Hemoglobin sickle cell disease complications: a clinical study of 179 cases - Wikidata - awgldk - TriplyDB

Hemoglobin sickle cell disease complications: a clinical study of 179 cases

Hemoglobin sickle cell disease complications: a clinical study of 179 cases

http://www.wikidata.org/entity/Q36132987

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2015 Clinical trials update in sickle cell anemia Human 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 disease Association 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 Brazil Outcome 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 disease Original Research: Use of hydroxyurea and phlebotomy in pediatric patients with hemoglobin SC disease Knowledge 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 disorder Pediatric sickle cell disease and obstructive sleep apnea: A cross-sectional study in a tertiary pediatric center in Saudi Arabia

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Hemoglobin sickle cell disease complications: a clinical study of 179 cases

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Hemoglobin sickle cell disease complications: a clinical study of 179 cases

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François Lionnet

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Gilles Grateau

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Jean-Philippe Haymann

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Katia Stankovic Stojanovic

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Nadjib Hammoudi

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Robert Girot

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Virginie Avellino

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P2860

The inherited diseases of hemoglobin are an emerging global health burden.

The paradox of hemoglobin SC disease

High prevalence of sickle cell trait in African Americans with ESRD.

Reconstructing sickle cell disease: a data-based analysis of the "hyperhemolysis paradigm" for pulmonary hypertension from the perspective of evidence-based medicine.

Glomerular hyperfiltration in adult sickle cell anemia: a frequent hemolysis associated feature

How I use hydroxyurea to treat young patients with sickle cell anemia.

Guidelines for the echocardiographic assessment of the right heart in adults: a report from the American Society of Echocardiography endorsed by the European Association of Echocardiography, a registered branch of the European Society of Cardiology,

Deconstructing sickle cell disease: reappraisal of the role of hemolysis in the development of clinical subphenotypes.

Iron in sickle cell disease: a review why less is better.

Role of phlebotomy in the management of hemoglobin SC disease: case report and review of the literature.

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