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

Year Number of Results
1970 3
1973 2
1974 5
1975 3
1979 2
1981 2
1983 2
1989 2
1990 1
1991 1
1992 1
1993 1
1994 2
1995 2
1996 3
1997 3
1998 6
1999 3
2000 7
2001 2
2002 4
2003 1
2004 2
2005 13
2006 9
2007 5
2008 7
2009 8
2010 14
2011 8
2012 4
2013 12
2014 12
2015 15
2016 16
2017 16
2018 16
2019 21
2020 5
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217 results
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Page 1
Recommendations regarding splenectomy in hereditary hemolytic anemias.
Iolascon A, Andolfo I, Barcellini W, Corcione F, Garçon L, De Franceschi L, Pignata C, Graziadei G, Pospisilova D, Rees DC, de Montalembert M, Rivella S, Gambale A, Russo R, Ribeiro L, Vives-Corrons J, Martinez PA, Kattamis A, Gulbis B, Cappellini MD, Roberts I, Tamary H; Working Study Group on Red Cells and Iron of the EHA. Iolascon A, et al. Haematologica. 2017 Aug;102(8):1304-1313. doi: 10.3324/haematol.2016.161166. Epub 2017 May 26. Haematologica. 2017. PMID: 28550188 Free PMC article.
Hereditary hemolytic anemias are a group of disorders with a variety of causes, including red cell membrane defects, red blood cell enzyme disorders, congenital dyserythropoietic anemias, thalassemia syndromes and hemoglobinopathies. ...
Hereditary hemolytic anemias are a group of disorders with a variety of causes, including red cell membrane defects, red blood cel
Association of Sickle Cell Trait With Hemoglobin A1c in African Americans.
Lacy ME, Wellenius GA, Sumner AE, Correa A, Carnethon MR, Liem RI, Wilson JG, Sacks DB, Jacobs DR Jr, Carson AP, Luo X, Gjelsvik A, Reiner AP, Naik RP, Liu S, Musani SK, Eaton CB, Wu WC. Lacy ME, et al. JAMA. 2017 Feb 7;317(5):507-515. doi: 10.1001/jama.2016.21035. JAMA. 2017. PMID: 28170479 Free PMC article.
IMPORTANCE: Hemoglobin A1c (HbA1c) reflects past glucose concentrations, but this relationship may differ between those with sickle cell trait (SCT) and those without it. ...DESIGN, SETTING, AND PARTICIPANTS: Retrospective cohort study using data collected from 7938 …
IMPORTANCE: Hemoglobin A1c (HbA1c) reflects past glucose concentrations, but this relationship may differ between those with sickle
Curing Hemoglobinopathies: Challenges and Advances of Conventional and New Gene Therapy Approaches.
Motta I, Ghiaccio V, Cosentino A, Breda L. Motta I, et al. Mediterr J Hematol Infect Dis. 2019 Nov 1;11(1):e2019067. doi: 10.4084/MJHID.2019.067. eCollection 2019. Mediterr J Hematol Infect Dis. 2019. PMID: 31700592 Free PMC article. Review.
Inherited hemoglobin disorders, including beta-thalassemia (BT) and sickle-cell disease (SCD), are the most common monogenic diseases worldwide, with a global carrier frequency of over 5%.1 With migration, they are becoming more common worldwide, making their manage …
Inherited hemoglobin disorders, including beta-thalassemia (BT) and sickle-cell disease (SCD), are the most common monogenic d …
Design of the patient navigator to Reduce Readmissions (PArTNER) study: A pragmatic clinical effectiveness trial.
Prieto-Centurion V, Basu S, Bracken N, Calhoun E, Dickens C, DiDomenico RJ, Gallardo R, Gordeuk V, Gutierrez-Kapheim M, Hsu LL, Illendula S, Joo M, Kazmi U, Mutso A, Pickard AS, Pittendrigh B, Sullivan JL, Williams M, Krishnan JA. Prieto-Centurion V, et al. Contemp Clin Trials Commun. 2019 Jul 19;15:100420. doi: 10.1016/j.conctc.2019.100420. eCollection 2019 Sep. Contemp Clin Trials Commun. 2019. PMID: 31440690 Free PMC article.
Previous work indicates the potential for community health workers and peer coaches serving as patient navigators to improve processes of care and health outcomes during care transitions, but have not been sufficiently tested to determine if such programs imp …
Previous work indicates the potential for community health workers and peer coaches serving as patient navigators to improve p …
Youth with Sickle Cell Disease: Genetic and Sexual Health Education Needs.
Housten AJ, Abel RA, Dadekian J, Schwieterman K, Jason D, King AA. Housten AJ, et al. Am J Health Behav. 2015 Nov;39(6):856-65. doi: 10.5993/AJHB.39.6.13. Am J Health Behav. 2015. PMID: 26450553 Free PMC article.
OBJECTIVES: Assess the need for and interest in a sexual health and sickle cell disease (SCD) inheritance educational program for youth with SCD. ...Nineteen (95%) demonstrated deficits in sexual health knowledge and/or requested sexual health e …
OBJECTIVES: Assess the need for and interest in a sexual health and sickle cell disease (SCD) inheritance educational p …
What motivates individuals with sickle cell disease to talk with others about their illness? Reasons for and against sickle cell disease disclosure.
Derlega VJ, Maduro RS, Janda LH, Chen IA, Goodman BM 3rd. Derlega VJ, et al. J Health Psychol. 2018 Jan;23(1):103-113. doi: 10.1177/1359105316649786. Epub 2016 May 26. J Health Psychol. 2018. PMID: 27235142
This interview study documented how individuals with sickle cell disease make decisions about who to talk with concerning their illness based on psychological and interpersonal issues that are important to them. Reasons for sickle cell disease disclosu …
This interview study documented how individuals with sickle cell disease make decisions about who to talk with concerning thei …
Technology use and preferences to support clinical practice guideline awareness and adherence in individuals with sickle cell disease.
Utrankar A, Mayo-Gamble TL, Allen W, Novak L, Kassim AA, Bonnet K, Schlundt D, Murry VM, Jackson GP, DeBaun M, Cronin RM. Utrankar A, et al. J Am Med Inform Assoc. 2018 Aug 1;25(8):976-988. doi: 10.1093/jamia/ocy036. J Am Med Inform Assoc. 2018. PMID: 29741695 Free PMC article.
OBJECTIVE: Sickle cell disease (SCD) is a chronic condition affecting over 100 000 individuals in the United States, predominantly from vulnerable populations. ...Current technology health uses included information access, care coordination, and …
OBJECTIVE: Sickle cell disease (SCD) is a chronic condition affecting over 100 000 individuals in the United States
Health Literacy in Adolescents With Sickle Cell Disease.
Perry EL, Carter PA, Becker HA, Garcia AA, Mackert M, Johnson KE. Perry EL, et al. J Pediatr Nurs. 2017 Sep-Oct;36:191-196. doi: 10.1016/j.pedn.2017.05.012. Epub 2017 Jul 7. J Pediatr Nurs. 2017. PMID: 28888502
PURPOSE: To evaluate health literacy in a cohort of 75 adolescents with sickle cell disease (SCD). DESIGN AND METHODS: This cross-sectional, descriptive correlational study included assessment of demographic measures and appraisal of data resulting from compl …
PURPOSE: To evaluate health literacy in a cohort of 75 adolescents with sickle cell disease (SCD). DESIGN AND METHODS: …
Engaging Patients With Sickle Cell Disease and Their Families in Disease Education, Research, and Community Awareness.
Hines J, Mitchell MJ, Crosby LE, Johnson A, Valenzuela JM, Kalinyak K, Joiner C. Hines J, et al. J Prev Interv Community. 2011;39(3):256-72. doi: 10.1080/10852352.2011.576976. J Prev Interv Community. 2011. PMID: 26308311
This article describes the planning, implementation, and evaluation of Research and Education Day, an event designed to promote education and awareness of sickle cell disease (SCD), while also fostering and increasing participation by families in research studies. . …
This article describes the planning, implementation, and evaluation of Research and Education Day, an event designed to promote education an …
Improving the Management of Vaso-Occlusive Episodes in the Pediatric Emergency Department.
Kavanagh PL, Sprinz PG, Wolfgang TL, Killius K, Champigny M, Sobota A, Dorfman D, Barry K, Miner R, Moses JM. Kavanagh PL, et al. Pediatrics. 2015 Oct;136(4):e1016-25. doi: 10.1542/peds.2014-3470. Epub 2015 Sep 21. Pediatrics. 2015. PMID: 26391933 Free article. Clinical Trial.
OBJECTIVES: Vaso-occlusive episodes (VOEs) account for the majority of emergency department (ED) visits for children with sickle cell disease (SCD). ...
OBJECTIVES: Vaso-occlusive episodes (VOEs) account for the majority of emergency department (ED) visits for children with sickle c
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