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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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Clinical Features and Genetic Analysis of Taiwanese Primary Immunodeficiency Patients with Prolonged Diarrhea and Monogenetic Inflammatory Bowel Disease

Journal of clinical immunology, 2023-08, Vol.43 (6), p.1455-1467

2023

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Distinct Lymphocyte Immunophenotyping and Quantitative Anti-Interferon Gamma Autoantibodies in Taiwanese HIV-Negative Patients with Non-Tuberculous Mycobacterial Infections

Journal of clinical immunology, 2023-05, Vol.43 (4), p.717-727

2023

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Development and validation of an expanded targeted sequencing panel for non-invasive prenatal diagnosis of sporadic skeletal dysplasia

BMC medical genomics, 2021-11, Vol.14 (Suppl 3), p.212-212, Article 212

2021

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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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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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Incomplete penetrance of NOD2 C483W mutation underlining Blau syndrome

Pediatric rheumatology online journal, 2022-10, Vol.20 (1), p.86-86, Article 86

2022

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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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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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Clinical Features of Female Taiwanese Carriers with X-linked Chronic Granulomatous Disease from 2004 to 2019

Journal of clinical immunology, 2021-08, Vol.41 (6), p.1303-1314

2021

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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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Age, gender, height and weight in relation to joint cartilage thickness among school-aged children from ultrasonographic measurement

Pediatric rheumatology online journal, 2021-05, Vol.19 (1), p.71-71, Article 71

2021

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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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Biomarkers associating endothelial Dysregulation in pediatric-onset systemic lupus erythematous

Pediatric rheumatology online journal, 2019-10, Vol.17 (1), p.69-69, Article 69

2019

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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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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

Clinical Features and Genetic Analysis of Taiwanese Primary Immunodeficiency Patients with Prolonged Diarrhea and Monogenetic Inflammatory Bowel Disease

Distinct Lymphocyte Immunophenotyping and Quantitative Anti-Interferon Gamma Autoantibodies in Taiwanese HIV-Negative Patients with Non-Tuberculous Mycobacterial Infections

Development and validation of an expanded targeted sequencing panel for non-invasive prenatal diagnosis of sporadic skeletal dysplasia

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

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

Incomplete penetrance of NOD2 C483W mutation underlining Blau syndrome

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

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

Clinical Features of Female Taiwanese Carriers with X-linked Chronic Granulomatous Disease from 2004 to 2019

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

Age, gender, height and weight in relation to joint cartilage thickness among school-aged children from ultrasonographic measurement

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

Biomarkers associating endothelial Dysregulation in pediatric-onset systemic lupus erythematous

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

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