Page last updated: 2024-08-26

nsc-172755 and alpha-Thalassemia

nsc-172755 has been researched along with alpha-Thalassemia in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (50.00)	18.2507
2000's	1 (50.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Ayadi, H; Fakhfakh, F; Frikha, M; Gargouri, J; Ghali, L; Harrabi, M; Labiadh, Z; Mseddi, S; Souissi, T	1
Ballas, SK; Sarnaik, SA	1

Other Studies

2 other study(ies) available for nsc-172755 and alpha-Thalassemia

Article	Year
[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
Molecular characteristics of pediatric patients with sickle cell anemia and stroke. American journal of hematology, 2001, Volume: 67, Issue:3 Topics: alpha-Thalassemia; Anemia, Sickle Cell; Benin; Cameroon; Central African Republic; Cerebral Infarction; Child; Child, Preschool; Cohort Studies; Comorbidity; DNA Mutational Analysis; Female; Gene Deletion; Gene Frequency; Genetic Predisposition to Disease; Genotype; Globins; Haplotypes; Hemoglobin, Sickle; Humans; Infant; Infant, Newborn; Male; Michigan; Risk Factors; Senegal; Sex Factors	2001

Article

Year

[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

Molecular characteristics of pediatric patients with sickle cell anemia and stroke.

American journal of hematology, 2001, Volume: 67, Issue:3

Topics: alpha-Thalassemia; Anemia, Sickle Cell; Benin; Cameroon; Central African Republic; Cerebral Infarction; Child; Child, Preschool; Cohort Studies; Comorbidity; DNA Mutational Analysis; Female; Gene Deletion; Gene Frequency; Genetic Predisposition to Disease; Genotype; Globins; Haplotypes; Hemoglobin, Sickle; Humans; Infant; Infant, Newborn; Male; Michigan; Risk Factors; Senegal; Sex Factors

2001