The cooperative study of sickle cell disease: review of study design and objectives.
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Evolving locally appropriate models of care for indian sickle cell diseaseSickle cell disease in childrenGenetic determinants of haemolysis in sickle cell anaemia.Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5' olfactory receptor gene clusterGenetic modifiers of the severity of sickle cell anemia identified through a genome-wide association studyA genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia.Venous thromboembolism incidence in the Cooperative Study of Sickle Cell Disease.Severe sickle cell anemia is associated with increased plasma levels of TNF-R1 and VCAM-1Increased reticulocytosis during infancy is associated with increased hospitalizations in sickle cell anemia patients during the first three years of life.The genetics of hemoglobin A2 regulation in sickle cell anemiaGenome-wide meta-analysis of systolic blood pressure in children with sickle cell diseaseAncestry of African Americans with sickle cell disease.BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia.Sickle cell leg ulcers: associations with haemolysis and SNPs in Klotho, TEK and genes of the TGF-beta/BMP pathway.Association between baseline fetal hemoglobin levels and incidence of severe vaso-occlusive pain episodes in children with sickle cell anemia.NT-pro brain natriuretic peptide levels and the risk of death in the cooperative study of sickle cell disease.Bayesian Polynomial Regression Models to Fit Multiple Genetic Models for Quantitative Traits.Sickle cell disease: old discoveries, new concepts, and future promise.Expression patterns of fetal hemoglobin in sickle cell erythrocytes are both patient- and treatment-specific during childhood.Asthma is associated with acute chest syndrome and pain in children with sickle cell anemiaA network model to predict the risk of death in sickle cell disease.Decades after the cooperative study: a re-examination of systemic blood pressure in sickle cell disease.Systematic review of interventional sickle cell trials registered in ClinicalTrials.gov.Sickle cell trait diagnosis: clinical and social implications.Health-related quality of life in adults with sickle cell disease (SCD): a report from the comprehensive sickle cell centers clinical trial consortium.Sibling history of asthma is a risk factor for pain in children with sickle cell anemiaEnuresis is a common and persistent problem among children and young adults with sickle cell anemia.Abnormal pulmonary function in adults with sickle cell anemiaSupporting family adaptation to presymptomatic and "untreatable" conditions in an era of expanded newborn screeningSickle cell anemia in sub-Saharan Africa: advancing the clinical paradigm through partnerships and research.Prediction of fetal hemoglobin in sickle cell anemia using an ensemble of genetic risk prediction modelsHydroxyurea therapy for sickle cell anemia.Hemolysis-associated priapism in sickle cell diseaseAssociation of klotho, bone morphogenic protein 6, and annexin A2 polymorphisms with sickle cell osteonecrosis.Genome-wide association study to identify variants associated with acute severe vaso-occlusive pain in sickle cell anemia.A ten year review of the sickle cell program in Muhimbili National Hospital, Tanzania
P2860
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P2860
The cooperative study of sickle cell disease: review of study design and objectives.
description
1982 nî lūn-bûn
@nan
1982年の論文
@ja
1982年論文
@yue
1982年論文
@zh-hant
1982年論文
@zh-hk
1982年論文
@zh-mo
1982年論文
@zh-tw
1982年论文
@wuu
1982年论文
@zh
1982年论文
@zh-cn
name
The cooperative study of sickle cell disease: review of study design and objectives.
@en
type
label
The cooperative study of sickle cell disease: review of study design and objectives.
@en
prefLabel
The cooperative study of sickle cell disease: review of study design and objectives.
@en
P1476
The cooperative study of sickle cell disease: review of study design and objectives
@en
P2093
P304
P577
1982-01-01T00:00:00Z