The Genetics Of Blood Disorders: Hereditary Hemoglobinopathies.

dc.creatorSonati, Maria de Fátima
dc.creatorCosta, Fernando Ferreira
dc.date2008-Aug
dc.date2015-11-27T13:13:11Z
dc.date2015-11-27T13:13:11Z
dc.date.accessioned2018-03-29T01:07:30Z
dc.date.available2018-03-29T01:07:30Z
dc.identifierJornal De Pediatria. v. 84, n. 4 Suppl, p. S40-51, 2008-Aug.
dc.identifier1678-4782
dc.identifierdoi:10.2223/JPED.1802
dc.identifierhttp://www.ncbi.nlm.nih.gov/pubmed/18791648
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/197975
dc.identifier18791648
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1298208
dc.descriptionTo summarize recently published data on the pathophysiology, diagnosis and treatment of sickle cell diseases and beta-thalassemias, the most relevant hereditary hemoglobinopathies in the global population. Searches were run on the MEDLINE and SCIELO databases, limited to the period from 2003 to May 2008, using the terms hereditary hemoglobinopathies, sickle cell diseases and beta-thalassemia. Two books and two chapters were also included. More than 2,000 articles were identified; those providing the most important information and broadest views were selected. Morbidity and mortality rates from sickle cell diseases and beta-thalassemia are still very high and represent an important challenge. Increased understanding of pathophysiological aspects has lead to significant improvements in treatment and prevention of these diseases.
dc.description84
dc.descriptionS40-51
dc.languageeng
dc.languagepor
dc.relationJornal De Pediatria
dc.relationJ Pediatr (Rio J)
dc.rightsaberto
dc.rights
dc.sourcePubMed
dc.subjectAnemia, Sickle Cell
dc.subjectAnimals
dc.subjectDisease Models, Animal
dc.subjectHumans
dc.subjectBeta-thalassemia
dc.titleThe Genetics Of Blood Disorders: Hereditary Hemoglobinopathies.
dc.typeArtículos de revistas


Este ítem pertenece a la siguiente institución