Parámetros hematológicos de pacientes con fibrosis 2133quística de la costa caribe colombiana: análisis y asociación con aislamiento de pseudomonas aeruginosa
Parámetros hematológicos de pacientes con fibrosis 2133quística de la costa caribe colombiana: análisis y asociación con aislamiento de pseudomonas aeruginosa
Issue
Section
Artículo Original
How to Cite
Rodríguez Escobar et al., Z. (2009). Parámetros hematológicos de pacientes con fibrosis 2133quística de la costa caribe colombiana: análisis y asociación con aislamiento de pseudomonas aeruginosa. NOVA, 7(11). https://doi.org/10.22490/24629448.1083
Dimensions
license
NOVA by http://www.unicolmayor.edu.co/publicaciones/index.php/nova is distributed under a license creative commons non comertial-atribution-withoutderive 4.0 international.
Furthermore, the authors keep their property intellectual rights over the articles.
Show authors biography
Article visits 169 | PDF visits 91
Downloads
Download data is not yet available.
- Ratjen F, Döring G. Cystic fibrosis. Lancet. 2003;361:681–689.
- Bobadilla J, Macek M, Fine J, Farrell P. Cystic fibrosis: a worldwide analysis of CFTR mutations: correlation with incidence data and application to screening. Hum Mutat. 2002;19:575-606.
- Keyeux G, Rodas MC, Bienvenu T, Garavito P, Vidaud, Sanchez D, et al. CFTR mutations in patients from Colombia: Implications for local and regional molecular diagnosis programs. Hum Mutat. 2003;22:259.
- Organización Mundial de la Salud (OMS). The molecular genetic epidemiology of cystic fibrosis. Ginebra: WHO; 2004.
- Instituto de Genética, Universidad Nacional de Colombia. Fibrosis quística, Fibrosis quística en Colombia. Disponible en: http://www.genetica.unal.edu.co/pages/fibrosis.html. Consultado: 11 de Julio 2008 .
- Heijerman H. Infection and inflammation in cystic fibrosis: A short review. J Cyst Fibros. 2005;4:3-5.
- Taccetti G, Campana S, Festini F, Mascherini M, Doring G. Early eradication therapy against Pseudomonas aeruginosa in cystic fibrosis patients. Eur Respir J. 2005;26:458–461.
- Jiménez TS, Bousoño GC, Ruiz DP. Protocolos de Patología respiratoria. Patología pulmonar en la fibrosis quística. Bol Soc Catalana Pediatr. 2007;47 Suppl 2:S7-13.
- Cystic Fibrosis Foundation Patient Registry, 2000. Annual Data Report. Bethesda, Maryland; 2001.
- Sánchez I, Perez M, Boza M, Lezana V, Vila M, Repetto G, et al. Consenso nacional de fibrosis quística. Rev Chil Pediatr. 2001;72:356–380.
- Girón R, Salcedo A, Casanova A. Antecedentes históricos y epidemiología. En: Girón R, Salcedo A, eds. Monografía de Fibrosis Quística. Madrid: Ergón; 2005. p. 9-20.
- Becker A. Interpretación del hemograma. Rev Chil Pediatr. 2001;72:460-465.
- García M, Garfia C, Manzanares J. Fibrosis quística. Monografías Neumomadrid. 1ª ed. Madrid: Ergón; 2005.
- Organización Mundial de la Salud (OMS). Iron deficiency anaemia: assessment, prevention, and control. A guide for program managers. Guía Tecnica. Ginebra: OMS; 2004. Xiii.
- Sinaasappel M, Stern M, Littlewood J, Wolfe S, Steinkamp G, Heijerman H, et al. Nutrition in patients with cystic fibrosis: a European consensus. J Cystic Fibrosis. 2002;1:51-75.
- Wilfond B, Farrell P, Laxova A. Severe haemolytic anemia associated with vitamine E deficiency in infants with cystic fibrosis. Clin Pediatr. 1994;33:2–7.
- Torres D. Estudio clínico epidemiológico de la fibrosis quística en el Instituto de Salud del Niño, Lima 1991 – 2002. Paediatrica. 2002;4:-15.
- Dowsett J, Tully O. Cystic fibrosis. En: Caballero B, Allen L, Prentice A, editores. Encyclopedia of Human Nutrition. 2°ed. Boston: Elsevier/Academic Press; 2005. p 494-501.
- Stoltzfus RJ. Iron-deficiency anemia: reexamining the nature and magnitude of the public health problem. Summary: implications for research and programs. J Nutr. 2001;131(2 Suppl 2): 697S-700S.
- Kahre T, Teder M, Panov M, Metspalu A. Severe CF manifestation with anaemia and failure to thrive in a 394delTT homozygous patient. J Cyst Fibros. 2004;3:58-60.
- Steven M. Rowe M, Miller S. Mechanisms of disease cystic fibrosis. N Engl J Med. 2001;352:1992-2001.
- Ramsey B, Accurso F, Cutting G, Welsh M. Cystic fibrosis. In: Valle D, Beaudet A, Vogelstein B, Kenneth K, Antonarakis S, Ballabio A editors. The metabolic and molecular bases of inherited disease. 1ª ed. Baltimore: Mc Graw Hill; 2007. p. 121- 88.
- Dodge JA, Turck D. Cystic fibrosis: nutritional consequences and management. Best Pract Res Clin Gastroenterol. 2006;20:531-546.
- Lancellotti L, D’Orazio C, Mastella G, Mazzi G, Lippi U. Deficiency of vitamins E and A in cystic fibrosis is independent of pancreatic function and current enzyme and vitamin supplementation. Eur J Pediatr. 1996;155:281-285.
- Swann IL, Kendra JR. Anaemia, vitamin E deficiency and failure to thrive in an infant. Clin Lab Haematol. 1998;20:61-63.
- Winklhofer-Roob BM. Cystic fibrosis: nutritional status and micronutrients. Curr Opin Clin Nutr Metab Care. 2000;3:293-297.
- Rodríguez J, Hernández R, López R. Aproximación al diagnostico de las anemias. BSCP Can Ped. 2001;25:251–255.
- Reid DW, Withers NJ, Francis L, Wilson JW, Kotsimbos TC. Iron deficiency in cystic fibrosis: relationship to lung disease severity and chronic Pseudomonas aeruginosa infection. Chest. 2002;121:48-54.
- O’connor TM, McGrath DS, Short C, O’donnell MJ, Sheehy M, Bredin CP. Subclinical anaemia of chronic disease in adult patients with cystic fibrosis. J Cyst Fibros. 2002;1:31-34.
- Segal E, Grenoville M, Macri C, Fernández A. Consenso de fibrosis quística. Arch argent Pediatr. 1999;97:188–219.
- Davies JC. Pseudomonas aeruginosa in cystic fibrosis: pathogenesis and persistence. Paediatr Respir Rev. 2002;3:128-134.
- Gómez MI, Prince A. Opportunistic infections in lung disease: Pseudomonas infections in cystic fibrosis. Curr Opin Pharmacol. 2007;7:244-251.
- Wesley A, Dawson K, Hewitt C, Kerr A. Clinical features of individuals with cystic fibrosis in New Zealand. N Z Med J. 1993;106:28-30.
- Canadian Cystic Fibrosis Foundation. Canadian patient data registry national report 1998. Toronto: Canadian Cystic Fibrosis Foundation; 2001.
- López S, Suarez M. Leucocitosis. Guías clínicas. 2006;6:1–4.
- Balke B, Schmoldt S, Häussler S, Suerbaum S, Heesemann J, Hogardt M. A German external quality survey of diagnostic microbiology of respiratory tract infections in patients with cystic fibrosis. J Cyst Fibros. 2008;7:7-14.
- Cantón R, Molina A, Máiz L. Fibrosis quística. Monografías Neumomadrid. 2ª ed. Madrid: Ergón; 2005.
- Wat D. Impact of respiratory viral infections on cystic fibrosis. Postgrad Med J. 2003;79:201-203.
- -------------------------------------------------------------------------------
- DOI: http://dx.doi.org/10.22490/24629448.1083