Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Eglė Sadauskienė"'
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:
Eglė Čiburienė, Sigita Aidietienė, Greta Ščerbickaitė, Eglė Sadauskienė, Diana Sudavičienė, Edita Baltruškevičienė, Birutė Brasiūnienė, Monika Drobnienė, Jelena Čelutkienė
Publikováno v:
Medicina, Vol 59, Iss 12, p 2140 (2023)
Background and Objectives: Cancer therapy containing anthracyclines is associated with cancer-treatment-related cardiac dysfunction and heart failure (HF). Conventional cardioprotective medications can be frequently complicated by their blood-pressur
Externí odkaz:
https://doaj.org/article/069a52e156ea4d158c99bca083ff5a26
Autor:
Lina Vencevičienė, Irena Butrimienė, Rimantas Vencevičius, Eglė Sadauskienė, Vytautas Kasiulevičius, Virginijus Šapoka
Publikováno v:
Medicina, Vol 51, Iss 5, Pp 272-279 (2015)
Objective: To explore the relationship between laboratory, functional, disease activity markers and bone mineral density (BMD) loss in patients with spondyloarthropathies (SpAs). Methods: A cohort of 41 SpA patients were followed up for 4 years. Dise
Externí odkaz:
https://doaj.org/article/ba052fb1ff9e4e72b822e8b77d3dad15
Autor:
Agnė Čerkauskaitė, Rimantė Čerkauskienė, Marius Miglinas, Arvydas Laurinavičius, Can Ding, Arndt Rolfs, Lina Vencevičienė, Jūratė Barysienė, Edita Kazėnaitė, Eglė Sadauskienė
Publikováno v:
Medicina, Vol 55, Iss 5, p 122 (2019)
Background: Fabry disease (FD) is a rare X-linked inherited lysosomal storage disorder caused by α-galactosidase A deficiency leading to intracellular glycosphingolipid accumulation. FD manifestation is multisystem, and can differ depending on disea
Externí odkaz:
https://doaj.org/article/f635e65036fa4506befa8ce45e9946cf
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:
Health Sciences. 30:112-117
Paveldimos kardiomiopatijos yra fenotipiškai ir genotipiškai heterogeninė retų ligų grupė. Šios ligos ilgą laiką gali būti besimptomės, tačiau sergant paveldimomis kardiomiopatijomis nustatoma padidėjusi staigios mirties rizika. Ta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9ed5e5a39faf657919fc085017c8d17d
https://doi.org/10.35988/sm-hs.2020.080
https://doi.org/10.35988/sm-hs.2020.080
Autor:
Eglė Sadauskienė, Vytautas Kasiulevičius, Virginijus Šapoka, Rimantas Vencevičius, Lina Vencevičienė, Irena Butrimienė
Publikováno v:
Medicina, Amsterdam : Elsevier, 2015, Vol. 51, No. 5, p. 272-279
Medicina; Volume 51; Issue 5; Pages: 272-279
Medicina, Vol 51, Iss 5, Pp 272-279 (2015)
Medicina
Volume 51
Issue 5
Pages 272-279
Medicina; Volume 51; Issue 5; Pages: 272-279
Medicina, Vol 51, Iss 5, Pp 272-279 (2015)
Medicina
Volume 51
Issue 5
Pages 272-279
Objective: To explore the relationship between laboratory, functional, disease activity markers and bone mineral density (BMD) loss in patients with spondyloarthropathies (SpAs). Methods: A cohort of 41 SpA patients were followed up for 4 years. Dise
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d43f6949aed82632607950fde1ac4a9f
https://repository.vu.lt/VU:ELABAPDB14500749&prefLang=en_US
https://repository.vu.lt/VU:ELABAPDB14500749&prefLang=en_US
