Genetic variation in CD36, HBA, NOS3 and VCAM1 is associated with chronic haemolysis level in sickle cell anaemia: a longitudinal study.
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Hemorheological alterations in sickle cell anemia and their clinical consequences - The role of genetic modulators.Minireview: Multiomic candidate biomarkers for clinical manifestations of sickle cell severity: Early steps to precision medicineMinireview: Genetic basis of heterogeneity and severity in sickle cell disease.The role of rs1984112_G at CD36 gene in increasing reticulocyte level among sickle cell disease patients.Variants in the non-coding region of the TLR2 gene associated with infectious subphenotypes in pediatric sickle cell anemia.Sickle cell anemia - Nitric oxide related genetic modifiers of hematological and biochemical parameters.
P2860
Genetic variation in CD36, HBA, NOS3 and VCAM1 is associated with chronic haemolysis level in sickle cell anaemia: a longitudinal study.
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name
Genetic variation in CD36, HBA ...... anaemia: a longitudinal study.
@en
Genetic variation in CD36, HBA ...... anaemia: a longitudinal study.
@nl
type
label
Genetic variation in CD36, HBA ...... anaemia: a longitudinal study.
@en
Genetic variation in CD36, HBA ...... anaemia: a longitudinal study.
@nl
prefLabel
Genetic variation in CD36, HBA ...... anaemia: a longitudinal study.
@en
Genetic variation in CD36, HBA ...... anaemia: a longitudinal study.
@nl
P2093
P2860
P50
P356
P1476
Genetic variation in CD36, HBA ...... anaemia: a longitudinal study.
@en
P2093
Alexandra Dias
Anabela Morais
Andreia Coelho
Emanuel Ferreira
Isabel Picanço
P2860
P304
P356
10.1111/EJH.12226
P577
2013-11-28T00:00:00Z