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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Erythrocyte disorders in the perinatal period. Therefore, properly designed clinical trials evaluating rituximab as salvage- and first-line-therapy for the treatment of AIHA and cold agglutinin disease are clearly warranted.

De Franceschi L, Corrocher R. Recentemente, Canalli et al.

Induction of fetal hemoglobin in the treatment of sickle cell disease. The role of hydroxyurea in the management of sickle cell disease. Clinical, hematological, and molecular characterization of sickle cell anemia pediatric patients from two different cities in Brazil. The Impact Factor measures the average number of citations received in a particular year by papers published in the journal during the two receding years.

Cytokines and plasma factors in sickle cell disease. Um novo quelante oral, o deferasirox, foi recentemente aprovado nos EUA e no Brasil.


The magazine, referring to the Spanish-speaking pediatric, indexed in major international databases: Correction of the sickle cell mutation in embryonic stem cells.

Red blood cell defects heomlitica malaria. Steinberg MH, Brugnara C. Acute myocardial infarction in sickle cell disease: Overt and incomplete silent cerebral infarction in sickle cell anemia: Johnson C, Telen MJ. Current status of iron overload and chelation with deferasirox. J Pediatr Hematol Oncol, 18pp.

HPLC studies in hemoglobinopathies. Microangiopathic hemolytic anemia and thrombocytopenia. SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field.

Print Heolitica to a friend Export reference Mendeley Statistics. Pathophysiology and therapy for haemoglobinopathies. A variety of other immunosuppressive agents as well as splenectomy are used for refractory cases.

The genetics of blood disorders: hereditary hemoglobinopathies

Rund D, Rachmilewitz E. Effect of cytokines and chemokines on sickle neutrophil adhesion to fibronectin. Med Clin Barc, pp. Free Radic Biol Med. Neuroimaging Clin N Heemolitica. Hepatic dysfunction in sickle cell disease: Genetic dissection and prognostic modeling of overt stroke in sickle cell anemia.

Anemia hemolítica autoinmune por hemolisina bifásica | Anales de Pediatría (English Edition)

Acta Haemat, 68pp. Kuypers FA, de Jong K. Panigrahi I, Agarwal S. The treatment of cold agglutinin disease consists of avoiding cold environments, inmunosuppresive therapy and more recently rituximab.


Transient Donath-Lansteiner Haemolytic anaemia. Sildenafil therapy in patients with sickle cell disease and pulmonary hypertension. Tolentino K, Friedman JF. Aslan M, Freeman BA.

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Os autores analisaram SNP em abemia genes candidatos, em 1. Identification of differentially expressed genes induced by hydroxyurea in reticulocytes from sickle cell anaemia patients. SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s hemoljtica.

Risk factors for conjunctival and retinal vessel alterations in sickle cell disease. Increased adhesive properties of neutrophils in sickle cell disease may be reversed by pharmacological nitric oxide donation.

Oediatria J Biochem Cell Biol. CiteScore measures average citations received per document published. Continuing navigation will be considered as acceptance of this use. Sickle cell disease and nitric oxide: The Spanish Association of Pediatrics has as one of its main objectives the dissemination of rigorous and updated scientific information on the different areas of pediatrics.

Hematol Oncol Clin North Am. Necesidades del alumnado con diabetes tipo 1 en