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

Year Number of Results
1972 2
1973 1
1974 2
1980 1
1981 3
1987 2
1988 2
1990 2
1992 2
1994 2
1995 2
1996 4
1997 5
1998 9
1999 4
2000 4
2001 6
2002 5
2003 3
2004 7
2005 12
2006 11
2007 17
2008 16
2009 14
2010 15
2011 16
2012 9
2013 12
2014 14
2015 14
2016 19
2017 11
2018 23
2019 14
2020 1
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253 results
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Page 1
Sickle cell disease.
Kato GJ, Piel FB, Reid CD, Gaston MH, Ohene-Frempong K, Krishnamurti L, Smith WR, Panepinto JA, Weatherall DJ, Costa FF, Vichinsky EP. Kato GJ, et al. Nat Rev Dis Primers. 2018 Mar 15;4:18010. doi: 10.1038/nrdp.2018.10. Nat Rev Dis Primers. 2018. PMID: 29542687 Free article. Review.
Early diagnosis is crucial to improve survival, and universal newborn screening programmes have been implemented in some countries but are challenging in low-income, high-burden settings....
Early diagnosis is crucial to improve survival, and universal newborn screening programmes have been implemented in some countries bu …
Sickle cell disease.
Ware RE, de Montalembert M, Tshilolo L, Abboud MR. Ware RE, et al. Lancet. 2017 Jul 15;390(10091):311-323. doi: 10.1016/S0140-6736(17)30193-9. Epub 2017 Feb 1. Lancet. 2017. PMID: 28159390 Review.
Recent advances include systematic universal screening for stroke risk, improved management of iron overload using oral chelators and non-invasive MRI measurements, and point-of-care diagnostic devices. ...
Recent advances include systematic universal screening for stroke risk, improved management of iron overload using oral chelators and …
Sickle cell disease.
Strouse J. Strouse J. Handb Clin Neurol. 2016;138:311-24. doi: 10.1016/B978-0-12-802973-2.00018-5. Handb Clin Neurol. 2016. PMID: 27637966 Review.
It is the most common serious genetic diseases in childhood, affecting approximately 1 in 2500 births and 100 000 individuals in the USA, in addition to 300 000 new cases globally each year. ...Among children with sickle cell anemia (HbSS), 11% had a stroke by age 18 years …
It is the most common serious genetic diseases in childhood, affecting approximately 1 in 2500 births and 100 000 individuals in the USA
Clinical Outcomes Associated With Sickle Cell Trait: A Systematic Review.
Naik RP, Smith-Whitley K, Hassell KL, Umeh NI, de Montalembert M, Sahota P, Haywood C Jr, Jenkins J, Lloyd-Puryear MA, Joiner CH, Bonham VL, Kato GJ. Naik RP, et al. Ann Intern Med. 2018 Nov 6;169(9):619-627. doi: 10.7326/M18-1161. Epub 2018 Oct 30. Ann Intern Med. 2018. PMID: 30383109 Free PMC article.
DATA SYNTHESIS: Of 7083 screened studies, 41 met inclusion criteria. High-strength evidence supported a positive association between SCT and risk for pulmonary embolism, proteinuria, and chronic kidney disease. ...
DATA SYNTHESIS: Of 7083 screened studies, 41 met inclusion criteria. High-strength evidence supported a positive association between …
Non-transfusion-dependent thalassemia and thalassemia intermedia: epidemiology, complications, and management.
Vichinsky E. Vichinsky E. Curr Med Res Opin. 2016;32(1):191-204. doi: 10.1185/03007995.2015.1110128. Epub 2015 Nov 25. Curr Med Res Opin. 2016. PMID: 26479125 Review.
CONCLUSIONS: Management of NTDT requires a comprehensive approach, beginning with screening and prenatal diagnosis, monitoring for iron overload and associated complications, and iron chelation therapy. ...
CONCLUSIONS: Management of NTDT requires a comprehensive approach, beginning with screening and prenatal diagnosis, monitoring for ir …
Pulmonary hypertension in chronic hemolytic anemias: Pathophysiology and treatment.
Haw A, Palevsky HI. Haw A, et al. Respir Med. 2018 Apr;137:191-200. doi: 10.1016/j.rmed.2018.02.020. Epub 2018 Feb 28. Respir Med. 2018. PMID: 29605204 Free article. Review.
Although most studies have been based on the use of echocardiography as a screening tool for pulmonary hypertension as opposed to the gold standard of right heart catheterization for definitive diagnosis, the association between chronic hemolytic anemia and pulmonary hyper …
Although most studies have been based on the use of echocardiography as a screening tool for pulmonary hypertension as opposed to the …
Sickle cell nephropathy: an update on pathophysiology, diagnosis, and treatment.
Hariri E, Mansour A, El Alam A, Daaboul Y, Korjian S, Aoun Bahous S. Hariri E, et al. Int Urol Nephrol. 2018 Jun;50(6):1075-1083. doi: 10.1007/s11255-018-1803-3. Epub 2018 Jan 30. Int Urol Nephrol. 2018. PMID: 29383580 Review.
Markers of renal injury, such as proteinuria and tubular dysfunction, have been associated with outcomes among patients with sickle cell nephropathy and provide means for early detection of nephropathy and screening prior to progression to renal failure. ...
Markers of renal injury, such as proteinuria and tubular dysfunction, have been associated with outcomes among patients with sickle cell nep …
Hydroxyurea for Children with Sickle Cell Anemia in Sub-Saharan Africa.
Tshilolo L, Tomlinson G, Williams TN, Santos B, Olupot-Olupot P, Lane A, Aygun B, Stuber SE, Latham TS, McGann PT, Ware RE; REACH Investigators. Tshilolo L, et al. N Engl J Med. 2019 Jan 10;380(2):121-131. doi: 10.1056/NEJMoa1813598. Epub 2018 Dec 1. N Engl J Med. 2019. PMID: 30501550 Free PMC article. Clinical Trial.
RESULTS: A total of 635 children were fully enrolled; 606 children completed screening and began receiving hydroxyurea at a mean (±SD) dose of 17.5±1.8 mg per kilogram per day. ...
RESULTS: A total of 635 children were fully enrolled; 606 children completed screening and began receiving hydroxyurea at a mean (±SD …
The current state of sickle cell trait: implications for reproductive and genetic counseling.
Pecker LH, Naik RP. Pecker LH, et al. Blood. 2018 Nov 29;132(22):2331-2338. doi: 10.1182/blood-2018-06-848705. Blood. 2018. PMID: 30487130 Free PMC article. Review.
Sickle cell trait (SCT) is unique among the carrier states that are identified during newborn screening. Unlike other heterozygous states for rare recessive diseases, SCT is exceedingly prevalent throughout regions of the world, making sickle cell disease one …
Sickle cell trait (SCT) is unique among the carrier states that are identified during newborn screening. Unlike other heterozy …
Treatment of dental and orthodontic complications in thalassaemia.
Mulimani P, Abas AB, Karanth L, Colombatti R, Kulkarni P. Mulimani P, et al. Cochrane Database Syst Rev. 2019 Aug 2;8(8):CD012969. doi: 10.1002/14651858.CD012969.pub2. Cochrane Database Syst Rev. 2019. PMID: 31425614
DATA COLLECTION AND ANALYSIS: Two review authors independently screened 35,202 titles from search results. We identified four unique randomised controlled trials, of which one seemed potentially relevant. ...
DATA COLLECTION AND ANALYSIS: Two review authors independently screened 35,202 titles from search results. We identified four unique …
253 results
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