Zobrazeno 1 - 10
of 178
pro vyhledávání: '"Ângelo Martins"'
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
Introduction and aimsRichter syndrome (RS) represents the clonal evolution of chronic lymphocytic leukemia with histological transformation into a high-grade B cell lymphoma (diffuse large B cell lymphoma - DLBCL) or Hodgkin lymphoma. Considering tha
Externí odkaz:
https://doaj.org/article/40da544e0c0f49a999763b87c0926627
Publikováno v:
HemaSphere, Vol 7, p e7469294 (2023)
Externí odkaz:
https://doaj.org/article/0c0e6c0ee7ea4a80acd07eff0b6dfd88
Autor:
Ana Maria Meireles, Leonardo Moço, Catarina Campos Costa, Dulcineia Pereira, Sérgio Chacim, Nelson Domingues, Ana Espírito Santo, Isabel Oliveira, Ângelo Martins, Ilídia Moreira, Luísa Viterbo, Gil Brás, Cláudia Moreira, Mário Mariz
Publikováno v:
HemaSphere, Vol 7, p e81356dd (2023)
Externí odkaz:
https://doaj.org/article/ca480e71bc09443499635b2261538394
Autor:
Mário Sousa-Pimenta, Maria Manuela Estevinho, Miguel Sousa Dias, Ângelo Martins, Letícia M. Estevinho
Publikováno v:
Antioxidants, Vol 12, Iss 4, p 936 (2023)
Mature lymphoid neoplasms arise de novo or by the transformation of more indolent lymphomas in a process that relies on the stepwise accumulation of genomic and transcriptomic alterations. The microenvironment and neoplastic precursor cells are heavi
Externí odkaz:
https://doaj.org/article/5ad144a3ccad46aca1e161991888460d
Autor:
Nuno Cerveira, Bruno Loureiro, Susana Bizarro, Cecília Correia, Lurdes Torres, Susana Lisboa, Joana Vieira, Rui Santos, Dulcineia Pereira, Cláudia Moreira, Sérgio Chacim, Nélson Domingues, Ana Espírito-Santo, Isabel Oliveira, Ilídia Moreira, Luísa Viterbo, Ângelo Martins, Manuel R. Teixeira, José M. Mariz
Publikováno v:
BMC Cancer, Vol 18, Iss 1, Pp 1-10 (2018)
Abstract Background Most patients with chronic myeloid leukemia (CML) treated with tyrosine kinase inhibitors (TKIs) will relapse if treatment is withdrawn, but various trials have recently demonstrated that a significant proportion of patients who a
Externí odkaz:
https://doaj.org/article/844beabb6bfa4c04860691966de11379
Publikováno v:
Serviço Social em Revista, Vol 16, Iss 1, Pp 193-210 (2013)
O objetivo do texto é analisar os discursos e práticas produzidos e voltados aos moradores de rua nas últimas três décadas e o impacto de tais práticas no que tange a mobilidade desses sujeitos nas cidades médias paulista. Partimos da ideia qu
Externí odkaz:
https://doaj.org/article/e10f2c3adfa5419b9f4011b7e9114fd3
Autor:
da Silva, Vanessa Telles, Ribeiro, Lucas de Angelo Martins, de Lemos, Willian Borges, Botelho, Sílvia Silva da Costa, Filho, Nelson Lopes Duarte, Pias, Marcelo Rita
The architecture, engineering and construction (AEC) sector extensively uses documents supporting product and process development. As part of this, organisations should handle big data of hundreds, or even thousands, of technical documents strongly l
Externí odkaz:
http://arxiv.org/abs/2302.08905
Autor:
Jose Manuel Martinez, Luís Leite, Daniela França, Rita Capela, Luísa Viterbo, Natalina Varajão, Ângelo Martins, Isabel Oliveira, Nélson Domingues, Ilídia Moreira, Ana Santo, Filipe Trigo, Jose Mariz
Publikováno v:
Acta Médica Portuguesa, Vol 28, Iss 4 (2015)
Introduction: The objective of the study was to reduce, by a bundle of interventions, the global bloodstream infections and catheterrelated bloodstream infections rates in neutropenic hematology patients with a long-term central venous catheter. Mate
Externí odkaz:
https://doaj.org/article/d7c28446f2984b8699dbe1af7fcdab73
Publikováno v:
Hematology Reports, Vol 6, Iss 4 (2014)
Celiac disease is an autoimmune disorder in which a genetic predisposition and the ingestion of wheat gluten triggers a deleterious immune response. This response is complex and may lead to manifestations other than enteropathyha: hepatitis, dermatit
Externí odkaz:
https://doaj.org/article/75304767478548eb8ca179dba0576247
Publikováno v:
Acta Médica Portuguesa, Vol 27, Iss 6 (2014)
Introdução: A histiocitose de células de Langerhans é uma doença heterogénea e mais frequente em crianças. Entre 1/2001 e 12/2013 admitimos 20 doentes com HCL nas duas instituições. O objectivo deste trabalho foi caracterizar esta populaçã
Externí odkaz:
https://doaj.org/article/24e3d005a25e449085efbe1ef548f1b3