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dc.contributor.authorCharrow, Joel
dc.contributor.authorGoodman, Stephen I.
dc.contributor.authorMcCabe, Edward R.G.
dc.contributor.authorRinaldo, Piero
dc.date.accessioned2014-08-07T17:58:29Z
dc.date.available2014-08-07T17:58:29Z
dc.date.issued2000
dc.identifier.urihttp://repositorio.ub.edu.ar/handle/123456789/2905
dc.description.abstractTandem mass spectrometry (MS/MS) has been used for sev-eral years to identify and measure carnitine esters in blood and urine of children suspected of having inborn errors of metab-olism. Indeed, acylcarnitine analysis is a better diagnostic test for disorders of fatty acid oxidation than organic acid analysis because it can often detect these conditions when the patient is not acutely ill.1 More recently, MS/MS has been used in pilot programs to screen newborns for these conditions and for dis-orders of amino and organic acid metabolism as well. The pur-pose of this article is to describe MS/MS and discuss its poten-tial role in newborn screening programs.es_ES
dc.language.isoenes_ES
dc.publisher.EditorUniversidad de Belgrano - Documentos CEEGMD - Centro para el estudio de enfermedades genéticas, metabólicas y discapacidades. Facultad de Ciencias Exactas
dc.relation.ispartofseriesACMG/ASHG statement;July/August 2000 - Vol. 2 z No. 4
dc.subjectTandem mass spectrometryes_ES
dc.subjectnewborn screeninges_ES
dc.subjectDisorderes_ES
dc.subjectTandem espectrometría de masases_ES
dc.subjectevaluación del recién nacidoes_ES
dc.subjectTrastornoes_ES
dc.titleTandem mass spectrometry in newborn screeninges_ES
dc.typeArticlees_ES


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