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Pure red cell aplasia and primary antiphospholipid syndrome: a unique association
(SPRINGER HEIDELBERGHEIDELBERG, 2013-08-02)
Pure red cell aplasia (PRCA) is a disease with important relationships to autoimmune mechanisms. Although some autoimmune diseases, such as rheumatoid arthritis and systemic lupus erythematosus, have been associated with ...
A Rare Case of Transfusion Transmission of Hepatitis A Virus to Two Patients with Haematological Disease
(Karger Publishers, 2016)
Haematological response of curimbas Prochilodus lineatus, naturally infected with Neoechinorhynchus curemai
(2013-04-01)
This study evaluated the haematological response of curimbas Prochilodus lineatus, naturally infected with Neoechinorhynchus curemai (Acanthocephala: Neoechinorhynchidae). Thirty-seven fish were captured in October 2010 ...
Haematological, biochemical and immunological biomarkers, antibacterial activity, and survival in Nile tilapia Oreochromis niloticus after treatment using antimicrobial peptide LL-37 against Streptococcus agalactiae
(2021-02-25)
Among the antimicrobial peptides (AMPs), which act as natural antibiotics in preventing the colonization of pathogens, LL-37 is noteworthy. It is a human cathelicidin characterized as a broad-spectrum antibiotic, with ...
Bovine Coronavirus (BoCV) Infection in Calves with Diarrhoea and Their Dams
(Universidade Federal do Rio Grande do Sul, 2016)
The Xmnl polymorphic site 5 ' to the gene G gamma in a Brazilian patient with sickle cell anaemia - fetal haemoglobin concentration, haematology and clinical features
(Termedia Publishing House Ltd, 2010-10-01)
We report a 20-year-old female with sickle cell anaemia and with an HbF concentration of 15.8%. The patient was not using hydroxyurea and was not receiving regular blood transfusions. The patient never had chronic ...
The Xmnl polymorphic site 5 ' to the gene G gamma in a Brazilian patient with sickle cell anaemia - fetal haemoglobin concentration, haematology and clinical features
(Termedia Publishing House Ltd, 2010-10-01)
We report a 20-year-old female with sickle cell anaemia and with an HbF concentration of 15.8%. The patient was not using hydroxyurea and was not receiving regular blood transfusions. The patient never had chronic ...