Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Lénia, Ferrão"'
Autor:
Lénia Ferrão, Maria Lurdes Lopes, Catarina Limbert, Bárbara Marques, Filomena Boieiro, Marisa Silva, Ramira Marques, João Lavinha, Amilcar Mota, João Gonçalves
Publikováno v:
Acta Médica Portuguesa, Vol 15, Iss 2 (2002)
The Turner syndrome (TS) has been described in association with different sex chromosome aberrations. Although most TS patients show no evidence of Y chromosome sequences, according to different authors some TS patients may have Y chromosome material
Externí odkaz:
https://doaj.org/article/c0a5c60c0c8045ed88dac63101c7e92f
Publikováno v:
American Journal of Hematology. 76:163-171
Antithrombin (AT), the most important coagulation serine proteases inhibitor, plays an important role in maintaining the hemostatic balance. Inherited AT deficiency, mainly characterized by predisposition to recurrent venous thromboembolism, is trans
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::79b483486c5739e67b21757c7cd931aa
https://doi.org/10.1002/ajh.20067
https://doi.org/10.1002/ajh.20067
Autor:
Luísa Romão, João Lavinha, Lénia Ferrão, Esmeraldina Correia Júnior, Paula Faustino, Helena Feliciano, Teresa Seixas, Armandina Miranda, Patrícia Pereira, Ana Batalha Reis, Isabel Picanço
Publikováno v:
American Journal of Hematology. 70:232-236
Homozygosity or compound heterozygosity for beta(0)-thalassemia mutations most commonly results in a transfusion-dependent thalassemia major phenotype. In this report, we describe a 55-year-old male, from Guinea-Bissau, that had been asymptomatic and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a606f1d7df88c31e18491b76745ced6b
https://doi.org/10.1002/ajh.10118
https://doi.org/10.1002/ajh.10118
Publikováno v:
Molecular cancer therapeutics. 9(8)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9f11a5f9d9030bf29940dc94788c0ab1
https://pubmed.ncbi.nlm.nih.gov/16093438
https://pubmed.ncbi.nlm.nih.gov/16093438
Autor:
Betsy J. Bricker, Cláudia Almendra, Ana C. Ferreira, Albano Beja-Pereira, Lénia Ferrão-Beck, Teresa Luísa Silva, Maria Inácia Corrêa de Sá, Gordon Luikart
Publikováno v:
Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases. 9(1)
We demonstrate that the ‘‘HOOF-Print’’ assay provides high power to discriminate among Brucella isolates collected on a small spatial scale (within Portugal). Additionally, we illustrate how haplotype identification using non-random associati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11bda1934c8ff6931d0ea5dba8e73192
https://pubmed.ncbi.nlm.nih.gov/19022402
https://pubmed.ncbi.nlm.nih.gov/19022402
Autor:
Maggy Grayon, Ana C. Ferreira, Michel S. Zygmunt, David Albert, Regina Cardoso, Bruno Garin-Bastuji, Clara Marin, Lénia Ferrão-Beck, Maria Inácia Sá, José M. Blasco, Pilar M. Muñoz, María Jesús de Miguel, Martine Thiébaud, Isabelle Jacques
Publikováno v:
Veterinary Microbiology
Veterinary Microbiology, Elsevier, 2006, 115 (1-3), pp.269-277. ⟨10.1016/j.vetmic.2006.02.002⟩
Veterinary Microbiology, Elsevier, 2006, 115 (1-3), pp.269-277. ⟨10.1016/j.vetmic.2006.02.002⟩
International audience; Swine brucellosis is caused by the biovars 1, 2 and 3 of Brucella suis the identification of which up to now relies on microbiological tests lacking adequate specificity together with time consuming and expensive molecular pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b97e93e4e4ce5c8e2015bde6b138bf0a
https://hal.inrae.fr/hal-02663371
https://hal.inrae.fr/hal-02663371
Autor:
Lénia, Ferrão, Maria Lurdes, Lopes, Catarina, Limbert, Bárbara, Marques, Filomena, Boieiro, Marisa, Silva, Ramira, Marques, João, Lavinha, Amilcar, Mota, João, Gonçalves
Publikováno v:
Acta medica portuguesa. 15(2)
The Turner syndrome (TS) has been described in association with different sex chromosome aberrations. Although most TS patients show no evidence of Y chromosome sequences, according to different authors some TS patients may have Y chromosome material
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c5eedf1239172d9d4a83fc36d6175a1b
https://pubmed.ncbi.nlm.nih.gov/15524154
https://pubmed.ncbi.nlm.nih.gov/15524154
Publikováno v:
American journal of hematology. 76(2)
Antithrombin (AT), the most important coagulation serine proteases inhibitor, plays an important role in maintaining the hemostatic balance. Inherited AT deficiency, mainly characterized by predisposition to recurrent venous thromboembolism, is trans
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7058684402caac608e934a42ebcb679f
https://pubmed.ncbi.nlm.nih.gov/15164384
https://pubmed.ncbi.nlm.nih.gov/15164384
Autor:
Paula, Faustino, Ana Batalha, Reis, Helena, Feliciano, Lénia, Ferrão, Patrícia, Pereira, Isabel, Picanço, Armandina, Miranda, Teresa, Seixas, Luísa, Romão, Esmeraldina Correia, Júnior, João, Lavinha
Publikováno v:
American journal of hematology. 70(3)
Homozygosity or compound heterozygosity for beta(0)-thalassemia mutations most commonly results in a transfusion-dependent thalassemia major phenotype. In this report, we describe a 55-year-old male, from Guinea-Bissau, that had been asymptomatic and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::beb6b11202f11c3b8d981e1be429d6b5
https://pubmed.ncbi.nlm.nih.gov/12111769
https://pubmed.ncbi.nlm.nih.gov/12111769
Publikováno v:
Molecular Cancer Therapeutics. 9:2856-2856
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8b4fc58dd44e27bf4f6f7d600e9c51d5
https://doi.org/10.1158/1535-7163.mct-10-0843
https://doi.org/10.1158/1535-7163.mct-10-0843