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Sickle Cell Disease 100 Years Later
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Comprehensive Handbook of Childhood Cancer and Sickle Cell Disease : A...
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Sickle Cell Disease by Graham R. Serjeant; Beryl E. Serjeant
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Pathology of Sickle Cell Disease.
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     Internet Search Results 

http://www.sicklecelldisease.org/
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Sickle-cell disease - Wikipedia
Sickle-cell disease (SCD) is a group of blood disorders typically inherited from a person's parents. The most common type is known as sickle-cell anaemia (SCA). It results in an abnormality in the oxygen-carrying protein haemoglobin found in red blood cells.

Sickle cell disease - Genetics Home Reference
Sickle cell disease is a group of disorders that affects hemoglobin, the molecule in red blood cells that delivers oxygen to cells throughout the body. People with this disorder have atypical hemoglobin molecules called hemoglobin S, which can distort red blood cells into a sickle, or crescent ...

Sickle Cell Disease | National Heart, Lung, and Blood ...
The term sickle cell disease (SCD) describes a group of inherited red blood cell disorders. People with SCD have abnormal hemoglobin, called hemoglobin S or sickle hemoglobin, in their red blood cells.

Home | Sickle Cell Disease | NCBDDD | CDC
Sickle cell disease (SCD) is a group of inherited red blood cell disorders. In SCD, the red blood cells become hard and sticky and look like a C-shaped farm tool called a “sickle.”

Sickle Cell Disease Association of Florida, Incorporated ...
Sickle Cell Disease Association of Florida is a 501(c)3 non profit advocacy organization established in 1976. The organization is committed to enhancing the lives of individuals and families impacted by sickle cell disease throughout the state of Florida

Welcome! The Annual Sickle Cell Disease Therapeutics ...
Welcome! The Annual Sickle Cell Disease Therapeutics Conference is a forum to discuss the latest advancements and future trends for treating patients with sickle cell disease.

Mortality In Sickle Cell Disease -- Life Expectancy and ...
Background Information on life expectancy and risk factors for early death among patients with sickle cell disease (sickle cell anemia, sickle cell-hemoglobin C disease, and the sickle cell-β-thalassemias) is needed to counsel patients, target therapy, and design clinical trials.

UpToDate
INTRODUCTION. Acute, painful episodes are the most common reason for individuals with sickle cell disease (SCD) to seek medical attention. The frequency of pain episodes is likely to be underestimated because these episodes are managed at home, especially as individuals with SCD grow older and learn how to manage pain on their own.

Voxelotor for Sickle Cell Disease | Global Blood Therapeutics
Voxelotor for Sickle Cell Disease Voxelotor (previously called GBT440), is being developed as an oral, once-daily therapy for patients with sickle cell disease (SCD).

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