Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Results by year

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 2
Text availability
Article attribute
Article type
Publication date

Search Results

240 results
Results by year
Filters applied: . Clear all
Page 1
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 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. ...KEYWORDS Sickle cell anemia, sickle cell disease, sickle cell disorders, hemolytic anemia, sickle cell trait, sickle
Sickle cell anemia is the most common hereditary disease in Cuba. ...KEYWORDS Sickle cell anemia,
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. ...A socioeconomic questionnaire a …
BACKGROUND: Sickle cell disease, the most common hereditary blood disease in the world, is the result of an atypical hemoglobi …
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. ...The authors further discuss the issues and dilemmas faced during prenatal …
OBJECTIVE: To study the issues and dilemmas in prenatal diagnosis of Sickle cell anemia (SCA) and to evaluate the role …
Prevalence and Genetic Analysis of α- and β-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. ...Our findings will be useful for developing an efficient control program and genetic counseli
This prospective study assessed the prevalence and genetic analysis of alpha- and beta-thalassemia and sickle cell a
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 geneti
OBJECTIVES: Assess the need for and interest in a sexual health and sickle cell disease (SCD) inheritance educational p …
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. This study assessed feasibility and efficacy of delivering basic genetic information to 101 adolescents with SCD. Participants completed a questionna
Sickle cell disease (SCD) genetic knowledge is important when individuals make reproductive decisions. This study asses
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
BACKGROUND AND AIM: Sickle cell syndrome is a group of inherited hematological disorders with varying degrees of anemia, jaundice, fatiguability along with hepatomegaly and splenomegaly. ...Sickle cell anemia is of prime importance becaus …
BACKGROUND AND AIM: Sickle cell syndrome is a group of inherited hematological disorders with varying degrees of anemia
Prenatal diagnosis of sickle cell anemia and beta-thalassemia in southern Turkey.
Cürük MA, Zeren F, Genç A, Ozavci-Aygün S, Kilinç Y, Aksoy K. Cürük MA, et al. Hemoglobin. 2008;32(6):525-30. doi: 10.1080/03630260802508269. Hemoglobin. 2008. PMID: 19065329
Hemoglobinopathies are the most common genetic diseases in Turkey. The incidence of sickle cell trait is 10.0% and beta-thalassemia (beta-thal) trait is 3.7% in the Cukurova region of southern Turkey. Sickle cell anemia is prevalent in th …
Hemoglobinopathies are the most common genetic diseases in Turkey. The incidence of sickle cell trait is 10.0% and beta …
240 results