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dc.contributor.authorShigematsu, Yosuke
dc.contributor.authorHirano, Satoko
dc.contributor.authorHata, Ikue
dc.contributor.authorTanaka, Yukie
dc.contributor.authorSudo, Masakatsu
dc.contributor.authorSakura, Nobuo
dc.contributor.authorTajima, Tsuyoshi
dc.contributor.authorYamaguchi, Seiji
dc.date.accessioned2014-08-05T18:58:58Z
dc.date.available2014-08-05T18:58:58Z
dc.date.issued2002
dc.identifier.urihttp://repositorio.ub.edu.ar/handle/123456789/2863
dc.description.abstractElectrospray tandem mass spectrometry was applied to detect a series of inherited metabolic disorders during a newborn-screening pilot study and a selective screening in Japan. In our mass screening of 102 200 newborns, five patients with propionic acidemia, two with methylmalonic acidemia, two with medium-chain acyl-CoA dehydrogenase deficiency, three with citrullinemia type II, and one with phenylketonuria were identified. In a selective screening of 164 patients with symptoms mainly related to hypoglycemia and/or hyperammonemia, 12 with fatty acid oxidation disorders and six with other disorders were found. The results indicated the importance of newborn screening using this technology in Japan.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.ispartofseriesJournal of Chromatography B, 776;year 2002. 39–48
dc.subjectNewborn mass screeninges_ES
dc.subjectInherited metabolic disorderses_ES
dc.subjectTrastornos metabólicos hereditarioses_ES
dc.subjectCribado poblacional del Recién Nacidoes_ES
dc.titleNewborn mass screening and selective screening using electrospray tandem mass spectrometry in Japanes_ES
dc.typeArticlees_ES


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