Literature DB >> 1686261

High prevalence of alpha-thalassemia in a black population of Brazil.

M F Sonati1, S B Farah, A S Ramalho, F F Costa.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1991        PMID： 1686261     DOI： 10.3109/03630269109027884

Source DB:  PubMed          Journal:  Hemoglobin        ISSN： 0363-0269            Impact factor:   0.849


× No keyword cloud information.
  11 in total

1.  Altered erythropoiesis and iron metabolism in carriers of thalassemia.

Authors:  Jacqueline S Guimarães; Juçara G Cominal; Ana Cristina Silva-Pinto; Gordana Olbina; Yelena Z Ginzburg; Vijay Nandi; Mark Westerman; Stefano Rivella; Ana Maria de Souza
Journal:  Eur J Haematol       Date:  2014-11-11       Impact factor: 2.997

2.  Prevalence of α-thalassemia 3.7 kb deletion in the adult population of Rio Grande do Norte, Brazil.

Authors:  Gustavo Henrique de Medeiros Alcoforado; Christiane Medeiros Bezerra; Telma Maria Araújo Moura Lemos; Denise Madureira de Oliveira; Elza Miyuki Kimura; Fernando Ferreira Costa; Maria de Fátima Sonati; Tereza Maria Dantas de Medeiros
Journal:  Genet Mol Biol       Date:  2012-07-26       Impact factor: 1.771

3.  Inherited hemoglobin disorders in an Afro-Amazonian community: Saracura.

Authors:  Greice Lemos Cardoso; Silvania Yukiko Lins Takanashi; João Farias Guerreiro
Journal:  Genet Mol Biol       Date:  2012-07-05       Impact factor: 1.771

4.  Prevalence of common α-thalassemia determinants in south Brazil: Importance for the diagnosis of microcytic anemia.

Authors:  Sandrine C Wagner; Simone M de Castro; Tatiana P Gonzalez; Ana P Santin; Leticia Filippon; Carina F Zaleski; Laura A Azevedo; Bruna Amorin; Sidia M Callegari-Jacques; Mara H Hutz
Journal:  Genet Mol Biol       Date:  2010-12-01       Impact factor: 1.771

5.  Response to the assessment of the Matos & Carvalho index by Hoffmann and Urrechaga.

Authors:  Januária F Matos; Luci M S Dusse; Karina B G Borges; Ricardo L V de Castro; Wendel Coura-Vital; Maria das G Carvalho
Journal:  Rev Bras Hematol Hemoter       Date:  2017-05-10

6.  Sickle cell disease: acute clinical manifestations in early childhood and molecular characteristics in a group of children in Rio de Janeiro.

Authors:  Isaac Lima da Silva Filho; Georgina Severo Ribeiro; Patrícia Gomes Moura; Monica Longo Vechi; Andréa Cony Cavalcante; Maria José de Andrada-Serpa
Journal:  Rev Bras Hematol Hemoter       Date:  2012

7.  Interaction between Hb SS and alpha thalassemia (3.7 kb deletion): a familial study.

Authors:  Eliana Litsuko Tomimatsu Shimauti; Paula Juliana Antoniato Zamaro; Claudia Regina Bonini-Domingos
Journal:  Rev Bras Hematol Hemoter       Date:  2011

8.  Molecular analysis and association with clinical and laboratory manifestations in children with sickle cell anemia.

Authors:  Roberta Faria Camilo-Araújo; Olga Maria Silverio Amancio; Maria Stella Figueiredo; Ana Carolina Cabanãs-Pedro; Josefina Aparecida Pellegrini Braga
Journal:  Rev Bras Hematol Hemoter       Date:  2014-07-09

9.  Prevalence of β(S)-globin gene haplotypes, α-thalassemia (3.7 kb deletion) and redox status in patients with sickle cell anemia in the state of Paraná, Brazil.

Authors:  Eliana LitsukoTomimatsu Shimauti; Danilo Grunig Humberto Silva; Eniuce Menezes de Souza; Eduardo Alves de Almeida; Francismar Prestes Leal; Claudia Regina Bonini-Domingos
Journal:  Genet Mol Biol       Date:  2015-08-21       Impact factor: 1.771

10.  Rare α0-thalassemia deletions detected by MLPA in five unrelated Brazilian patients.

Authors:  Natália O Mota; Elza M Kimura; Roberta D Ferreira; Gisele A Pedroso; Dulcinéia M Albuquerque; Daniela M Ribeiro; Magnun N N Santos; Cristina M Bittar; Fernando F Costa; Maria de Fatima Sonati
Journal:  Genet Mol Biol       Date:  2017-10-02       Impact factor: 1.771
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.