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Interventions for treating pulmonary hypertension in people with sickle cell disease or thalassaemiaHemoglobin variants: biochemical properties and clinical correlatesInflammation in Sickle Cell Disease: Differential and Down-Expressed Plasma Levels of Annexin A1 ProteinComments on: "Clinical, hematological and genetic data of a cohort of children with hemoglobin SD".Associations between environmental factors and hospital admissions for sickle cell disease.Anti-Toxoplasma gondii antibodies in patients with beta-hemoglobinopathies: the first report in the AmericasA diagnostic role for dense cells in sickle cell disease.Management of sickle cell disease: a review for physician education in Nigeria (sub-saharan Africa).The invisibility of sickle cell disease in Brazil: lessons from a study in MaranhãoRed blood cell indices and prevalence of hemoglobinopathies and glucose 6 phosphate dehydrogenase deficiencies in male Tanzanian residents of Dar es Salaam.Correction of the sickle cell disease mutation in human hematopoietic stem/progenitor cellsA rapid paper-based test for quantifying sickle hemoglobin in blood samples from patients with sickle cell disease.Neonatal Screening and the Clinical Outcome in Children with Sickle Cell Disease in Central IndiaUpdated Mechanisms of Sickle Cell Disease-Associated Chronic painKnowledge and awareness of personal sickle cell genotype among parents of children with sickle cell disease in southeast Nigeria.Effect of Age on Blood Rheology in Sickle Cell Anaemia and Sickle Cell Haemoglobin C Disease: A Cross-Sectional StudyLongitudinal Analysis of Patient Specific Predictors for Mortality in Sickle Cell Disease.Sickle Cell Trait Worsens Oxidative Stress, Abnormal Blood Rheology, and Vascular Dysfunction in Type 2 DiabetesFebrile Convulsion among Hospitalized Children Aged Six Months to Five Years and Its Association With Haemoglobin Electrophoretic PatternDifferences of microparticle patterns between sickle cell anemia and hemoglobin SC patients.Sickle cell disease and pregnancy outcomes: a study of the community-based hospital in a tribal block of Gujarat, IndiaClinical and laboratory profile of patients with sickle cell anemia.Classification of the disorders of hemoglobinPerspectives in Pediatric Pathology, Chapter 22. Testicular Involvement in Systemic Diseases.Hemoglobin inhibits albumin uptake by proximal tubule cells: implications for sickle cell disease.The epidemiology of sickle cell disease in Germany following recent large-scale immigration.Use of genome-editing tools to treat sickle cell disease.Insulin Secretion and Resistance in Normoglycemic Patients with Sickle Cell Disease.Improved hydroxyurea effect with the use of text messaging in children with sickle cell anemia.Survival of children with sickle cell disease in the comprehensive newborn screening programme in Minas Gerais, Brazil.Prostacyclin, thromboxane and glomerular filtration rate are abnormal in sickle cell pregnancy.The compound state: Hb S/beta-thalassemiaVery mild forms of Hb S/beta(+)-thalassemia in Brazilian children.Hydroxycarbamide in children with sickle cell anaemia after first-dose vs. chronic therapy: pharmacokinetics and predictive models for drug exposure.Novel genetic polymorphisms associated with severe malaria and under selective pressure in North-eastern Tanzania.Comprehensive management reduces incidence and mortality of acute chest syndrome in patients with sickle cell disease.Genetic Basis and Genetic Modifiers of β-Thalassemia and Sickle Cell Disease.Haemoglobin F, A2, and S levels in subjects with or without sickle cell trait in south-eastern Gabon.Progressive glomerular and tubular damage in sickle cell trait and sickle cell anemia mouse models.Oxidative Stress in Diabetic Patients with Sickle-Cell Anemia: A Warning Call for Endemic Areas.
P2860
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P2860
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on October 2013
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
The natural history of sickle cell disease.
@en
The natural history of sickle cell disease.
@nl
type
label
The natural history of sickle cell disease.
@en
The natural history of sickle cell disease.
@nl
prefLabel
The natural history of sickle cell disease.
@en
The natural history of sickle cell disease.
@nl
P2860
P1476
The natural history of sickle cell disease.
@en
P2093
Graham R Serjeant
P2860
P304
P356
10.1101/CSHPERSPECT.A011783
P577
2013-10-01T00:00:00Z