SciELO Analytics (Beta)
Brasil
Brazilian Journal of Medical and Biological Research (0100-879X)
alpha-Globin genes: thalassemic and structural alterations in a Brazilian population

Received Citations (11)

publishing year previous first author document title
2005 Revista Brasileira de Hematologia e Hemoterapia Silva Filho, Isaac L. Screening of abnormal hemoglobin and the evaluation of oxidative degeneration of hemoglobin among workers with the sickle cell trait (HbAS), exposed to occupational hazards
2001 Brazilian Journal of Medical and Biological Research Borges, E. High prevalence of alpha-thalassemia among individuals with microcytosis and hypochromia without anemia
2005 Cadernos de Saúde Pública Adorno, Elisângela Vitória Hemoglobinopatias em recém-nascidos de Salvador, Bahia, Nordeste do Brasil
2013 Revista Brasileira de Hematologia e Hemoterapia Silva, Marcilene Rezende Alpha chain hemoglobins with electrophoretic mobility similar to that of hemoglobin S in a newborn screening program
2013 Revista Brasileira de Hematologia e Hemoterapia Sonati, Maria de Fátima α-chain hemoglobin variants with electrophoretic mobility similar to that of hemoglobin S in newborn screening programs
2015 Genetics and Molecular Biology Shimauti, Eliana LitsukoTomimatsu Prevalence of βS-globin gene haplotypes, α-thalassemia (3.7 kb deletion) and redox status in patients with sickle cell anemia in the state of Paraná, Brazil
2003 Brazilian Journal of Medical and Biological Research Jorge, S.B. Screening for mutations in human alpha-globin genes by nonradioactive single-strand conformation polymorphism
2012 Revista Brasileira de Hematologia e Hemoterapia Neves, Fabia Hematological differences between patients with different subtypes of sickle cell disease on hydroxyurea treatment
2015 Revista Brasileira de Hematologia e Hemoterapia Kimura, Elza Miyuki Investigating alpha-globin structural variants: a retrospective review of 135,000 Brazilian individuals
2011 Brazilian Journal of Medical and Biological Research Suemasu, C.N. Characterization of alpha thalassemic genotypes by multiplex ligation-dependent probe amplification in the Brazilian population
2017 Revista Brasileira de Hematologia e Hemoterapia Ferreira, Roberta Dorta A combination of the -α3.7 and --MEDII alleles causing hemoglobin H disease in a Brazilian patient
This tool is under development and it is available in Beta Test version
This tool is under development and it was published with the objective to test the usage and performance. All the indicators are real and they are gradually being loaded. Slowness and out of service problems may occur in this version.

SciELO - Scientific Electronic Library Online
FAPESP CNPq BIREME FapUnifesp

Avenida Onze de Junho, 269 - Vila Clementino 04041-050 São Paulo

Tel.: +55 11 5083-3639/59 - Email: scielo@scielo.org

Help

Developments

Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 International License.