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2 results on '"Pope, Shammara"'

1. Vital Signs: Use of Recommended Health Care Measures to Prevent Selected Complications of Sickle Cell Anemia in Children and Adolescents--Selected U.S. States, 2019

Author

Schieve, Laura A., Simmons, Gretchen M., Payne, Amanda B., Abe, Karon, Hsu, Lewis L., Hulihan, Mary, Pope, Shammara, Rhie, Sarah, Dupervil, Brandi, and Hooper, W. Craig

Subjects
United States. National Heart, Lung and Blood Institute -- Analysis, Sickle cell anemia -- Complications and side effects -- Genetic aspects, Medical care -- Utilization -- Quality management, Hydroxyurea -- Complications and side effects, Patient compliance -- Analysis, Medicaid -- Analysis, Health care industry -- Analysis, Children -- Health aspects, African Americans -- Analysis, Health care industry, Health
Abstract

Introduction Sickle cell disease (SCD), a group of inherited blood disorders characterized by abnormal hemoglobin, reduces life expectancy by >20 years (1). SCD primarily affects persons whose ancestors came from [...]

Published
2022

2. Incidence of sickle cell trait--United States, 2010

Author

Ojodu, Jelili, Hulihan, Mary M., Pope, Shammara N., and Grant, Althea M.

Subjects
Sickle cell anemia, Hemoglobin, Health
Abstract

Persons with sickle cell trait (SCT) are heterozygous carriers of an abnormal [beta]-globin gene that results in the production of an abnormal hemoglobin, Hb S, which can distort red blood [...]

Published
2014

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