Anemia de células falciformes

Autores:: Chaves, Walter
Amador, Dolly
Sánchez, Jorge

Tipo de recurso:: Article of journal

Fecha de publicación:: 2014

Institución:: Fundación Universitaria de Ciencias de la Salud - FUCS

Repositorio:: Repositorio Digital Institucional ReDi

Idioma:: spa

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dc.title.spa.fl_str_mv	Anemia de células falciformes
dc.title.translated.eng.fl_str_mv	Sickle cell anemia
title	Anemia de células falciformes
spellingShingle	Anemia de células falciformes drepanocitosis anemia de células falciformes hemoglobinopatías hemoglobina S sickle cell disease sickle cell anemia hemoglobinopathies hemoglobin S
title_short	Anemia de células falciformes
title_full	Anemia de células falciformes
title_fullStr	Anemia de células falciformes
title_full_unstemmed	Anemia de células falciformes
title_sort	Anemia de células falciformes
dc.creator.fl_str_mv	Chaves, Walter Amador, Dolly Sánchez, Jorge
dc.contributor.author.spa.fl_str_mv	Chaves, Walter Amador, Dolly Sánchez, Jorge
dc.subject.spa.fl_str_mv	drepanocitosis anemia de células falciformes hemoglobinopatías hemoglobina S
topic	drepanocitosis anemia de células falciformes hemoglobinopatías hemoglobina S sickle cell disease sickle cell anemia hemoglobinopathies hemoglobin S
dc.subject.eng.fl_str_mv	sickle cell disease sickle cell anemia hemoglobinopathies hemoglobin S
publishDate	2014
dc.date.accessioned.none.fl_str_mv	2014-09-01 00:00:00 2022-06-29T19:35:59Z
dc.date.issued.none.fl_str_mv	2014-09-01
dc.date.available.none.fl_str_mv	2014-09-01 00:00:00 2022-06-29T19:35:59Z
dc.type.spa.fl_str_mv	Artículo de revista
dc.type.eng.fl_str_mv	Journal article
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dc.relation.references.spa.fl_str_mv	Rees DC, Williams TN, Gladwin MT. Sickle-cell disease. Lancet. 2010;376(9757):2018-31. Bender MA, Hobbs W. Sickle cell disease. In: Pagon RA, Adam MP, Ardinger HH, Bird TD, Dolan CR, Fong CT, et al. GeneReviewsTM[monografía en Internet]. Washington, Seattle; 1993-2014 [citado 9 Jul 2014]. Disponible en: http://www.ncbi.nlm.nih.gov/books/NBK1377/ Denis M. Sickle cell anemia. In: Miller LP, editor. Blood diseases of infancy and childhood. 7th ed. St. Louis, Toronto: Mosby; 1995. p. 415. Platt OS, Brambilla DJ, Rosse WF, Milner PF, Castro O, Steinberg MH, et al. Mortality in sickle cell disease. Life expectancy and risk factors for early death. N Engl J Med. 1994;330(23):1639-44. Lane PA, O’Connell JL, Lear JL, Rogers ZR, Woods GM, Hassell KL, et al. Functional asplenia in hemoglobin SC disease. Blood. 1995;85(8):2238-44. Tsaras G, Owusu-Ansah A, Boateng FO, Amoateng-Adjepong Y. Complications associated with sickle cell trait: a brief narrative review. Am J Med. 2009;122(6):507-12. Gong L, Parikh S, Rosenthal PJ, Greenhouse B. Biochemical and immunological mechanisms by which sickle cell trait protects against malaria. Malar J. 2013;12(1):317. Durán CL, Morales OL, Echeverri SJ, Isaza M. Haplotipos del gen de la globina beta en portadores de hemoglobina S en Colombia. Biomedica. 2012;32(1):103-11. Solanki DL, Kletter GG, Castro O. Acute splenic sequestration crises in adults with sickle cell disease. Am J Med. 1986;80(5):985-90. Powars D, Wilson B, Imbus C, Pegelow C, Allen J. The natural history of stroke in sickle cell disease. Am J Med. 1978;65(3):461-71. Minter KR, Gladwin MT. Pulmonary complications of sickle cell anemia. A need for increased recognition, treatment, and research. Am J Respir Crit Care Med. 2001;164(11):2016-9. Ballas SK, Lieff S, Benjamin LJ, Dampier CD, Heeney MM, Hoppe C, et al. Definitions of the phenotypic manifestations of sickle cell disease. Am J Hematol. 2010;85(1):6-13. Nagalla S, Ballas SK. Drugs for preventing red blood cell dehydration in people with sickle cell disease. Cochrane Database Syst Rev. 2012;7:CD003426. Vichinsky E, Williams R, Das M, Earles AN, Lewis N, Adler A, et al. Pulmonary fat embolism: a distinct cause of severe acute chest syndrome in sickle cell anemia. Blood. 1994;83(11):3107-12. Vichinsky EP, Neumayr LD, Earles AN, Williams R, Lennette ET, Dean D, et al. Causes and outcomes of the acute chest syndrome in sickle cell disease. National Acute Chest Syndrome Study Group. N Engl J Med. 2000;342(25):1855-65. National Institute of Health, National Heart Lung and Blood Institute. The management of sickle cell disease [monografía en Internet]. Washington: The Institute; 2004 [citado 9 Jul 2014]. Disponible en: http://www.nhlbi.nih.gov/health/prof/blood/sickle/sc_mngt.pdf Davies S, Olujohungbe A. Hydroxyurea for sickle cell disease. Cochrane Database Syst Rev. 2001(2):CD002202. Segal JB, Strouse JJ, Beach MC, et al. Hydroxyurea for the treatment of sickle cell disease [monografía en Internet]. Rockville (MD): Agency for Healthcare Research and Quality; 2008 [citado 9 Jul 2014]. Disponible en: http://www.ncbi.nlm.nih.gov/books/NBK38503/ Halsey C, Roberts IA. The role of hydroxyurea in sickle cell disease. Br J Haematol. 2003;120(2):177-86. Platt OS. Hydroxyurea for the treatment of sickle cell anemia. N Engl J Med. 2008;358(13):1362-9. Ortega Aramburu JJ. [Sickle-cell anemia: an emerging disease in Spain]. An Pediatr (Barc). 2003;58(2):93-4. Wilson RE, Krishnamurti L, Kamat D. Management of sickle cell disease in primary care. Clin Pediatr (Phila). 2003;42(9):753-61. Ruggeri A, Eapen M, Scaravadou A, Cairo MS, Bhatia M, Kurtzberg J, et al. Umbilical cord blood transplantation for children with thalassemia and sickle cell disease. Biol Blood Marrow Transplant. 2011;17(9):1375-82.
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dc.relation.citationedition.spa.fl_str_mv	Núm. 3 , Año 2014 : Julio – Septiembre
dc.relation.citationendpage.none.fl_str_mv	225
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dc.relation.citationvolume.spa.fl_str_mv	23
dc.relation.ispartofjournal.spa.fl_str_mv	Revista Repertorio de Medicina y Cirugía
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spelling	Chaves, Walterf68f7a620f26a75d133a0df7e3188463500Amador, Dollyc71bf48a8e77d8950d3ab872db991662300Sánchez, Jorgea7b399307962dc36fc0b4935afd0174f2014-09-01 00:00:002022-06-29T19:35:59Z2014-09-012014-09-01 00:00:002022-06-29T19:35:59ZSociedad de Cirugía de Bogotá, Hospital de San José y Fundación Universitaria de Ciencias de la SaludFundación Universitaria de Ciencias de la Salud FUCS - 0info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/4.0/http://purl.org/coar/access_right/c_abf2https://revistas.fucsalud.edu.co/index.php/repertorio/article/view/715drepanocitosisanemia de células falciformeshemoglobinopatíashemoglobina Ssickle cell diseasesickle cell anemiahemoglobinopathieshemoglobin SAnemia de células falciformesSickle cell anemiaapplication/pdfArtículo de revistaJournal articlehttp://purl.org/coar/resource_type/c_6501http://purl.org/coar/resource_type/c_6501http://purl.org/coar/resource_type/c_2df8fbb1info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionTexthttp://purl.org/redcol/resource_type/ARTREFhttp://purl.org/coar/version/c_970fb48d4fbd8a8510.31260/RepertMedCir.v23.n3.2014.7150121-7372https://repositorio.fucsalud.edu.co/handle/001/27392462-991Xhttps://doi.org/10.31260/RepertMedCir.v23.n3.2014.715spaRees DC, Williams TN, Gladwin MT. Sickle-cell disease. Lancet. 2010;376(9757):2018-31.Bender MA, Hobbs W. Sickle cell disease. In: Pagon RA, Adam MP, Ardinger HH, Bird TD, Dolan CR, Fong CT, et al. GeneReviewsTM[monografía en Internet]. Washington, Seattle; 1993-2014 [citado 9 Jul 2014]. Disponible en: http://www.ncbi.nlm.nih.gov/books/NBK1377/Denis M. Sickle cell anemia. In: Miller LP, editor. Blood diseases of infancy and childhood. 7th ed. St. Louis, Toronto: Mosby; 1995. p. 415.Platt OS, Brambilla DJ, Rosse WF, Milner PF, Castro O, Steinberg MH, et al. Mortality in sickle cell disease. Life expectancy and risk factors for early death. N Engl J Med. 1994;330(23):1639-44.Lane PA, O’Connell JL, Lear JL, Rogers ZR, Woods GM, Hassell KL, et al. Functional asplenia in hemoglobin SC disease. Blood. 1995;85(8):2238-44.Tsaras G, Owusu-Ansah A, Boateng FO, Amoateng-Adjepong Y. Complications associated with sickle cell trait: a brief narrative review. Am J Med. 2009;122(6):507-12.Gong L, Parikh S, Rosenthal PJ, Greenhouse B. Biochemical and immunological mechanisms by which sickle cell trait protects against malaria. Malar J. 2013;12(1):317.Durán CL, Morales OL, Echeverri SJ, Isaza M. Haplotipos del gen de la globina beta en portadores de hemoglobina S en Colombia. Biomedica. 2012;32(1):103-11.Solanki DL, Kletter GG, Castro O. Acute splenic sequestration crises in adults with sickle cell disease. Am J Med. 1986;80(5):985-90.Powars D, Wilson B, Imbus C, Pegelow C, Allen J. The natural history of stroke in sickle cell disease. Am J Med. 1978;65(3):461-71.Minter KR, Gladwin MT. Pulmonary complications of sickle cell anemia. A need for increased recognition, treatment, and research. Am J Respir Crit Care Med. 2001;164(11):2016-9.Ballas SK, Lieff S, Benjamin LJ, Dampier CD, Heeney MM, Hoppe C, et al. Definitions of the phenotypic manifestations of sickle cell disease. Am J Hematol. 2010;85(1):6-13.Nagalla S, Ballas SK. Drugs for preventing red blood cell dehydration in people with sickle cell disease. Cochrane Database Syst Rev. 2012;7:CD003426.Vichinsky E, Williams R, Das M, Earles AN, Lewis N, Adler A, et al. Pulmonary fat embolism: a distinct cause of severe acute chest syndrome in sickle cell anemia. Blood. 1994;83(11):3107-12.Vichinsky EP, Neumayr LD, Earles AN, Williams R, Lennette ET, Dean D, et al. Causes and outcomes of the acute chest syndrome in sickle cell disease. National Acute Chest Syndrome Study Group. N Engl J Med. 2000;342(25):1855-65.National Institute of Health, National Heart Lung and Blood Institute. The management of sickle cell disease [monografía en Internet]. Washington: The Institute; 2004 [citado 9 Jul 2014]. Disponible en: http://www.nhlbi.nih.gov/health/prof/blood/sickle/sc_mngt.pdfDavies S, Olujohungbe A. Hydroxyurea for sickle cell disease. Cochrane Database Syst Rev. 2001(2):CD002202.Segal JB, Strouse JJ, Beach MC, et al. Hydroxyurea for the treatment of sickle cell disease [monografía en Internet]. Rockville (MD): Agency for Healthcare Research and Quality; 2008 [citado 9 Jul 2014]. Disponible en: http://www.ncbi.nlm.nih.gov/books/NBK38503/Halsey C, Roberts IA. The role of hydroxyurea in sickle cell disease. Br J Haematol. 2003;120(2):177-86.Platt OS. Hydroxyurea for the treatment of sickle cell anemia. N Engl J Med. 2008;358(13):1362-9.Ortega Aramburu JJ. [Sickle-cell anemia: an emerging disease in Spain]. An Pediatr (Barc). 2003;58(2):93-4.Wilson RE, Krishnamurti L, Kamat D. Management of sickle cell disease in primary care. Clin Pediatr (Phila). 2003;42(9):753-61.Ruggeri A, Eapen M, Scaravadou A, Cairo MS, Bhatia M, Kurtzberg J, et al. Umbilical cord blood transplantation for children with thalassemia and sickle cell disease. Biol Blood Marrow Transplant. 2011;17(9):1375-82.https://revistas.fucsalud.edu.co/index.php/repertorio/article/download/715/754Núm. 3 , Año 2014 : Julio – Septiembre225322123Revista Repertorio de Medicina y CirugíaPublicationOREORE.xmltext/xml2608https://repositorio.fucsalud.edu.co/bitstreams/6433b0a0-0aa9-4968-bf9a-61a082769c3c/downloadd88b2c8a8266c4269f064d9df867dc85MD51001/2739oai:repositorio.fucsalud.edu.co:001/27392024-02-02 13:07:17.994https://creativecommons.org/licenses/by-nc-sa/4.0/Fundación Universitaria de Ciencias de la Salud FUCS - 0metadata.onlyhttps://repositorio.fucsalud.edu.coRepositorio Digital de la Fundación Universitaria de Ciencias de la Saludredi@fucsalud.edu.co

Anemia de células falciformes

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