Ziga Iztok Remec
Overview
Explore the profile of Ziga Iztok Remec including associated specialties, affiliations and a list of published articles.
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Articles
8
Citations
53
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0
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Recent Articles
1.
Drole Torkar A, Klinc A, Remec Z, Rankovic B, Bartolj K, Bertok S, et al.
Int J Neonatal Screen
. 2025 Feb;
11(1).
PMID: 39982343
Mitochondrial trifunctional protein (MTP) and long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiencies have been a part of the Slovenian newborn screening (NBS) program since 2018. We describe a case of early lethal...
2.
Levstek T, Bahcic E, Vujkovac B, Cokan Vujkovac A, Tesovnik T, Remec Z, et al.
Cells
. 2025 Feb;
14(3).
PMID: 39937009
Fabry nephropathy is a life-threatening complication of Fabry disease characterized by complex and incompletely understood pathophysiological processes possibly linked to premature aging. We aimed to investigate leukocyte telomere length (LTL),...
3.
Berlic M, Korosec M, Remec Z, Cuk V, Battelino T, Repic Lampret B
Eur J Pediatr
. 2024 Apr;
183(7):3085-3094.
PMID: 38658398
As children spend up to 9 h a day in kindergarten, the main purpose of our study was to evaluate the effect of antioxidant-rich kindergarten meals on oxidative stress biomarkers...
4.
Mlinaric M, Bonham J, Kozich V, Kolker S, Majek O, Battelino T, et al.
Int J Neonatal Screen
. 2023 Apr;
9(2).
PMID: 37092515
The COVID-19 pandemic affected many essential aspects of public health, including newborn screening programs (NBS). Centers reported missing cases of inherited metabolic disease as a consequence of decreased diagnostic process...
5.
Perko D, Groselj U, Cuk V, Remec Z, Zerjav Tansek M, Drole Torkar A, et al.
Int J Mol Sci
. 2023 Feb;
24(3).
PMID: 36768810
Phenylketonuria (PKU) was the first disease to be identified by the newborn screening (NBS) program. Currently, there are various methods for determining phenylalanine (Phe) values, with tandem mass spectrometry (MS/MS)...
6.
Perko D, Repic Lampret B, Remec Z, Zerjav Tansek M, Drole Torkar A, Krhin B, et al.
Genes (Basel)
. 2022 Mar;
13(3).
PMID: 35328070
Phenylketonuria (PKU) was the first disorder for which newborn screening (NBS) was introduced in the early 1960s. Slovenia started the NBS program for PKU in 1979, and the fluorimetric method...
7.
Sikonja J, Brecelj J, Zerjav Tansek M, Repic Lampret B, Drole Torkar A, Klemencic S, et al.
Mol Genet Metab Rep
. 2022 Mar;
30:100836.
PMID: 35242570
Tyrosinemia type 1 (HT1) is an inborn error of tyrosine catabolism that leads to severe liver, kidney, and neurological dysfunction. Newborn screening (NBS) can enable a timely diagnosis and early...
8.
Koracin V, Mlinaric M, Baric I, Brincat I, Djordjevic M, Drole Torkar A, et al.
Front Pediatr
. 2021 May;
9:648939.
PMID: 34026686
Significant part of Southeastern Europe (with a population of 76 million) has newborn screening (NBS) programs non-harmonized with developed European countries. Initial survey was conducted in 2013/2014 among 11 countries...
9.
Repic Lampret B, Remec Z, Drole Torkar A, Zerjav Tansek M, Smon A, Koracin V, et al.
Zdr Varst
. 2020 Nov;
59(4):256-263.
PMID: 33133282
Introduction: In the last two decades, the introduction of tandem mass spectrometry in clinical laboratories has enabled simultaneous testing of numerous acylcarnitines and amino acids from dried blood spots for...
10.
Lovrecic L, Remec Z, Volk M, Rudolf G, Writzl K, Peterlin B
BMC Med Genet
. 2016 Nov;
17(1):81.
PMID: 27846804
Background: The objective of reported study was to evaluate the clinical utility of prenatal microarray testing for submicroscopic genomic imbalances in routine prenatal settings and to stratify the findings according...