Zobrazeno 1 - 10
of 27
pro vyhledávání: '"M.H. Estienne"'
Autor:
A. Cosson, Marc Zandecki, Pierre Fenaux, Pascale Lepelley, M.H. Estienne, G. Torpier, S. Paquet, B. Lerche
Publikováno v:
European Journal of Haematology. 39:77-81
A total lack of EPO was fortuitously discovered in a 63-yr-old woman from the north of France who had primary refractory anaemia, but without dysgranulopoiesis; MPO activity was normal. Her twin sister, whose blood count was normal, also had EPO defi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af9c34e276e7e97f88b4e9173972cde5
https://doi.org/10.1111/j.1600-0609.1987.tb00169.x
https://doi.org/10.1111/j.1600-0609.1987.tb00169.x
Autor:
A. Cosson, J. L. Lai, Claude Preudhomme, P. Lepelley, Marc Zandecki, P. Fenaux, M.H. Estienne
Publikováno v:
Clinical and laboratory haematology. 12(1)
The prognostic value of cytological features was assessed in 132 patients with de novo acute myeloid leukaemia (AML) treated by anthracycline-cytosine-arabinoside combination chemotherapy. Of these patients, 98 (75%) achieved complete remission (CR).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9592448810bddbececc4fed50108e3cb
https://pubmed.ncbi.nlm.nih.gov/2344717
https://pubmed.ncbi.nlm.nih.gov/2344717
Autor:
Pierre Fenaux, Jenny Goudemand, Claudine Caron, Thierry Facon, Marc Zandecki, M.H. Estienne, A. Cosson
Publikováno v:
British Journal of Haematology. 74:542-543
We report on a patient having grey platelet syndrome without myelofibrosis, but with idiopathic pulmonary fibrosis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c6843c1c9632de45ebba5e46a41d98a
https://doi.org/10.1111/j.1365-2141.1990.tb06350.x
https://doi.org/10.1111/j.1365-2141.1990.tb06350.x
Autor:
M.H. Estienne, Francis Bauters, M. Deminatti, Pierre Fenaux, Jean-Luc Laï, J.B. Savary, Marc Zandecki, Jean-Pierre Jouet
Publikováno v:
Cancer Genetics and Cytogenetics. 29:311-314
We report a promyelocytic blast crisis in a case of Ph-positive thrombocythemia with both t(9;22) and t(15;17). Our patient confirms the specificity of t(15;17) in malignant proliferation of promyelocytes and suggests its appearance as a second genet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f6d33e672f7a52b4af366b60f05a0d6
https://doi.org/10.1016/0165-4608(87)90241-x
https://doi.org/10.1016/0165-4608(87)90241-x
Autor:
P. Lepelley, M.H. Estienne, Jean-Luc Laï, Francis Bauters, M. Deminatti, Pierre Fenaux, J.J. Huart
Publikováno v:
Cancer Genetics and Cytogenetics. 39:45-53
We report two cases of translocation t(10;17)(p13;q12) found in a series of 278 cytogenetically studied acute nonlymphocytic leukemia cases. Blast cells, in both cases, were undifferentiated and had phagocytic properties. These patients might represe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::444a8bdaeab25968128bb702c9b6187e
https://doi.org/10.1016/0165-4608(89)90228-8
https://doi.org/10.1016/0165-4608(89)90228-8
Autor:
J.P. Pollet, J.J. Huart, J.B. Savary, Pierre Fenaux, M.H. Estienne, Jean-Luc Laï, M. Deminatti
Publikováno v:
Cancer Genetics and Cytogenetics. 33:99-109
Childhood acute lymphocytic leukemia (ALL) with partial deletion of the short arm of chromosome 9 (9p−), particularly in the p21–22 region, associated with bulky disease, has been regarded as a possible subgroup of ALL. We have reviewed clinical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::557701599e1807058bba166015808650
https://doi.org/10.1016/0165-4608(88)90055-6
https://doi.org/10.1016/0165-4608(88)90055-6
Autor:
M.H. Estienne, Brigitte Nelken, Jean-Luc Laï, Pierre Fenaux, Francis Bauters, M. Deminatti, P. Lepelley, Jean-Pierre Jouet, J.B. Savary, J.J. Huart
Publikováno v:
Cancer Genetics and Cytogenetics. 37:9-17
We report clinical, immunologic, and cytogenetic characteristics of six patients with a t(1;19)(q23;p13) that was balanced in one case and of the unbalanced type [−19,der (19)t(1;19)(q23;p13)] in the remaining five cases. Intracytoplasmic immunoglo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6f6d719b02f33c55466f423bffb021c4
https://doi.org/10.1016/0165-4608(89)90068-x
https://doi.org/10.1016/0165-4608(89)90068-x
Autor:
Francis Bauters, Jean-Luc Laï, Pierre Fenaux, R. Beuscart, M.H. Estienne, B. Dupriez, J P Jouet
Publikováno v:
La Revue de Médecine Interne. 10:323-329
Resume Nous rapportons une serie de 39 anemies sideroblastiques acquises idiopathiques, representant 12 p. 100 des 330 syndromes myelodysplasiques diagnostiques dans notre service en six ans. L'âge moyen est tres eleve (70,8 ans). L'anemie, quasi co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::17567cccb31bf8dc94c5d081ce75832e
https://doi.org/10.1016/s0248-8663(89)80030-x
https://doi.org/10.1016/s0248-8663(89)80030-x
Publikováno v:
XIth International Congress on Thrombosis and Haemostasis.
A 46 yr old Caucasian woman has been diagnosed as having a congenital deficiency of platelet a-granules (gray platelet syndrome - GPS) associated with an extensive idiopathic pulmonary fibrosis (IPF). The patient had a life long history of bleeding t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0de76b1ee9eecafa597e5b16940e7aa5
https://doi.org/10.1055/s-0038-1644559
https://doi.org/10.1055/s-0038-1644559
Autor:
Jean-Pierre Jouet, Pascale Lepelley, Marc Zandecki, Pierre Fenaux, Jean-Luc Laï, M.H. Estienne, R. Beuscart, A. Cosson, Francis Bauters
Publikováno v:
European journal of haematology. 40(4)
Between 1980 and 1986, we diagnosed refractory anaemia (RA), according to the FAB classification, in 69 patients, who constituted 22% of the 312 cases of myelodysplastic syndromes (MDS) seen over that period. The haematological features were variable
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07299cd6528a4d241aca14f8c331588c
https://pubmed.ncbi.nlm.nih.gov/3366222
https://pubmed.ncbi.nlm.nih.gov/3366222