Hemolytic Anemia
Mostrando 13-24 de 209 artigos, teses e dissertações.
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13. Prevalence of the American College of Rheumatology hematological classification criteria and associations with serological and clinical variables in 460 systemic lupus erythematosus patients
Objective: To study systemic lupus erythematosus in a Brazilian population using the American College of Rheumatology hematological classification criteria and report associations of the disease with serological and clinical profiles. Methods: This is a retrospective study of 460 systemic lupus erythematosus patients followed in a single rheumatologic cen
Rev. Bras. Hematol. Hemoter.. Publicado em: 2015-04
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14. Tuberculosis associated with transient hemolytic anemia responsive to tuberculosis chemotherapy: a case report
Braz J Infect Dis. Publicado em: 2013-02
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15. Hb Southampton [B106(G8)Leu→PRO, CTG→CCG] in a Uruguayan woman
Hemoglobin Southampton (also known as hemoglobin Casper) is a rare hemoglobin structural variant resulting from a substitution of a leucine residue for proline at codon beta106 [beta106(G8)Leu→Pro, CTG→CCG]. It is very unstable and associated with severe hemolytic anemia. We detected this mutation in a 37-year-old Uruguayan woman with a history of severe
Rev. Bras. Hematol. Hemoter.. Publicado em: 2013
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16. Isotipos IgG e IgM anti-dsDNA em pacientes com lúpus eritematoso sistêmico
IgG anti-dsDNA antibodies are associated to lupus nephritis. Recent data suggest that IgM isotype is nephroprotector. We evaluated the frequency of IgG anti-dsDNA in patients with Systemic lupus erythemathosus (SLE) and its relation between IgG/IgM proportion and clinical manifestations of the disease. This transversal study included 137 SLE patients accordi
IBICT - Instituto Brasileiro de Informação em Ciência e Tecnologia. Publicado em: 28/03/2012
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17. Clinical course of 63 children with hereditary spherocytosis: a retrospective study
BACKGROUND: Hereditary spherocytosis (HS) is an inherited hemolytic anemia that is caused by deficiency or dysfunction of erythrocyte cytoskeletal proteins. AIM: The aim of this study was to describe the clinical course of hereditary spherocytosis in patients treated in the Pediatric Hematology Unit, Hospital das Clínicas, Universidade Federal de Minas Gera
Revista Brasileira de Hematologia e Hemoterapia. Publicado em: 2012
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18. Wilson's disease: an analysis of 28 Brazilian children
OBJECTIVES: Clinical-laboratory and evolutionary analysis of twenty-eight patients with Wilson's disease. METHODS: Twenty-eight children (twelve females and sixteen males) with Wilson's disease were evaluated retrospectively between 1987 and 2009, with a follow-up of 72 months (1 - 240 months). The clinical, laboratory, and histologic features at diagnosis w
Clinics. Publicado em: 2012
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19. Correlation of low levels of nitrite and high levels of fetal hemoglobin in patients with sickle cell disease at baseline
BACKGROUND: Sickle cell disease is a hemoglobinopathy characterized by hemolytic anemia, increased susceptibility to infections and recurrent vaso-occlusive crises that reduces the quality of life of sufferers. OBJECTIVE: To evaluate the correlation of the levels of lactate dehydrogenase, malonaldehyde and nitrite to fetal hemoglobin in patients with sickle
Rev. Bras. Hematol. Hemoter.. Publicado em: 2012
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20. Predição da hemólise fetal em gestantes aloimunizadas / Prediction of fetal hemolysis in alloimmunized pregnancies
OBJETIVO: O objetivo deste estudo foi avaliar fatores clínicos, laboratoriais, dopplervelocimétricos e hematimétricos preditivos da velocidade de hemólise entre a primeira e a segunda transfusões intrauterinas em gestantes aloimunizadas. MÉTODOS: Este estudo retrospectivo compreendeu gestações únicas, com fetos não hidrópicos, submetidos à primei
IBICT - Instituto Brasileiro de Informação em Ciência e Tecnologia. Publicado em: 15/06/2011
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21. Cytokines and T-Lymphocute count in patients in the acute and chronic phases of Bartonella bacilliformis infection in an endemic area in peru: a pilot study
Human Bartonellosis has an acute phase characterized by fever and hemolytic anemia, and a chronic phase with bacillary angiomatosis-like lesions. This cross-sectional pilot study evaluated the immunology patterns using pre- and post-treatment samples in patients with Human Bartonellosis. Patients between five and 60 years of age, from endemic areas in Peru,
Revista do Instituto de Medicina Tropical de São Paulo. Publicado em: 2011-06
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22. Valores de transaminasas en cabras criollas infectadas con Trypanosoma vivax.
La presente comunicación reporta los valores de las enzimas transaminasas, Aspartatoaminotransferasa (AST) y Alaninaamino-transferasa (ALT) encontrados en sueros de cabras infectadas con la cepa de Trypanosoma vivax Stock (TvIIV) y sus controles. Las determinaciones se realizaron durante un lapso experimental de diez semanas, divididos en dos períodos igua
Pesquisa Agropecuária Brasileira. Publicado em: 2011
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23. Allium species poisoning in dogs and cats
Dogs and cats are the animals that owners most frequently seek assistance for potential poisonings, and these species are frequently involved with toxicoses due to ingestion of poisonous food. Feeding human foodstuff to pets may prove itself dangerous for their health, similarly to what is observed in Allium species toxicosis. Allium species toxicosis is rep
Journal of Venomous Animals and Toxins including Tropical Diseases. Publicado em: 2011
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24. Molecular characterization of glucose-6-phosphate dehidrogenase deficiency in patients from the southern brazilian city of Porto Alegre, RS
Glucose-6-phosphate dehydrogenase (G6PDH; EC 1.1.1.49) deficiency is one of the most common human enzymopathies throughout the world. Although most affected individuals are asymptomatic, there is a risk of neonatal jaundice and acute hemolytic anemia which can be triggered by infection, some pharmaceuticals and, in older individuals, eating fava beans. We ch
Publicado em: 2010