Recent advances in “sickle and niche” research-Tribute to Dr. Paul S Frenette

LS Torres, N Asada, MJ Weiss, A Trumpp, T Suda… - Stem Cell Reports, 2022 - cell.com
In this retrospective, we review the two research topics that formed the basis of the
outstanding career of Dr. Paul S. Frenette. In the first part, we focus on sickle cell disease …

Linking labile heme with thrombosis

MT Hopp, D Imhof - Journal of clinical medicine, 2021 - mdpi.com
Thrombosis is one of the leading causes of death worldwide. As such, it also occurs as one
of the major complications in hemolytic diseases, like hemolytic uremic syndrome …

VWF–ADAMTS13 axis dysfunction in children with sickle cell disease treated with hydroxycarbamide vs blood transfusion

H Fogarty, A Ahmad, F Atiq, D Doherty, S Ward… - Blood …, 2023 - ashpublications.org
Previous studies have reported elevated von Willebrand factor (VWF) levels in patients with
sickle cell disease (SCD) and demonstrated a key role for the VWF-ADAMTS13 axis in the …

Atrial arrhythmia in adults with sickle cell anemia: a missing link toward understanding and preventing strokes

T d'Humières, Z Sadraoui, L Savale, L Boyer… - Blood …, 2024 - ashpublications.org
Although patients with homozygous sickle cell anemia (SCA) carry both significant left atrial
(LA) remodeling and an increased risk of stroke, the prevalence of atrial arrhythmia (AA) has …

How we approach thrombosis risk in children with COVID‐19 infection and MIS‐C

AA Sharathkumar, EVS Faustino… - Pediatric blood & …, 2021 - Wiley Online Library
Thrombosis within the microvasculature and medium to large vessels is a serious and
common complication among critically ill individuals with coronavirus disease 2019 (COVID …

P-selectin blockade in the treatment of painful vaso-occlusive crises in sickle cell disease: a spotlight on crizanlizumab

NR Karki, A Kutlar - Journal of Pain Research, 2021 - Taylor & Francis
Microvascular vaso-occlusion driven pain crisis is the hallmark of sickle cell disease with
profound morbidity and increased mortality. Selectins, most notably P-selectins have an …

Hypercoagulability in hemoglobinopathies: Decoding the thrombotic threat

R Bou‐Fakhredin, MD Cappellini… - American Journal of …, 2025 - Wiley Online Library
Beta (β)‐thalassemia and sickle cell disease (SCD) are characterized by a hypercoagulable
state, which can significantly influence organ complication and disease severity. While red …

Iron deficiency anemia and thrombosis risk in children—Revisiting an old hypothesis

H Kalff, H Cario, S Holzhauer - Frontiers in Pediatrics, 2022 - frontiersin.org
Iron deficiency anemia has a high prevalence in children and has repeatedly been
implicated as a risk factor for arterial and venous thrombosis. As an effective therapy for iron …

Extracellular vesicles in sickle cell disease: Plasma concentration, blood cell types origin distribution and biological properties

E Nader, Y Garnier, P Connes, M Romana - Frontiers in Medicine, 2021 - frontiersin.org
Prototype of monogenic disorder, sickle cell disease (SCD) is caused by a unique single
mutation in the β-globin gene, leading to the production of the abnormal hemoglobin S …

COVID-19 and venous thromboembolism risk in patients with sickle cell disease

A Singh, AM Brandow, T Wun, AS Shet - Blood advances, 2022 - ashpublications.org
Venous thromboembolism (VTE) is a life-threatening complication observed among patients
with sickle cell disease (SCD) and also among those with severe COVID-19 infection …