| scholarly article | Q13442814 |
| review article | Q7318358 |
| P356 | DOI | 10.1016/S0268-960X(03)00037-7 |
| P698 | PubMed publication ID | 14684149 |
| P2093 | author name string | Iheanyi Okpala | |
| P2860 | cites work | Sickle cell anemia, a molecular disease | Q7507635 |
| Insights into the molecular basis of leukocyte tethering and rolling revealed by structures of P- and E-selectin bound to SLe(X) and PSGL-1 | Q27628438 | ||
| Traffic signals for lymphocyte recirculation and leukocyte emigration: the multistep paradigm | Q29547181 | ||
| Relationship between the clinical manifestations of sickle cell disease and the expression of adhesion molecules on white blood cells | Q33185017 | ||
| Cellular and molecular mechanisms of inflammation and thrombosis | Q33636061 | ||
| Complement haemolytic activity, circulating immune complexes and the morbidity of sickle cell anaemia | Q33706818 | ||
| Glycoprotein IV mediates thrombospondin-dependent platelet-monocyte and platelet-U937 cell adhesion | Q33848191 | ||
| Microvascular sites and characteristics of sickle cell adhesion to vascular endothelium in shear flow conditions: pathophysiological implications | Q33854510 | ||
| Management of cerebral vasculopathy in children with sickle cell anaemia | Q33904379 | ||
| Pathophysiology of sickle cell disease. | Q33953635 | ||
| Indications for red cell transfusion in sickle cell disease | Q34156013 | ||
| Adhesion receptors on haematopoietic progenitor cells | Q34190479 | ||
| The distribution of the sickle-cell trait in East Africa and elsewhere, and its apparent relationship to the incidence of subtertian malaria | Q34235933 | ||
| Pathophysiology of sickle cell disease: role of cellular and genetic modifiers | Q34404450 | ||
| Sickle cell vaso-occlusion: multistep and multicellular paradigm | Q34530995 | ||
| Neutrophils use both shared and distinct mechanisms to adhere to selectins under static and flow conditions | Q35764552 | ||
| Ethnic and sex differences in the total and differential white cell count and platelet count | Q37220258 | ||
| Neutrophil-neutrophil interactions under hydrodynamic shear stress involve L-selectin and PSGL-1. A mechanism that amplifies initial leukocyte accumulation of P-selectin in vitro | Q37359036 | ||
| Two-step model of leukocyte-endothelial cell interaction in inflammation: distinct roles for LECAM-1 and the leukocyte beta 2 integrins in vivo | Q37583902 | ||
| Hydroxyurea corrects the dysregulated L-selectin expression and increased H(2)O(2) production of polymorphonuclear neutrophils from patients with sickle cell anemia | Q38903694 | ||
| PECAM-1: its expression and function as a cell adhesion molecule on hemopoietic and endothelial cells. | Q40958086 | ||
| The pathophysiology of vascular obstruction in the sickle syndromes | Q41155071 | ||
| Pathophysiology of vaso-occlusion | Q41257222 | ||
| Role of erythrocyte phosphatidylserine in sickle red cell-endothelial adhesion | Q43893061 | ||
| Genetic neutropenia in people of African origin | Q46670225 | ||
| Silent cerebral infarcts in sickle cell anemia: a risk factor analysis. The Cooperative Study of Sickle Cell Disease | Q48274342 | ||
| Acute phase reactants and severity of homozygous sickle cell disease | Q50671971 | ||
| PECULIAR ELONGATED AND SICKLE-SHAPED RED BLOOD CORPUSCLES IN A CASE OF SEVERE ANEMIA | Q54087043 | ||
| Fatal sickle cell crisis after granulocyte colony-stimulating factor administration. | Q55034829 | ||
| Mortality in sickle cell disease. Life expectancy and risk factors for early death. | Q55065788 | ||
| An abnormality of the alternate pathway of complement activation in sickle-cell disease | Q70034822 | ||
| Benign clinical course in homozygous sickle cell disease: a search for predictors | Q73271841 | ||
| Hydroxyurea therapy decreases the in vitro adhesion of sickle erythrocytes to thrombospondin and laminin | Q73883387 | ||
| Peripheral blood neutrophil count and candidacidal activity correlate with the clinical severity of sickle cell anaemia (SCA) | Q74526017 | ||
| Granulocytosis causing sickle-cell crisis | Q77292395 | ||
| P433 | issue | 1 | |
| P921 | main subject | sickle-cell disease | Q185034 |
| lymphocyte | Q715347 | ||
| P304 | page(s) | 65-73 | |
| P577 | publication date | 2004-03-01 | |
| P1433 | published in | Blood Reviews | Q15724415 |
| P1476 | title | The intriguing contribution of white blood cells to sickle cell disease - a red cell disorder | |
| P478 | volume | 18 |
| Q36528046 | A novel hemoglobin-binding peptide reduces cell-free hemoglobin in murine hemolytic anemia |
| Q41347905 | A prospective study of the association between sickle cell disease and hepatobiliary effects in Bahrain |
| Q38861043 | A randomized trial of artesunate-amodiaquine versus artemether-lumefantrine in Ghanaian paediatric sickle cell and non-sickle cell disease patients with acute uncomplicated malaria |
| Q52877179 | Acute gastrointestinal vaso-occlusive ischemia in sickle cell disease: CT imaging features and clinical outcome. |
| Q55013382 | Adult Sickle Cell Anaemia Patients in Bone Pain Crisis have Elevated Pro-Inflammatory Cytokines. |
| Q34255075 | Aggregation of mononuclear and red blood cells through an {alpha}4{beta}1-Lu/basal cell adhesion molecule interaction in sickle cell disease |
| Q37413923 | An observational study of children with sickle cell disease in Kilifi, Kenya |
| Q34013495 | Arginase levels and their association with Th17-related cytokines, soluble adhesion molecules (sICAM-1 and sVCAM-1) and hemolysis markers among steady-state sickle cell anemia patients |
| Q38857629 | Association of circulating transcriptomic profiles with mortality in sickle cell disease |
| Q91625821 | Correlating transcranial arterial Doppler velocities with haematologic parameters and haemolytic indices of Nigerian children with sickle cell anaemia |
| Q37045665 | Effect of automated red cell exchanges on oxygen saturation on-air, blood parameters and length of hospitalization in sickle cell disease patients with acute chest syndrome |
| Q37146392 | Effect of propranolol as antiadhesive therapy in sickle cell disease |
| Q38804432 | Emerging point-of-care technologies for sickle cell disease screening and monitoring. |
| Q46565372 | Erythroid adhesion molecules in sickle cell disease: effect of hydroxyurea |
| Q50580233 | Evaluation of clinical and laboratory correlates of sickle leg ulcers. |
| Q50652273 | Fibronectin bridges monocytes and reticulocytes via integrin alpha4beta1. |
| Q48304119 | Haemoglobin oxygen saturation, leucocyte count and lactate dehydrogenase are predictors of elevated cerebral blood flow velocity in Nigerian children with sickle cell anaemia. |
| Q59135231 | Hematological parameters in Ghanaian sickle cell disease patients |
| Q57805625 | Hemoglobin F as a predictor of health-related quality of life in children with sickle cell anemia |
| Q83835647 | High levels of neopterin and interleukin-3 in sickle cell disease patients |
| Q33886410 | Higher rates of hemolysis are not associated with albuminuria in Jamaicans with sickle cell disease |
| Q37406275 | Inhaled carbon monoxide reduces leukocytosis in a murine model of sickle cell disease |
| Q36543049 | Investigational agents for sickle cell disease |
| Q38253064 | Investigational selectin-targeted therapy of sickle cell disease |
| Q34133852 | Levels of high-density lipoprotein cholesterol (HDL-C) among children with steady-state sickle cell disease |
| Q24193246 | Magnesium for treating sickle cell disease |
| Q29994630 | Magnesium for treating sickle cell disease |
| Q39219659 | Microfluidics for investigating vaso-occlusions in sickle cell disease |
| Q34750520 | Participation of Mac-1, LFA-1 and VLA-4 integrins in the in vitro adhesion of sickle cell disease neutrophils to endothelial layers, and reversal of adhesion by simvastatin |
| Q37275858 | Perspectives on thrombosis in essential thrombocythemia and polycythemia vera: is leukocytosis a causative factor? |
| Q35987429 | Phase 1 Study of a Sulforaphane-Containing Broccoli Sprout Homogenate for Sickle Cell Disease |
| Q28540243 | Phase 1 study of the E-selectin inhibitor GMI 1070 in patients with sickle cell anemia |
| Q33722654 | Placenta growth factor in sickle cell disease: association with hemolysis and inflammation |
| Q33598716 | Plasma interleukin-1beta concentration is associated with stroke in sickle cell disease |
| Q57624377 | Platelet count as a predictor of the severity of sickle cell disease during pregnancy |
| Q42759417 | Priapism in homozygous sickle cell patients: important clinical and laboratory associations |
| Q34478678 | Red blood cells, platelets and polymorphonuclear neutrophils of patients with sickle cell disease exhibit oxidative stress that can be ameliorated by antioxidants |
| Q52647102 | Shear dependent red blood cell adhesion in microscale flow. |
| Q36941118 | Sickle red cells induce adhesion of lymphocytes and monocytes to endothelium |
| Q38882070 | Splenic enlargement in adults with homozygous sickle cell disease: the Jamaican experience |
| Q36012888 | Tapered oral dexamethasone for the acute chest syndrome of sickle cell disease |
| Q33758996 | Telomere length correlates with disease severity and inflammation in sickle cell disease. |
| Q37811628 | The paradox of the neutrophil's role in tissue injury |
| Q45072571 | The prevalence of abnormal leukocyte count, and its predisposing factors, in patients with sickle cell disease in Saudi Arabia |
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