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Anemia haemolitic

Silvina Mazaira
Almost all clases of psychiatric drugs (typical and atypical antipsychotics, antidepressants, mood stabilizers, benzodiazepines) have been reported as possible causes of haematological toxicity. This is a review of the literature in which different clinical situations involving red blood cells, white blood cells, platelets and impaired coagulation are detailed and the drugs more frequently involved are listed. The haematological adverse reactions detailed here include: aplastic anemia, haemolitic anemia, leukopenia, agranulocytosis, leukocytosis, eosinophilia, thrombocytosis, thrombocytopenia, disordered platelet function and impaired coagulation...
November 2008: Vertex: Revista Argentina de Psiquiatriá
G Schaison
Sickle cell anemia is a congenital haemolitic anemia. The replacement of the hydrophilic glutamine residue at the 6 position of the beta chain by the hydrophobic valine leads to severe conformation change in the molecule resulting in sickling. The consequences are haemolysis, vascular stasis and thrombotic crisis. Infection triggers thrombosis and vice-versa. Clinical manifestation is anemia punctuated by intermittent crisis producing infarction. Pneumococcal and salmonella infections are frequent mainly in the lungs and bones...
1983: Revue de Stomatologie et de Chirurgie Maxillo-faciale
F Dambrosio, M A Giacomoni, F Cattaneo
No abstract text is available yet for this article.
February 1969: Annali di Ostetricia, Ginecologia, Medicina Perinatale
A Notario, M Ricetti, U Comin, A Cardenà, E Grandi, P Bernini
A study of membrane proteins in pernicious anaemia and other haemolitic and anhaemolytic erythropathies is reported. Cellulose acetate and acrylamide gel electrophoresis was carried out and acid, neutral and basic amino acid contents were determined. Relatively specific alterations were noted. Chromatographic analysis of the amino acids suggested that in pernicious anaemia, as in other conditions, structural changes take place in the red cell membrane, though these may be confined to certain sectors. A constant alteration related to the concomitance or otherwise of erythrocyte hyperhaemolysis, however, could not be discerned...
March 24, 1977: Minerva Medica
D Korać, E Stojimirović, S Miletić
In patients with hereditary haematologic diseases risk of repetition of these anomalies in brothers and sisters of probands and their progenies was assessed. In haemiphilia and Wiskott-Aldrich's. thrombocytopenia, both caused by a mutant gene in an X chromosome, prenatal pole determination was consulted in order to have a pregnancy with a male fetus interrupted due to high risk. Dominantly hereditary spherocytosis, eliptocytosis, chronic benign neutropenia are the diseases which do not appear in such a severe form that ceasation of further pregnancies should be consulted, instead, an early postnatal diagnosis is suggested to the families with increased risk of these anomalies...
1977: Bilten za Hematologiju i Transfuziju
D Negovanović, N Dograjić, R Konecni, R Jokanović, E Stojimirović
During the last ten years twenty children with hereditary haemolitic anemia were admitted to the Children's University Hospital. As hyperbilirubinemia is one of the factors influencing calculi formation, we made systematic examination of the biliary and urinary pathways, because throughout these the excretory activity of bilirubin and its compound urobilinogen is performed. Owing to such a procedure, out of twenty children ten were discovered to have biliary calculi and other ten biliary and urinary calculi...
1977: Bilten za Hematologiju i Transfuziju
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