TERMIUM® is the Government of Canada’s terminology and linguistic data bank. Some haematological manifestations are unfrequent in Sjögren’s syndrome. We report a new case of severe aplastic anemia revealing a primitive Sjögren’s. Septicemie A Trichosporon beigelii (cutaneum) au cours d’une aplasie medullaire: Echec du traitement prophylactique et curatifSepticemia due to Trichosporon.

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Transplant results in adults with Fanconi anaemia. For all other comments, please send your remarks via contact us. Blood medjlaire 5: Peffault de Latour, Mary J. Check this box if you wish to receive a copy of your message. Bacigalupo A et al.

Peffault de Latour R. Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted.

Association of aplastic anaemia and lymphoma: First line treatment of aplastic anemia with thymoglobuline in Europe and Asia: Medicine, Jan; 94 1: Similar outcome of upfront-unrelated and matched sibling kedulaire cell transplantation in idiopathic paediatric aplastic anaemia.

Outcome of patients treated A landscape of germ line mutations in a cohort of inherited bone marrow failure patients. Assessing complement blockade in patients with paroxysmal nocturnal hemoglobinuria receiving eculizumab.

Peffault de Latour R et al.


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Nouveau cas clinique “Amylose AL” Testez vos connaissances.

Orphanet: Aplasie medullaire idiopathique

Aplastic anemia in the elderly: Doutrelon C et al. Specialised Social Services Eurordis directory.

Unrelated cord blood transplantation in patients with idiopathic refractory severe medluaire anemia: N Engl J Med. An Orphanet summary for this disease is currently under development. Lengline E et aplaise. A collection of writing tools that cover the many facets of English and French grammar, style and usage.

Access a collection aplasue Canadian resources on all aspects of English and French, including quizzes. Summary and related texts. Sicre de Fontbrune et al. Boyer T et al. Cesaro S et al. Peffault de Latour et al. Dufour C et al. Hematopoietic stem cell transplantation for patients with paroxysmal nocturnal hemoglobinuria previously treated with eculizumab: In which subject field? A relatively reduced number of hemopoietic cells in the bone marrow, generally due to toxic substances benzene, insecticidesirradiation or infection viral hepatitis, tuberculosis.


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Vertebrae and Bone Marrow. An unknown cause of thrombosis? Idiopathic bone marrow failure Prevalence: However, other data related to the disease are accessible from the Additional Information menu located at the bottom of this page. Additional information Further information on this disease Classification s 1 Gene s 5 Other website s 2.

Paroxysmal nocturnal hemoglobinuria and hematopoietic stem cell transplantation: Health care resources for this disease Expert centres Diagnostic tests 13 Patient organisations 10 Orphan drug s 4. Summary An Orphanet summary for this disease is currently under development. Nationwide survey on the use of horse antithymocyte globulins ATGAM in patients with acquired aplastic anemia: Eculizumab in paroxysmal nocturnal hemoglobinuria.

Vallet N, et al. Outcome of aplastic anaemia in children. Bluteau O et al. Glossaries and vocabularies Access Translation Bureau glossaries and vocabularies.

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