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  2. Sickle cell disease - Wikipedia

    en.wikipedia.org/wiki/Sickle_cell_disease

    Sickle cell disease (SCD), also simply called sickle cell, is a group of hemoglobin-related blood disorders typically inherited. The most common type is known as sickle cell anemia. It results in an abnormality in the oxygen-carrying protein haemoglobin found in red blood cells.

  3. Sickle cell trait - Wikipedia

    en.wikipedia.org/wiki/Sickle_cell_trait

    Sickle cell trait describes a condition in which a person has one abnormal allele of the hemoglobin beta gene (is heterozygous), but does not display the severe symptoms of sickle cell disease that occur in a person who has two copies of that allele (is homozygous).

  4. James B. Herrick - Wikipedia

    en.wikipedia.org/wiki/James_B._Herrick

    Herrick studied and taught at various Chicago hospitals. His first discovery, in 1910, was that of sickle-shaped red blood cells on the blood film of a dental student from Grenada. His description of the student's disease was known for many years as Herrick's syndrome, and is now known as sickle-cell disease.

  5. Anthony Clifford Allison - Wikipedia

    en.wikipedia.org/wiki/Anthony_Clifford_Allison

    Sickle-cell disease and resistance to malaria. In 1949 Allison participated in a vocational Oxford University Expedition to Mount Kenya. He took up the task of collecting blood samples from Kenyans for analyses of blood groups and genetic markers such as for sickle-cell disease.

  6. Sickle cell-beta thalassemia - Wikipedia

    en.wikipedia.org/wiki/Sickle_cell-beta_thalassemia

    Sickle cell-beta thalassemia is caused by inheritance of a sickle cell allele from one parent and a beta thalassemia allele from the other. Mutations. A sickle allele is always the same mutation of the beta-globin gene (glutamic acid to valine at amino acid six). In contrast, beta-thalassemia alleles can be created by many different mutations ...

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  7. Harvey Itano - Wikipedia

    en.wikipedia.org/wiki/Harvey_Itano

    Harvey Akio Itano (Japanese: ハーベイ・アキオ・イタノ, November 3, 1920 – May 8, 2010) was an American biochemist best known for his work on the molecular basis of sickle cell anemia and other diseases.

  8. Victoria Gray - Wikipedia

    en.wikipedia.org/wiki/Victoria_Gray

    Victoria Gray was the first patient ever to be treated with the gene-editing tool CRISPR for sickle-cell disease. [1] This marked the initial indication that a cure is attainable for individuals born with sickle-cell disease and another severe blood disorder, beta-thalassemia .

  9. Elizabeth Anionwu - Wikipedia

    en.wikipedia.org/wiki/Elizabeth_Anionwu

    Website. www .elizabethanionwu .co .uk. Dame Elizabeth Nneka Anionwu OM DBE FRCN (born Elizabeth Mary Furlong; 2 July 1947) is a British nurse, health care administrator, lecturer, and Emeritus Professor of Nursing at the University of West London . In 1979, Anionwu became the United Kingdom's first sickle-cell and thalassemia nurse specialist ...

  10. Roland B. Scott - Wikipedia

    en.wikipedia.org/wiki/Roland_B._Scott

    Roland Boyd Scott (April 18, 1909 – December 10, 2002) was an American researcher, pediatrician and authority on sickle cell disease. [1] Scott authored a key paper in 1948 describing the incidence of sickle cell in infants that eventually led to the establishment of routine screening for newborns. [1] He established the Howard University ...

  11. Transfusion therapy (Sickle-cell disease) - Wikipedia

    en.wikipedia.org/wiki/Transfusion_therapy...

    Transfusion therapy for sickle-cell disease entails the use of red blood cell transfusions in the management of acute cases of sickle cell disease and as a prophylaxis to prevent complications by decreasing the number of red blood cells (RBC) that can sickle by adding normal red blood cells.