Zobrazeno 1 - 10
of 77
pro vyhledávání: '"M. Spyropoulou-Vlachou"'
Minimal residual disease (MRD) was monitored in 52 patients with sustained CR (≥2 years) after frontline therapy using next-generation flow (NGF) cytometry. 25% of patients initially MRD- reversed to MRD+. 56% of patients in sustained CR were MRD+;
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::83d36b15edaf4f5826a88cd466373c48
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3105362
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3105362
Autor:
C. Papasteriades, Dário Ligeiro, Jean-Marie Tiercy, Jose Manuel Nunes, A. Tordai, B. Vidan-Jeras, Alicia Sanchez-Mazas, M. Spyropoulou-Vlachou, M. Ivanova, Francesca Poli, Marte K. Viken, Valérie Dubois, Marja-Liisa Lokki, S. Wenda, Zorana Grubic, Stéphane Buhler, Taina Jaatinen
Publikováno v:
Tissue Antigens
Tissue Antigens, Vol. 84 (2014) pp. 459-464
Tissue Antigens, Vol. 84 (2014) pp. 459-464
Within the framework of the EU-funded HLA-NET action, an analysis of three G-group alleles, HLA-B*44:02:01G, DRB1*14:01:01G and DQB1*03:01:01G, was undertaken in 12 European populations. Ambiguities were resolved by polymerase chain reaction-sequence
Autor:
M. Spyropoulou-Vlachou, A. Dinou, F. Dempegioti, M. Varla-Leftherioti, P. LeBouteiller, Theodora Keramitsoglou
Publikováno v:
Advances in Neuroimmune Biology. 2:99-103
In the frame of EMBIC study, maternal KIR and trophoblastic HLA-C matching was estimated in 39 randomly selected cases of women who were undergoing vacuum uterine curettage for therapeutic termination of first trimester missed pregnancy (Group A = 19
Akademický článek
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Akademický článek
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Autor:
N. Kanellias, Meletios A. Dimopoulos, Lia A. Moulopoulos, Anna Tasidou, Magdalini Migkou, Maria Gavriatopoulou, M Spyropoulou-Vlachou, Maria Roussou, E. Terpos, Efstathios Kastritis, Evangelos Eleftherakis-Papaiakovou, Maria Gkotzamanidou
Publikováno v:
Leukemia. 27(4)
Asymptomatic multiple myeloma (AMM) is characterized by a constant risk of progression to symptomatic myeloma. To evaluate previously recognized risk factors and to identify high-risk features we analyzed 96 patients with AMM and at least 18 months o
Autor:
E. Terpos, Despoina Mparmparoussi, Maria Roussou, M Spyropoulou-Vlachou, Meletios A. Dimopoulos, Maria Gkotzamanidou, Charis Matsouka, Nikitas Nikitas, Erasmia Psimenou, Efstathios Kastritis
Publikováno v:
Leukemia. 27(2)
The role of thalidomide, bortezomib and lenalidomide in multiple myeloma patients presenting with renal impairment was evaluated in 133 consecutive newly diagnosed patients who were treated with a novel agent-based regimen. A significant improvement
Autor:
J.-F. Eliaou, E. Eglite, Denisa Mendonça, U Bekmane, A. Dormoy, G. Sulcebe, Søren Buus, B. Martins da Silva, Zorana Grubic, Francesca Poli, Jose Manuel Nunes, M. L. Lokki, Frans H.J. Claas, A.-M. van Walraven, Maria Eugenia Riccio, M. Ivanova, M. Toungouz Nevessignsky, C. Papasteriades, D. Papioannou Voniatis, Dário Ligeiro, Faviel F. Gonzalez-Galarza, AM Little, Valérie Dubois, Benedicte A. Lie, Alicia Sanchez-Mazas, Jean-Marie Tiercy, Gottfried Fischer, B. Vidan-Jeras, M. Spyropoulou Vlachou, Stéphane Buhler, Christelle Vangenot, Susan Tonks, Derek Middleton, J. Martorell
Publikováno v:
International Journal of Immunogenetics, Vol. 39, No 6 (2012) pp. 459-476
International journal of immunogenetics
International journal of immunogenetics, 39 (6
International Journal of Immunogenetics
International Journal of Immunogenetics, 39(6), 459-476
International journal of immunogenetics
International journal of immunogenetics, 39 (6
International Journal of Immunogenetics
International Journal of Immunogenetics, 39(6), 459-476
HLA-NET (a European COST Action) aims at networking researchers working in bone marrow transplantation, epidemiology and population genetics to improve the molecular characterization of the HLA genetic diversity of human populations, with an expected
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::488e06254bcb48ca274913e129e6a837
https://archive-ouverte.unige.ch/unige:21982
https://archive-ouverte.unige.ch/unige:21982
Autor:
Z T, Karageorgaki, G K, Bertsias, C P, Mavragani, H D, Kritikos, M, Spyropoulou-Vlachou, A A, Drosos, D T, Boumpas, H M, Moutsopoulos
Publikováno v:
Clinical and experimental rheumatology. 27(1 Suppl 52)
Takayasu arteritis (TA) is an uncommon disease with clinical heterogeneity across different ethnic groups. We aimed to evaluate the epidemiological, clinical, and immuno-genetic features of TA in Greece.Demographic, clinical, laboratory, angiographic
Publikováno v:
Journal of Reproductive Immunology. 111:20