Ildiko Szatmari
Overview
Explore the profile of Ildiko Szatmari including associated specialties, affiliations and a list of published articles.
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Articles
14
Citations
161
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0
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Recent Articles
1.
Mikos B, Molnar M, Szatmari I, Monostori P, Bereczki C, Szabo A, et al.
Orv Hetil
. 2024 Jul;
165(29):1122-1129.
PMID: 39033493
No abstract available.
2.
Nemeth K, Szatmari I, Tokesi V, Szabo P
Curr Issues Mol Biol
. 2023 Dec;
45(12):9354-9367.
PMID: 38132432
In neonatal screening, amino acids have a significant diagnostic role. Determination of their values may identify abnormal conditions. Early diagnosis and continuous monitoring of amino acid disorders results in a...
3.
Xue A, Lenart I, Kincs J, Szabo H, Parniczky A, Balogh I, et al.
Int J Neonatal Screen
. 2023 Sep;
9(3).
PMID: 37754773
The aim of this study is to evaluate the strategy of the cystic fibrosis newborn screening (CFNBS) programme in Hungary based on the results of the first year of screening....
4.
Monostori P, Godejohann M, Janda J, Galla Z, Racz G, Klinke G, et al.
Clin Biochem
. 2022 Oct;
111:72-80.
PMID: 36202155
Objectives: Determination of methylmalonic acid (MMA) from dried blood spots (DBS) is commonly performed in clinical diagnostics and newborn screening for propionic acidemia (PA) and methylmalonic acidemia. Isobaric compounds of...
5.
Becsei D, Kiss E, Szatmari I, Arato A, Reusz G, Szabo A, et al.
Mol Genet Metab Rep
. 2022 Jul;
32:100897.
PMID: 35845719
Background: Patients with phenylketonuria (PKU) must maintain a lifelong natural protein-restricted diet to prevent neuro-cognitive damage. Early diagnosis is established with newborn screening, with diet subsequently controlled by regular phenylalanine...
6.
Becsei D, Hiripi R, Kiss E, Szatmari I, Arato A, Reusz G, et al.
Mol Genet Metab Rep
. 2021 Dec;
29:100823.
PMID: 34900594
Background: Phenylketonuria (PKU) is an inherited error of metabolism, screened at 48-72 h of life since 1975 in Hungary. The patients have to keep a strict lifelong protein-restricted diet, resulting...
7.
Gal A, Grosz Z, Borsos B, Szatmari I, Sebok A, Javor L, et al.
Life (Basel)
. 2021 Jun;
11(6).
PMID: 34072668
Pompe disease is caused by the accumulation of glycogen in the lysosomes due to a deficiency of the lysosomal acid-α-glucosidase (GAA) enzyme. Depending on residual enzyme activity, the disease manifests...
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.
Loeber J, Platis D, Zetterstrom R, Almashanu S, Boemer F, Bonham J, et al.
Int J Neonatal Screen
. 2021 Apr;
7(1).
PMID: 33808002
Neonatal screening (NBS) was initiated in Europe during the 1960s with the screening for phenylketonuria. The panel of screened disorders ("conditions") then gradually expanded, with a boost in the late...
10.
[Changes of lactate levels in diabetic ketoacidosis and in newly diagnosed type 1 diabetes mellitus]
Jenei K, Szatmari I, Szabo E, Mariam A, Luczay A, Zsidegh P, et al.
Orv Hetil
. 2019 Nov;
160(45):1784-1790.
PMID: 31680540
It is known that lactate concentration is increased in diabetic ketoacidosis (DKA), however, the pathophysiology and kinetics of lactate changes are still unclear. Normally, L-lactate is the major form in...