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Leslie Naesens

Ghent University
H指数:15
被引数:3,275

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A Novel Heterozygous Variant in AICDA Impairs Ig Class Switching and Somatic Hypermutation in Human B Cells and is Associated with Autosomal Dominant HIGM2 Syndrome

AICDA中的一种新的杂合变体会损害人b细胞中的Ig类别转换和体细胞超突变,并与常染色体显性HIGM2综合征相关

2024-02-160
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Loss of GM-CSF-dependent instruction of alveolar macrophages in COVID-19 provides a rationale for inhaled GM-CSF treatment
2022-12-0123
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GTF3A mutations predispose to herpes simplex encephalitis by disrupting biogenesis of the hostderived RIG-I ligand RNA5SP141

GTF3A突变通过破坏宿主衍生的rig-i配体RNA5SP141的生物发生而易患单纯疱疹病毒性脑炎

2022-11-2518
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Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)
2022-05-2320
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Mutations in RNU7-1 Weaken Secondary RNA Structure, Induce MCP-1 and CXCL10 in CSF, and Result in Aicardi-Goutieres Syndrome with Severe End-Organ Involvement
2022-03-2314
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TIM3+TRBV11-2 T cells and IFNγ signature in patrolling monocytes and CD16+ NK cells delineate MIS-C
2021-12-1654
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Effect of anti-interleukin drugs in patients with COVID-19 and signs of cytokine release syndrome (COV-AID): a factorial, randomised, controlled trial
2021-12-0195
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Case Report: Convalescent Plasma, a Targeted Therapy for Patients with CVID and Severe COVID-19
2020-11-2045
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A human immune dysregulation syndrome characterized by severe hyperinflammation with a homozygous nonsense Roquin-1 mutation (vol 10, 4779 , 2019)
2019-11-201
OAAI
A human immune dysregulation syndrome characterized by severe hyperinflammation with a homozygous nonsense Roquin-1 mutation

人类免疫失调综合征,其特征是具有纯合无义Roquin-1突变的严重过度炎症

2019-10-2142
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