Clinical relevance of cytogenetic abnormalities at diagnosis of acquired aplastic anaemia in adults
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.2006.06105.x/fullpdf
Reference12 articles.
1. Abnormal cytogenetic clones in patients with aplastic anaemia: response to immunosuppressive therapy
2. Estimation of failure probabilities in the presence of competing risks: new representations of old estimators
3. A third course of anti-thymocyte globulin in aplastic anaemia is only beneficial in previous responders
4. Aplastic anaemia with 13q-: a benign subset of bone marrow failure responsive to immunosuppressive therapy
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1. Diagnosis and management of acquired aplastic anemia in childhood. Guidelines from the Marrow Failure Study Group of the Pediatric Haemato-Oncology Italian Association (AIEOP);Blood Cells, Molecules, and Diseases;2024-09
2. The state of the art in the treatment of severe aplastic anemia: immunotherapy and hematopoietic cell transplantation in children and adults;Frontiers in Immunology;2024-04-05
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4. Cytogenetics in the management of bone marrow failure syndromes: Guidelines from the Groupe Francophone de Cytogénétique Hématologique (GFCH);Current Research in Translational Medicine;2023-10
5. Allogeneic hematopoietic stem cell transplantation for acquired severe aplastic anemia: a summary of a 20-year experience;Polish Archives of Internal Medicine;2023-02-28
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