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Minireview: Prognostic factors and the response to hydroxurea treatment in sickle cell disease.

Minireview: Prognostic factors and the response to hydroxurea treatment in sickle cell disease.

http://www.wikidata.org/entity/Q37107206

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Sickle cell disease severity: an introduction.Influence of Study Design on Developmental and Reproductive Toxicology Study Outcomes.Fetal hemoglobin induction in sickle erythroid progenitors using a synthetic zinc finger DNA-binding domain

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Minireview: Prognostic factors and the response to hydroxurea treatment in sickle cell disease.

http://www.wikidata.org/entity/Q37107206

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article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 29 March 2016

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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Minireview: Prognostic factors ...... atment in sickle cell disease.

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Minireview: Prognostic factors ...... atment in sickle cell disease.

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Minireview: Prognostic factors ...... atment in sickle cell disease.

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Minireview: Prognostic factors ...... atment in sickle cell disease.

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Minireview: Prognostic factors ...... atment in sickle cell disease.

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Minireview: Prognostic factors ...... atment in sickle cell disease.

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Experimental Biology and Medicine

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Minireview: Prognostic factors ...... atment in sickle cell disease.

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P2860

Hydroxyurea induces fetal hemoglobin by the nitric oxide-dependent activation of soluble guanylyl cyclase

Genomic approaches to identifying targets for treating β hemoglobinopathies

Whole exome sequencing identifies novel genes for fetal hemoglobin response to hydroxyurea in children with sickle cell anemia

Management of sickle cell disease: summary of the 2014 evidence-based report by expert panel members.

Hydroxyurea therapy of a murine model of sickle cell anemia inhibits the progression of pneumococcal disease by down-modulating E-selectin

Genetic and biochemical markers of hydroxyurea therapeutic response in sickle cell anemia.

Risk factors for death in 632 patients with sickle cell disease in the United States and United Kingdom

Improved survival of children and adolescents with sickle cell disease.

The risks and benefits of long-term use of hydroxyurea in sickle cell anemia: A 17.5 year follow-up.

How I use hydroxyurea to treat young patients with sickle cell anemia.

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