Cargando…
The evaluation of phenylalanine levels in Estonian phenylketonuria patients during eight years by electronic laboratory records
Blood phenylalanine (Phe) values from the dried blood spots of all Estonian phenylketonuria (PKU) patients have been deposited into a unified electronic laboratory database for eight years, providing an opportunity to assess the adherence of the patients to dietary recommendations over time and to o...
Autores principales: | Lilleväli, Hardo, Reinson, Karit, Muru, Kai, Saarsalu, Siret, Künnapas, Kadi, Kahre, Tiina, Murumets, Ülle, Õunap, Katrin |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6434493/ https://www.ncbi.nlm.nih.gov/pubmed/30963030 http://dx.doi.org/10.1016/j.ymgmr.2019.100467 |
Ejemplares similares
-
High incidence of low vitamin B12 levels in Estonian newborns
por: Reinson, Karit, et al.
Publicado: (2018) -
FLAD1‐associated multiple acyl‐CoA dehydrogenase deficiency identified by newborn screening
por: Muru, Kai, et al.
Publicado: (2019) -
The prevalence of inherited metabolic disorders in Estonian population over 30 years: A significant increase during study period
por: Tiivoja, Elis, et al.
Publicado: (2022) -
The prevalence of germline pathogenic variants in Estonian colorectal cancer patients: results from routine clinical setting 2016–2021
por: Roht, Laura, et al.
Publicado: (2022) -
Genome sequencing identifies a homozygous inversion disrupting QDPR as a cause for dihydropteridine reductase deficiency
por: Lilleväli, Hardo, et al.
Publicado: (2020)