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Profil bibliographique

Charlotte F.J. Van Tuijn

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

42Publications signalées
574Citations signalées
2Affiliations récentes

Les institutions déclarées

Les domaines associés

Hemoglobinopathies and Related DisordersIron Metabolism and DisordersMyeloproliferative Neoplasms: Diagnosis and TreatmentBlood groups and transfusionFolate and B Vitamins Research

Les publications récentes

Accès ouvert 2025 article OpenAlex

Humoral and cellular immune response after COVID-19 vaccination in patients with sickle cell disease on hydroxyurea

Sabine Haggenburg, Cilia R. Pothast, Quincy Hofsink, Nienke J.E. Haverkate et autres

ABSTRACT: Patients with sickle cell disease (SCD) are at increased risk of COVID-19-related mortality compared with healthy individuals, even after vaccination. To what extent impaired vaccine-induced immunity contributes to this risk is unknown. We prospectively investigated vaccine immunogenicity in 31 patients with …

nl, us (code pays fourni par la source)

0 citations Blood Advances
Accès ouvert 2025 article OpenAlex

Changes in the quality of life of adults with sickle cell disease following allogeneic stem cell transplantation: A mixed‐methods, prospective cohort study

Elisabeth Dovern, Sterre J.A.M. Nijland, Annemarie Braamse, Maud M. van Muilekom et autres

Abstract Advances in conditioning regimens have made non‐myeloablative allogeneic hematopoietic stem cell transplantation (HSCT) a viable curative option for adults with sickle cell disease (SCD). However, prospective studies comparing pre‐ and post‐transplant patient‐reported health outcomes are scarce. Therefore, in a prospective, mixed‐methods …

nl, us (code pays fourni par la source)

9 citations HemaSphere
Accès ouvert 2024 article OpenAlex

Azathioprine/hydroxyurea preconditioning prior to nonmyeloablative matched sibling donor hematopoietic stem cell transplantation in adults with sickle cell disease: A prospective observational cohort study

Elisabeth Dovern, Mesire Aydin, Mette D. Hazenberg, Man Tang et autres

Nonmyeloablative, matched sibling donor hematopoietic stem cell transplantation with alemtuzumab/total body irradiation (TBI) conditioning is a curative therapy with low toxicity for adults with sickle cell disease (SCD). However, relatively low donor chimerism levels and graft rejection remain important challenges. We hypothesized …

nl, ch, gb (code pays fourni par la source)

10 citations American Journal of Hematology
Accès ouvert 2023 article OpenAlex

A multimodal pain protocol for treatment of vaso‐occlusive crisis in patients with sickle cell disease: Implementation and evaluation

Manouk Admiraal, Jonathan van Daalen, Michael W J Ritt, Joost Dekker et autres

OBJECTIVES: Pain management during a vaso-occlusive crisis (VOC) for patients with sickle cell disease (SCD) remains a major challenge and strongly depends on opioids. We developed a multimodality pain protocol for rapid, opioid-sparing pain treatment of VOC and evaluated its feasibility. METHODS: …

nl (code pays fourni par la source)

7 citations European Journal Of Haematology
Accès ouvert 2023 article OpenAlex

The association between renal function decline and disease severity in sickle cell disease

Aafke E. Gaartman, Charlotte F.J. Van Tuijn, Erfan Nur, Liffert Vogt et autres

In sickle cell disease (SCD), reduced estimated glomerular filtration rate (eGFR) and albuminuria are frequently seen and associated with increased mortality in SCD.1 In non-SCD patients, a decline of renal function over time is a risk factor for cardiovascular morbidity and mortality.2 …

nl (code pays fourni par la source)

1 citation American Journal of Hematology
2022 article OpenAlex

Protocol Adherence for Adult Sickle Cell Patients Presenting with Vaso-Occlusive Crises on a Tertiary Teaching Hospital Emergency Department

Charlotte F.J. Van Tuijn, Mitchel E. van Straaten, Erfan Nur, Bart J. Biemond et autres

Background Patients with Sickle cell disease (SCD) suffer from frequent vaso-occlusive crises (VOC) that heavily contribute to morbidity and mortality. VOC's constitute the principal cause of emergency department (ED) presentation and hospital admission and the ED visit serves to diagnose underlying disorders, …

nl (code pays fourni par la source)

0 citations Blood
2022 article OpenAlex

Movement Behavior in Adults with Sickle Cell Disease Compared to Healthy Adults: Preliminary Results

Aaron Heeren, Charlotte F.J. Van Tuijn, Myrthe J. van Dijk, Eduard J. van Beers et autres

Background Sickle cell disease (SCD) is one of the most common monogenic disorders in the world. People with SCD experience pain due to blood flow obstruction and have musculoskeletal and cardiopulmonary complications, which correspond to different chronic conditions. In other chronic diseases, …

nl (code pays fourni par la source)

0 citations Blood
2022 article OpenAlex

Improved T-Cell Chimerism and Successful Withdrawal of Immunosuppression after Non-Myeloablative Stem Cell Transplantation for Sickle Cell Disease with Azathioprine/Hydroxyurea Preconditioning Added to Alemtuzumab/TBI Conditioning

Elisabeth Dovern, Mesire Aydin, Man Tang, Liesbeth E.M. Suijk et autres

Background: Allogeneic hematopoietic stem cell transplantation (HSCT) is currently the only established curative treatment option for sickle cell disease (SCD). In adult SCD patients, myeloablative conditioning is associated with significant toxicity, primarily because of cumulative organ damage. Recently, matched sibling donor (MSD) …

nl, ch (code pays fourni par la source)

1 citation Blood
Accès ouvert 2021 conference-abstract OpenAlex

Incidence of Sars-COV-2 Infection in Sickle Cell Patients Presenting with a Painful Crisis, a 12 Month Prospective Cohort Study

Kadère Konté, Erfan Nur, Man Tang, Jarom Heijmans et autres

Abstract Background: Sickle cell disease (SCD) is frequently complicated by painful vaso-occlusive crises (VOCs) often resulting in healthcare utilization including hospital admission. A vaso-occlusive crisis (VOC) can be induced by multiple factors including infection, exposure to cold, physical exercise, dehydration and stress. …

nl (code pays fourni par la source)

0 citations Blood
Accès ouvert 2021 article OpenAlex

Incidence of SARS‐COV‐2 infection in sickle cell patients presenting with a painful crisis: A 12‐month prospective cohort study

Kadère Konté, Erfan Nur, Man Tang, Jarom Heijmans et autres

Sickle cell disease (SCD) is frequently complicated by painful vaso-occlusive crises (VOCs) often resulting in healthcare utilization including hospital admission. A vaso-occlusive crisis (VOC) can be induced by multiple factors including infection, exposure to cold, physical exercise, dehydration, and stress. Given the …

nl (code pays fourni par la source)

2 citations International Journal of Laboratory Hematology

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