Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Albertina Nunes"'
Autor:
Ana Carolina Freitas, Tiago Maia, Joana Desterro, Francesca Pierdomenico, Albertina Nunes, Isabelina Ferreira, José Cabeçadas, Maria Gomes da Silva
Publikováno v:
Hematology Reports, Vol 15, Iss 1, Pp 212-219 (2023)
Myelodysplastic/myeloproliferative neoplasms (MDS/MPN) are not a single disease, but rather a heterogenous group of entities which are increasingly subclassified according to recurrent genetic abnormalities. Chromosomal translocations involving menin
Externí odkaz:
https://doaj.org/article/88f00ab111be4926932753d62d05f78c
Autor:
Luís Landeiro, Tiago Neto Gonçalves, Margarida Proença, Albertina Nunes, Alexandra Bayão Horta
Publikováno v:
European Journal of Case Reports in Internal Medicine (2022)
A myeloid sarcoma is an extramedullary tumour arising from infiltration by leukemic cells at an anatomic site other than the bone marrow. Most commonly it precedes acute myeloid leukaemia but occasionally occurs simultaneously. It may also be associa
Externí odkaz:
https://doaj.org/article/4010b6e3ba7d470f8de3e0096fb97ef2
Autor:
Luís Landeiro, Ana Carolina Freitas, Margarida Proença, José Cabeçadas, Albertina Nunes, Alexandra Bayão Horta
Publikováno v:
European Journal of Case Reports in Internal Medicine (2021)
Multicentric Castleman disease (MCD) represents a group of poorly understood lymphoproliferative disorders related to proinflammatory hypercytokinaemia. In immunocompetent patients its etiology is still unknown, hence the designation of idiopathic mu
Externí odkaz:
https://doaj.org/article/89eee749381647aea23497852fc5c0d2
Autor:
Filipa Moita, Isabel Bogalho, Helena Alaiz, Joana Parreira, Maria Jesus Frade, Albertina Nunes, Maria Gomes da Silva
Publikováno v:
Case Reports in Hematology, Vol 2013 (2013)
Hypereosinophilia, either clonal or reactive, has been described in association with multiple hematological malignancies. We describe a case of a patient presenting with hypereosinophilia that evolved into T-cell lymphoblastic lymphoma. Complete remi
Externí odkaz:
https://doaj.org/article/da6f4c4b1bd048a7941849d6a0e4cfb1
Autor:
Sónia Matos, Paulo Bernardo, Susana Esteves, Aida Botelho de Sousa, Marcos Lemos, Patrícia Ribeiro, Madalena Silva, Albertina Nunes, Joana Lobato, Maria de Jesus Frade, Maria Gomes da Silva, Sérgio Chacim, José Mariz, Graça Esteves, João Raposo, Ana Espadana, José Carda, Pedro Barbosa, Vânia Martins, Maria Carmo-Fonseca, Joana Desterro
Publikováno v:
Cancers; Volume 14; Issue 13; Pages: 3236
Although mutation profiling of defined genes is recommended for classification of acute myeloid leukemia (AML) patients, screening of targeted gene panels using next-generation sequencing (NGS) is not always routinely used as standard of care. The ob
Autor:
José Cabeçadas, Luís Landeiro, Alexandra Bayão Horta, Margarida Proença, Albertina Nunes, Ana Carolina Freitas
Publikováno v:
Eur J Case Rep Intern Med
European Journal of Case Reports in Internal Medicine (2021)
European Journal of Case Reports in Internal Medicine (2021)
Multicentric Castleman disease (MCD) represents a group of poorly understood lymphoproliferative disorders related to proinflammatory hypercytokinaemia. In immunocompetent patients the aetiology is still unknown, hence the designation of idiopathic M
Autor:
Marcus Hentrich, Jordi Esteve, Matteo G. Della Porta, Mar Tormo, Sigrid Machherndl-Spandl, Ana Garrido, Sonia Matos, Annika Dufour, Olga Salamero, Jorge Sierra, Marta Pratcorona, Lisa Pleyer, Federico Lussana, Maria Carmo-Fonseca, Francesco Passamonti, Paola Fazi, Albertina Nunes, Sonja Heibl, Susana Vives, Christoph Sippel, Nicola Stefano Fracchiolla, Alfonso Piciocchi, Joana M. P. Desterro, Montserrat Arnan, Pamela Acha, Erica Travaglino, Aida Botelho de Sousa, Friedrich Stölzel, Maria Teresa Voso, Giulia Maggioni, Christian Thiede, Claudia Basilico, Cristina Astrid Tentori, Francesc Solé, Karsten Spiekermann, Marcos Lemos, Klaus H. Metzeler, Elisabetta Todisco, Bernhard Heilmeier, Jan Moritz Middeke, Marina Diaz, Valentina Mancini, David Gallardo
Publikováno v:
Blood. 136:30-31
Introduction. Mutations in genes encoding the metabolic enzymes isocitrate dehydrogenase (IDH) 1 and 2 are found in 10-20% of patients with acute myeloid leukemia (AML). Recently, IDH inhibitors have shown good clinical response in patient's refracto
Publikováno v:
Annals of Oncology. 31:S652
Publikováno v:
Gastroenterology. 154:S12