Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Nomeda Valevičienė"'
Autor:
Dovilė Žebrauskienė, Eglė Sadauskienė, Rūta Masiulienė, Sigita Aidietienė, Agnė Šiaudinienė, Valdas Pečeliūnas, Gabrielė Žukauskaitė, Edvardas Žurauskas, Nomeda Valevičienė, Jūratė Barysienė, Eglė Preikšaitienė
Publikováno v:
Medicina, Vol 60, Iss 2, p 237 (2024)
Background and Objectives: Hereditary transthyretin amyloidosis (ATTRv) is a rare disease caused by pathogenic variants in the transthyretin (TTR) gene. More than 140 different disease-causing variants in TTR have been reported. Only a few individual
Externí odkaz:
https://doaj.org/article/57465c76c7cc4fb89e6e8c5b8cdbfbc7
Autor:
Giedrė Balčiūnaitė, Darius Palionis, Edvardas Žurauskas, Viktor Skorniakov, Vilius Janušauskas, Aleksejus Zorinas, Tomas Zaremba, Nomeda Valevičienė, Audrius Aidietis, Pranas Šerpytis, Kęstutis Ručinskas, Peter Sogaard, Sigita Glaveckaitė
Publikováno v:
BMC Cardiovascular Disorders, Vol 20, Iss 1, Pp 1-10 (2020)
Abstract Background Adverse cardiac remodeling with a myocardial fibrosis as a key pathophysiologic component may be associated to worse survival in aortic stenosis (AS) patients. Therefore, with the application of advanced cardiac imaging we aim to
Externí odkaz:
https://doaj.org/article/a880b6af5efd4722995fdb3c45966467
Autor:
Dovilė Gabartaitė, Dovilė Jančauskaitė, Violeta Mikštienė, Eglė Preikšaitienė, Rimvydas Norvilas, Nomeda Valevičienė, Germanas Marinskis, Audrius Aidietis, Jūratė Barysienė
Publikováno v:
Acta Medica Lituanica, Vol 28, Iss 1 (2021)
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 pathogenic variants o
Externí odkaz:
https://doaj.org/article/1e023c6293134de8a1475d28a4390c83
Publikováno v:
Hellenic Journal of Cardiology, Vol 57, Iss 6, Pp 428-434 (2016)
Objective: The natural history, management, and outcome of Takotsubo (stress) cardiomyopathy (TTC) is not clear. The aim of this study was to investigate clinical features, define prognostic predictors, and assess the clinical course and outcomes of
Externí odkaz:
https://doaj.org/article/0aa7d01ab86f42dbbb5d17f949521cf2
Autor:
Donatas Austys, Andrej Dobrovolskij, Valerija Jablonskienė, Valerij Dobrovolskij, Nomeda Valevičienė, Rimantas Stukas
Publikováno v:
Medicina, Vol 55, Iss 8, p 456 (2019)
Background and Objectives: Epicardial adipose tissue (EAT) is shown to be an important factor in the development of coronary artery disease, but numerous pathophysiological mechanisms of its action are still only partially understood. There is a lack
Externí odkaz:
https://doaj.org/article/c7b31d5e0c2a421389aceccdff38e06d
Autor:
Rokas Šerpytis, Mindaugas Lizaitis, Egle Majauskienė, Petras Navickas, Sigita Glaveckaitė, Žaneta Petrulionienė, Nomeda Valevičienė, Aleksandras Laucevičius, Qin M. Chen, Joseph S. Alpert, Pranas Šerpytis
Publikováno v:
Advances in Therapy. 40:2471-2480
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8614475b54eecf93336ff3c488a2dfc4
https://doi.org/10.1007/s12325-023-02485-2
https://doi.org/10.1007/s12325-023-02485-2
Autor:
Giedrė Balčiūnaitė, Justinas Besusparis, Darius Palionis, Edvardas Žurauskas, Viktor Skorniakov, Vilius Janušauskas, Aleksejus Zorinas, Tomas Zaremba, Nomeda Valevičienė, Pranas Šerpytis, Audrius Aidietis, Kęstutis Ručinskas, Peter Sogaard, Sigita Glaveckaitė
Publikováno v:
Balčiūnaitė, G, Besusparis, J, Palionis, D, Žurauskas, E, Skorniakov, V, Janušauskas, V, Zorinas, A, Zaremba, T, Valevičienė, N, Šerpytis, P, Aidietis, A, Ručinskas, K, Sogaard, P & Glaveckaitė, S 2022, ' Exploring myocardial fibrosis in severe aortic stenosis : echo, CMR and histology data from FIB-AS study ', International Journal of Cardiovascular Imaging, vol. 38, no. 7, pp. 1555-1568 . https://doi.org/10.1007/s10554-022-02543-w
PurposeMyocardial fibrosis in aortic stenosis (AS) is associated with worse survival following aortic valve replacement (AVR). We assessed myocardial fibrosis in severe AS patients, integrating echocardiographic, cardiovascular magnetic resonance (CM
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8cb789e5c78f267c665abc1e959905c4
https://doi.org/10.1007/s10554-022-02543-w
https://doi.org/10.1007/s10554-022-02543-w
Autor:
Dovile Zebrauskiene, Egle Sadauskiene, Justas Dapkunas, Visvaldas Kairys, Joris Balciunas, Aleksandras Konovalovas, Ruta Masiuliene, Gunda Petraityte, Nomeda Valeviciene, Mindaugas Mataciunas, Jurate Barysiene, Violeta Mikstiene, Migle Tomkuviene, Egle Preiksaitiene
Publikováno v:
Clinical Epigenetics, Vol 16, Iss 1, Pp 1-15 (2024)
Abstract 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, an
Externí odkaz:
https://doaj.org/article/1c9dd59da3c14eceb348640c7603e7f9
Publikováno v:
Medicina, Vol 60, Iss 7, p 1162 (2024)
Background and Objectives: Over the past decade, there has been increasing attention paid to advanced and innovative cardiovascular magnetic resonance (CMR) modalities, such as T1 and T2 mapping, which play a major role in diagnosing diffuse myocardi
Externí odkaz:
https://doaj.org/article/3a6584c2b53c4d5da210a2dbbbe621b7
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