Faustino P - Search Results

1

Prevalence Rate of Thalassemia Carriers among Individuals with Microcytosis or Hypochromia in Portugal.

Santos D, Barreto M, Kislaya I, Mendonça J, P Machado M, Lopes P, Matias Dias C, Faustino P. Santos D, et al. Among authors: p machado m, faustino p. Acta Med Port. 2023 Jul 3;36(7-8):467-474. doi: 10.20344/amp.19162. Epub 2023 Mar 10. Acta Med Port. 2023. PMID: 36898140 Free article.

2

An African origin for an "American black" beta zero-thalassemia mutation?

Gonçalves J, Faustino P, Lavinha J, Rosado L, Peres MJ, Martins MC. Gonçalves J, et al. Among authors: faustino p. Am J Hematol. 1994 Aug;46(4):373-4. doi: 10.1002/ajh.2830460425. Am J Hematol. 1994. PMID: 8037197 No abstract available.

3

Sickle cell disease severity scoring: a yet unsolved problem.

Coelho A, Dias A, Morais A, Nunes B, Faustino P, Lavinha J. Coelho A, et al. Among authors: faustino p. Eur J Haematol. 2012 Dec;89(6):501-2. doi: 10.1111/ejh.12011. Epub 2012 Oct 26. Eur J Haematol. 2012. PMID: 22938536 No abstract available.

4

Epidemiology of haemoglobin disorders in Europe: an overview.

Modell B, Darlison M, Birgens H, Cario H, Faustino P, Giordano PC, Gulbis B, Hopmeier P, Lena-Russo D, Romao L, Theodorsson E. Modell B, et al. Among authors: faustino p. Scand J Clin Lab Invest. 2007;67(1):39-69. doi: 10.1080/00365510601046557. Scand J Clin Lab Invest. 2007. PMID: 17365984 Review.

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

The hepcidin gene promoter nc.-1010C > T; -582A > G haplotype modulates serum ferritin in individuals carrying the common H63D mutation in HFE gene.

Silva B, Pita L, Gomes S, Gonçalves J, Faustino P. Silva B, et al. Among authors: faustino p. Ann Hematol. 2014 Dec;93(12):2063-6. doi: 10.1007/s00277-014-2160-7. Ann Hematol. 2014. PMID: 25015054

7

beta-Thalassemia mutation at -90C-->T impairs the interaction of the proximal CACCC box with both erythroid and nonerythroid factors.

Faustino P, Lavinha J, Marini MG, Moi P. Faustino P, et al. Blood. 1996 Oct 15;88(8):3248-9. Blood. 1996. PMID: 8874232 Free article. No abstract available.

8

[The molecular basis of dominantly inherited beta-thalassemia].

Faustino P, Barbot J, Gonçalves J, Peres MJ, Lavinha J. Faustino P, et al. Acta Med Port. 1999 Jul-Nov;12(7-11):293-6. Acta Med Port. 1999. PMID: 10707468 Free article. Portuguese.

9

Genetic modulators of fetal hemoglobin expression and ischemic stroke occurrence in African descendant children with sickle cell anemia.

Nicolau M, Vargas S, Silva M, Coelho A, Ferreira E, Mendonça J, Vieira L, Kjöllerström P, Maia R, Silva R, Dias A, Ferreira T, Morais A, Soares IM, Lavinha J, Faustino P. Nicolau M, et al. Among authors: faustino p. Ann Hematol. 2019 Dec;98(12):2673-2681. doi: 10.1007/s00277-019-03783-y. Epub 2019 Sep 2. Ann Hematol. 2019. PMID: 31478061 Clinical Trial.

10

Biomarkers and genetic modulators of cerebral vasculopathy in sub-Saharan ancestry children with sickle cell anemia.

Silva M, Vargas S, Coelho A, Ferreira E, Mendonça J, Vieira L, Maia R, Dias A, Ferreira T, Morais A, Soares IM, Lavinha J, Silva R, Kjöllerström P, Faustino P. Silva M, et al. Among authors: faustino p. Blood Cells Mol Dis. 2020 Jul;83:102436. doi: 10.1016/j.bcmd.2020.102436. Epub 2020 Apr 13. Blood Cells Mol Dis. 2020. PMID: 32434137

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