Jurate Barysiene
Overview
Explore the profile of Jurate Barysiene including associated specialties, affiliations and a list of published articles.
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19
Citations
47
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Recent Articles
1.
Zebrauskiene D, Sadauskiene E, Dapkunas J, Kairys V, Balciunas J, Konovalovas A, et al.
Clin Epigenetics
. 2024 Jun;
16(1):76.
PMID: 38845031
Tatton-Brown-Rahman syndrome (TBRS) is a rare congenital genetic disorder caused by autosomal dominant pathogenic variants in the DNA methyltransferase DNMT3A gene. Typical TBRS clinical features are overgrowth, intellectual disability, and...
2.
Aliosaitiene U, Petrulioniene Z, Rinkuniene E, Mainelis A, Barysiene J, Smailyte U, et al.
J Cardiovasc Dev Dis
. 2024 Mar;
11(3).
PMID: 38535114
Background: Familial hypercholesterolemia (FH) is a genetic disorder that manifests as impaired low-density lipoprotein cholesterol (LDL-C) metabolism, resulting in lifelong exposure to high cholesterol levels and increased risk of cardiovascular...
3.
Zebrauskiene D, Sadauskiene E, Masiuliene R, Aidietiene S, Siaudiniene A, Peceliunas V, et al.
Medicina (Kaunas)
. 2024 Feb;
60(2).
PMID: 38399526
Hereditary transthyretin amyloidosis (ATTRv) is a rare disease caused by pathogenic variants in the transthyretin () gene. More than 140 different disease-causing variants in have been reported. Only a few...
4.
Uzdavinyte Gateliene E, Cesnaite G, Sadauskiene E, Barysiene J
Eur Heart J Case Rep
. 2023 Nov;
7(10):ytad486.
PMID: 37908547
Background: Kawasaki disease (KD) is an acute systemic vasculitis syndrome, mostly targeting children under 5 years old. If untreated, coronary artery abnormalities develop to approximately one out of four patients...
5.
Jukneviciene R, Simonavicius J, Mikalauskas A, cerlinskaite-Bajore K, Arrigo M, Juknevicius V, et al.
BMJ Open
. 2022 Dec;
12(9):e061611.
PMID: 36581965
Objectives: To evaluate the potential of soluble cluster of differentiation 146 (sCD146) in the detection and grading of congestion in patients with acute dyspnoea. Design: Subanalysis of the prospective observational...
6.
Jukneviciene R, Juknevicius V, Jasiunas E, Rasciute B, Barysiene J, Mataciunas M, et al.
Medicine (Baltimore)
. 2022 Jul;
101(29):e29579.
PMID: 35866759
High-sensitivity troponin assay brought new challenges as we detect elevated concentration in many other diseases, and it became difficult to distinguish the real cause of this elevation. In this notion,...
7.
Jakaite R, Peceliunas V, Aidietiene S, Bertasiute A, Bileisiene N, Mickeviciute O, et al.
J Electrocardiol
. 2021 Aug;
68:157-163.
PMID: 34455115
Background: ST/T abnormalities recognized as electrocardiographic (ECG) left ventricular (LV) strain pattern are known as a marker of myocyte death and reduced survival. The purpose of this study was to...
8.
Gabartaite D, Jancauskaite D, Mikstiene V, Preiksaitiene E, Norvilas R, Valeviciene N, et al.
Acta Med Litu
. 2021 Aug;
28(1):127-135.
PMID: 34393635
Summary Background: Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a heritable cardiomyopathy, characterized by fibrofatty replacement of myocytes in the right ventricular, left ventricular or both ventricles. It is caused by...
9.
Bileisiene N, Barysiene J, Mikstiene V, Preiksaitiene E, Marinskis G, Kezeviciute M, et al.
Medicina (Kaunas)
. 2021 Aug;
57(7).
PMID: 34357002
Congenital long QT syndrome (LQTS) is a hereditary ion channelopathy associated with ventricular arrhythmia and sudden cardiac death starting from young age due to prolonged cardiac repolarization, which is represented...
10.
Paleviciute E, Gumbiene L, Jureviciene E, Simbelyte T, Lauceviciene I, Laucevicius A, et al.
Respiration
. 2021 May;
100(10):949-957.
PMID: 34044412
Background: Pulmonary hypertension (PH) is a severe progressive disease, associated with reduced exercise capacity and poor quality of life. Although scientific evidence supports the incorporation of specialized training in the...