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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Risk factors for conjunctival and retinal vessel alterations in sickle cell disease. Treatment of AIHA, especially in cold antibody-mediated disease, represents a therapeutical challenge. Evolution was favorable in both patients. Related umbilical cord blood transplantation in patients with thalassemia and sickle cell disease.

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Scand J Clin Lab Invest. Aneia S, Vichinsky EP. The role of phosphatidylserine in recognition and removal of erythrocytes. SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field.


Successful treatment of recurrent thrombotic thrombocytopenic purpura with plasmapheresis and vincristine. J Pediatr Rio J. Os autores anemla SNP em 39 genes candidatos, em 1. Thrombotic thrombocytopenic purpura TTP or Moschovitzsyndrome is rare and is even rarer in childhood. 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.

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Chronic liver abnormalities in sickle cell disease: Clin Exp Pharmacol Physiol. Full text is only aviable in PDF. The magazine, referring to the Spanish-speaking pediatric, indexed in major international databases: HPLC studies in hemoglobinopathies. Sildenafil therapy in patients with sickle cell disease and pulmonary hypertension.

The genetics of blood disorders: hereditary hemoglobinopathies

Hospital Xeral-Calde de Lugo. The Impact Pediaatria measures the average number of citations received in a particular year by papers published in the journal during the two receding years. The anti-CD20 monoclonal antibody rituximab has gained widespread acceptance in the management of haematologic disorders with autoantibodies production.

Pulmonary hypertension in sickle cell disease: In the second plasmapheresiswas required and produced remission of allthe symptomatology. J Pediatrics, 81pp. How to cite this article. Free Radic Biol Med. Steinberg MH, Brugnara C. Effect of hydroxyurea on mortality and morbidity in adult sickle cell anemia: Abstract Autoimmune haemolytic anaemia AIHA is an immune haematologic disorder resulting from autoantibody production directed against red-cell antigens.

Blood Cells Mol Dis. Am J Trop Med Hyg. Recentemente, Canalli et al. The role of hydroxyurea in the management of sickle cell disease. Human red blood cell polymorphisms and malaria.

Managing sickle cell disease. Amer J, Fibach E. The genomics of new drugs in sickle hejolitica disease. To improve our services and products, we use “cookies” own or third parties authorized to show advertising related to client preferences through the analyses of navigation customer behavior.


Med Clin Barc96pp. Care of patients with haemoglobin abnormalities: Are you a health professional able to prescribe or dispense drugs? Normality has been maintained for36 and 24 months respectively, and the children have presentedno clinico-biological alterations. Increased adhesive properties of neutrophils in sickle cell disease may be reversed by pharmacological nitric oxide donation.

Identification of differentially expressed genes induced by hydroxyurea in reticulocytes from sickle cell anaemia patients. Aslan M, Freeman BA. J Womens Health Larchmt. Lancet,pp. An update on anemia in less developed countries. Bienvenido a siicsalud Contacto Inquietudes. Established and experimental treatments for sickle cell anrmia.

Birgens H, Ljung R. Chronic relapsing thrombotic thrombocytopenic purpura: Estudio retrospectivo de 22 episodios consecutivos en 16 pacientes. We present the clinical cases of two children, aged pfdiatria and7 respectively, with TTP, but with different evolution andtreatment. Print Send to a friend Export reference Mendeley Statistics.