Zobrazeno 1 - 10
of 373
pro vyhledávání: '"Morkūnienė A"'
Publikováno v:
Balkan Journal of Medical Genetics, Vol 19, Iss 2, Pp 95-100 (2016)
Barth syndrome (BTHS) is a rare X-linked disease characterized by dilated cardiomyopathy, proximal skeletal myopathy and cyclic neutropenia. It is caused by various mutations in the tafazzin (TAZ) gene located on Xq28 that results in remodeling of ca
Externí odkaz:
https://doaj.org/article/c60d0733477943c7bdc6eb033d1368b8
Autor:
Finsterer J, Stollberger C, Bakšienė M, Benušienė E, Morkūnienė A, Ambrozaitytė L, Utkus A, Kučinskas V
Publikováno v:
Balkan Journal of Medical Genetics, Vol 20, Iss 2, Pp 91-93 (2017)
Externí odkaz:
https://doaj.org/article/625d16b7c26f4247a8adcddd523244b4
Autor:
Kristina Morkūnienė, Justina Dambrauskaitė, Renata Bižienė, Ramutė Mišeikienė, Nijolė Pečiulaitienė, Laimutis Kučinskas, Ugnė Dudonytė
Publikováno v:
Journal of Advanced Veterinary and Animal Research, Vol 11, Iss 3, Pp 738-745 (2024)
Objective: Diabetes mellitus (DM) is a prevalent endocrine condition found in cats. Recent research has identified a connection between a higher risk of diabetes in cats and genetic factors. This genetic susceptibility to type 2 diabetes is associate
Externí odkaz:
https://doaj.org/article/430cf785c0524fb795bfd74e809ff36d
Publikováno v:
Journal of CO2 Utilization, Vol 85, Iss , Pp 102890- (2024)
Valorisation of fruit processing by-products and waste is an important task for increasing the sustainability of agro-food sector. In this study, pitted sour cherry pomace was mechanically pre-fractionated into the 6 different particle size (>10, 4
Externí odkaz:
https://doaj.org/article/fc03b87353c34fda86071923e3183cb1
Publikováno v:
In Journal of CO2 Utilization July 2024 85
Publikováno v:
Lietuvos Chirurgija, Vol 22, Iss 4 (2023)
Liver biopsy is the most accurate interventional procedure to diagnose hepatic diseases. According to the information provided by the Institute of Hygiene, 968 percutaneous liver biopsies were performed in Lithuania in 2022. The Lithuanian scientific
Externí odkaz:
https://doaj.org/article/1a809f7693d342f99ff0907617d1ae89
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Samiatina-Morkūnienė, Diana1,2,3,4 dsamiatina@yahoo.de, Silickytė, Rūta5,6 ruta.silickyte@stud.lsmu.lt, Jankauskaitė, Gabija5,6 gabija.jankauskaite@stud.lsmu.lt
Publikováno v:
Lithuanian Surgery / Lietuvos Chirurgija. 2023, Vol. 22 Issue 4, p245-248. 4p.
Autor:
Morkūnienė, Kristina, Dambrauskaitė, Justina, Bižienė, Renata, Mišeikienė, Ramutė, Pečiulaitienė, Nijolė, Kučinskas, Laimutis, Dudonytė, Ugnė
Publikováno v:
Journal of Advanced Veterinary & Animal Research; Sep2024, Vol. 11 Issue 3, p738-745, 8p
Autor:
Evelina Siavrienė, Gunda Petraitytė, Birutė Burnytė, Aušra Morkūnienė, Violeta Mikštienė, Tautvydas Rančelis, Algirdas Utkus, Vaidutis Kučinskas, Eglė Preikšaitienė
Publikováno v:
BMC Musculoskeletal Disorders, Vol 22, Iss 1, Pp 1-8 (2021)
Abstract Background Autosomal recessive limb–girdle muscular dystrophy-1 (LGMDR1), also known as calpainopathy, is a genetically heterogeneous disorder characterised by progression of muscle weakness. Homozygous or compound heterozygous variants in
Externí odkaz:
https://doaj.org/article/9fa109b82e7f4d818b1ad473453435d8