Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Elaine Whitworth"'
Autor:
Christopher L. Edwards, Sharena Scott, Michaela Boggan, Jordan Meek, Kiera Alston, Aiden Pearson, Alexandria McDougald, McKenzie Broadnax, Mary Wood, Camela S. Barker, Jessica Miller, Elaine Whitworth, Osaffo James, John J. Sollers III, W. Jeff Bryson, Roland Thorpe, Goldie Byrd, Keith E. Whitfield, Shiv Sudhakar, Debra O. Parker, Jonathan Livingston, Nirmish Shah, Kenyon Railey
Publikováno v:
Journal of the National Medical Association. 115:26-37
Objective To delineate the etiology, symptomatology, and treatment of sickle cell intrahepatic cholestasis (SCIC). Sickle cell disease (SCD) is the most frequently inherited hematologic disease, and SCIC is one rare and often fatal complication and c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2b07ba7b9b7e57a597dfa3044acccfc
https://doi.org/10.1016/j.jnma.2022.12.004
https://doi.org/10.1016/j.jnma.2022.12.004
Autor:
Christopher L. Edwards, Shani Harris-Peterson, Gary G. Bennett, Mary Wood, Alvin Killough, Charles Loughlin, Elaine Whitworth, Mischca T. Scales, Laura M. De Castro, Stephanie Johnson, Ojinga Harrison, Miriam Feliu, Mary Abrams
Publikováno v:
International Journal of Behavioral Medicine. 12:171-179
Sickle cell disease (SCD) is the most common genetic disorder of the blood. The disease produces significantly abnormal hemoglobin (Hgb) molecules in red blood cells (RBCs). The sickling of RBCs occurs when partially or totally deoxygenated Hgb molec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aec280c76f809301c62a3c49bf440718
https://doi.org/10.1207/s15327558ijbm1203_6
https://doi.org/10.1207/s15327558ijbm1203_6
Publikováno v:
Journal of Health & Social Policy. 5:141-160
Individuals with sickle cell disease experience a variety of psychosocial issues, some of which lead to maladjustments. To gather baseline data on coping and adjustment by a group of individuals over 30 years of age, a pilot study was conducted with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8351c9c285c291f0559e168b365c2a6
https://doi.org/10.1300/j045v05n03_09
https://doi.org/10.1300/j045v05n03_09
Publikováno v:
Journal of pediatric hematology/oncology. 33(5)
We implemented the Duke Sickle Cell Disease (SCD) Transition Program for adolescents with SCD and investigated the knowledge about SCD; concerns and emotions about transitioning; and the initial impact of the Transition Program. Thirty-three adolesce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::609661b9fcad674af5a6efa86becec3a
https://pubmed.ncbi.nlm.nih.gov/21602723
https://pubmed.ncbi.nlm.nih.gov/21602723