Please use this identifier to cite or link to this item:
http://hdl.handle.net/20.500.12188/11113| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Mirjana Kocova | en_US |
| dc.contributor.author | Violeta Anastasovska | en_US |
| dc.date.accessioned | 2021-03-22T09:13:36Z | - |
| dc.date.available | 2021-03-22T09:13:36Z | - |
| dc.date.issued | 2016 | - |
| dc.identifier.uri | http://hdl.handle.net/20.500.12188/11113 | - |
| dc.description.abstract | Phenylketonuria is an autosomal recessive inborn error of metabolism which can be prevented by early and continuous treatment. Therefore newborn screening for phenylketonuria has been introduced in many countries. We present here the results of the selective newborn screening for inborn errors of metabolism, including PKU, performed by tandem mass spectrometry which has been introduced in Macedonia since 2011. | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | BMC Part of Springer Nature | en_US |
| dc.relation.ispartof | Orphanet Journal of Rare Diseases | en_US |
| dc.title | Phenylketonuria screening in the Republic of Macedonia | en_US |
| dc.type | Article | en_US |
| dc.identifier.doi | 10.1186/s13023-016-0483-2 | - |
| dc.identifier.url | http://link.springer.com/content/pdf/10.1186/s13023-016-0483-2.pdf | - |
| dc.identifier.volume | 11 | - |
| dc.identifier.issue | 1 | - |
| item.fulltext | No Fulltext | - |
| item.grantfulltext | none | - |
| crisitem.author.dept | Faculty of Medicine | - |
| crisitem.author.dept | Faculty of Medicine | - |
| Appears in Collections: | Faculty of Medicine: Journal Articles | |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.