[HTML][HTML] Blood rheology: key parameters, impact on blood flow, role in sickle cell disease and effects of exercise

E Nader, S Skinner, M Romana, R Fort… - Frontiers in …, 2019 - frontiersin.org
Blood viscosity is an important determinant of local flow characteristics, which exhibits shear
thinning behavior: it decreases exponentially with increasing shear rates. Both hematocrit …

The role of blood rheology in sickle cell disease

P Connes, T Alexy, J Detterich, M Romana… - Blood reviews, 2016 - Elsevier
Studies performed in the last decades have highlighted the need to better understand the
contribution of the endothelium, vascular function, oxidative stress, inflammation …

Impact of sickle cell disease on patientsʼ daily lives, symptoms reported, and disease management strategies: Results from the international Sickle Cell World …

I Osunkwo, B Andemariam, CP Minniti… - American Journal of …, 2021 - Wiley Online Library
Sickle cell disease (SCD) is a genetic disorder, characterized by hemolytic anemia and vaso‐
occlusive crises (VOCs). Data on the global SCD impact on quality of life (QoL) from the …

Vaso-occlusive crisis in sickle cell disease: current paradigm on pain management

SN Uwaezuoke, AC Ayuk, IK Ndu, CI Eneh… - Journal of pain …, 2018 - Taylor & Francis
This narrative review aims to highlight the current paradigm on pain management in sickle
cell vaso-occlusive crisis. It specifically examines the pathophysiologic mechanisms of sickle …

Whole blood viscosity and red blood cell adhesion: Potential biomarkers for targeted and curative therapies in sickle cell disease

E Kucukal, Y Man, A Hill, S Liu, A Bode… - American journal of …, 2020 - Wiley Online Library
Sickle cell disease (SCD) is a recessive genetic blood disorder exhibiting abnormal blood
rheology. Polymerization of sickle hemoglobin, due to a point mutation in the β‐globin gene …

Haemolysis and abnormal haemorheology in sickle cell anaemia

P Connes, Y Lamarre, X Waltz… - British journal of …, 2014 - Wiley Online Library
Although pulmonary hypertension, leg ulcers, priapism, stroke and glomerulopathy in sickle
cell anaemia (SCA) result from the adverse effects of chronic haemolysis on vascular …

End points for sickle cell disease clinical trials: patient-reported outcomes, pain, and the brain

AT Farrell, J Panepinto, CP Carroll, DS Darbari… - Blood …, 2019 - ashpublications.org
To address the global burden of sickle cell disease (SCD) and the need for novel therapies,
the American Society of Hematology partnered with the US Food and Drug Administration to …

Advances in understanding the pathogenesis of cerebrovascular vasculopathy in sickle cell anaemia

P Connes, S Verlhac… - British journal of …, 2013 - Wiley Online Library
Cerebral vasculopathy is the most severe complication to affect children with sickle cell
anaemia and its pathophysiology is complex. Traditionally, small‐vessel occlusion by …

[HTML][HTML] Quelle morale pour la corruption?

G Koenig - Revue internationale et stratégique, 2016 - cairn.info
Pourtant, quand l'on tente de cerner de plus près la corruption en tant que concept, elle
semble s' évanouir. Si la corruption consiste à «se» vendre, n'est-elle pas au cœur des …

[HTML][HTML] Hemorheological risk factors of acute chest syndrome and painful vaso-occlusive crisis in children with sickle cell disease

Y Lamarre, M Romana, X Waltz… - …, 2012 - ncbi.nlm.nih.gov
Hemorheological risk factors of acute chest syndrome and painful vaso-occlusive crisis in
children with sickle cell disease - PMC Back to Top Skip to main content NIH NLM Logo Access …