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Lambertus P. van den Heuvel

radboud university medical center
H-index:64
Citation Count:1.4万
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Characterizing Properdin-Inhibited C3 Nephritic Factors in Patients with Complement-Mediated Kidney Diseases

表征补体介导肾脏疾病患者中properdin抑制的C3肾炎性因子

2026-07-300
OA
APOL1-mediated kidney disease: a narrative review of the lessons learnt from the past 15 years

APOL1介导的肾脏疾病:过去15年经验教训的叙事性综述

2025-12-170
PRE
Commentary: Complement genetic variants and FH desialylation in S. pneumoniae-haemolytic uraemic syndrome

评论:补体基因变异和S. pneumoniae-溶血尿毒症综合征中的FH去唾液酸化

2025-11-200
OAAI
Publisher Correction: Performance of creatinine and cystatin C-based equations to estimate glomerular filtration rate in African children with sickle cell anemia

出版商更正:基于肌酐和胱抑素C的方程在非洲镰状细胞贫血儿童中估算肾小球滤过率的表现

2025-11-100
PRE
Performance of creatinine and cystatin C-based equations to estimate glomerular filtration rate in African children with sickle cell anemia

基于肌酐和胱抑素C的方程在非洲镰状细胞贫血儿童中估算肾小球滤过率的表现

2025-10-160
PRE
Glycoproteomics analysis of complement factor H and its complement-regulatory function during Streptococcus pneumoniae-associated hemolytic uremic syndrome

肺炎链球菌相关溶血尿毒综合征中补体因子H的糖蛋白质组学分析及其补体调节功能

2025-08-210
OA
Model-Informed Precision Dosing of Eculizumab in Patients with Paroxysmal Nocturnal Hemoglobinuria

基于模型的精准用药:对阵发性夜间血红蛋白尿症患者使用Eculizumab的剂量确定

2025-06-250
OAAI
IdeZ protease does not prevent convertase stabilization by C3 nephritic factors in C3 glomerulopathy

IdeZ蛋白酶不会阻止C3肾毒因子在C3肾小球病中对转化酶的稳定化作用

2025-04-120
PRE
Targeting oxidative stress-induced lipid peroxidation enhances podocyte function in cystinosis
2025-02-200
OAAI
Posttraumatic stress disorder is characterized by functional dysregulation of dermal fibroblasts
2024-10-010
OAAI
APOL 1 RISK GENOTYPE IS ASSOCIATED WITH ALBUMINURIA IN SUB-SAHARAN AFRICAN WITHOUT HYPERTENSION: A CASE STUDY OF TRYPANOSOMA BRUCEI GAMBIENSE ENDEMIC AREA
2024-09-010
PRE
MFSD12 depletion reduces cystine accumulation without improvement in proximal tubular function in experimental models for cystinosis
2024-06-010
PRE
Biallelic Variants of MRPS36 Cause a New Form of Leigh Syndrome

MRPS36的双等位基因变体导致Leigh综合征的新形式

2024-04-300
PRE
Impact of preterm birth on kidney health and development
2024-03-276
OAAI
Ex Vivo Test of Complement Dysregulation in Atypical Hemolytic Uremic Syndrome Kidney Transplant patients: A Pilot Study
2024-01-015
OAAI
Evaluation of the efficacy of cystinosin supplementation through CTNS mRNA delivery in experimental models for cystinosis
2023-11-285
OAAI
Levamisole Modulation of Podocytes' Actin Cytoskeleton in Nephrotic Syndrome
2023-11-132
OAAI
Functional evaluation of complement factor I variants by immunoassays and SDS-PAGE

利用免疫测定和SDS-PAGE对补体因子I变异体的功能性评估

2023-10-261
OAAI
Modeling complement activation on human glomerular microvascular endothelial cells
2023-10-250
OAAI
Proteinuria and Exposure to Eculizumab in Atypical Hemolytic Uremic Syndrome
2023-04-105
OA