Hemostatic alterations in sickle cell disease: relationships to disease pathophysiology.
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Deconstructing sickle cell disease: reappraisal of the role of hemolysis in the development of clinical subphenotypes.Endothelial activation by platelets from sickle cell anemia patients.Tissue factor-positive monocytes in children with sickle cell disease: correlation with biomarkers of haemolysis.Platelet activation in patients with sickle disease, hemolysis-associated pulmonary hypertension, and nitric oxide scavenging by cell-free hemoglobinGenetic diminution of circulating prothrombin ameliorates multiorgan pathologies in sickle cell disease miceCharacterization of the hypercoagulable state in patients with sickle cell disease.Skull bone infarctive crisis and deep vein thrombosis in homozygous sickle cell disease- case report and review of the literature.A phase 1 study of prasugrel in patients with sickle cell disease: pharmacokinetics and effects on ex vivo platelet reactivityCoagulation abnormalities of sickle cell disease: Relationship with clinical outcomes and the effect of disease modifying therapies.Sickle cell disease at the dawn of the molecular era.Role of the hemostatic system on sickle cell disease pathophysiology and potential therapeuticsInterplay between coagulation and vascular inflammation in sickle cell disease.Prasugrel hydrochloride for the treatment of sickle cell disease.Thrombin generation and cell-dependent hypercoagulability in sickle cell disease.Identification of the Ca²⁺ entry pathway involved in deoxygenation-induced phosphatidylserine exposure in red blood cells from patients with sickle cell diseaseHemolysis-associated hypercoagulability in sickle cell disease: the plot (and blood) thickens!Coagulation profile of Sudanese children with homozygous sickle cell disease and the effect of treatment with omega-3 fatty acid on the coagulation parameters.Sleep-disordered breathing in patients with sickle cell disease.Computational imaging analysis of fibrin matrices with the inclusion of erythrocytes from homozygous SS blood reveals agglomerated and amorphous structures.Relationship between clotting activity and phosphatidylserine expression on erythrocyte membranes in polycythemia vera patients with the JAK2 V617F mutation.
P2860
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P2860
Hemostatic alterations in sickle cell disease: relationships to disease pathophysiology.
description
2001 nî lūn-bûn
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2001 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Hemostatic alterations in sickle cell disease: relationships to disease pathophysiology.
@ast
Hemostatic alterations in sickle cell disease: relationships to disease pathophysiology.
@en
type
label
Hemostatic alterations in sickle cell disease: relationships to disease pathophysiology.
@ast
Hemostatic alterations in sickle cell disease: relationships to disease pathophysiology.
@en
prefLabel
Hemostatic alterations in sickle cell disease: relationships to disease pathophysiology.
@ast
Hemostatic alterations in sickle cell disease: relationships to disease pathophysiology.
@en
P2860
P1476
Hemostatic alterations in sickle cell disease: relationships to disease pathophysiology.
@en
P2093
P2860
P356
10.1080/15513810109168816
P577
2001-01-01T00:00:00Z