| No. | Código | Descripción |
| 1 |
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Aproximaci贸n matem谩tica para la correcci贸n de la influencia de la hem贸lisis en pruebas frecuentes del laboratorio cl铆nico
Pineda,D., Mart铆nez,C., Mench茅n, A., y Fern谩ndez, E.. (2010). Aproximaci贸n matem谩tica para la correcci贸n de la influencia de la hem贸lisis en pruebas frecuentes del laboratorio cl铆nico. Revista del laboratorio Cl铆nico. 3(1). 25 Pineda,D., Mart铆nez,C., Mench茅n, A., y Fern谩ndez, E. |
2 |
|
Six Sigma: determinaci贸n de metas anal铆ticas con base en la variabilidad biol贸gica y la evoluci贸n tecnol贸gica
Arturo,M.. (2006). Six Sigma: determinaci贸n de metas anal铆ticas con base en la variabilidad biol贸gica y la evoluci贸n tecnol贸gica. Revista Mexicana de patolog铆a Cl铆nica. 54(1). 28 Arturo,M. |
3 |
|
Assuring Control Quality for Quality Controls
Diiulio,R.. (2009). Assuring Control Quality for Quality Controls. TestingDiagnostics. 1. 1 Diiulio,R. |
4 |
|
Biological variation and reference change values: an essential piece of the puzzle of laboratory testing
Plebani,M., y Lippi,G.. (2012). Biological variation and reference change values: an essential piece of the puzzle of laboratory testing. Clinical Chemistry Laboratory Medical, 50(2). DOI 10.1515/CCLM.2011.751. 50(2). 751 Plebani,M., y Lippi,G. |
5 |
|
Within-subject and between-subject biological variation of prothrombin time and activated partial thromboplastin time
Dot,D., Mir贸,J., y Arderiu,F. . (1992). Within-subject and between-subject biological variation of prothrombin time and activated partial thromboplastin time. Annals of Clinical聽Biochemistry. 29. 422 Dot,D., Mir贸,J., y Arderiu,F. |
6 |
|
Calculating Uncertainty of Measurement for Serology Assays by Use of Precision and Bias
Dimech,W., Francis,B., Kox,J., y Roberts,G.. (2006). Calculating Uncertainty of Measurement for Serology Assays by Use of Precision and Bias. Clinical Chemistry. 52(3). 1 Dimech,W., Francis,B., Kox,J., y Roberts,G. |