Faustino P - Search Results

1

Non-classical hereditary hemochromatosis in Portugal: novel mutations identified in iron metabolism-related genes.

Mendes AI, Ferro A, Martins R, Picanço I, Gomes S, Cerqueira R, Correia M, Nunes AR, Esteves J, Fleming R, Faustino P. Mendes AI, et al. Among authors: faustino p. Ann Hematol. 2009 Mar;88(3):229-34. doi: 10.1007/s00277-008-0572-y. Epub 2008 Sep 2. Ann Hematol. 2009. PMID: 18762941

2

Importation route of the sickle cell trait into Portugal: contribution of molecular epidemiology.

Lavinha J, Gonçalves J, Faustino P, Romão L, Osório-Almeida L, Peres MJ, Picanço I, Martins MC, Ducrocq R, Labie D, et al. Lavinha J, et al. Among authors: faustino p. Hum Biol. 1992 Dec;64(6):891-901. Hum Biol. 1992. PMID: 1427745

3

Asymptomatic homozygous deletional beta(0)-thalassemia in an African individual.

Faustino P, Reis AB, Feliciano H, Ferrão L, Pereira P, Picanço I, Miranda A, Seixas T, Romão L, Júnior EC, Lavinha J. Faustino P, et al. Am J Hematol. 2002 Jul;70(3):232-6. doi: 10.1002/ajh.10118. Am J Hematol. 2002. PMID: 12111769 Free article.

4

Compound heterozygosity for Hb Spanish town [alpha27(B8)Glu-->Val], Hb S [beta6(A3)Glu-->Val] and the -alpha(3.7kb) thalassemia deletion.

Faustino P, Picanço I, Miranda A, Seixas T, Ferrão A, Morais A, Lavinha J, Romão L. Faustino P, et al. Hemoglobin. 2002 May;26(2):185-9. doi: 10.1081/hem-120005458. Hemoglobin. 2002. PMID: 12144063 No abstract available.

5

Genetic studies suggest a novel Portuguese origin for hemoglobin Porto Alegre.

Faustino P, Miranda A, Picanço I, Kimura EM, Ferreira Costa F, de Fátima Sonati M. Faustino P, et al. Haematologica. 2004 Aug;89(8):1009-10. Haematologica. 2004. PMID: 15339686

6

Hb Yaoundé [beta134(H12)Val-->Ala] in association with Hb C [beta6(A3)Glu-->Lys] in a Caucasian Portuguese family.

Faustino P, Miranda A, do Céu Silva M, Alves C, Picanço I, Ferreira C, Seixas MT, Pina F, Romão L. Faustino P, et al. Hemoglobin. 2004 Aug;28(3):229-35. doi: 10.1081/hem-120040259. Hemoglobin. 2004. PMID: 15481891

7

The role of HFE mutations on iron metabolism in beta-thalassemia carriers.

Martins R, Picanço I, Fonseca A, Ferreira L, Rodrigues O, Coelho M, Seixas T, Miranda A, Nunes B, Costa L, Romão L, Faustino P. Martins R, et al. Among authors: faustino p. J Hum Genet. 2004;49(12):651-655. doi: 10.1007/s10038-004-0202-z. Epub 2004 Nov 5. J Hum Genet. 2004. PMID: 15538648

8

HFE gene mutations are extremely rare in Western sub-Saharan Africa.

Martins R, Picanço I, Nunes B, Romão L, Faustino P. Martins R, et al. Among authors: faustino p. Ann Hematol. 2005 Oct;84(10):686-8. doi: 10.1007/s00277-005-1036-2. Epub 2005 Apr 15. Ann Hematol. 2005. PMID: 15834568 No abstract available.

9

Human alpha2-globin nonsense-mediated mRNA decay induced by a novel alpha-thalassaemia frameshift mutation at codon 22.

Pereira FJ, do Céu Silva M, Picanço I, Seixas MT, Ferrão A, Faustino P, Romão L. Pereira FJ, et al. Among authors: faustino p. Br J Haematol. 2006 Apr;133(1):98-102. doi: 10.1111/j.1365-2141.2006.05971.x. Br J Haematol. 2006. PMID: 16512835 Free article.

10

Hemoglobin Loves Park [beta68 (E12) Leu-->Phe]: report of five cases including one originating from a de novo mutation.

Ferreira C, Hoyer JD, Miranda A, Picanço I, Almendra V, Seixas MT, Almeida T, Romão L, Faustino P. Ferreira C, et al. Among authors: faustino p. Am J Hematol. 2006 Apr;81(4):256-61. doi: 10.1002/ajh.20548. Am J Hematol. 2006. PMID: 16550507 Free article.

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