Design of the multicenter study of hydroxyurea in sickle cell anemia. Investigators of the Multicenter Study of Hydroxyurea.
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Mutations and polymorphisms in hemoglobin genes and the risk of pulmonary hypertension and death in sickle cell diseaseSystematic review: Hydroxyurea for the treatment of adults with sickle cell diseaseHealth related quality of life in sickle cell patients: the PiSCES projectImputation of missing genotypes: an empirical evaluation of IMPUTE.Usability testing of a Smartphone for accessing a web-based e-diary for self-monitoring of pain and symptoms in sickle cell diseaseComorbidity, Pain, Utilization, and Psychosocial Outcomes in Older versus Younger Sickle Cell Adults: The PiSCES ProjectAssessing the quality of healthcare provided to children.High incarceration rates among black men enrolled in clinical studies may compromise ability to identify disparitiesThe risks and benefits of long-term use of hydroxyurea in sickle cell anemia: A 17.5 year follow-up.Correction of the sickle cell mutation in embryonic stem cellsHydroxyurea for sickle cell disease.Severe painful vaso-occlusive crises and mortality in a contemporary adult sickle cell anemia cohort study.Crystallographic analysis of human hemoglobin elucidates the structural basis of the potent and dual antisickling activity of pyridyl derivatives of vanillin.Markers of severe vaso-occlusive painful episode frequency in children and adolescents with sickle cell anemia.Ion transport pathology in the mechanism of sickle cell dehydration.Pain site frequency and location in sickle cell disease: the PiSCES projectProcalcitonin as a biomarker of bacterial infection in sickle cell vaso-occlusive crisisHydroxyurea (hydroxycarbamide) for sickle cell disease.Clinical pharmacology and clinical trials of ribonucleotide reductase inhibitors: is it a viable cancer therapy?Hydroxyurea downregulates endothelin-1 gene expression and upregulates ICAM-1 gene expression in cultured human endothelial cells.Combined endpoints: can we use them?Predictive Ability of Intermittent Daily Sickle Cell Pain Assessment: The PiSCES Project.Treating pain in sickle cell disease with opioids: clinical advances, ethical pitfalls.Fetal hemoglobin and alpha thalassemia modulate the phenotypic expression of HbSD-Punjab.Fetal hemoglobin in sickle cell anemia: genetic determinants of response to hydroxyurea
P2860
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P2860
Design of the multicenter study of hydroxyurea in sickle cell anemia. Investigators of the Multicenter Study of Hydroxyurea.
description
1995 nî lūn-bûn
@nan
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
1995年论文
@zh
1995年论文
@zh-cn
name
Design of the multicenter stud ...... ticenter Study of Hydroxyurea.
@en
type
label
Design of the multicenter stud ...... ticenter Study of Hydroxyurea.
@en
prefLabel
Design of the multicenter stud ...... ticenter Study of Hydroxyurea.
@en
P2093
P1476
Design of the multicenter stud ...... ticenter Study of Hydroxyurea.
@en
P2093
Charache S
McMahon RP
Waclawiw M
P304
P356
10.1016/S0197-2456(95)00098-4
P407
P577
1995-12-01T00:00:00Z