La anemia hemolítica autoinmune (AHAI) es una alteración hematológica autoinmune producida por la síntesis de autoanticuerpos contra los antígenos propios. Estas representam as formas mais comuns de anemia hemolítica hereditária. .. quanto ao seu potencial carcinogênico67 em relação à população pediátrica. Recibido para publicación: Aceptado para publicación: Introducción. La anemia hemolítica microangiopática se describió por prime-.
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Med Clin Barc96pp. Pulmonary hypertension in sickle cell disease.
Anemia hemolítica autoinmune por hemolisina bifásica | Anales de Pediatría (English Edition)
Modifier genes and sickle cell anemia. Normality has been maintained for36 and 24 months respectively, and the children have presentedno clinico-biological alterations. A variety of other immunosuppressive agents as well as splenectomy are used for refractory cases.
Previous article Next article. Kuypers FA, de Jong K. J Pediatr,pp. Moi P, Sadelain M. Acta Haemat, 68pp.
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hmeolitica De Franceschi L, Corrocher R. The role of hydroxyurea in the hemolktica of sickle cell disease. Amer J, Fibach E. J Womens Health Larchmt. We present the clinical cases of two children, aged 4 and7 respectively, with TTP, but with different evolution andtreatment. Subscribe to our Newsletter. Sickle cell disease and nitric oxide: Corticoids represent the standard frontline therapeutic option for warm autoantibodies haemolytic anaemia.
J Pediatrics, 81pp. Thrombotic thrombocytopenic purpura TTP or Moschovitzsyndrome is rare and is even rarer in childhood.
The role of phosphatidylserine in recognition and removal of erythrocytes.
Peripheral blood versus bone marrow as a source of hematopoietic stem cells for allogeneic transplantation in children with class I and II beta thalassemia major. Care of patients with haemoglobin abnormalities: Predicting clinical severity in sickle cell anaemia.
Am J Trop Med Hyg. Current status of iron overload and chelation with deferasirox. Placenta growth factor activates monocytes and correlates with sickle cell disease severity. Chronic liver abnormalities in sickle cell disease: Fathallah H, Atweh GF. Eur J Pediatr,pp. Continuing navigation will be considered as acceptance of this use.
All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License. Overt and incomplete silent cerebral infarction in sickle cell anemia: Familial infantile thrombotic thrombocytopenic purpura. HPLC studies in hemoglobinopathies.
Genetic insights into the clinical diversity of beta thalassaemia. Hemoliica Aguado b. Remission after cis retinoic acid in thrombotic thrombocytopenic purpura. High levels of GDF15 in thalassemia suppress expression of the iron regulatory protein hepcidin. Adhesion molecules and pwdiatria in the pathophysiology of sickle cell disease.
Choudhry VP, Naithani R. Abstract Autoimmune haemolytic anaemia AIHA is an immune haematologic disorder resulting from autoantibody production directed against red-cell antigens. Scand J Clin Lab Invest.
Sangre, 28pp. Free Radic Biol Med. Blood Cells Mol Dis. Franchini M, Veneri D. Managing sickle cell disease.