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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1970 2
1973 1
1974 4
1975 3
1979 2
1981 2
1983 1
1985 1
1987 3
1989 1
1990 2
1991 2
1992 1
1993 1
1994 5
1995 3
1996 6
1997 6
1998 10
1999 3
2000 6
2001 11
2002 6
2003 3
2004 4
2005 23
2006 9
2007 14
2008 12
2009 14
2010 19
2011 13
2012 9
2013 15
2014 16
2015 22
2016 19
2017 14
2018 20
2019 18
2020 16
2021 7
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321 results
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Page 1
Genetics and ESKD Disparities in African Americans.
Umeukeje EM, Young BA. Umeukeje EM, et al. Am J Kidney Dis. 2019 Dec;74(6):811-821. doi: 10.1053/j.ajkd.2019.06.006. Epub 2019 Oct 10. Am J Kidney Dis. 2019. PMID: 31606237 Free PMC article. Review.
Do Words Matter? Stigmatizing Language and the Transmission of Bias in the Medical Record.
P Goddu A, O'Conor KJ, Lanzkron S, Saheed MO, Saha S, Peek ME, Haywood C Jr, Beach MC. P Goddu A, et al. J Gen Intern Med. 2018 May;33(5):685-691. doi: 10.1007/s11606-017-4289-2. Epub 2018 Jan 26. J Gen Intern Med. 2018. PMID: 29374357 Free PMC article.
OBJECTIVE: To assess whether stigmatizing language written in a patient medical record is associated with a subsequent physician-in-training's attitudes towards the patient and clinical decision-making. DESIGN: Randomized vignette study of two chart notes employing stigmat …
OBJECTIVE: To assess whether stigmatizing language written in a patient medical record is associated with a subsequent physician-in-training …
Management of Sickle Cell Disease: Recommendations from the 2014 Expert Panel Report.
Yawn BP, John-Sowah J. Yawn BP, et al. Am Fam Physician. 2015 Dec 15;92(12):1069-76. Am Fam Physician. 2015. PMID: 26760593 Free article.
This overview highlights some of the most important clinical activities that can and should be carried out in the community care setting. Children with sickle cell anemia should receive prophylactic penicillin from birth through at least five years of age, and all p …
This overview highlights some of the most important clinical activities that can and should be carried out in the community care setting. Ch …
Impact of sickle cell disease on patients' daily lives, symptoms reported, and disease management strategies: Results from the international Sickle Cell World Assessment Survey (SWAY).
Osunkwo I, Andemariam B, Minniti CP, Inusa BPD, El Rassi F, Francis-Gibson B, Nero A, Trimnell C, Abboud MR, Arlet JB, Colombatti R, de Montalembert M, Jain S, Jastaniah W, Nur E, Pita M, DeBonnett L, Ramscar N, Bailey T, Rajkovic-Hooley O, James J. Osunkwo I, et al. Am J Hematol. 2021 Apr 1;96(4):404-417. doi: 10.1002/ajh.26063. Epub 2021 Feb 25. Am J Hematol. 2021. PMID: 33264445 Free PMC article.
Sickle cell disease (SCD) is a genetic disorder, characterized by hemolytic anemia and vaso-occlusive crises (VOCs). ...A substantial proportion of patients reported that SCD caused a high negative impact on emotions (60%) and school achievement (51%)
Sickle cell disease (SCD) is a genetic disorder, characterized by hemolytic anemia and vaso-occlusive crises (VOCs). ...A subs
The cost of health care for children and adults with sickle cell disease.
Kauf TL, Coates TD, Huazhi L, Mody-Patel N, Hartzema AG. Kauf TL, et al. Am J Hematol. 2009 Jun;84(6):323-7. doi: 10.1002/ajh.21408. Am J Hematol. 2009. PMID: 19358302 Free article.
Although sickle cell disease (SCD) is marked by high utilization of medical resources, the full cost of care for patients with SCD, including care not directly related to SCD, is unknown. ...
Although sickle cell disease (SCD) is marked by high utilization of medical resources, the full cost of care for patien …
Improving self-management in adolescents with sickle cell disease.
Crosby LE, Hood A, Kidwell K, Nwankwo C, Peugh J, Strong H, Quinn C, Britto MT. Crosby LE, et al. Pediatr Blood Cancer. 2020 Oct;67(10):e28492. doi: 10.1002/pbc.28492. Epub 2020 Jul 22. Pediatr Blood Cancer. 2020. PMID: 32697889 Clinical Trial.
BACKGROUND: Sickle cell disease (SCD) is associated with significant medical challenges that often worsen in adolescence when caregivers are beginning to transfer responsibility for disease management. ...Each SCHealthEd participant (N = 27) received six weekly phon …
BACKGROUND: Sickle cell disease (SCD) is associated with significant medical challenges that often worsen in adolescence when …
Disease Self-Efficacy and Health-Related Quality of Life in Adolescents With Sickle Cell Disease.
Goldstein-Leever A, Peugh JL, Quinn CT, Crosby LE. Goldstein-Leever A, et al. J Pediatr Hematol Oncol. 2020 Mar;42(2):141-144. doi: 10.1097/MPH.0000000000001363. J Pediatr Hematol Oncol. 2020. PMID: 30499909 Free PMC article.
Adolescents and young adults (AYA) with sickle cell disease (SCD) are at risk for poor health-related quality of life (HRQOL). ...
Adolescents and young adults (AYA) with sickle cell disease (SCD) are at risk for poor health-related quality of life (HRQOL). …
Increasing Educational Attainment in Adolescents with Sickle Cell Disease.
Harris KM, Dadekian JN, Abel RA, Jones B, Housten A, Ddamulira B, Chadwick-Mansker K, King AA. Harris KM, et al. Soc Work Public Health. 2019;34(6):468-482. doi: 10.1080/19371918.2019.1629142. Epub 2019 Jun 30. Soc Work Public Health. 2019. PMID: 31258020 Free PMC article.
Adolescents with sickle cell disease (SCD), a chronic condition primarily impacting African Americans, experience challenges graduating high school. ...This study aimed to examine 1) educational attainment for adolescents with SCD, 2) neighborho …
Adolescents with sickle cell disease (SCD), a chronic condition primarily impacting African Americans, experience challenges g …
Sickle cell crisis and pregnancy.
Parrish MR, Morrison JC. Parrish MR, et al. Semin Perinatol. 2013 Aug;37(4):274-9. doi: 10.1053/j.semperi.2013.04.006. Semin Perinatol. 2013. PMID: 23916026 Review.
Access to high-risk obstetric care, patient education, and close follow-up is important to minimize maternal morbidity and mortality. A high index of suspicion and good diagnostic acumen is necessary to obtain optimal results in the pregnant patient affected …
Access to high-risk obstetric care, patient education, and close follow-up is important to minimize maternal morbidity and mor …
Perceptions of US Adolescents and Adults With Sickle Cell Disease on Their Quality of Care.
Kanter J, Gibson R, Lawrence RH, Smeltzer MP, Pugh NL, Glassberg J, Masese RV, King AA, Calhoun C, Hankins JS, Treadwell M. Kanter J, et al. JAMA Netw Open. 2020 May 1;3(5):e206016. doi: 10.1001/jamanetworkopen.2020.6016. JAMA Netw Open. 2020. PMID: 32469413 Free PMC article.
IMPORTANCE: Sickle cell disease (SCD) is the most common inherited red blood cell disorder in the United States, and previous studies have shown that individuals with SCD are affected by multiple health disparities, including stigmatization, ine …
IMPORTANCE: Sickle cell disease (SCD) is the most common inherited red blood cell disorder in the United Stat
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