Zobrazeno 1 - 10
of 84
pro vyhledávání: '"J. Buisine"'
Autor:
F. Mielot, J. Buisine, E. Duchayne, O. Fenneteau, J. Goasguen, A. M. Guitard, M. Maierredelsperger, M. Malet, A. M. Manel, B. Bader-meunier, G. Tchernia
Publikováno v:
Leukemia & Lymphoma. 28:531-540
We reviewed the peripheral blood and bone marrow smears of 81 children with myelodysplastic syndrome (MDS). The morphological FAB classification was applicable in 59 children (72,8%): RAEB and RAEBt were the most frequent, 32 cases (39,5%). CMML was
Autor:
Brigitte Bader-Meunier, Danièle Sommelet, F. Mielot, Jean-Paul Dommergues, G. Tchernia, J. Buisine
Publikováno v:
Archives de Pédiatrie. 4:561-567
Myelodysplastic syndromes (MDS) in children constitute a heterogeneous disorder, including 'primary' MDS and MDS associated with constitutional abnormalities. The Franco-American-British (FAB) cytological classification for adults can be applied for
Autor:
S, Dimicoli, A, Fohlen-Walter, L, Mansuy, J, Buisine, M-J, Grégoire, T, Lecompte, P, Bordigoni, P, Jonveaux, J-F, Lesesve
Publikováno v:
Annales de biologie clinique. 61(3)
The clinical, hematological, and cytogenetic data from a 4 year-old child with acute myeloid (AML-M1) and basophilia is reported. Interestingly, cytogenetic investigations revealed the presence of the translocation t(6;9) (p23;q34). This abnormality
Autor:
V, Latger-Cannard, B, Bibes, A, Dao, A, Fohlen-Walter, J, Buisine, C, Rabaud, T, May, M, Marchand-Arvier, J F, Lesesve, T, Lecompte
Publikováno v:
Annales de biologie clinique. 60(2)
Publikováno v:
Annales de biologie clinique. 59(3)
Autor:
A, Fohlen-Walter, J F, Lesesve, C, Jacob, V, Latger-Cannard, E, de Maistre, C, Hulin, J M, Merseille, J, Buisine, T, Lecompte
Publikováno v:
Annales de biologie clinique. 59(1)
Autor:
J F, Lesesve, J, Buisine, M J, Grégoire, P, Raby, P, Lederlin, M C, Béné, N, Froment, E, Labouyrie
Publikováno v:
Clinical and laboratory haematology. 22(5)
The history of a 28-year-old woman with anaplastic large cell lymphoma (ALCL) in the first trimester of her pregnancy is reported. Investigations allowed to diagnose a T-cell CD30 positive ALCL, which appearance is rare during pregnancy. Moreover, th
Publikováno v:
Annales de biologie clinique. 58(4)
Leukoagglutination is a rare EDTA-dependent phenomenon resulting in a spurious minoration of the leukocyte count performed using automated analyzers. We described seven cases. The leukocyte agglutination was detected by unstable WBC count, abnormal W
Publikováno v:
Clinical and laboratory haematology. 22(1)
Autor:
R, Garand, J, Goasguen, A, Brizard, J, Buisine, A, Charpentier, J F, Claisse, E, Duchayne, M, Lagrange, C, Segonds, X, Troussard, G, Flandrin
Publikováno v:
British journal of haematology. 103(2)
T-prolymphocytic leukaemia (T-PLL) is a rare disorder with a poor outcome. Presentation features were studied in 78 T-PLL cases. Although 53 patients (group A) presented with typical progressive disease including rapidly increasing leucocytosis. 25 p