Hemoglobin sickle cell disease complications: a clinical study of 179 cases
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2015 Clinical trials update in sickle cell anemiaHuman bulbar conjunctival hemodynamics in hemoglobin SS and SC disease.Elevated hypercoagulability markers in hemoglobin SC disease.Plasma levels of some coagulation parameters in steady state HBSC disease patients.The clinical significance of K-Cl cotransport activity in red cells of patients with HbSC diseaseAssociation between oxidative stress and vascular reactivity in children with sickle cell anaemia and sickle haemoglobin C disease.Hemorheological risk factors of acute chest syndrome and painful vaso-occlusive crisis in children with sickle cell disease.Differences of microparticle patterns between sickle cell anemia and hemoglobin SC patients.Hemoglobin sickle cell disease in BrazilOutcome and challenges of kidney transplant in patients with sickle cell disease.Risk factors for venous thromboembolism in adults with hemoglobin SC or Sβ(+) thalassemia genotypes.Hematologic and hemorheological determinants of resting and exercise-induced hemoglobin oxygen desaturation in children with sickle cell diseaseOriginal Research: Use of hydroxyurea and phlebotomy in pediatric patients with hemoglobin SC diseaseKnowledge insufficient: the management of haemoglobin SC disease.Cohort study of adult patients with haemoglobin SC disease: clinical characteristics and predictors of mortality.Laboratory and Genetic Biomarkers Associated with Cerebral Blood Flow Velocity in Hemoglobin SC Disease.Management of refractory ischemic priapism: current perspectives.[Hemoglobin disorders].Impaired blood rheology plays a role in the chronic disorders associated with sickle cell-hemoglobin C disease.Beneficial Effect of the Nitric Oxide Donor Compound 3-(1,3-Dioxoisoindolin-2-yl)Benzyl Nitrate on Dysregulated Phosphodiesterase 5, NADPH Oxidase, and Nitrosative Stress in the Sickle Cell Mouse Penis: Implication for Priapism Treatment.A proposed treatment algorithm for adults with Haemoglobin SC disease.Red cell exchange transfusion halts progressive proliferative sickle cell retinopathy in a teenaged patient with hemoglobin SC disease.Rheology of red blood cells in patients with HbC disease.Subclinical left ventricular systolic impairment in steady state young adult patients with sickle-cell anemia.Lipid profiles in French West Indies sickle cell disease cohorts, and their general population.Association between relative systemic hypertension and otologic disorders in patients with sickle cell-hemoglobin C disorderPediatric sickle cell disease and obstructive sleep apnea: A cross-sectional study in a tertiary pediatric center in Saudi Arabia
P2860
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P2860
Hemoglobin sickle cell disease complications: a clinical study of 179 cases
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
@zh
2012年论文
@zh-cn
name
Hemoglobin sickle cell disease complications: a clinical study of 179 cases
@ast
Hemoglobin sickle cell disease complications: a clinical study of 179 cases
@en
type
label
Hemoglobin sickle cell disease complications: a clinical study of 179 cases
@ast
Hemoglobin sickle cell disease complications: a clinical study of 179 cases
@en
prefLabel
Hemoglobin sickle cell disease complications: a clinical study of 179 cases
@ast
Hemoglobin sickle cell disease complications: a clinical study of 179 cases
@en
P2093
P2860
P1433
P1476
Hemoglobin sickle cell disease complications: a clinical study of 179 cases
@en
P2093
François Lionnet
Gilles Grateau
Jean-Philippe Haymann
Katia Stankovic Stojanovic
Nadjib Hammoudi
Robert Girot
Virginie Avellino
P2860
P304
P356
10.3324/HAEMATOL.2011.055202
P577
2012-02-07T00:00:00Z