Search Results - "Justica, Benvindo"

Clinicobiological, Immunophenotypic, and Molecular Characteristics of Monoclonal CD56 −/+dim Chronic Natural Killer Cell Large Granular Lymphocytosis by Lima, Margarida, Almeida, Julia, Montero, Andrés García, Teixeira, Maria dos Anjos, Queirós, Maria Luís, Santos, Ana Helena, Balanzategui, Ana, Estevinho, Alexandra, Algueró, Maria del Cármen, Barcena, Paloma, Fonseca, Sónia, Amorim, Maria Luís, Cabeda, José Manuel, Pinho, Luciana, Gonzalez, Marcos, Miguel, Jesus San, Justiça, Benvindo, Orfão, Alberto

“…Indolent natural killer (NK) cell lymphoproliferative disorders include a heterogeneous group of patients in whom persistent expansions of mature, typically…”
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Clinical and genetic heterogeneity in hereditary haemochromatosis: association between lymphocyte counts and expression of iron overload by Porto, Graça, Cardoso, Carla S., Gordeuk, Victor, Cruz, Eugénia, Fraga, José, Areias, Jorge, Oliveira, José Carlos, Bravo, Fernanda, Gangaidzo, Innocent T., MacPhail, A.P., Gomo, Zvenyika A.R., Moyo, Victor M., Melo, Graça, Silva, Cidália, Justiça, Benvindo, De Sousa, Maria

“…: To identify a new marker of expression of disease, independent of HFE genotype in patients with hereditary haemochromatosis (HHC), the total peripheral blood…”
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TCRαβ+/CD4+ large granular lymphocytosis: A new clonal T-cell lymphoproliferative disorder by LIMA, Margarida, ALMEIDA, Julia, BUENO, Clara, JUSTICA, Benvindo, GONZALEZ, Marcos, SAN MIGUEL, Jesus F, ORFAO, Alberto, TEIXEIRA, Maria Dos, ALGUERO, Maria Del, SANTOS, Ana Helena, BALANZATEGUI, Ana, QUEIROS, Maria Luis, BARCENA, Paloma, IZARRA, Antonio, FONSECA, Sonia

“…Large granular lymphocyte (LGL) leukemia is a well-recognized disease of mature T-CD8 + or less frequently natural killer cells; in contrast, monoclonal…”
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Guess what: Chronic 13q14.3+/CD5−/CD23+ lymphocytic leukemia in blood and t(11;14)(q13;q32)+/CD5+/CD23− mantle cell lymphoma in lymph nodes by Lima, Margarida, Pinto, Luísa, Dos Anjos Teixeira, Maria, Canelhas, Áurea, Mota, Alexandra, Cabeda, José Manuel, Silva, Cidália, Queirós, Maria Luís, Fonseca, Sónia, Santos, Ana Helena, Brochado, Paulo, Justiça, Benvindo

“…We report a case of a patient with two B‐cell lymphoproliferative disorders: CD5−/CD23+ B‐cell chronic lymphocytic leukemia and CD5+/CD23− mantle cell…”
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Immunophenotypic analysis of the TCR-Vβ repertoire in 98 persistent expansions of CD3+/TCR-αβ+ large granular lymphocytes : Utility in assessing clonality and insights into the pathogenesis of the disease by LIMA, Margarida, ALMEIDA, Julia, ORFAO, Alberto, SANTOS, Ana Helena, DOS ANJOS TEIXEIRA, Maria, DEL CARMEN ALGUERO, Maria, QUEIROS, Maria Luis, BALANZATEGUI, Ana, JUSTICA, Benvindo, GONZALEZ, Marcos, SAN MIGUEL, Jesus F

“…At present, a major challenge in the initial diagnosis of leukemia of large granular lymphocytes (LGLs) is to establish the clonal nature of the expanded…”
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Unexpected pattern of β‐globin mutations in β‐thalassaemia patients from northern Portugal by Cabeda, José M., Correia, Cristina, Estevinho, Alexandra, Simões, Carla, Amorim, Maria Luis, Pinho, Luciana, JustiçA, Benvindo

“…We characterized the genetic nature of β‐thalassaemia in northern Portugal. Of the 164 patients studied three were β‐thalassaemia major cases (one IVS‐1‐6/β°39…”
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The “ex Vivo” Patterns of CD2/CD7, CD57/CD11c, CD38/CD11b, CD45RA/CD45RO, and CD11a/HLA-DR Expression Identify Acute/Early and Chronic/Late NK-Cell Activation States by Lima, Margarida, Almeida, Julia, dos Anjos Teixeira, Maria, Queirós, Maria Luı́s, Justiça, Benvindo, Orfão, Alberto

“…ABSTRACT To define a dynamic sequence of phenotypic changes related to early and late phases of NK-cell activation, we have analyzed by four-color flow…”
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Major histocompatibility complex class I associations in iron overload: evidence for a new link between the HFE H63D mutation, HLA-A29, and non-classical forms of hemochromatosis by Porto, G, Alves, H, Rodrigues, P, Cabeda, J M, Portal, C, Ruivo, A, Justiça, B, Wolff, R, De Sousa, M

“…The present study is an analysis of the frequencies of HFE mutations in patients with different forms of iron overload compared with the frequencies found in…”
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Expansions of CD8+CD28- and CD8+TcRVβ5.2+ T cells in peripheral blood of heavy alcohol drinkers by AROSA, Fernando A, PORTO, Graca, BRAVO, Fernanda, OLIVEIRA, José Carlos, ALVES, Helena, FRAGA, José, JUSTICA, Benvindo, DE SOUSA, Maria, CABEDA, Josh Manuel, LACERDA, Rosa, RESENDE, Dolores, CRUZ, Eugenia, CARDOSO, Carla, FONSECA, Mafalda, SIMOES, Carla, RODRIGUES, Pedro

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Utility of flow cytometry immunophenotyping and DNA ploidy studies for diagnosis and characterization of blood involvement in CD4+ Sezary's syndrome by Lima, M, Almeida, J, dos Anjos Teixeira, M, Queiros, ML, Santos, AH, Fonseca, S, Balanzategui, A, Justica, B, Orfao, A

“…Servico de Hematologia, Unidade de Citometria, Hospital Geral de Santo Antonio, Rua D Manuel II, s/n, 4099-001 Porto, Portugal. mmc.lima@clix.pt BACKGROUND AND…”
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Dominantly transmitted β-thalassemia arising from the production of several aberrant mRNA species and one abnormal peptide by FAUSTINO, P, OSORIO-ALMEIDA, L, ROMAO, L, BARBOT, J, FERNANDES, B, JUSTICA, B, LAVINHA, J

“…We describe a dominantly inherited beta-thalassemia intermedia phenotype observed in a five-generation Portuguese family. Carriers are characterized by…”
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Review of the quality monitoring methods used by countries using or implementing universal leukoreduction by Beckman, Neil, Sher, Graham, Masse, Maurice, Richter, Ekkehard, Ringwald, Juergen, Rebulla, Paolo, van Der Meer, Pieter, Justica, Benvindo, Walker, Brian, Rowe, Graham

“…Several countries are implementing or have implemented universal leukoreduction (ULR). Specifications, leukocyte counting, and monitoring methods were…”
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Mutations in the β3 gene giving rise to type I Glanzmann thrombasthenia in two families in Portugal by Garcia, Loida Corbillon, Breillat, Christelle, Lima, Margarida, Combrié, Robert, Morais, Sara, Teixera, Maria dos Anjos, Campos, Manuel, Justica, Benvindo, Nurden, Alan T.

“…Glazzmann thrombasthenia is an inherited bleeding syndrome in which an absence of platelet aggregation is associated with quantitative or qualitative…”
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Mutations in the beta3 gene giving rise to type I Glanzmann thrombasthenia in two families in Portugal by Garcia, Loida Corbillon, Breillat, Christelle, Lima, Margarida, Combrié, Robert, Morais, Sara, Teixera, Maria dos Anjos, Campos, Manuel, Justica, Benvindo, Nurden, Alan T

“…Glazzmann thrombasthenia is an inherited bleeding syndrome in which an absence of platelet aggregation is associated with quantitative or qualitative…”
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Atopic Dermatitis-Like Non-Erythrodermic Leukemic Variant of CD3 sub(-/+dim) CD4 sub(+) Cutaneous T-Cell Lymphoma Preceded by Cutaneous Papular Xanthomatosis by Lima, Margarida, Velho, Gloria, Alves, Rosario, Cunha, Manuel, Maria dos Anjos Teixeira, Canelhas, Aurea, Almeida, Julia, Sachse, Fernanda, Queiros, Maria Luis, Santos, Ana Helena, Fonseca, Sonia, Goncalves, Vicente, Massa, Antonio, Orfao, Alberto, Benvindo Justica

“…We report a patient with cutaneous papular xanthomatosis who 4 years later developed a CD3 sub(-/+dim)/CD4 sub(+) T-cell lymphoma. Pruritic xerotic non-…”
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Immunophenotypic Analysis of the TCR-V{beta} Repertoire in 98 Persistent Expansions of CD3+/TCR-{alpha}{beta}+ Large Granular Lymphocytes : Utility in Assessing Clonality and Insights into the Pathogenesis of the Disease by Lima, Margarida, Almeida, Julia, Santos, Ana Helena, dos Anjos Teixeira, Maria, del Carmen Alguero, Maria, Queiros, Maria Luis, Balanzategui, Ana, Justica, Benvindo, Gonzalez, Marcos, San Miguel, Jesus F, Orfao, Alberto

“…At present, a major challenge in the initial diagnosis of leukemia of large granular lymphocytes (LGLs) is to establish the clonal nature of the expanded…”
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Unexpected pattern of β-globin mutations in β-thalassaemia patients from northern Portugal by CABEDA, J. M, CORREIA, C, ESTEVINBO, A, SIMÖES, C, AMORIM, M. L, PINHO, L, JUSTICA, B

“…We characterized the genetic nature of beta-thalassaemia in northern Portugal. Of the 164 patients studied three were beta-thalassaemia major cases (one…”
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TCR{alpha}{beta}+/CD4+ Large Granular Lymphocytosis: A New Clonal T-Cell Lymphoproliferative Disorder by Lima, Margarida, Almeida, Julia, dos Anjos Teixeira, Maria, Alguero, Maria del Carmen, Santos, Ana Helena, Balanzategui, Ana, Queiros, Maria Luis, Barcena, Paloma, Izarra, Antonio, Fonseca, Sonia, Bueno, Clara, Justica, Benvindo, Gonzalez, Marcos, San Miguel, Jesus F, Orfao, Alberto

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Immunophenotype and TCR-Vβ repertoire of peripheral blood T-cells in acute infectious mononucleosis by Lima, Margarida, Teixeira, Maria dos Anjos, Queirós, Maria L.uís, Santos, Ana Helena, Gonçalves, Cristina, Correia, J.oão, Farinha, F.átima, Mendonça, Fernanda, Soares, José Manuel Neves, Almeida, J.úlia, Orfão, Alberto, Justiça, Benvindo

“…Although a number of studies on the phenotypic changes that occur after T-cell activation have already been published, the specific immunophenotypic features…”
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Relative impact of HLA phenotype and CD4-CD8 ratios on the clinical expression of hemochromatosis by Porto, G, Vicente, C, Teixeira, MA, Martins, O, Cabeda, JM, Lacerda, R, Gonçalves, C, Fraga, J, Macedo, G, Silva, BM, Alves, H, Justiça, B, de Sousa, M

“…Hemochromatosis is a hereditary iron-overload disease linked to HLA. The clinical expression of hemochromatosis is influenced by sex and age. However, other…”
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