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An Update on XMEN Disease

Journal of clinical immunology, 2020-07, Vol.40 (5), p.671-681

2020

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Tocilizumab-induced hypofibrinogenemia in patients with systemic-onset juvenile idiopathic arthritis

Scientific reports, 2023-06, Vol.13 (1), p.9050-9050, Article 9050

2023

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A New Patient with NOCARH Syndrome Due to CDC42 Defect

Journal of clinical immunology, 2020-05, Vol.40 (4), p.571-575

2020

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Haploinsufficiency of A20 Due to Novel Mutations in TNFAIP3

Journal of clinical immunology, 2020-07, Vol.40 (5), p.741-751

2020

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Systemic inflammation and chronic kidney disease in a patient due to the RNASEH2B defect

Pediatric rheumatology online journal, 2021-01, Vol.19 (1), p.9-9, Article 9

2021

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JAK inhibitors in systemic juvenile idiopathic arthritis

Frontiers in pediatrics, 2023-04, Vol.11, p.1134312-1134312

2023

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Macrophage activation syndrome in children with Kikuchi-Fujimoto disease

Pediatric rheumatology online journal, 2023-01, Vol.21 (1), p.10-10, Article 10

2023

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Elevated serum IFN-γand IFN-γ/IL-6 ratio in Kikuchi-Fujimoto disease

Pediatric rheumatology online journal, 2023-08, Vol.21 (1), p.88-88, Article 88

2023

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Acquired Hemophilia A in Wiskott–Aldrich Syndrome

Journal of clinical immunology, 2021-07, Vol.41 (5), p.1119-1122

2021

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Canakinumab in the treatment of systemic juvenile idiopathic arthritis: a retrospective single center study in China

Frontiers in pediatrics, 2024-03, Vol.12, p.1349907-1349907

2024

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LACC1 deficiency leading to juvenile arthritis and anemia

Clinical immunology (Orlando, Fla.), 2024-08, Vol.265, p.110290, Article 110290

2024

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Kawasaki disease associated pulmonary involvement in infants

Pediatric pulmonology, 2021-10, Vol.56 (10), p.3389-3394

2021

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Elevated serum IFN-[gamma]and IFN-[gamma]/IL-6 ratio in Kikuchi-Fujimoto disease

Pediatric rheumatology online journal, 2023-08, Vol.21 (1)

2023

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Characterization of a Novel Pathogenic PLCG2 Variant Leading to APLAID Syndrome Responsive to a TNF Inhibitor

Arthritis & rheumatology (Hoboken, N.J.), 2024-08

2024

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Identification of a novel de novo gain-of-function mutation of PIK3CD in a patient with activated phosphoinositide 3-kinase δ syndrome

Clinical immunology (Orlando, Fla.), 2018-12, Vol.197, p.60-67

2018

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Defective glycosylation and multisystem abnormalities characterize the primary immunodeficiency XMEN disease

The Journal of clinical investigation, 2020-01, Vol.130 (1), p.507-522

2020

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Talaromyces marneffei Infections in 8 Chinese Children with Inborn Errors of Immunity

Mycopathologia (1975), 2022-12, Vol.187 (5-6), p.455-467

2022

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Homozygous IL37 mutation associated with infantile inflammatory bowel disease

Proceedings of the National Academy of Sciences - PNAS, 2021-03, Vol.118 (10), p.1

2021

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Novel mutations of TYK2 leading to divergent clinical phenotypes

Pediatric allergy and immunology, 2022-01, Vol.33 (1), p.e13671-n/a

2022

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Targeted next‐generation sequencing for genetic diagnosis of 160 patients with primary immunodeficiency in south China

Pediatric allergy and immunology, 2018-12, Vol.29 (8), p.863-872

2018

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AKTIN - The German Emergency Department Data Registry - real-time data from emergency medicine : Implementation and first results from 15 emergency departments with focus on Federal Joint Committee's guidelines on acuity assessment

Medizinische Klinik, Intensivmedizin und Notfallmedizin, 2022-02, Vol.117 (1), p.24-33

2022

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Clinical features and mutational analysis of a case with Sensenbrenner syndrome

Zhonghua yi xue yi chuan xue za zhi, 2018-06, Vol.35 (3), p.426

2018

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A New Patient with NOCARH Syndrome Due to CDC42 Defect

Journal of clinical immunology, 2020, Vol.40 (4), p.571-575

2020

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Acquired Hemophilia A in Wiskott-Aldrich Syndrome

Journal of clinical immunology, 2021, Vol.41 (5), p.1119-1122

2021

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Online Identification of Power System Dynamic Signature Using PMU Measurements and Data Mining

IEEE transactions on power systems, 2016-05, Vol.31 (3), p.1760-1768

2016

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An Update on XMEN Disease

Tocilizumab-induced hypofibrinogenemia in patients with systemic-onset juvenile idiopathic arthritis

A New Patient with NOCARH Syndrome Due to CDC42 Defect

Haploinsufficiency of A20 Due to Novel Mutations in TNFAIP3

Systemic inflammation and chronic kidney disease in a patient due to the RNASEH2B defect

JAK inhibitors in systemic juvenile idiopathic arthritis

Macrophage activation syndrome in children with Kikuchi-Fujimoto disease

Elevated serum IFN-γand IFN-γ/IL-6 ratio in Kikuchi-Fujimoto disease

Acquired Hemophilia A in Wiskott–Aldrich Syndrome

Canakinumab in the treatment of systemic juvenile idiopathic arthritis: a retrospective single center study in China

LACC1 deficiency leading to juvenile arthritis and anemia

Kawasaki disease associated pulmonary involvement in infants

Elevated serum IFN-[gamma]and IFN-[gamma]/IL-6 ratio in Kikuchi-Fujimoto disease

Characterization of a Novel Pathogenic PLCG2 Variant Leading to APLAID Syndrome Responsive to a TNF Inhibitor

Identification of a novel de novo gain-of-function mutation of PIK3CD in a patient with activated phosphoinositide 3-kinase δ syndrome

Defective glycosylation and multisystem abnormalities characterize the primary immunodeficiency XMEN disease

Talaromyces marneffei Infections in 8 Chinese Children with Inborn Errors of Immunity

Homozygous IL37 mutation associated with infantile inflammatory bowel disease

Novel mutations of TYK2 leading to divergent clinical phenotypes

Targeted next‐generation sequencing for genetic diagnosis of 160 patients with primary immunodeficiency in south China

AKTIN - The German Emergency Department Data Registry - real-time data from emergency medicine : Implementation and first results from 15 emergency departments with focus on Federal Joint Committee's guidelines on acuity assessment

Clinical features and mutational analysis of a case with Sensenbrenner syndrome

A New Patient with NOCARH Syndrome Due to CDC42 Defect

Acquired Hemophilia A in Wiskott-Aldrich Syndrome

Online Identification of Power System Dynamic Signature Using PMU Measurements and Data Mining

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