Výsledky vyhledávání - "Marie-José Grange"

Temporal differences in membrane loss lead to distinct reticulocyte features in hereditary spherocytosis and in immune hemolytic anemia

Autor: Gil Tchernia, Marie-José Grange, Narla Mohandas, Martin Sorette, Thérèse Cynober, Lydie Da Costa

Publikováno v: Blood. 98:2894-2899

Spherocytic red cells with reduced membrane surface area are a feature of hereditary spherocytosis (HS) and some forms of autoimmune hemolytic anemia (AIHA). It is generally assumed that membrane loss in spherocytic red cells occurs during their sojo

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19e249f965de696fee6f6479227cc448
https://doi.org/10.1182/blood.v98.10.2894

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Hydroxyl Radical as a Potential Intracellular Mediator of Polymorphonuclear Neutrophil Apoptosis

Autor: Marie-José Grange, Catherine Pasquier, Emmanuelle Rollet-Labelle, Claude Marquetty, Carole Elbim, Marie-Anne Gougerot-Pocidalo

Publikováno v: Free Radical Biology and Medicine. 24:563-572

We investigated reactive oxygen species (ROS) involvement in polymorphonuclear neutrophilic leukocyte (neutrophil) apoptosis triggering. Neutrophils were incubated with xanthine oxidase (XO), which produces superoxide anion (O2.-) and hydrogen peroxi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6345f96394b19ca0154d26dadfd13522
https://doi.org/10.1016/s0891-5849(97)00292-x

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Risk of Leukaemia, Carcinoma, and Myelofibrosis in32P- or Chemotherapy-Treated Patients with Polycythaemia Vera: a Prospective Analysis of 682 Cases

Autor: Marie Echard, Jean-Didier Rain, Yves Najean, Françoise Lejeune, Alain Goguel, Dresch C, Marie-José Grange

Publikováno v: Leukemia & Lymphoma. 22:111-119

An analysis of the risk of progression towards leukemia, carcinoma and myelofibrosis was performed in 93 patients treated by 32P alone (PVSG protocols) since 1970-1979, 395 patients over the age of 65 years treated by 32P with or without maintenance

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::a0355af44fdb087fb6cfd904e17b08f5
https://doi.org/10.3109/10428199609074368

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Priapism in a patient with unstable hemoglobin: hemoglobin Köln

Autor: Valérie, Andrieu, Olivier, Dumonceau, Marie-José, Grange

Publikováno v: American journal of hematology. 74(1)

We report a case of severe priapism occurring in a patient with unstable hemoglobin, hemoglobin Köln, and underline several factors that may have contributed to this complication: abnormal plasticity of red cells, splenectomy, and cytomegalovirus in

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::7091845d1f8bcf482855581da9966307
https://pubmed.ncbi.nlm.nih.gov/12949895

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[Bernard-Soulier thrombopathy: a diagnostic pitfall]

Autor: Kadoudja, Chemlal, Marie-José, Grange, Marie-Geneviève, Huisse

Publikováno v: Annales de medecine interne. 153(5)

First described in 1948, Bernard-Soulier syndrome is an uncommon hereditary thrombopathy characterized by abnormal expression of the GPIb-IX-V complex which inhibits platelet migration to the site of endothelial trauma. Our case illustrates the patho

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::32458f7edcae2999e626b4e9e400ccee
https://pubmed.ncbi.nlm.nih.gov/12442081

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Intravenous immunoglobulin or high-dose methylprednisolone, with or without oral prednisone, for adults with untreated severe autoimmune thrombocytopenic purpura: a randomised, multicentre trial

Autor: Sylvie Chevret, Stéphane Cheze, Bertrand Godeau, François Bassompierre, Bruno Varet, Olivier Fain, Eric Legouffe, Philippe Bierling, Marie-José Grange, Cyrille Hulin, François Lefrère, Jean-Marc Zini

Publikováno v: Lancet (London, England). 359(9300)

Summary Background Treatment of adults with autoimmune thrombocytopenic purpura (AITP) is based more on individual experience than on results of controlled studies. We compared intravenous immunoglobulin with high-dose methylprednisolone in untreated

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::746729da72349e8f976a5e855a367a93
https://pubmed.ncbi.nlm.nih.gov/12103322

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Peg IFNα-2a in Polycythemia Vera (PV). Results of a Phase 2 Study by the French 'PV-NORD' Group

Autor: Nathalie Cambier, Pascal Turlure, Murielle Roussel, Bernard Grandchamp, Bruno Cassinat, Jean-Didier Rain, Sylvia Bellucci, Pierre Fenaux, Jean-Jacques Kiladjian, Christine Chomienne, Marie-José Grange

Publikováno v: Blood. 108:670-670

Background: IFNα can control erythrocytosis in 75% of PV while avoiding leukemogenicity of myelosuppressive drugs, but 20–25% of patients stop therapy due to side effects. Peg IFNα −2b, allowing weekly use, showed similar efficacy but no better

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::a25bcb95379314281ccb65437a864be5
https://doi.org/10.1182/blood.v108.11.670.670

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PVN1: A Phase 2 Study of Pegylated Interferon-α2a in Polycythemia Vera (PV) by the 'PV-Nord' Group. Preliminary Report of Efficacy and Safety

Autor: Christine Chomienne, Nathalie Cambier, Pascal Turlure, Murielle Roussel, Sylvia Bellucci, Jean-Didier Rain, Jean-Jacques Kiladjian, Pierre Fenaux, Marie-José Grange, Bruno Cassinat

Publikováno v: Blood. 106:4940-4940

Background: Interferon-α (IFN) can control erythrocytosis in about 75% of PV patients and may even induce cytogenetic remission while avoiding the leukemogenic potential of myelosuppressive drugs. However, 20–25% of patients discontinue therapy du

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::796e286d5f31cf55bc6e251cfe73dc64
https://doi.org/10.1182/blood.v106.11.4940.4940

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