Page last updated: 2024-08-26

nsc-172755 and Sickle Cell Trait

nsc-172755 has been researched along with Sickle Cell Trait in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19901 (20.00)18.7374
1990's2 (40.00)18.2507
2000's0 (0.00)29.6817
2010's2 (40.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Bouscaillou, J; Choudat, I; Cottrell, G; Garcia, A; Guerra, J; Koura, GK; Le Port, A; Massougbodji, A; Ouedraogo, S; Rachas, A; Watier, L1
Cottrell, G; Garcia, A; Koura, KG; Le Port, A; Massougbodji, A; Ouédraogo, S1
Ayadi, H; Fakhfakh, F; Frikha, M; Gargouri, J; Ghali, L; Harrabi, M; Labiadh, Z; Mseddi, S; Souissi, T1
Akogbeto, M; Castel, J; Chippaux, JP; Massougbodji, A; Zohoun, I; Zohoun, T1
Agboton, Y; Auvert, B; Chauliac, M; Devanlay, M; Dupin, H; Galan, P; Hercberg, S; Masse-Raimbault, AM; Soustre, Y; Zohoun, I1

Other Studies

5 other study(ies) available for nsc-172755 and Sickle Cell Trait

ArticleYear
Anaemia during pregnancy: impact on birth outcome and infant haemoglobin level during the first 18 months of life.
    Tropical medicine & international health : TM & IH, 2012, Volume: 17, Issue:3

    Topics: Adolescent; Adult; Anemia; Benin; Family; Feeding Behavior; Female; Follow-Up Studies; Hemoglobins; Humans; Infant; Infant, Low Birth Weight; Infant, Newborn; Infant, Newborn, Diseases; Malaria; Marriage; Pregnancy; Pregnancy Complications, Hematologic; Pregnancy Outcome; Premature Birth; Prevalence; Prospective Studies; Sex Factors; Sickle Cell Trait; Young Adult

2012
Maternal anaemia at delivery and haemoglobin evolution in children during their first 18 months of life using latent class analysis.
    PloS one, 2012, Volume: 7, Issue:11

    Topics: Adult; Analysis of Variance; Anemia; Benin; Developing Countries; Female; Hemoglobins; Humans; Infant; Infant, Newborn; Malaria; Male; Maternal Age; Plasmodium falciparum; Pregnancy; Prospective Studies; Risk Factors; Rural Population; Sickle Cell Trait

2012
[Hemoglobin beta S haplotype in the Kebili region (southern Tunisia)].
    Transfusion clinique et biologique : journal de la Societe francaise de transfusion sanguine, 1998, Volume: 5, Issue:2

    Topics: Adolescent; Adult; alpha-Thalassemia; Anemia, Sickle Cell; Benin; Child; Consanguinity; Ethnicity; Female; Fetal Hemoglobin; Gene Frequency; Genetic Heterogeneity; Globins; Haplotypes; Hemoglobin, Sickle; Humans; Male; Polymorphism, Restriction Fragment Length; Severity of Illness Index; Sickle Cell Trait; Tunisia

1998
[Plasmodium falciparum or P. malariae parasitemia in carriers of sickle cell trait in various Benin biotypes].
    Revue d'epidemiologie et de sante publique, 1992, Volume: 40, Issue:4

    Topics: Animals; Antibodies, Protozoan; Benin; Child; Child, Preschool; Ecology; Hemoglobin A; Hemoglobin, Sickle; Heterozygote; Humans; Infant; Malaria; Malaria, Falciparum; Phenotype; Plasmodium malariae; Population Density; Sickle Cell Trait

1992
Prevalence of iron deficiency and iron-deficiency anaemia in Benin.
    Public health, 1988, Volume: 102, Issue:1

    Topics: Adolescent; Adult; Anemia, Hypochromic; Benin; Child; Child, Preschool; Female; Humans; Infant; Iron Deficiencies; Malaria; Male; Middle Aged; Random Allocation; Rural Population; Sickle Cell Trait; Urban Population

1988