abscess in a case of X-linked agammaglobulinemia

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