L’hémoglobinurie paroxystique nocturne est une maladie liée à une mutation somatique entraînant l’expansion de clones cellulaires déficients pour des. Site Internet de la filière de santé maladies rares MaRIH, Publications Aplasie médullaire/Hémoglobinurie paroxystique nocturne/Anémie de Fanconi. Many translated example sentences containing “hémoglobinurie paroxystique nocturne” – English-French dictionary and search engine for English translations.

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Transplant results in adults with Fanconi anaemia.

Change the order of display of the official languages of Canada English first French first Option to display the non-official languages Noctyrne or Portuguese Neither Spanish Portuguese Display definitions, contexts, etc. Bierings M et al. Access a collection of Canadian resources on all aspects of English and French, including quizzes.

Elevated levels of circulating procoagulant microparticles in patients with paroxysmal nocturnal hemoglobinuria and aplastic anemia.

Access to the text HTML. Immunosuppressive therapy remains an important treatment modality in this subcategory for patients without a donor or ineligible for BMT. A phase I study of oxidized raffinose cross-linked human hemoglobin. The treatment of severe acquired aplastic anemia. FAQ Frequently asked questions Display options.

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Outline Masquer le plan. Bacigalupo A et al. Alterations in both the hematopoietic microenvironment and the progenitor cell population follow the recovery from myeloablative therapy and bone marrow transplantation. Evidence for a metabolic shift of arginine metabolism in sickle cell disease.

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John Libbey Eurotext – Hématologie – Hémoglobinurie paroxystique nocturne

Outcome of aplastic anaemia in children. Gene expression profiling in CD34 cells to identify differences between aplastic anemia patients and healthy volunteers.

Recurrent thrombotic paroxyxtique remains even now associated with bad prognosis, whatever the form of the disease. Worse outcome and more chronic GVHD with peripheral blood progenitor cells than bone marrow in HLA-matched sibling donor transplants for young patients with severe acquired aplastic anemia.

Peffault de Latour aZ. A collection of writing tools that cover the many facets of English and French grammar, style and usage. Paroxysmal nocturnal hemoglobinuria and hematopoietic stem cell transplantation: Access to the PDF text. Multicenter phase 3 study of the complement inhibitor eculizumab for the treatment of patients with paroxysmal nocturnal hemoglobinuria.

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You can move this window by clicking on the headline. Multicenter randomized study comparing cyclosporine-A alone and antithymocyte globulin with prednisone for treatment of severe aplastic anemia. Boyer T et hmoglobinuriw. Personal information regarding our website’s visitors, including their identity, is confidential.

The clinical sequelae of intravascular hemolysis and extracellular plasma hemoglobin: Top of the page – Article Outline. Hematopoietic stem cell transplantation in childhood inherited bone marrow failure syndrome.

Peffault de Latour et al. The hematopoietic defect in aplastic anemia assessed by long-term marrow culture. First line noccturne of aplastic anemia with thymoglobuline in Europe and Asia: A study by the severe aplastic anaemia and paediatric disease working parties of the European group blood and bone marrow transplant.


Nationwide survey on the use of horse antithymocyte globulins ATGAM in patients with acquired aplastic anemia: Eculizumab in paroxysmal nocturnal hemoglobinuria. Peffault de Latour R. Natural history of paroxysmal nocturnal haemoglobinuria using modern diagnostic assays. If you want to subscribe to this journal, see our rates You can purchase this item in Paroystique Per View: Characterization paroxyatique T-cell repertoire of the bone marrow in immune-mediated aplastic anemia: Outcome of patients with acquired aplastic anemia given first line bone marrow transplantation or immunosuppressive treatment in the last decade: Unrelated stem cell transplantation for severe acquired aplastic anemia: Benajiba L et al.

From earlier descriptions, the clinical polymorphism of PNH has been recognized by paroxystiqke presentations; one form, predominantly haemolytic without overt marrow failure, referred to classic PNH and the other one, with marrow failure, was often described as the aplastic anemia PNH syndrome AA-PNH.

Peffault de Latour, Mary J. Second allogeneic stem cell transplant for aplastic anaemia: Pneumocystose pulmonaire ou simple colonisation? Amoura bG. Clinical course and flow cytometric analysis of paroxysmal nocturnal hemoglobinuria in the United States parodystique Japan. Previous Article PCR Pneumocystis jirovecii positive chez les patients atteints de maladie auto-immune: Hmoglovinurie, Jan; 94 1:

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