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Dupilumab for STAT3-Hyper-IgE Syndrome With Refractory Intestinal Complication

Pediatrics (Evanston), 2021-09, Vol.148 (3), p.1

2021

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Lipopolysaccharide stimulation test on cultured PBMCs assists the discrimination of cryopyrin-associated periodic syndrome from systemic juvenile idiopathic arthritis

Scientific reports, 2021-06, Vol.11 (1), p.11903-11903, Article 11903

2021

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Cytotoxic Function and Cytokine Production of Natural Killer Cells and Natural Killer T-Like Cells in Systemic Lupus Erythematosis Regulation with Interleukin-15

Mediators of inflammation, 2019-01, Vol.2019 (2019), p.1-12

2019

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Anti–IFN-γ autoantibodies are strongly associated with HLA-DR15:02/16:02 and HLA-DQ05:01/05:02 across Southeast Asia

Journal of allergy and clinical immunology, 2016-03, Vol.137 (3), p.945-948.e8

2016

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Clinical effects of dupilumab: A novel treatment for Kimura disease

Immunity, Inflammation and Disease, 2023-11, Vol.11 (11), p.e1084-n/a

2023

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Total serum IgE in a population-based study of Asian children in Taiwan: reference value and significance in the diagnosis of allergy

PloS one, 2013-11, Vol.8 (11), p.e80996-e80996

2013

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Diminished toll-like receptor response in febrile infection-related epilepsy syndrome (FIRES)

Biomedical Journal, 2020-06, Vol.43 (3), p.293-304

2020

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Pulmonary function evaluation in pediatric patients with primary immunodeficiency complicated by bronchiectasis

Journal of microbiology, immunology and infection, 2020-12, Vol.53 (6), p.1014-1020

2020

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Prevalence and oncologic impact of chronic kidney disease for upper tract urothelial carcinoma in endemic area

Journal of the Formosan Medical Association, 2024-07, Vol.123 (7), p.758-763

2024

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A Nationwide Study of Severe and Protracted Diarrhoea in Patients with Primary Immunodeficiency Diseases

Scientific reports, 2017-06, Vol.7 (1), p.3669-11, Article 3669

2017

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Clinical features and outcomes of patients with chronic granulomatous disease in Taiwan

Journal of microbiology, immunology and infection, 2023-02, Vol.56 (1), p.130-138

2023

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Human uracil-DNA glycosylase deficiency associated with profoundly impaired immunoglobulin class-switch recombination

Nature immunology, 2003-10, Vol.4 (10), p.1023-1028

2003

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Novel Mutations of the Tetratricopeptide Repeat Domain 7A Gene and Phenotype/Genotype Comparison

Frontiers in immunology, 2017-09, Vol.8, p.1066-1066

2017

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Current Perspectives and Unmet Needs of Primary Immunodeficiency Care in Asia Pacific

Frontiers in immunology, 2020-08, Vol.11, p.1605-1605

2020

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Lower T Regulatory and Th17 Cell Populations Predicted by RT-PCR-Amplified FOXP3 and ROR γ t Genes Are Not Rare in Patients With Primary Immunodeficiency Diseases

Frontiers in immunology, 2020-06, Vol.11, p.1111-1111

2020

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Novel Compound Heterozygous Mutations in CRTAP Cause Rare Autosomal Recessive Osteogenesis Imperfecta

Frontiers in genetics, 2020-08, Vol.11, p.897-897

2020

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Incidence of severe combined immunodeficiency through newborn screening in a Chinese population

Journal of the Formosan Medical Association, 2015-01, Vol.114 (1), p.12-16

2015

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Laser therapy for twin–twin transfusion syndrome in a dizygotic monochorionic twin pregnancy: A case report

Taiwanese journal of obstetrics & gynecology, 2021-07, Vol.60 (4), p.791-793

2021

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A Novel CD3G Mutation in a Taiwanese Patient With Normal T Regulatory Function Presenting With the CVID Phenotype Free of Autoimmunity-Analysis of all Genotypes and Phenotypes

Frontiers in immunology, 2019-12, Vol.10, p.2833-2833

2019

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Effect of azithromycin on natural killer cell function

International immunopharmacology, 2012-05, Vol.13 (1), p.8-14

2012

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Distinct Clinical Features and Novel Mutations in Taiwanese Patients With X-Linked Agammaglobulinemia

Frontiers in immunology, 2020-09, Vol.11, p.2001-2001

2020

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Quantitative trait analysis suggests polymorphisms of estrogen-related genes regulate human sperm concentrations and motility

Human reproduction (Oxford), 2011-06, Vol.26 (6), p.1585-1596

2011

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Immune defects in active mycobacterial diseases in patients with primary immunodeficiency diseases (PIDs)

Journal of the Formosan Medical Association, 2011-12, Vol.110 (12), p.750-758

2011

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A single-nucleotide polymorphism of the DAZL gene promoter confers susceptibility to spermatogenic failure in the Taiwanese Han

Human reproduction (Oxford), 2012-09, Vol.27 (9), p.2857-2865

2012

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Patients with inhibitory and neutralizing auto-antibodies to interferon-γ resemble the sporadic adult-onset phenotype of Mendelian Susceptibility to Mycobacterial Disease (MSMD) lacking Bacille Calmette–Guerin (BCG)-induced diseases

Immunobiology (1979), 2013-05, Vol.218 (5), p.762-771

2013

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Dupilumab for STAT3-Hyper-IgE Syndrome With Refractory Intestinal Complication

Lipopolysaccharide stimulation test on cultured PBMCs assists the discrimination of cryopyrin-associated periodic syndrome from systemic juvenile idiopathic arthritis

Cytotoxic Function and Cytokine Production of Natural Killer Cells and Natural Killer T-Like Cells in Systemic Lupus Erythematosis Regulation with Interleukin-15

Anti–IFN-γ autoantibodies are strongly associated with HLA-DR15:02/16:02 and HLA-DQ05:01/05:02 across Southeast Asia

Clinical effects of dupilumab: A novel treatment for Kimura disease

Total serum IgE in a population-based study of Asian children in Taiwan: reference value and significance in the diagnosis of allergy

Diminished toll-like receptor response in febrile infection-related epilepsy syndrome (FIRES)

Pulmonary function evaluation in pediatric patients with primary immunodeficiency complicated by bronchiectasis

Prevalence and oncologic impact of chronic kidney disease for upper tract urothelial carcinoma in endemic area

A Nationwide Study of Severe and Protracted Diarrhoea in Patients with Primary Immunodeficiency Diseases

Clinical features and outcomes of patients with chronic granulomatous disease in Taiwan

Human uracil-DNA glycosylase deficiency associated with profoundly impaired immunoglobulin class-switch recombination

Novel Mutations of the Tetratricopeptide Repeat Domain 7A Gene and Phenotype/Genotype Comparison

Current Perspectives and Unmet Needs of Primary Immunodeficiency Care in Asia Pacific

Lower T Regulatory and Th17 Cell Populations Predicted by RT-PCR-Amplified FOXP3 and ROR γ t Genes Are Not Rare in Patients With Primary Immunodeficiency Diseases

Novel Compound Heterozygous Mutations in CRTAP Cause Rare Autosomal Recessive Osteogenesis Imperfecta

Incidence of severe combined immunodeficiency through newborn screening in a Chinese population

Laser therapy for twin–twin transfusion syndrome in a dizygotic monochorionic twin pregnancy: A case report

A Novel CD3G Mutation in a Taiwanese Patient With Normal T Regulatory Function Presenting With the CVID Phenotype Free of Autoimmunity-Analysis of all Genotypes and Phenotypes

Effect of azithromycin on natural killer cell function

Distinct Clinical Features and Novel Mutations in Taiwanese Patients With X-Linked Agammaglobulinemia

Quantitative trait analysis suggests polymorphisms of estrogen-related genes regulate human sperm concentrations and motility

Immune defects in active mycobacterial diseases in patients with primary immunodeficiency diseases (PIDs)

A single-nucleotide polymorphism of the DAZL gene promoter confers susceptibility to spermatogenic failure in the Taiwanese Han

Patients with inhibitory and neutralizing auto-antibodies to interferon-γ resemble the sporadic adult-onset phenotype of Mendelian Susceptibility to Mycobacterial Disease (MSMD) lacking Bacille Calmette–Guerin (BCG)-induced diseases

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