Determining oxidative and non-oxidative genotoxic effects driven by estuarine sediment contaminants on a human hepatoma cell line
Pinto, M., Costa, P.M., Louro, H., Costa, M.H., Lavinha, J., Caeiro, S., Silva, M.J.
Published in The Science of the total environment (15.04.2014)
Published in The Science of the total environment (15.04.2014)
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Human hepatoma cells exposed to estuarine sediment contaminant extracts permitted the differentiation between cytotoxic and pro-mutagenic fractions
PINTO, M, COSTA, P. M, LOURO, H, COSTA, M. H, LAVINHA, J, CAEIRO, S, SILVA, M. J
Published in Environmental pollution (1987) (01.02.2014)
Published in Environmental pollution (1987) (01.02.2014)
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Ethnic heterogeneity of the factor XIII Val34Leu polymorphism
Attié-Castro, F A, Zago, M A, Lavinha, J, Elion, J, Rodriguez-Delfin, L, Guerreiro, J F, Franco, R F
Published in Thrombosis and haemostasis (01.10.2000)
Published in Thrombosis and haemostasis (01.10.2000)
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Swyer Syndrome and 46,XY Partial Gonadal Dysgenesis Associated with 9p Deletions in the Absence of Monosomy-9p Syndrome
Veitia, R.A., Nunes, M., Quintana-Murci, L., Rappaport, R., Thibaud, E., Jaubert, F., Fellous, M., McElreavey, K., Gonçalves, J., Silva, M., Cidade Rodrigues, J., Caspurro, M., Boieiro, F., Marques, R., Lavinha, J.
Published in American journal of human genetics (01.09.1998)
Published in American journal of human genetics (01.09.1998)
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Cystic fibrosis patients with the 3272-26A>G splicing mutation have milder disease than F508del homozygotes: a large European study
Amaral, Margarida D, Pacheco, Paula, Beck, Sebastian, Farinha, Carlos M, Penque, Deborah, Nogueira, Paulo, Barreto, Celeste, Lopes, Beatriz, Casals, Teresa, Dapena, Javier, Gartner, Silvia, Vásquez, Carlos, Pérez-Frías, Javier, Olveira, Casilda, Cabanas, Rodrigo, Estivill, Xavier, Tzetis, Maria, Kanavakis, Emmanuel, Doudounakis, Stavros, Dörk, Thilo, Tümmler, Burkhard, Girodon-Boulandet, Emmanuelle, Cazeneuve, Cécile, Goossens, Michel, Blayau, Martine, Verlingue, Claudine, Vieira, Isabel, Féréc, Claude, Claustres, Mireille, Georges, Marie des, Clavel, Christine, Birembaut, Philippe, Hubert, Dominique, Bienvenu, Thierry, Adoun, Michèle, Chomel, Jean-Claude, De Boeck, Kris, Cuppens, Harry, Lavinha, João
Published in Journal of medical genetics (01.11.2001)
Published in Journal of medical genetics (01.11.2001)
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Molecular genetic analysis of factor XI deficiency: identification of five novel gene alterations and the origin of type II mutation in Portuguese families
Ventura, C, Santos, A I, Tavares, A, Gago, T, Lavinha, J, McVey, J H, David, D
Published in Thrombosis and haemostasis (01.11.2000)
Published in Thrombosis and haemostasis (01.11.2000)
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Long-term follow-up of a family with autosomal dominant polycystic kidney disease type 3
de Almeida, E, Martins Prata, M, de Almeida, S, Lavinha, J
Published in Nephrology, dialysis, transplantation (01.03.1999)
Published in Nephrology, dialysis, transplantation (01.03.1999)
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Iron deficiency anaemia among 6-to-36-month children from northern Angola
Fançony, Cláudia, Soares, Ânia, Lavinha, João, Barros, Henrique, Brito, Miguel
Published in BMC pediatrics (17.06.2020)
Published in BMC pediatrics (17.06.2020)
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Haplotypic heterogeneity of beta-thalassaemia IVS I-1 (G-->A) mutation in southern Portugal
Pacheco, P, Loureiro, P, Faustino, P, Lavinha, J
Published in British journal of haematology (01.09.1996)
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Published in British journal of haematology (01.09.1996)
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Population genetics of IFITM3 in Portugal and Central Africa reveals a potential modifier of influenza severity
David, Susana, Correia, Vanessa, Antunes, Liliana, Faria, Ricardo, Ferrão, José, Faustino, Paula, Nunes, Baltazar, Maltez, Fernando, Lavinha, João, Rebelo de Andrade, Helena
Published in Immunogenetics (New York) (01.03.2018)
Published in Immunogenetics (New York) (01.03.2018)
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Biomarkers and genetic modulators of cerebral vasculopathy in sub-Saharan ancestry children with sickle cell anemia
Silva, Marisa, Vargas, Sofia, Coelho, Andreia, Ferreira, Emanuel, Mendonça, Joana, Vieira, Luís, Maia, Raquel, Dias, Alexandra, Ferreira, Teresa, Morais, Anabela, Soares, Isabel Mota, Lavinha, João, Silva, Rita, Kjöllerström, Paula, Faustino, Paula
Published in Blood cells, molecules, & diseases (01.07.2020)
Published in Blood cells, molecules, & diseases (01.07.2020)
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Variants in the non-coding region of the TLR2 gene associated with infectious subphenotypes in pediatric sickle cell anemia
David, Susana, Aguiar, Pedro, Antunes, Liliana, Dias, Alexandra, Morais, Anabela, Sakuntabhai, Anavaj, Lavinha, João
Published in Immunogenetics (New York) (2018)
Published in Immunogenetics (New York) (2018)
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Anemia in preschool children from Angola: a review of the evidence
Fançony, Cláudia, Lavinha, João, Brito, Miguel, Barros, Henrique
Published in Porto biomedical journal (2020)
Published in Porto biomedical journal (2020)
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Environmental risk assessment in a contaminated estuary: An integrated weight of evidence approach as a decision support tool
Caeiro, S., Vaz-Fernandes, P., Martinho, A.P., Costa, P.M., Silva, M.J., Lavinha, J., Matias-Dias, C., Machado, A., Castanheira, I., Costa, M.H.
Published in Ocean & coastal management (01.07.2017)
Published in Ocean & coastal management (01.07.2017)
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Beta-thalassaemia unlinked to the beta-globin gene interacts with sickle-cell trait in a Portuguese family
Pacheco, P, Peres, M J, Faustino, P, Pischedda, C, Gonçalves, J, Carvajales-Ramos, M, Seixas, T, Martins, M C, Moi, P, Lavinha, J
Published in British journal of haematology (01.09.1995)
Published in British journal of haematology (01.09.1995)
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Missense mutation R1066C in the second transmembrane domain of CFTR causes a severe cystic fibrosis phenotype: Study of 19 heterozygous and 2 homozygous patients
Casals, T, Pacheco, P, Barreto, C, Giménez, J, Ramos, MD, Pereira, S, Pinheiro, JA, Cobos, N, Curvelo, A, Vázquez, C, Rocha, H, Séculi, JL, Pérez, E, Dapena, J, Carrilho, E, Duarte, A, Palacio, AM, Nunes, V, Lavinha, J, Estivill, X
Published in Human mutation (1997)
Published in Human mutation (1997)
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δ-Thalassemia due to a Mutation in an Erythroid-Specific Binding Protein Sequence 3’ to the δ-Globin Gene
Moi, P., Loudianos, G., Lavinha, J., Murru, S., Cossu, P., Casu, R., Oggiano, L., Longinotti, M., Cao, A., Pirastu, M.
Published in Blood (15.01.1992)
Published in Blood (15.01.1992)
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Genetic variation in CD36, HBA, NOS3 and VCAM1 is associated with chronic haemolysis level in sickle cell anaemia: a longitudinal study
Coelho, Andreia, Dias, Alexandra, Morais, Anabela, Nunes, Baltazar, Ferreira, Emanuel, Picanço, Isabel, Faustino, Paula, Lavinha, João
Published in European journal of haematology (01.03.2014)
Published in European journal of haematology (01.03.2014)
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