Literature DB >> 8892732

Human alpha-thalassemia syndromes: detection of molecular defects.

A C Kattamis1, C Camaschella, P Sivera, S Surrey, P Fortina.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1996        PMID： 8892732     DOI： 10.1002/(SICI)1096-8652(199610)53:2<81::AID-AJH5>3.0.CO;2-#

Source DB:  PubMed          Journal:  Am J Hematol        ISSN： 0361-8609            Impact factor:   10.047


× No keyword cloud information.
  10 in total

1.  PCR-based analysis of alpha-thalassemia in Southern Taiwan.

Authors:  Tyen-Po Chen; Ta-Chih Liu; Chao-Sung Chang; Jang-Gowth Chang; Hui-Jen Tsai; Sheng-Fung Lin
Journal:  Int J Hematol       Date:  2002-04       Impact factor: 2.490

Review 2.  Carrier screening and genetic counselling in beta-thalassemia.

Authors:  Antonio Cao
Journal:  Int J Hematol       Date:  2002-08       Impact factor: 2.490

Review 3.  Alpha-thalassaemia.

Authors:  Cornelis L Harteveld; Douglas R Higgs
Journal:  Orphanet J Rare Dis       Date:  2010-05-28       Impact factor: 4.123

4.  CRISPR/Cas9 gene correction of HbH-CS thalassemia-induced pluripotent stem cells.

Authors:  Xie Yingjun; Xie Yuhuan; Chen Yuchang; Li Dongzhi; Wang Ding; Song Bing; Yang Yi; Lu Dian; Xue Yanting; Xiong Zeyu; Liu Nengqing; Chen Diyu; Sun Xiaofang
Journal:  Ann Hematol       Date:  2019-09-09       Impact factor: 3.673

5.  Hb H disease resulting from the association of an α-thalassemia allele [-(α)] with an unstable α-globin variant [Hb Icaria]: First report on the occurrence in Brazil.

Authors:  Elza M Kimura; Denise M Oliveira; Kleber Fertrin; Valéria R Pinheiro; Susan E D C Jorge; Fernando F Costa; Maria de Fátima Sonati
Journal:  Genet Mol Biol       Date:  2009-12-01       Impact factor: 1.771

6.  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

7.  Investigating alpha-globin structural variants: a retrospective review of 135,000 Brazilian individuals.

Authors:  Elza Miyuki Kimura; Denise Madureira Oliveira; Susan Elisabeth Jorge; Daniela Maria Ribeiro; Tânia Regina Zaccariotto; Magnun Nueldo Nunes Santos; Vanessa Almeida; Dulcinéia Martins Albuquerque; Fernando Ferreira Costa; Maria de Fátima Sonati
Journal:  Rev Bras Hematol Hemoter       Date:  2015-01-31

8.  Alpha thalassemia and alpha-MRE haplotypes in Uruguayan patients with microcytosis and hypochromia without anemia.

Authors:  Ana María Soler; Bruna Facanali Piellusch; Lorena da Silveira; Gisele Audrei Pedroso; Pablo López; Enrique Savio; María de Fatima Sonati; Julio da Luz
Journal:  Genet Mol Biol       Date:  2021-03-26       Impact factor: 1.771

9.  Frequency and spectrum of hemoglobinopathy mutations in a Uruguayan pediatric population.

Authors:  Julio Da Luz; Amalia Avila; Sandra Icasuriaga; María Gongóra; Luis Castillo; Alejandra Serrón; Elza Miyuki Kimura; Fernando Ferreira Costa; Mónica Sans; Maria de Fátima Sonati
Journal:  Genet Mol Biol       Date:  2013-07-19       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
  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.