Therapeutic advances in sickle cell disease in the last decade.

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Therapeutic advances in sickle cell disease in the last decade.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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2017年學術文章

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Therapeutic advances in sickle cell disease in the last decade.

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Therapeutic advances in sickle cell disease in the last decade.

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Item

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Therapeutic advances in sickle cell disease in the last decade.

@en

Therapeutic advances in sickle cell disease in the last decade.

@nl

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Therapeutic advances in sickle cell disease in the last decade.

@en

Therapeutic advances in sickle cell disease in the last decade.

@nl

P1476

Therapeutic advances in sickle cell disease in the last decade.

@en

P2093

Arun S Shet

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P2860

Transfusion independence and HMGA2 activation after gene therapy of human β-thalassaemia

MicroRNA-15a and -16-1 act via MYB to elevate fetal hemoglobin expression in human trisomy 13

GBT440 increases haemoglobin oxygen affinity, reduces sickling and prolongs RBC half-life in a murine model of sickle cell disease

Sickle cell disease: when and how to transfuse.

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

The HDAC inhibitors trichostatin A and suberoylanilide hydroxamic acid exhibit multiple modalities of benefit for the vascular pathobiology of sickle transgenic mice.

Translating scientific advances to improved outcomes for children with sickle cell disease: a timely opportunity.

Reactivation of developmentally silenced globin genes by forced chromatin looping.

Effect of hydroxyurea on the frequency of painful crises in sickle cell anemia. Investigators of the Multicenter Study of Hydroxyurea in Sickle Cell Anemia.

Hydroxycarbamide in very young children with sickle-cell anaemia: a multicentre, randomised, controlled trial (BABY HUG).

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708-712

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scholarly article

editorial

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10.4103/IJMR.IJMR_1153_17

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English

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P478

145

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P50

Swee Lay Thein

P577

2017-06-01T00:00:00Z

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P698

29067969

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5674537

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