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Year Number of Results
2013 1
2015 1
2016 2
2017 1
2019 4
2020 2
2021 5
2022 2
2023 2
2024 0

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Page 1
Genome Editing in Medicine: Tools and Challenges.
Petraitytė G, Preikšaitienė E, Mikštienė V. Petraitytė G, et al. Among authors: mikstiene v. Acta Med Litu. 2021;28(2):205-219. doi: 10.15388/Amed.2021.28.2.8. Epub 2021 Aug 17. Acta Med Litu. 2021. PMID: 35637939 Free PMC article. Review.
Autosomal recessive hypercholesterolemia: Case report.
Petrulioniene Z, Gargalskaite U, Mikstiene V, Norvilas R, Skiauteryte E, Utkus A. Petrulioniene Z, et al. Among authors: mikstiene v. J Clin Lipidol. 2019 Nov-Dec;13(6):887-893. doi: 10.1016/j.jacl.2019.09.009. Epub 2019 Sep 23. J Clin Lipidol. 2019. PMID: 31734096 Free article.
Molecular and Functional Characterisation of a Novel Intragenic 12q24.21 Deletion Resulting in MED13L Haploinsufficiency Syndrome.
Siavrienė E, Petraitytė G, Mikštienė V, Maldžienė Ž, Sasnauskienė A, Žitkutė V, Ambrozaitytė L, Rančelis T, Utkus A, Kučinskas V, Preikšaitienė E. Siavrienė E, et al. Among authors: mikstiene v. Medicina (Kaunas). 2023 Jun 29;59(7):1225. doi: 10.3390/medicina59071225. Medicina (Kaunas). 2023. PMID: 37512036 Free PMC article.
Novel GLI3 variant causes Greig cephalopolysyndactyly syndrome in three generations of a Lithuanian family.
Siavrienė E, Mikštienė V, Radzevičius D, Maldžienė Ž, Rančelis T, Petraitytė G, Tamulytė G, Kavaliauskienė I, Šarkinas L, Utkus A, Kučinskas V, Preikšaitienė E. Siavrienė E, et al. Among authors: mikstiene v. Mol Genet Genomic Med. 2019 Sep;7(9):e878. doi: 10.1002/mgg3.878. Epub 2019 Jul 20. Mol Genet Genomic Med. 2019. PMID: 31325247 Free PMC article.
PIGN-Related Disease in Two Lithuanian Families: A Report of Two Novel Pathogenic Variants, Molecular and Clinical Characterisation.
Siavrienė E, Maldžienė Ž, Mikštienė V, Petraitytė G, Rančelis T, Dapkūnas J, Burnytė B, Benušienė E, Sasnauskienė A, Grikinienė J, Griškevičiūtė E, Utkus A, Preikšaitienė E. Siavrienė E, et al. Among authors: mikstiene v. Medicina (Kaunas). 2022 Oct 26;58(11):1526. doi: 10.3390/medicina58111526. Medicina (Kaunas). 2022. PMID: 36363484 Free PMC article.
Etiological profile of hearing loss amongst Lithuanian pediatric cochlear implant users.
Byckova J, Mikstiene V, Kiveryte S, Mickeviciene V, Gromova M, Cernyte G, Mataityte-Dirziene J, Stumbrys D, Utkus A, Lesinskas E. Byckova J, et al. Among authors: mikstiene v. Int J Pediatr Otorhinolaryngol. 2020 Jul;134:110043. doi: 10.1016/j.ijporl.2020.110043. Epub 2020 Apr 10. Int J Pediatr Otorhinolaryngol. 2020. PMID: 32305661
Donor Splice Site Variant in SLC9A6 Causes Christianson Syndrome in a Lithuanian Family: A Case Report.
Petraitytė G, Mikštienė V, Siavrienė E, Cimbalistienė L, Maldžienė Ž, Rančelis T, Vaitėnienė EM, Ambrozaitytė L, Dapkūnas J, Dzindzalieta R, Pranckevičienė E, Kučinskas V, Utkus A, Preikšaitienė E. Petraitytė G, et al. Among authors: mikstiene v. Medicina (Kaunas). 2022 Feb 26;58(3):351. doi: 10.3390/medicina58030351. Medicina (Kaunas). 2022. PMID: 35334527 Free PMC article.
20 results