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

Year Number of Results
1971 1
1972 6
1973 4
1974 16
1975 6
1976 5
1977 4
1978 4
1979 3
1980 2
1981 4
1982 2
1983 5
1984 5
1985 3
1986 4
1987 1
1988 5
1989 6
1990 3
1991 2
1992 3
1993 2
1994 3
1995 5
1996 5
1997 7
1998 5
1999 5
2000 4
2001 1
2002 3
2003 4
2004 5
2005 6
2006 7
2007 5
2008 7
2009 4
2010 2
2011 9
2012 5
2013 14
2014 12
2015 11
2016 6
2017 5
2018 5
2019 6
2020 4
2021 2
2022 3
2023 5
2024 2

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247 results

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Page 1
Sickle cell trait diagnosis: clinical and social implications.
Naik RP, Haywood C Jr. Naik RP, et al. Hematology Am Soc Hematol Educ Program. 2015;2015(1):160-7. doi: 10.1182/asheducation-2015.1.160. Hematology Am Soc Hematol Educ Program. 2015. PMID: 26637716 Free PMC article. Review.
In 1949, homozygous Hb S or sickle cell disease (SCD) became the first inherited condition identified at the molecular level; however, since then, both SCD and heterozygous Hb S, sickle cell trait (SCT), have endured a long and complicated history. ... …
In 1949, homozygous Hb S or sickle cell disease (SCD) became the first inherited condition identified at the molecular level; …
Sickle Cell Anemia in Cuba: Prevention and Management, 1982-2018.
Marcheco-Teruel B. Marcheco-Teruel B. MEDICC Rev. 2019 Oct;21(4):34-38. doi: 10.37757/MR2019.V21.N4.6. MEDICC Rev. 2019. PMID: 32335567 Free article.
Sickle cell anemia is the most common hereditary disease in Cuba. ...The Cuban experience shows that a middle-income country can mitigate the impact of a genetic disease through a universal preventive program based in primary care, which also pays particular …
Sickle cell anemia is the most common hereditary disease in Cuba. ...The Cuban experience shows that a middle-income co …
Sexuality and sickle cell anemia.
Côbo Vde A, Chapadeiro CA, Ribeiro JB, Moraes-Souza H, Martins PR. Côbo Vde A, et al. Rev Bras Hematol Hemoter. 2013;35(2):89-93. doi: 10.5581/1516-8484.20130027. Rev Bras Hematol Hemoter. 2013. PMID: 23741184 Free PMC article.
BACKGROUND: Sickle cell disease, the most common hereditary blood disease in the world, is the result of an atypical hemoglobin called S (Hb S) which, when homozygous (Hb SS) is the cause of sickle cell anemia. ...METHODS: Twenty male and female …
BACKGROUND: Sickle cell disease, the most common hereditary blood disease in the world, is the result of an atypical hemoglobi …
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 dise …
Sickle cell trait (SCT) is unique among the carrier states that are identified during newborn screening. Unlike other heterozy …
Sickle cell anemia--molecular diagnosis and prenatal counseling: SGPGI experience.
Kumar R, Panigrahi I, Dalal A, Agarwal S. Kumar R, et al. Indian J Pediatr. 2012 Jan;79(1):68-74. doi: 10.1007/s12098-011-0510-1. Epub 2011 Jun 29. Indian J Pediatr. 2012. PMID: 21713598
OBJECTIVE: To study the issues and dilemmas in prenatal diagnosis of Sickle cell anemia (SCA) and to evaluate the role of genetic modifiers in counseling the families. ...CONCLUSIONS: The knowledge of the relationship between genotype and phenotype, effect of …
OBJECTIVE: To study the issues and dilemmas in prenatal diagnosis of Sickle cell anemia (SCA) and to evaluate the role …
Reproductive Health Counseling among Youth with Sickle Cell Disease.
Stanek CJ, Reich J, Theroux CI, Creary SE, Quinn GP, Nahata L. Stanek CJ, et al. J Pediatr Adolesc Gynecol. 2023 Aug;36(4):393-398. doi: 10.1016/j.jpag.2023.03.002. Epub 2023 Mar 18. J Pediatr Adolesc Gynecol. 2023. PMID: 36934802
STUDY OBJECTIVE: Reproductive health counseling is important for youth with sickle cell disease (SCD) given that they experience potential infertility risks from SCD and its treatments and high rates of unplanned pregnancies. ...Only 57% of youth received contracept …
STUDY OBJECTIVE: Reproductive health counseling is important for youth with sickle cell disease (SCD) given that they experien …
Genetic modifiers of sickle cell disease.
Thein SL. Thein SL. Hemoglobin. 2011;35(5-6):589-606. doi: 10.3109/03630269.2011.615876. Epub 2011 Oct 3. Hemoglobin. 2011. PMID: 21967611 Review.
Sickle cell disease is one of the best characterized human monogenic disorders. ...This review highlights the more recent genetic association studies that have been applied to unravel the genetic modifiers of sickle cell disease including Hb F genet …
Sickle cell disease is one of the best characterized human monogenic disorders. ...This review highlights the more recent gene …
A study of spectrum of sickle cell anemia and thalassemia in a teaching institute of South India.
Sabitha Rani SS, Vamshidhar IS, Bangaru S, John NA, John J. Sabitha Rani SS, et al. Niger J Clin Pract. 2022 Apr;25(4):490-495. doi: 10.4103/njcp.njcp_1742_21. Niger J Clin Pract. 2022. PMID: 35439909 Free article.
The clinical presentations can be may vary and therefore require thorough investigations. We tried to evaluate the spectrum of sickle cell anemia and thalassemia in pediatric patients of our hospital. ...Sickle cell anemia is of prime imp …
The clinical presentations can be may vary and therefore require thorough investigations. We tried to evaluate the spectrum of sickle …
Genetic counseling and carrier screening in candidates for gamete donation at a Portuguese center.
Soares CA, Tkachenko N, Vale-Fernandes E, Barreiro M, Abreu M, Reis CF, Soares G, Fortuna AM, Soares AR. Soares CA, et al. JBRA Assist Reprod. 2023 Jun 22;27(2):180-184. doi: 10.5935/1518-0557.20220012. JBRA Assist Reprod. 2023. PMID: 35916466 Free PMC article.
OBJECTIVE: Genetic counseling and carrier screening are part of the gamete donation process by healthy individuals. ...Of 97 candidates tested, 16.5% presented anomalous laboratory results (16/97): ten candidates were carriers for an autosomal recessive disorder - c …
OBJECTIVE: Genetic counseling and carrier screening are part of the gamete donation process by healthy individuals. ...Of 97 c …
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. ...The mean age was 16.91.8 years (range 13-19). Of the 20 participants, 100% expressed interest in SCD genetic …
OBJECTIVES: Assess the need for and interest in a sexual health and sickle cell disease (SCD) inheritance educational program …
247 results