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

Year Number of Results
1973 1
1975 1
1979 1
1983 2
1984 1
1988 1
1989 2
1990 2
1991 2
1992 2
1993 4
1994 3
1995 3
1996 7
1997 7
1998 6
1999 7
2000 5
2001 6
2002 6
2003 8
2004 7
2005 16
2006 12
2007 5
2008 15
2009 19
2010 24
2011 28
2012 27
2013 32
2014 25
2015 31
2016 21
2017 24
2018 28
2019 29
2020 42
2021 18
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417 results
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Page 1
Alpha and beta thalassemia.
Muncie HL Jr, Campbell J. Muncie HL Jr, et al. Am Fam Physician. 2009 Aug 15;80(4):339-44. Am Fam Physician. 2009. PMID: 19678601 Free article. Review.
Bone marrow transplants can be curative for some children with beta thalassemia major. Persons with thalassemia should be referred for preconception genetic counseling, and persons with alpha thalassemia trait should consider chorionic villus sampling to diagnose infants w …
Bone marrow transplants can be curative for some children with beta thalassemia major. Persons with thalassemia should be referred fo …
Management of sickle cell disease: summary of the 2014 evidence-based report by expert panel members.
Yawn BP, Buchanan GR, Afenyi-Annan AN, Ballas SK, Hassell KL, James AH, Jordan L, Lanzkron SM, Lottenberg R, Savage WJ, Tanabe PJ, Ware RE, Murad MH, Goldsmith JC, Ortiz E, Fulwood R, Horton A, John-Sowah J. Yawn BP, et al. JAMA. 2014 Sep 10;312(10):1033-48. doi: 10.1001/jama.2014.10517. JAMA. 2014. PMID: 25203083 Review.
IMPORTANCE: Sickle cell disease (SCD) is a life-threatening genetic disorder affecting nearly 100,000 individuals in the United States and is associated with many acute and chronic complications requiring immediate medical attention. ...Strong recommen …
IMPORTANCE: Sickle cell disease (SCD) is a life-threatening genetic disorder affecting nearly 100,000 individuals in the Un
Sickle cell disease: A primary care update.
Onimoe G, Rotz S. Onimoe G, et al. Cleve Clin J Med. 2020 Jan;87(1):19-27. doi: 10.3949/ccjm.87a.18051. Epub 2020 Jan 2. Cleve Clin J Med. 2020. PMID: 31990651 Free article. Review.
Sickle cell disease (SCD) is the most common hemoglobinopathy in the United States and causes significant disease-related morbidity including multiorgan damage, chronic anemia, and debilitating pain crises. ...
Sickle cell disease (SCD) is the most common hemoglobinopathy in the United States and causes significant
Pathophysiology and treatment of pulmonary hypertension in sickle cell disease.
Gordeuk VR, Castro OL, Machado RF. Gordeuk VR, et al. Blood. 2016 Feb 18;127(7):820-8. doi: 10.1182/blood-2015-08-618561. Epub 2016 Jan 12. Blood. 2016. PMID: 26758918 Free PMC article. Review.
Pulmonary hypertension affects 10% of adult patients with sickle cell disease (SCD), particularly those with the homozygous genotype. ...Patients with hemodynamics of pulmonary arterial hypertension should be referred to specialized centers and considered for …
Pulmonary hypertension affects 10% of adult patients with sickle cell disease (SCD), particularly those with the homozygous ge …
Drug Therapies for the Management of Sickle Cell Disease.
Rai P, Ataga KI. Rai P, et al. F1000Res. 2020 Jun 11;9:F1000 Faculty Rev-592. doi: 10.12688/f1000research.22433.1. eCollection 2020. F1000Res. 2020. PMID: 32765834 Free PMC article. Review.
Sickle cell disease (SCD) afflicts millions of people worldwide but is referred to as an orphan disease in the United States. ...While most individuals with SCD in resource-rich countries survive into adulthood, the life expectancy of patients w
Sickle cell disease (SCD) afflicts millions of people worldwide but is referred to as an orphan disease in the Unite
Current and novel therapies for the prevention of vaso-occlusive crisis in sickle cell disease.
Osunkwo I, Manwani D, Kanter J. Osunkwo I, et al. Ther Adv Hematol. 2020 Sep 29;11:2040620720955000. doi: 10.1177/2040620720955000. eCollection 2020. Ther Adv Hematol. 2020. PMID: 33062233 Free PMC article. Review.
Individuals with sickle cell disease (SCD) are living further into adulthood in high-resource countries. ...With increased understanding of the pathophysiology of VOCs, there are several new potential therapies that specifically target the pathologic process of vaso …
Individuals with sickle cell disease (SCD) are living further into adulthood in high-resource countries. ...With increased und …
Microvascular thrombosis: experimental and clinical implications.
Bray MA, Sartain SE, Gollamudi J, Rumbaut RE. Bray MA, et al. Transl Res. 2020 Nov;225:105-130. doi: 10.1016/j.trsl.2020.05.006. Epub 2020 May 23. Transl Res. 2020. PMID: 32454092 Free PMC article. Review.
.); however, thrombosis is often present in the microcirculation in a variety of significant human diseases, such as disseminated intravascular coagulation, thrombotic microangiopathy, sickle cell disease, and others. Further, microvascular thrombosis has recently b …
.); however, thrombosis is often present in the microcirculation in a variety of significant human diseases, such as disseminated intravascu …
Effect of donor type and conditioning regimen intensity on allogeneic transplantation outcomes in patients with sickle cell disease: a retrospective multicentre, cohort study.
Eapen M, Brazauskas R, Walters MC, Bernaudin F, Bo-Subait K, Fitzhugh CD, Hankins JS, Kanter J, Meerpohl JJ, Bolaños-Meade J, Panepinto JA, Rondelli D, Shenoy S, Williamson J, Woolford TL, Gluckman E, Wagner JE, Tisdale JF. Eapen M, et al. Lancet Haematol. 2019 Nov;6(11):e585-e596. doi: 10.1016/S2352-3026(19)30154-1. Epub 2019 Sep 5. Lancet Haematol. 2019. PMID: 31495699 Free PMC article.
BACKGROUND: Donors other than matched siblings and low-intensity conditioning regimens are increasingly used in haematopoietic stem cell transplantation. We aimed to compare the relative risk of donor type and conditioning regimen intensity on the transplantation outcomes …
BACKGROUND: Donors other than matched siblings and low-intensity conditioning regimens are increasingly used in haematopoietic stem cell
Sickle cell disease: an international survey of results of HLA-identical sibling hematopoietic stem cell transplantation.
Gluckman E, Cappelli B, Bernaudin F, Labopin M, Volt F, Carreras J, Pinto Simões B, Ferster A, Dupont S, de la Fuente J, Dalle JH, Zecca M, Walters MC, Krishnamurti L, Bhatia M, Leung K, Yanik G, Kurtzberg J, Dhedin N, Kuentz M, Michel G, Apperley J, Lutz P, Neven B, Bertrand Y, Vannier JP, Ayas M, Cavazzana M, Matthes-Martin S, Rocha V, Elayoubi H, Kenzey C, Bader P, Locatelli F, Ruggeri A, Eapen M; Eurocord, the Pediatric Working Party of the European Society for Blood and Marrow Transplantation, and the Center for International Blood and Marrow Transplant Research. Gluckman E, et al. Blood. 2017 Mar 16;129(11):1548-1556. doi: 10.1182/blood-2016-10-745711. Epub 2016 Dec 13. Blood. 2017. PMID: 27965196 Free PMC article.
Despite advances in supportive therapy to prevent complications of sickle cell disease (SCD), access to care is not universal. Hematopoietic cell transplantation is, to date, the only curative therapy for SCD, but its application is limited by availability of …
Despite advances in supportive therapy to prevent complications of sickle cell disease (SCD), access to care is not universal. …
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.
DESIGN: Randomized vignette study of two chart notes employing stigmatizing versus neutral language to describe the same hypothetical patient, a 28-year-old man with sickle cell disease. PARTICIPANTS: A total of 413 physicians-in-training: medical students and resid …
DESIGN: Randomized vignette study of two chart notes employing stigmatizing versus neutral language to describe the same hypothetical patien …
417 results
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