The delay time in sickle cell disease after 40 years: A paradigm assessed.

The delay time in sickle cell disease after 40 years: A paradigm assessed.

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http://www.wikidata.org/entity/Q38341763
2015 Clinical trials update in sickle cell anemiaKinetic assay shows that increasing red cell volume could be a treatment for sickle cell disease.Treating sickle cell disease by targeting HbS polymerizationEffect of Age on Blood Rheology in Sickle Cell Anaemia and Sickle Cell Haemoglobin C Disease: A Cross-Sectional StudyDifferences of microparticle patterns between sickle cell anemia and hemoglobin SC patients.Probing the Twisted Structure of Sickle Hemoglobin Fibers via Particle Simulations.GBT440 Inhibits Sickling of Sickle Cell Trait Blood Under In Vitro Conditions Mimicking Strenuous Exercise.Universality of supersaturation in protein-fiber formation.New developments in anti-sickling agents: can drugs directly prevent the polymerization of sickle haemoglobin in vivo?A microfluidic platform to study the effects of vascular architecture and oxygen gradients on sickle blood flow.Deamidation of Human γS-Crystallin Increases Attractive Protein Interactions: Implications for Cataract.
P2860

The delay time in sickle cell disease after 40 years: A paradigm assessed.

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http://www.wikidata.org/entity/Q38341763
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2015 nî lūn-bûn
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The delay time in sickle cell disease after 40 years: A paradigm assessed.
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The delay time in sickle cell disease after 40 years: A paradigm assessed.
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The delay time in sickle cell disease after 40 years: A paradigm assessed.
@en
P1433
P1476
P2093
P2860
P304
P31
P356
P433
P478
P577
P5875
P698
P921
P356
P1433
P1476
The delay time in sickle cell disease after 40 years: A paradigm assessed.
@en
P2093
P2860
P304
P31
P356
P433
P478
P577
P5875
P698
P921