Zobrazeno 1 - 10
of 1 889
pro vyhledávání: '"D. Catovsky"'
Publikováno v:
Annals of Oncology. 26:v100-v107
No abstract available
Autor:
David Torrents, David Martín-García, Renée Beekman, D. Catovsky, J.M. Allan, X.S. Puente, Helen E. Speedy, P.J. Law, Guillem Clot, R.S. Houlston, Vicente Chapaprieta, Montserrat Puiggròs, Jesús Gutiérrez-Abril, C. López-Otín, Sílvia Beà, Elias Campo, Giulia Orlando, José I. Martín-Subero
Publikováno v:
HemaSphere. 3:129
Publikováno v:
Scandinavian Journal of Haematology. 35:343-347
A case of acute leukaemia is described in which the blast cells showed Sudan Black and terminal deoxynucleotidyl transferase (TdT) positivity at presentation and did not react with the monoclonal antibodies (McAb) My9 (anti-myeloid) and J5 (anti-CALL
Autor:
M.C. del Cañizo, D. Catovsky, Estela Matutes, Ríos A, Juliana Salazar, J F San Miguel, Letizia Foroni, M. Gonzalez
Publikováno v:
ResearcherID
An atypical case of lymphoproliferative disorder in which T- and B-cell antigens were coexpressed in the neoplastic cells is described. The disease was characterised by hepatosplenomegaly, lymphadenopathy, a low WBC (5 X 10(9)/l) and bone marrow infi
Publikováno v:
European Journal of Haematology. 39:349-352
Hairy cell leukaemia affecting primarily the spleen is a very rare feature of this disease at presentation. Splenectomy in such cases would seem to provide a cure. We report a case of primary splenic hairy cell leukaemia in which clinical and haemato
Publikováno v:
Scandinavian Journal of Haematology. 32:417-422
The monoclonal antibody RFB1, which reacts with early haemopoietic precursors in human bone marrow and peripheral T-lymphocytes, but not with pre-B cells and mature peripheral blood and marrow B lymphocytes, was tested in blood from 60 patients with
Autor:
E. Matutes, Martin J. S. Dyer, Martin Yuille, D. Catovsky, V. Brito-Babapulle, P. J. J. C. De Schouwer
Publikováno v:
British Journal of Haematology. 110:831-838
T-cell prolymphocytic leukaemia (T-PLL) is a sporadic, mature T-cell disorder in which there is usually an aberrant T-cell receptor alpha (TCRA) rearrangement that activates the TCL1 or MTCP1-B1 oncogenes. As mutations of the Ataxia Telangiectasia (A
Publikováno v:
British Journal of Haematology. 109:794-799
B-cell chronic lymphocytic leukaemia (CLL) is the most common form of leukaemia. To gain insight into the role of inherited factors in the disease, we have conducted a survey of the family histories of 268 CLL patients and have reviewed published fam
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
R. L. Powles, Ricardo Morilla, K Owusu-Ankomah, Alison Morilla, N Farahat, Jennifer Treleaven, Estela Matutes, CR Pinkerton, D. Catovsky
Publikováno v:
British Journal of Haematology. 101:158-164
The clinical significance of detecting minimal residual disease (MRD) in B-lineage acute lymphoblastic leukaemia (ALL) was evaluated by quantitative flow cytometry using a combination of TdT with CD10 and CD19. 53 patients with B-cell precursor ALL w