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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, p.4236562-12

2019

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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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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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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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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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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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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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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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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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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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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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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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Effect of azithromycin on natural killer cell function

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

2012

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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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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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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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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

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

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

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

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

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

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

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

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

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

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

Effect of azithromycin on natural killer cell function

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

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

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

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