Detalhe da pesquisa
1.
Characterization of a cohort of Angolan children with sickle cell anemia treated with hydroxyurea.
Blood Cells Mol Dis
; 105: 102822, 2024 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-38215581
2.
Differential expression of adhesion molecules in sickle cell anemia and gut microbiome effect.
Ann Hematol
; 103(2): 409-419, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38153527
3.
Ancestry of the major long-range regulatory site of the α-globin genes in the Portuguese population with the common 3.7 kb α-thalassemia deletion.
Mol Biol Rep
; 51(1): 612, 2024 May 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-38704770
4.
Are Genetic Modifiers the Answer to Different Responses to Hydroxyurea Treatment?-A Pharmacogenetic Study in Sickle Cell Anemia Angolan Children.
Int J Mol Sci
; 24(10)2023 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-37240136
5.
Microbial gut evaluation in an angolan paediatric population with sickle cell disease.
J Cell Mol Med
; 26(21): 5360-5368, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-36168945
6.
How Hydroxyurea Alters the Gut Microbiome: A Longitudinal Study Involving Angolan Children with Sickle Cell Anemia.
Int J Mol Sci
; 23(16)2022 Aug 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-36012325
7.
Co-Inheritance of alpha-thalassemia and sickle cell disease in a cohort of Angolan pediatric patients.
Mol Biol Rep
; 47(7): 5397-5402, 2020 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-32632780
8.
Widening the spectrum of deletions and molecular mechanisms underlying alpha-thalassemia.
Ann Hematol
; 96(11): 1921-1929, 2017 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-28887661
9.
Genetic Modifiers of Sickle Cell Anemia Phenotype in a Cohort of Angolan Children.
Genes (Basel)
; 15(4)2024 Apr 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-38674403
10.
Genotypic Diversity among Angolan Children with Sickle Cell Anemia.
Int J Environ Res Public Health
; 18(10)2021 05 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-34069401
11.
Hb Evora [alpha2-35 (B16), Ser-->Pro], a novel hemoglobin variant associated with an alpha-thalassemia phenotype.
Haematologica
; 92(2): 252-3, 2007 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-17296578
12.
Genetic studies suggest a novel Portuguese origin for hemoglobin Porto Alegre.
Haematologica
; 89(8): 1009-10, 2004 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-15339686
13.
Mutational spectrum of delta-globin gene in the Portuguese population.
Eur J Haematol
; 79(5): 422-8, 2007 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-17916081
14.
Hemoglobin Loves Park [beta68 (E12) Leu-->Phe]: report of five cases including one originating from a de novo mutation.
Am J Hematol
; 81(4): 256-61, 2006 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-16550507
15.
Clinical and laboratory effects of hydroxyurea in children and adolescents with sickle cell anemia: a Portuguese hospital study.
Hemoglobin
; 29(3): 171-80, 2005.
Artigo
em Inglês
| MEDLINE | ID: mdl-16114180
16.
The role of HFE mutations on iron metabolism in beta-thalassemia carriers.
J Hum Genet
; 49(12): 651-655, 2004.
Artigo
em Inglês
| MEDLINE | ID: mdl-15538648
17.
Hb Yaoundé [beta134(H12)Val-->Ala] in association with Hb C [beta6(A3)Glu-->Lys] in a Caucasian Portuguese family.
Hemoglobin
; 28(3): 229-35, 2004 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-15481891
18.
Asymptomatic homozygous deletional beta(0)-thalassemia in an African individual.
Am J Hematol
; 70(3): 232-6, 2002 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-12111769
19.
Compound heterozygosity for Hb Spanish town [alpha27(B8)Glu-->Val], Hb S [beta6(A3)Glu-->Val] and the -alpha(3.7kb) thalassemia deletion.
Hemoglobin
; 26(2): 185-9, 2002 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-12144063