Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Ausra Matuleviciene"'
Autor:
Evaldas Kazlauskas, Giedre Smailyte, Ingrida Domarkienė, Vaidutis Kučinskas, Aušra Matulevičienė, Ask Elklit, Gabrielė Žukauskaitė, Laima Ambrozaitytė
Publikováno v:
Global Health Action, Vol 16, Iss 1 (2023)
The adverse effects on the health of the Chornobyl nuclear power plant accident clean-up workers have been reported previously. However, there is a lack of studies on the mental health of Chornobyl clean-up workers. The current study explored psychol
Externí odkaz:
https://doaj.org/article/9333e712054e46e39656e30667df911d
Autor:
Gabrielė Žukauskaitė, Ingrida Domarkienė, Aušra Matulevičienė, Svetlana Dauengauer-Kirlienė, Vaidutis Kučinskas, Laima Ambrozaitytė
Publikováno v:
Current Issues in Molecular Biology, Vol 45, Iss 4, Pp 2972-2983 (2023)
Some people resist or recover from health challenges better than others. We studied Lithuanian clean-up workers of the Chornobyl nuclear disaster (LCWC) who worked in the harshest conditions and, despite high ionising radiation doses as well as other
Externí odkaz:
https://doaj.org/article/1a544d481aee4f9194f1628e420efa57
Autor:
Gunda Petraitytė, Kamilė Šiaurytė, Violeta Mikštienė, Loreta Cimbalistienė, Dovilė Kriaučiūnienė, Aušra Matulevičienė, Algirdas Utkus, Eglė Preikšaitienė
Publikováno v:
BMC Endocrine Disorders, Vol 21, Iss 1, Pp 1-6 (2021)
Abstract Background Acrodysostosis is a rare hereditary disorder described as a primary bone dysplasia with or without hormonal resistance. Pathogenic variants in the PRKAR1A and PDE4D genes are known genetic causes of this condition. The latter gene
Externí odkaz:
https://doaj.org/article/98a20fbf7d584d77a7fc98e358505ab6
Autor:
Sigita Lesinskienė, Darja Rojaka, Rūta Praninskienė, Aušra Morkūnienė, Aušra Matulevičienė, Algirdas Utkus
Publikováno v:
Journal of Medical Case Reports, Vol 14, Iss 1, Pp 1-5 (2020)
Abstract Background Huntington’s disease is a rare, autosomal dominant neurodegenerative disease characterized by motor, cognitive, and psychiatric symptoms. Usually, the disease symptoms first appear around the age of 40, but in 5–10% of cases,
Externí odkaz:
https://doaj.org/article/3d18abf713fb47fb9eb0ffe19591bf4a
Autor:
Adelė Butėnaitė, Robertas Strumila, Aistė Lengvenytė, Indrė Kotryna Pakutkaitė, Aušra Morkūnienė, Aušra Matulevičienė, Edgaras Dlugauskas, Algirdas Utkus
Publikováno v:
Acta Medica Lituanica, Vol 28, Iss 1 (2021)
Background: In Huntington’s disease psychiatric symptoms may manifest prior to motor dysfunction. Such symptoms negatively impact people’s quality of life and can worsen the course of the primary disease. The aim of the present study was to asses
Externí odkaz:
https://doaj.org/article/d5102af535b34e2eac1559d9a29d35b4
Publikováno v:
Computational Science and Techniques, Vol 1, Iss 2, Pp 141-154 (2013)
In this paper, we present a comparative analysis of hierarchical clustering and multidimensional scaling methods for genotype and phenotype data analysis. Fisher's exact test was applied to determinate dependencies between congenital anomalies. In or
Externí odkaz:
https://doaj.org/article/c2fcd37aeee54d91a0e947882f7291ca
Publikováno v:
European journal of medical genetics, Amsterdam : Elsevier, 2023, vol. 66, iss. 6, art. no. 104763, p. [1-5]
Gastrointestinal (GI) problems are common in Phelan-McDermid syndrome (PMS). Chewing and swallowing difficulties, dental problems, reflux disease, cyclic vomiting, constipation, incontinence, diarrhoea, and nutritional deficiencies have been most fre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa560be2617ab545186f692ddad3ff8d
https://doi.org/10.1016/j.ejmg.2023.104763
https://doi.org/10.1016/j.ejmg.2023.104763
Autor:
Alina Urnikyte, Laura Pranckeniene, Ingrida Domarkiene, Svetlana Dauengauer-Kirliene, Alma Molyte, Ausra Matuleviciene, Ingrida Pilypiene, Vaidutis Kučinskas
Publikováno v:
Genes; Volume 13; Issue 4; Pages: 569
Genes, Basel : MDPI, 2022, vol. 13, iss. 4, art. no. 569, p. [1-12]
Genes, Basel : MDPI, 2022, vol. 13, iss. 4, art. no. 569, p. [1-12]
Most genetic variants are rare and specific to the population, highlighting the importance of characterizing local population genetic diversity. Many countries have initiated population-based whole-genome sequencing (WGS) studies. Genomic variation w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4fb959073cf3ecf5671cdd89be5c358
Autor:
Thomas Eggermann, Matthias Begemann, Ausra Matuleviciene, Florian Kraft, Robert Meyer, Asmaa Kenawy, Miriam Elbracht, Laima Ambrozaityte, Christian Thomas Hübner
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 105:2401-2407
Context Silver-Russell syndrome (SRS) is a clinical and molecular heterogeneous disorder associated with short stature, typical facial gestalt, and body asymmetry. Though molecular causes of SRS can be identified in a significant number of patients,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::736bd66fc03f8280b32912339be4190f
https://doi.org/10.1210/clinem/dgaa273
https://doi.org/10.1210/clinem/dgaa273
Autor:
Ausra Matuleviciene, Vaidutis Kučinskas, Gabriele Zukauskaite, Laima Ambrozaityte, Ingrida Domarkiene, Justas Arasimavičius
Publikováno v:
Book of Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cee562b1ad494d5d08c8d60a459da716
https://doi.org/10.21175/rad.abstr.book.2021.6.2
https://doi.org/10.21175/rad.abstr.book.2021.6.2