Bento C - Search Results

1

The use of capillary blood samples in a large scale screening approach for the detection of beta-thalassemia and hemoglobin variants.

Bento C, Relvas L, Vazão H, Campos J, Rebelo U, Ribeiro ML. Bento C, et al. Haematologica. 2006 Nov;91(11):1565. Haematologica. 2006. PMID: 17082015

2

Genetic heterogeneity of beta-thalassemia in populations of the Iberian Peninsula.

Ribeiro ML, Gonçalves P, Cunha E, Bento C, Almeida H, Pereira J, Núñez GM, Tamagnini GP. Ribeiro ML, et al. Among authors: bento c. Hemoglobin. 1997 May;21(3):261-9. doi: 10.3109/03630269708997387. Hemoglobin. 1997. PMID: 9140722 No abstract available.

3

Consequences at mRNA level of the PKLR gene splicing mutations IVS10(+1)G-->C and IVS8(+2)T-->G causing pyruvate kinase deficiency.

Manco L, Bento C, Ribeiro ML, Tamagnini G. Manco L, et al. Among authors: bento c. Br J Haematol. 2002 Sep;118(3):927-8. Br J Haematol. 2002. PMID: 12181074 Free article. No abstract available.

4

Chronic haemolytic anaemia because of pyruvate kinase (PK) deficiency in a child heterozygous for haemoglobin S and no clinical features of sickle cell disease.

Manco L, Vagace JM, Relvas L, Rebelo U, Bento C, Villegas A, Letícia Ribeiro M. Manco L, et al. Among authors: bento c. Eur J Haematol. 2010 Jan 1;84(1):89-90. doi: 10.1111/j.1600-0609.2009.01353.x. Epub 2009 Sep 16. Eur J Haematol. 2010. PMID: 19758413 Review. No abstract available.

5

Chronic hemolytic anemia is associated with a new glucose-6-phosphate dehydrogenase in-frame deletion in an older woman.

Manco L, Pereira J, Relvas L, Rebelo U, Crisóstomo AI, Bento C, Ribeiro ML. Manco L, et al. Among authors: bento c. Blood Cells Mol Dis. 2011 Apr 15;46(4):288-93. doi: 10.1016/j.bcmd.2011.02.001. Epub 2011 Mar 11. Blood Cells Mol Dis. 2011. PMID: 21397531

6

High prevalence of hemoglobin disorders and glucose-6-phosphate dehydrogenase (G6PD) deficiency in the Republic of Guinea (West Africa).

Millimono TS, Loua KM, Rath SL, Relvas L, Bento C, Diakite M, Jarvis M, Daries N, Ribeiro LM, Manco L, Kaeda JS. Millimono TS, et al. Among authors: bento c. Hemoglobin. 2012;36(1):25-37. doi: 10.3109/03630269.2011.600491. Epub 2011 Sep 19. Hemoglobin. 2012. PMID: 21929367

7

β Thalassemia major due to acquired uniparental disomy in a previously healthy adolescent.

Bento C, Maia TM, Milosevic JD, Carreira IM, Kralovics R, Ribeiro ML. Bento C, et al. Haematologica. 2013 Jan;98(1):e4-6. doi: 10.3324/haematol.2012.064097. Epub 2012 Aug 8. Haematologica. 2013. PMID: 22875618 Free PMC article. No abstract available.

8

Transient neonatal cyanosis associated with a new Hb F variant: Hb F viseu.

Bento C, Magalhães Maia T, Carvalhais I, Moita F, Abreu G, Relvas L, Pereira A, Farela Neves J, Ribeiro ML. Bento C, et al. J Pediatr Hematol Oncol. 2013 Mar;35(2):e77-80. doi: 10.1097/MPH.0b013e3182667be3. J Pediatr Hematol Oncol. 2013. PMID: 22935660

9

Hb Iberia [α104(G11)Cys → Arg,TGC>CGC (α2) (HBA2:c.313T>C)], a new α-thalassemic hemoglobin variant found in the Iberian Peninsula: report of six cases.

Bento C, Oliveira AC, Neves J, Gameiro M, Cunha E, Coucelo M, Costa RM, Barbot J, Costa E, Fernández-Lago C, Ribeiro ML. Bento C, et al. Hemoglobin. 2012;36(6):517-25. doi: 10.3109/03630269.2012.742911. Hemoglobin. 2012. PMID: 23181747

10

Hb Plasencia [α125(H8)Leu→Arg (α2)] is a frequent cause of α+-thalassemia in the Portuguese population.

Cunha E, Bento C, Oliveira A, Relvas L, Neves J, Gameiro M, Barros C, Araújo A, Macedo A, Rocha P, Costa R, Maia T, Ribeiro ML. Cunha E, et al. Among authors: bento c. Hemoglobin. 2013;37(2):183-7. doi: 10.3109/03630269.2013.763822. Epub 2013 Jan 31. Hemoglobin. 2013. PMID: 23368878 Free article.

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