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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 3
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 6
1998 4
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 4
2018 5
2019 6
2020 4
2021 2
2022 3
2023 5
2024 2

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243 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. ... 鈥�
In 1949, homozygous Hb S or sickle cell disease (SCD) became the first inherited condition identified at the molecular level; 鈥�
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. On average, 1 in 33 Cubans is a carrier of this severe hemolytic anemia that can cause early death. ...The Cuban experience shows that a middle-income country can mitigate the impact of 鈥�
Sickle cell anemia is the most common hereditary disease in Cuba. On average, 1 in 33 Cubans is a carrier of this sever 鈥�
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 鈥�
Sickle cell trait (SCT) is unique among the carrier states that are identified during newborn screening. Unlike other heterozy 鈥�
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 鈥�
OBJECTIVE: To study the issues and dilemmas in prenatal diagnosis of Sickle cell anemia (SCA) and to evaluate the role 鈥�
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. METHODS: Using a cross-sectional approach, qualitative data were collected during interviews of youth with SCD between a 鈥�
OBJECTIVES: Assess the need for and interest in a sexual health and sickle cell disease (SCD) inheritance educational program 鈥�
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.
Thalassemia was prevalent at the rate of 3.96%, sickle cell anemia had a prevalence of 1.98% sickle thalassemia was 0.89%. N = 20 pairs of Parents recognized genetic counseling i.e., with a single child or who wanted further children read 鈥�
Thalassemia was prevalent at the rate of 3.96%, sickle cell anemia had a prevalence of 1.98% sickle thalassemia 鈥�
Sexuality and sickle cell anemia.
C么bo Vde A, Chapadeiro CA, Ribeiro JB, Moraes-Souza H, Martins PR. C么bo 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 鈥�
BACKGROUND: Sickle cell disease, the most common hereditary blood disease in the world, is the result of an atypical hemoglobi 鈥�
Prevalence and Genetic Analysis of alpha- and beta-Thalassemia and Sickle Cell Anemia in Southwest Iran.
Nezhad FH, Nezhad KH, Choghakabodi PM, Keikhaei B. Nezhad FH, et al. J Epidemiol Glob Health. 2018 Dec;8(3-4):189-195. doi: 10.2991/j.jegh.2018.04.103. J Epidemiol Glob Health. 2018. PMID: 30864762 Free PMC article.
This prospective study assessed the prevalence and genetic analysis of alpha- and beta-thalassemia and sickle cell anemia (SCA) in Southwest Iran. Hematological indices were measured in 17,581 couples living in Khuzestan Province, Southwest Iran. ...Our findi 鈥�
This prospective study assessed the prevalence and genetic analysis of alpha- and beta-thalassemia and sickle cell anemia 鈥�
Genetic counseling in sickle cell anemia: experiences with couples at risk.
Neal-Cooper F, Scott RB. Neal-Cooper F, et al. Public Health Rep. 1988 Mar-Apr;103(2):174-8. Public Health Rep. 1988. PMID: 3128834 Free PMC article.
Beginning in 1970, a cohort of 74 sickle trait-carrying couples was identified who risked producing children with sickle cell anemia or other serious hemoglobinopathies. ...In young couples, concern for producing a child with sickle cell 鈥�
Beginning in 1970, a cohort of 74 sickle trait-carrying couples was identified who risked producing children with sickle ce 鈥�
Genetic education and sickle cell disease: feasibility and efficacy of a program tailored to adolescents.
Porter JS, Matthews CS, Carroll YM, Anderson SM, Smeltzer MP, Hankins JS. Porter JS, et al. J Pediatr Hematol Oncol. 2014 Oct;36(7):572-7. doi: 10.1097/MPH.0000000000000226. J Pediatr Hematol Oncol. 2014. PMID: 25089602
Sickle cell disease (SCD) genetic knowledge is important when individuals make reproductive decisions. ...Participants with HbSS/HbSbeta0-thal genotype and participants with more prior pain episodes exhibited a smaller increase in median scores than those with HbSC/ 鈥�
Sickle cell disease (SCD) genetic knowledge is important when individuals make reproductive decisions. ...Participants with Hb 鈥�
243 results