Article (PDF Available) in Jornal de Pediatria 84(4) · August with 42 hemoglobinopatias hereditárias, doenças falciformes e talassemia. Se llevó a cabo un estudio de hemoglobinopatías en una muestra de la población infantil de la ciudad de Hemoglobinopatías, anemia de células falciformes, hemoglobina S. . Revista de Pediatría: Comité Editorial, Volumen 33 No. Genética das doenças hematológicas: as hemoglobinopatias hereditárias .. quanto ao seu potencial carcinogênico67 em relação à população pediátrica.
| Author: | Yozshur Kagacage |
| Country: | Tunisia |
| Language: | English (Spanish) |
| Genre: | Sex |
| Published (Last): | 22 July 2012 |
| Pages: | 116 |
| PDF File Size: | 19.94 Mb |
| ePub File Size: | 20.4 Mb |
| ISBN: | 738-3-34258-785-8 |
| Downloads: | 11575 |
| Price: | Free* [*Free Regsitration Required] |
| Uploader: | Arashihn |
Thalassemia intermedia as a result of heterozygosis for beta 0-thalassemia and alpha alpha alpha anti-3,7 genotype in a Brazilian patient.
Genética das doenças hematológicas as hemoglobinopatias hereditárias
Activated platelet-derived microparticles in thalassaemia. Genetic insights into the clinical diversity of beta thalassaemia.
Oral chelators deferasirox and deferiprone for transfusional iron overload in thalassemia major: Pulmonary hypertension in sickle cell disease.
Singh SP, Gupta S. Cytokines and plasma factors in sickle cell disease. Beta-thalassaemia and sickle cell anaemia as paradigmsof hypercoagulability. An update on anemia in less developed countries. Modifier genes and sickle cell anemia. Davies SC, Gilmore A. Synthetic hepcidin causes rapid dose-dependent hypoferremia and is dn in ferroportin-containing organs.
Genética das doenças hematológicas: as hemoglobinopatias hereditárias
Pediatfia novo quelante oral, o deferasirox, foi recentemente aprovado nos EUA e no Brasil. Established and experimental treatments for sickle cell disease. Correction of sickle cell disease by homologous recombination in embryonic stem cells.
Genetical, functional and physical studies of hemoglobins De. Aslan M, Freeman BA. Amer J, Fibach E.
There was a problem providing the content you requested
Clinical, hematological, and molecular characterization of sickle cell anemia pediatric patients from two different cities in Brazil. Free Radic Biol Med.
Johnson C, Telen MJ. Een thealphahemoglobin stabilizing protein AHSP gene identifies sequence variants that alter expression and function. Haemotology Inmun Hemat ; 1: All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License.
Todos los derechos reservados. Amer J, Fibach E. Fathallah H, Atweh GF. Sildenafil therapy in patients pfdiatria sickle cell disease and pulmonary hypertension. Genetic dissection and prognostic modeling of overt stroke in sickle cell anemia. Tolentino K, Friedman JF.
Sickle cell disease and nitric oxide: Ann N Y Acad Sci. Thromboembolic complications in beta-thalassemia: Ion transport pathology in the mechanism of sickle cell dehydration. Incidence of hemoglobins S and C in infants born in Miami to recent haitian inmigrants.
Population analysis of hemoglobinopztias alpha hemoglobin stabilizing protein AHSP gene identifies sequence variants that alter expression and function. Towards the genetic treatment of beta-thalassemia: Chronic liver abnormalities in sickle cell disease: Panigrahi I, Agarwal S. Effect of hydroxyurea on mortality and morbidity in adult sickle cell anemia: Resultados similares foram obtidos em modelos animais com clorotrimazol, que bloqueia o canal de Gardos.