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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L’hémoglobinurie paroxystique nocturne – EM|consulte
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Recurrent thrombotic events remains even now associated with bad prognosis, whatever the form of the disease. Antithymocyte globulin with or without cyclosporin A: Unrelated cord blood transplantation in patients with idiopathic refractory severe aplastic anemia: Peffault de Latour R et al. Immunosuppressive therapy remains an important treatment modality in this subcategory for patients without a donor or ineligible for BMT.
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Access to the text HTML. Access a collection of Proxystique resources on all aspects of English and French, including quizzes. Paroxysmal nocturnal hemoglobinuria and hematopoietic stem cell transplantation: In which subject field? Better results in ? Med Sci Paris ; 25 12 Granulocyte-stimulating factor and severe aplastic anemia: Doutrelon C et al.
Journal page Archives Contents list. Peffault de Latour aZ. Second allogeneic stem cell transplant for aplastic anaemia: Effect of eculizumab on hemolysis and transfusion requirements in patients with paroxysmal nocturnal hemoglobinuria. If you want to subscribe to this journal, see our rates You can purchase this item in Pay Per View: Glossaries and vocabularies Access Translation Bureau glossaries and vocabularies. Prospective randomized multicenter study comparing cyclosporin alone versus the combination of antithymocyte globulin and cyclosporin for treatment of patients with nonsevere aplastic anemia: In classic PNH, recent studies have focused on inhibiting the complement cascade with encouraging clinical results using eculizumab, a C5-inhibitor humanized monoclonal antibody.
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paroxysgique Blood ; 5: Vallet N, et al. Access to the full text of this article requires a subscription. The hematopoietic defect in aplastic anemia assessed by long-term marrow culture. The treatment of severe acquired aplastic anemia. A rare disorder characterized by hemolysis and hemoglobinuria, the latter accentuated during sleep.
Thrombotic events are characterized by involvement of unusual sites hepatic, mesenteric, cerebral, dermal veins. Marchiafava Micheli syndrome Marchiafava-Micheli’s syndrome.
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Publications Aplasie médullaire/Hémoglobinurie paroxystique nocturne/Anémie de Fanconi
Bluteau O et al. A collection of writing tools that cover the noxturne facets of English and French grammar, style and usage. Thromboses remain a major life threatening complication affecting outcomes in both disease subcategories.
Natural history of paroxysmal nocturnal haemoglobinuria using modern diagnostic assays. Worse outcome and more chronic GVHD with peripheral blood progenitor cells than bone marrow in HLA-matched sibling donor transplants for young patients jmoglobinurie severe acquired aplastic anemia.
Medicine, Jan; 94 1: Primary prophylaxis with warfarin prevents thrombosis in paroxysmal nocturnal hemoglobinuria PNH. Peffault de Latour et al.
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