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G

Gregor Dückers

Helios Kliniken
H指数:21
被引数:2,532

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Infant-onset juvenile idiopathic arthritis: a multicentre retrospective study

婴儿期起病的幼年特发性关节炎:一项多中心回顾性研究

2025-11-010
PRE
Inhibition of lysosomal degradation increases expression of mutant ADA2 in DADA2 monocytes

溶酶体降解的抑制增加了DADA2单核细胞中突变型ADA2的表达

2025-06-200
OAAI
IRF2BP2 deficiency: An important form of common variable immunodeficiency with inflammation

IRF2BP2 缺陷:一种伴有炎症的常见可变免疫缺陷的重要形式

2025-03-140
PRE
UNC93B1 variants underlie TLR7-dependent autoimmunity
2024-02-2321
PRE
Detrimental NFKB1 missense variants affecting the Rel-homology domain of p105/p50

有害的NFKB1错义变体影响p105/p50的Rel同源结构域

2022-08-295
OAAI
Rubella vaccine-induced granulomas are a novel phenotype with incomplete penetrance of genetic defects in cytotoxicity

风疹疫苗诱导的肉芽肿是一种新型表型,其细胞毒性遗传缺陷的外显率不完全。

2022-01-0112
OAAI
A distinct CD38+CD45RA+ population of CD4+, CD8+, and double-negative T cells is controlled by FAS

CD4,CD8和双阴性T细胞的独特CD38 CD45RA群体受FAS控制

2020-11-1033
OAAI
Incidence of SCID in Germany from 2014 to 2015 an ESPED* Survey on Behalf of the API*** Erhebungseinheit fur Seltene Padiatrische Erkrankungen in Deutschland (German Paediatric Surveillance Unit) ** Arbeitsgemeinschaft Padiatrische Immunologie
2020-05-2610
PREAI
The German National Registry of Primary Immunodeficiencies (2012-2017)
2019-07-1968
OAAI
A combined immunodeficiency with severe infections, inflammation, and allergy caused by ARPC1B deficiency

由ARPC1B缺陷引起的联合免疫缺陷与严重感染,炎症和过敏

2019-06-0180
OAAI
Lung disease in STAT3 hyper-IgE syndrome requires intense therapy

STAT3高IgE综合征中的肺部疾病需要强化治疗

2019-04-0419
PREAI
Phenotype, penetrance, and treatment of 133 cytotoxic T-lymphocyte antigen 4-insufficient subjects
2018-12-01313
OAAI
Long-term follow-up of IPEX syndrome patients after different therapeutic strategies: An international multicenter retrospective study
2018-03-01211
OAAI
Human RAD52-a novel player in DNA repair in cancer and immunodeficiency
2016-12-157
OAAI
Key findings to expedite the diagnosis of hyper-IgE syndromes in infants and young children
2016-01-2642
PREAI
The Extended Clinical Phenotype of 26 Patients with Chronic Mucocutaneous Candidiasis due to Gain-of-Function Mutations in STAT1
2015-11-25107
OAAI
Novel mutations in TNFRSF7/CD27: Clinical, immunologic, and genetic characterization of human CD27 deficiency
2015-09-01107
PREAI
DOCK8 Deficiency: Clinical and Immunological Phenotype and Treatment Options - a Review of 136 Patients
2015-01-28225
PREAI