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Evaluation of quality of life after paediatric cochlear implantation.
Acta Med Litu. 2018;25(3):173-184. doi: 10.6001/actamedica.v25i3.3865.
Acta Med Litu. 2018.
PMID: 30842707
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.
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
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Thiamine responsive megaloblastic anemia syndrome: a novel homozygous SLC19A2 gene mutation identified.
Mikstiene V, Songailiene J, Byckova J, Rutkauskiene G, Jasinskiene E, Verkauskiene R, Lesinskas E, Utkus A.
Mikstiene V, et al. Among authors: byckova j.
Am J Med Genet A. 2015 Jul;167(7):1605-9. doi: 10.1002/ajmg.a.37015. Epub 2015 Feb 23.
Am J Med Genet A. 2015.
PMID: 25707023
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The high frequency of GJB2 gene mutation c.313_326del14 suggests its possible origin in ancestors of Lithuanian population.
Mikstiene V, Jakaitiene A, Byckova J, Gradauskiene E, Preiksaitiene E, Burnyte B, Tumiene B, Matuleviciene A, Ambrozaityte L, Uktveryte I, Domarkiene I, Rancelis T, Cimbalistiene L, Lesinskas E, Kucinskas V, Utkus A.
Mikstiene V, et al. Among authors: byckova j.
BMC Genet. 2016 Feb 19;17:45. doi: 10.1186/s12863-016-0354-9.
BMC Genet. 2016.
PMID: 26896187
Free PMC article.
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A novel CHD7 variant disrupting acceptor splice site in a patient with mild features of CHARGE syndrome: a case report.
Siavrienė E, Petraitytė G, Mikštienė V, Rančelis T, Maldžienė Ž, Morkūnienė A, Byčkova J, Utkus A, Kučinskas V, Preikšaitienė E.
Siavrienė E, et al. Among authors: byckova j.
BMC Med Genet. 2019 Jul 17;20(1):127. doi: 10.1186/s12881-019-0859-y.
BMC Med Genet. 2019.
PMID: 31315586
Free PMC article.
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