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M

Minke A.E. Rab

University Medical Center Utrecht
H指数:16
被引数:743

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Novel oxygenscan parameters differentiate unique hemolytic and inflammatory profiles associated with sickle cell disease genotypes

新型氧扫描参数可区分与镰状细胞病基因型相关的独特溶血和炎症表型

2026-08-030
OA
Undetectable Hydroxyurea Levels in the Majority of Sickle Cell Disease Patients, Especially in Young Children

在大多数镰状细胞病患者中检测不到羟基脲水平,尤其是在幼儿中

2026-07-030
OAAI
Metabolomics in sickle cell disease: Current knowledge and gaps – A scoping review

镰状细胞病中的代谢组学:现有知识及空白——一篇范围综述

2025-09-060
PREAI
Iron Deficiency in HbSC Disease Treated With Repetitive Phlebotomy Is Associated With Fewer Sickle Cell Disease-Related Complications

HbSC疾病患者经反复放血治疗后,缺铁与较少的镰状细胞病相关并发症相关。

2025-09-040
OAAI
Satisfy: A Eurobloodnet Multicenter, Single-Arm Phase 2 Trial of Mitapivat in Adult Patients with Erythrocyte Membranopathies and Congenital Dyserythropoietic Anemia Type II- Results from the 8-Week Dose-Escalation Period

满足:一项Eurobloodnet多中心、单臂II期临床试验,评估米塔吡范在成人红细胞膜病和先天性红细胞生成障碍性贫血II型患者中的应用——8周剂量递增期结果

BLOOD
IF23.1
2024-11-050
PRE
Metabolic blood profile and response to treatment with the pyruvate kinase activator mitapivat in patients with sickle cell disease
2024-06-250
OAAI
A novel missense variant in ATP11C is associated with reduced red blood cell phosphatidylserine flippase activity and mild hereditary hemolytic anemia
2023-09-062
OAAI
Characterization of genetic variants in the EGLN1/PHD2 gene identified in a European collection of patients with erythrocytosis
2023-06-155
OAAI