Lavinha J - Search Results

1

Hb Himeji [alpha 2 beta 2(140)(H18)Ala----Asp] is linked to different haplotypes in Japanese and Portuguese families.

Lavinha J, Faustino P, Osório-Almeida L, Hattori Y, Ohba Y, Martins MC. Lavinha J, et al. Hemoglobin. 1991;15(1-2):137-8. doi: 10.3109/03630269109072496. Hemoglobin. 1991. PMID: 1680833 No abstract available.

2

Molecular basis of alpha-thalassemia in Portugal.

Peres MJ, Romão L, Carreiro H, Picanço I, Batalha L, Magalhães HA, Martins MC, Lavinha J. Peres MJ, et al. Among authors: lavinha j. Hemoglobin. 1995;19(6):343-52. doi: 10.3109/03630269509005826. Hemoglobin. 1995. PMID: 8718693

3

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. Among authors: lavinha j. Hemoglobin. 2002 May;26(2):185-9. doi: 10.1081/hem-120005458. Hemoglobin. 2002. PMID: 12144063 No abstract available.

4

Beta-thalassaemia unlinked to the beta-globin gene interacts with sickle-cell trait in a Portuguese family.

Pacheco P, Peres MJ, Faustino P, Pischedda C, Gonçalves J, Carvajales-Ramos M, Seixas T, Martins MC, Moi P, Lavinha J. Pacheco P, et al. Among authors: lavinha j. Br J Haematol. 1995 Sep;91(1):85-9. doi: 10.1111/j.1365-2141.1995.tb05249.x. Br J Haematol. 1995. PMID: 7577658

5

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

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

6

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. Hum Biol. 1992 Dec;64(6):891-901. Hum Biol. 1992. PMID: 1427745

7

Novel promoter and splice junction defects add to the genetic, clinical or geographic heterogeneity of beta-thalassaemia in the Portuguese population.

Faustino P, Osório-Almeida L, Barbot J, Espírito-Santo D, Gonçalves J, Romão L, Martins MC, Marques MM, Lavinha J. Faustino P, et al. Among authors: lavinha j. Hum Genet. 1992 Jul;89(5):573-6. doi: 10.1007/BF00219188. Hum Genet. 1992. PMID: 1634236

8

Unusual molecular basis of Hb H disease in the Azores Islands, Portugal.

Romão L, Olim G, Martins MC, Rodrigues V, Coutinho-Gomes MP, Lavinha J. Romão L, et al. Among authors: lavinha j. Hemoglobin. 1990;14(6):607-16. doi: 10.3109/03630269009046969. Hemoglobin. 1990. PMID: 2101837

9

A novel rearrangement of the human fetal globin genes leading to a six gamma-globin gene haplotype.

Gonçalves I, Lavinha J, Ducrocq R, Osório-Almeida L. Gonçalves I, et al. Among authors: lavinha j. Br J Haematol. 2002 Feb;116(2):454-7. Br J Haematol. 2002. PMID: 11841451 Free article.

10

A novel mosaic Bantu/Benin/Bantu beta s haplotype found in several African populations.

Gonçalves I, Gonçalves J, Périchon B, Osório-Almeida L, Krishnamoorthy R, Lavinha J. Gonçalves I, et al. Among authors: lavinha j. Hum Genet. 1994 Jul;94(1):101-3. doi: 10.1007/BF02272853. Hum Genet. 1994. PMID: 8034287

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