(Q48919012)

16 February 2018

title

Genetic variation in CD36, HBA, NOS3 and VCAM1 is associated with chronic haemolysis level in sickle cell anaemia: a longitudinal study. (English)

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4

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Paula Faustino

object named as

Paula Faustino

7

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João Lavinha

object named as

João Lavinha

8

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author name string

Andreia Coelho

1

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16 February 2018

Alexandra Dias

2

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Anabela Morais

3

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Emanuel Ferreira

5

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Isabel Picanço

6

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publication date

28 November 2013

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European Journal of Haematology

published in

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16 February 2018

volume

92

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issue

3

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page(s)

237-243

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Hemoglobinopathy Learning Collaborative: using quality improvement (QI) to achieve equity in health care quality, coordination, and outcomes for sickle cell disease

cites work

1 reference

Climatic and geographic temporal patterns of pain in the Multicenter Study of Hydroxyurea

21 January 2018

1 reference

Genetic modifiers of sickle cell disease

21 January 2018

1 reference

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

21 January 2018

1 reference

Rapid analysis of -alpha 3.7 thalassaemia and alpha alpha alpha anti 3.7 triplication by enzymatic amplification analysis

21 January 2018

1 reference

Multiple testing in large-scale genetic studies

21 January 2018

1 reference

Severe sickle cell anemia is associated with increased plasma levels of TNF-R1 and VCAM-1

21 January 2018

1 reference

Variants in the VCAM1 gene and risk for symptomatic stroke in sickle cell disease

21 January 2018

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Balanced polymorphism selected by genetic versus infectious human disease

21 January 2018

1 reference

Modulation of erythroid adhesion receptor expression by hydroxyurea in children with sickle cell disease

21 January 2018

1 reference

Plasma thrombospondin-1 is increased during acute sickle cell vaso-occlusive events and associated with acute chest syndrome, hydroxyurea therapy, and lower hemolytic rates

21 January 2018

1 reference

Polymorphisms in the CD36/FAT gene are associated with plasma vitamin E concentrations in humans.

21 January 2018

1 reference

Shear stress insensitivity of endothelial nitric oxide synthase expression as a genetic risk factor for coronary heart disease

21 January 2018

1 reference

The -786C/T single-nucleotide polymorphism in the promoter of the gene for endothelial nitric oxide synthase: insensitivity to physiologic stimuli as a risk factor for rheumatoid arthritis

21 January 2018

1 reference

Genetic determinants of haemolysis in sickle cell anaemia

21 January 2018

1 reference

Genetic variants in genes related to lipid metabolism and atherosclerosis, dyslipidemia and atorvastatin response

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1111/EJH.12226

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16 February 2018

PubMed ID

24168396

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16 February 2018