dc.contributor.author | Shigematsu, Yosuke | |
dc.contributor.author | Hirano, Satoko | |
dc.contributor.author | Hata, Ikue | |
dc.contributor.author | Tanaka, Yukie | |
dc.contributor.author | Sudo, Masakatsu | |
dc.contributor.author | Sakura, Nobuo | |
dc.contributor.author | Tajima, Tsuyoshi | |
dc.contributor.author | Yamaguchi, Seiji | |
dc.date.accessioned | 2014-08-05T18:58:58Z | |
dc.date.available | 2014-08-05T18:58:58Z | |
dc.date.issued | 2002 | |
dc.identifier.uri | http://repositorio.ub.edu.ar/handle/123456789/2863 | |
dc.description.abstract | Electrospray 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.iso | en | es_ES |
dc.publisher.Editor | Universidad de Belgrano - Documentos CEEGMD - Centro para el estudio de enfermedades genéticas, metabólicas y discapacidades. Facultad de Ciencias Exactas | |
dc.relation.ispartofseries | Journal of Chromatography B, 776;year 2002. 39–48 | |
dc.subject | Newborn mass screening | es_ES |
dc.subject | Inherited metabolic disorders | es_ES |
dc.subject | Trastornos metabólicos hereditarios | es_ES |
dc.subject | Cribado poblacional del Recién Nacido | es_ES |
dc.title | Newborn mass screening and selective screening using electrospray tandem mass spectrometry in Japan | es_ES |
dc.type | Article | es_ES |