Dasa Perko

Ljubljana, 1000, Slovenia

Last Updated: 09/26/2026

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Found 12 publications

Current Status of Newborn Screening in Southeastern and Central Europe.

Current Status of Newborn Screening in Southeastern and Central Europe.

Journal: International journal of neonatal screening

Published: December 30, 2025

International Survey on Phenylketonuria Newborn Screening.

International Survey on Phenylketonuria Newborn Screening.

Journal: International journal of neonatal screening

Published: January 30, 2025

Sudden Death of a Four-Day-Old Newborn Due to Mitochondrial Trifunctional Protein/Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiencies and a Systematic Literature Review of Early Deaths of Neonates with Fatty Acid Oxidation Disorders.

Sudden Death of a Four-Day-Old Newborn Due to Mitochondrial Trifunctional Protein/Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiencies and a Systematic Literature Review of Early Deaths of Neonates with Fatty Acid Oxidation Disorders.

Journal: International journal of neonatal screening

Published: November 05, 2024

Newborn Screening in a Pandemic-Lessons Learned.

Newborn Screening in a Pandemic-Lessons Learned.

Journal: International journal of neonatal screening

Published: February 27, 2023

Comparison of Tandem Mass Spectrometry and the Fluorometric Method-Parallel Phenylalanine Measurement on a Large Fresh Sample Series and Implications for Newborn Screening for Phenylketonuria.

Comparison of Tandem Mass Spectrometry and the Fluorometric Method-Parallel Phenylalanine Measurement on a Large Fresh Sample Series and Implications for Newborn Screening for Phenylketonuria.

Journal: International journal of molecular sciences

Published: December 08, 2022

Optimizing the Phenylalanine Cut-Off Value in a Newborn Screening Program.

Optimizing the Phenylalanine Cut-Off Value in a Newborn Screening Program.

Journal: Genes

Published: December 17, 2021

Very Long-Chain Acyl-CoA Dehydrogenase Deficiency: High Incidence of Detected Patients With Expanded Newborn Screening Program.

Very Long-Chain Acyl-CoA Dehydrogenase Deficiency: High Incidence of Detected Patients With Expanded Newborn Screening Program.

Journal: Frontiers in genetics

Published: December 31, 2020

Expanded Newborn Screening Program in Slovenia using Tandem Mass Spectrometry and Confirmatory Next Generation Sequencing Genetic Testing.

Expanded Newborn Screening Program in Slovenia using Tandem Mass Spectrometry and Confirmatory Next Generation Sequencing Genetic Testing.

Journal: Zdravstveno varstvo

Published: April 17, 2020

PIK3AP1 and SPON2 Genes Are Differentially Methylated in Patients With Periodic Fever, Aphthous Stomatitis, Pharyngitis, and Adenitis (PFAPA) Syndrome.

PIK3AP1 and SPON2 Genes Are Differentially Methylated in Patients With Periodic Fever, Aphthous Stomatitis, Pharyngitis, and Adenitis (PFAPA) Syndrome.

Journal: Frontiers in immunology

Published: March 04, 2020

Next generation sequencing as a follow-up test in an expanded newborn screening programme.

Next generation sequencing as a follow-up test in an expanded newborn screening programme.

Journal: Clinical biochemistry

Published: June 07, 2017

Clinical features and genetic background of the periodic Fever syndrome with aphthous stomatitis, pharyngitis, and adenitis: a single center longitudinal study of 81 patients.

Clinical features and genetic background of the periodic Fever syndrome with aphthous stomatitis, pharyngitis, and adenitis: a single center longitudinal study of 81 patients.

Journal: Mediators of inflammation

Published: November 26, 2014

The carrier rate and spectrum of MEFV gene mutations in central and southeastern European populations.

The carrier rate and spectrum of MEFV gene mutations in central and southeastern European populations.

Journal: Clinical and experimental rheumatology

Published: September 14, 2014

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Last Updated: 09/26/2026