Autoimmune Anemia Hemolytic
Mostrando 1-12 de 24 artigos, teses e dissertações.
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1. Evans syndrome in male lupus patient: case report
RESUMO A síndrome de Evans (SE) é uma doença autoimune rara de etiologia desconhecida; ocorre quando há combinação de anemia hemolítica autoimune (AHAI) com trombocitopenia, acompanhada ou não de neutropenia imune. Essa síndrome se enquadra em um tipo variável especial da AHAI a quente, podendo se relacionar com doenças reumatológicas, como lúpu
J. Bras. Patol. Med. Lab.. Publicado em: 02/09/2019
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2. Autoimmune hemolytic anemia and hyperglobulinemia leading to the diagnosis of multiple myeloma
Rev. Bras. Hematol. Hemoter.. Publicado em: 2017-12
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3. Drug reaction with eosinophilia and systemic symptoms (DRESS) and its relation with autoimmunity in a reference center in Mexico
Abstract: BACKGROUND: Drug reaction with eosinophilia and systemic symptoms is a severe adverse drug reaction, with a reported mortality of 10%. Long-term outcomes involve organic failure and autoimmune diseases in some populations. OBJECTIVE: To evaluate the clinical prognosis of patients with drug reaction with eosinophilia and systemic symptoms. METHOD
An. Bras. Dermatol.. Publicado em: 2017-02
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4. Mycoplasma pneumoniae associated with severe autoimmune hemolytic anemia: case report and literature review
Brazilian Journal of Infectious Diseases. Publicado em: 2009-02
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5. Expressão de SIRP alfa e SPH-1 na anemia hemolitica autoimune / SIP-alpha and SHP-1 expression in autoimmune hemolytic anemia
SIRP alfa (Signal Regulatory Protein alfa ) é um receptor que medeia funções inibidoras em fagócitos. Sua ativação e conseqüente fosforilação dos ITIMs ocorre pela ligação ao CD47 presente na membrana dos eritrócitos, e permite o recrutamento e a ativação de SHP-1, a qual desfosforila substratos específicos envolvidos na mediação de diversos
Publicado em: 2009
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6. Evaluation of the red cell deformability through ektacytometry in iron deficiency / Avaliação da deformidade eritrocitária através da ectacitometria na deficiência de ferro
The deformability allows the 7 to 8 cm red cell to circulate through capillaries of 3 cm. This phenomenon depends on cellular geometry, internal viscosity and viscoelastic properties of the membrane. Among the various techniques of erytrocyte deformability (ED) analysis such as: micropipette aspiration, filtration and reoscopy, we chose ektacytometry. This t
Publicado em: 2002
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7. Alterações tireoideanas em pacientes com beta-talassemia maior submetidos a hipertransfusão sanguinea
Among several clinical presentations of thalassemia syndromes, beta¬thalassemia major (Cooley s disease) is one of the great severity. The clinical features consist of chronic hemolytic anemia, from the early years of life, and severe hypoxia, requiring a regimen of chronic blood transfusions to survive. Treatment with chronic regular transfusions leads to
Publicado em: 1999
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8. Autoimmune hemolytic anemia occurred prior to evident nephropathy in a patient with chronic hepatitis C virus infection: case report
BioMed Central.
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9. Exacerbation of Autoantibody-Mediated Hemolytic Anemia by Viral Infection
Strong enhancement of the pathogenicity of an antierythrocyte monoclonal antibody was observed after infection of mice with lactate dehydrogenase-elevating virus. While injection of the antierythrocyte antibody alone induced only moderate anemia, concomitant infection with this virus, which is harmless in most normal mice, led to a dramatic drop in the hemat
American Society for Microbiology.
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10. Autoimmune hemolytic anemia in chronic mucocutaneous candidiasis.
Chronic mucocutaneous candidiasis is an immunodeficiency disease characterized by T-cell dysregulation and chronic superficial candidal infections. We report on three patients with chronic mucocutaneous candidiasis who developed autoantibodies to erythrocytes. Our first patient, a 19-year-old female, developed autoimmune hemolytic anemia (AIHA) that required
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11. The diagnostic significance of a positive direct antiglobulin test in anemic cats.
The preparation of a feline Coombs serum (rabbit antifeline gamma globulin) is described. The direct antiglobulin test using this serum was performed on 20 anemic and 20 healthy control cats. Red cell membrane antibodies were detected in cats with feline leukemia virus infection and in others with inflammatory and neoplastic diseases. A low titre of cold agg
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12. Quantitative studies of ferritinlike iron in erythrocytes of thalassemia, sickle-cell anemia, and hemoglobin Hammersmith with Mössbauer spectroscopy.
By using the technique of recoil-free absorption (Mössbauer effect) in iron, we found large amounts of iron, yielding a well-defined spectrum different from that of oxy- or deoxyhemoglobin, in whole erythrocytes of 13 patients with beta-thalassemia major and intermedia, 3 with hemoglobin H disease, 2 with sickle-cell anemia, and 1 with unstable hemoglobin H