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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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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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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

Volltextzugriff (PDF)

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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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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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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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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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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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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Immunologic difference between hypersensitivity to mosquito bite and hemophagocytic lymphohistiocytosis associated with Epstein-Barr virus infection

PloS one, 2013-10, Vol.8 (10), p.e76711

2013

Volltextzugriff (PDF)

Differences in Disease Features Between Childhood-Onset and Adult-Onset Systemic Lupus Erythematosus Patients Presenting with Acute Abdominal Pain

Seminars in arthritis and rheumatism, 2011-04, Vol.40 (5), p.447-454

2011

Volltextzugriff (PDF)

Stronger Toll-like receptor 1/2, 4, and 7/8 but less 9 responses in peripheral blood mononuclear cells in non-infectious exacerbated asthmatic children

Immunobiology (1979), 2013-02, Vol.218 (2), p.192-200

2013

Volltextzugriff (PDF)

Central nervous system infections in patients with systemic lupus erythematosus

Journal of rheumatology, 2005-01, Vol.32 (1), p.40

2005

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Polymorphisms of estrogen-related genes jointly confer susceptibility to human spermatogenic defect

Fertility and sterility, 2010, Vol.93 (1), p.141-149

2010

Volltextzugriff (PDF)

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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

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

Incomplete penetrance of NOD2 C483W mutation underlining Blau syndrome

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

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

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

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

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

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

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

Immunologic difference between hypersensitivity to mosquito bite and hemophagocytic lymphohistiocytosis associated with Epstein-Barr virus infection

Differences in Disease Features Between Childhood-Onset and Adult-Onset Systemic Lupus Erythematosus Patients Presenting with Acute Abdominal Pain

Stronger Toll-like receptor 1/2, 4, and 7/8 but less 9 responses in peripheral blood mononuclear cells in non-infectious exacerbated asthmatic children

Central nervous system infections in patients with systemic lupus erythematosus

Polymorphisms of estrogen-related genes jointly confer susceptibility to human spermatogenic defect

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