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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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Carlos Gomes, cj. Resultados similares foram obtidos em modelos animais com clorotrimazol, que bloqueia o canal de Gardos. Continuing navigation will be considered as acceptance of this hemoliticz.

SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact. De Franceschi L, Corrocher R. Overt and incomplete silent cerebral infarction in sickle cell anemia: Choudhry VP, Naithani R. Peripheral blood versus bone marrow as a source peduatria hematopoietic stem cells for allogeneic transplantation in children with class I and II beta thalassemia major.

Fathallah H, Atweh GF. SRJ is a prestige metric based on the idea that not all citations are the same.


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J Pediatr Rio J. Birgens H, Ljung R. Modification of globin gene expression by RNA targeting strategies.

The treatment of these autoimmune haemolytic anaemias with rituximab requires authorisation by the Spanish Ministry of Health for compassionate use. Print Send to a friend Export reference Mendeley Statistics.

Neuroimaging Clin N Am. J Pediatr,pp.

Cytokines and plasma factors in sickle cell disease. Um novo quelante oral, o deferasirox, foi recentemente aprovado nos EUA e no Brasil. Erythrocyte disorders in the perinatal period. SNIP pediztria contextual citation impact by wighting citations based on the total number of citations in a subject field.

Sickle cell disease and nitric oxide: Distinct HLA associations by stroke subtype in children with sickle cell anemia. Previous article Next article.

The acute form is more frequent, and in most casesthe course is fulminant if treatment is not initiated. J Womens Health Larchmt. We present the clinical cases of two children, aged 4 and7 respectively, with TTP, but with different evolution andtreatment. Singh SP, Gupta S.

Thefirst child recovered spontaneously.



Material and methods We present the clinical cases of two children, aged 4 and7 respectively, with TTP, but with different evolution andtreatment. J Med Assoc Thai. Prdiatria Rev Mol Med. N Engl J Med. Abstract Autoimmune haemolytic anaemia AIHA is an immune haematologic disorder resulting from autoantibody production directed against red-cell antigens. Davies SC, Gilmore A.

How to cite this article. Moi P, Sadelain M. Clinically, it is characterized by microangiopathic hemolyticanemia, thrombocytopenia, neurologic abnormalities,fever and renal dysfunction. Therapy with hydroxyurea is associated with reduced adhesion molecule gene and protein expression in sickle red cells with a concomitant reduction in adhesive properties.

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In the second plasmapheresiswas required and produced remission of allthe symptomatology. The genomics of new drugs in sickle cell disease. Necesidades del alumnado con diabetes tipo 1 en