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Author/Creator Mikstiene, Violeta

1. Case Report of Extremely Rare Autosomal Recessive Familial Hypercholesterolemia. (June 2018)

Authors:
Petrulioniene, Zaneta; Skiauteryte, Egle; Gargalskaite, Urte; Kutkiene, Sandra; Rinkuniene, Egidija; Dzenkeviciute, Vilma; Mikstiene, Violeta; Preiksaitiene, Egle; Norvilas, Rimvydas; Griskevicius, Antanas; Petrulionyte, Ema; Utkus, Algirdas
Journal:
Atherosclerosis
Issue:
Volume 32(2018)
Page Start:
52
Record Type:
Journal Article
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2. Etiological profile of hearing loss amongst Lithuanian pediatric cochlear implant users. (July 2020)

Authors:
Byckova, Jekaterina; Mikstiene, Violeta; Kiveryte, Silvija; Mickeviciene, Vaiva; Gromova, Margarita; Cernyte, Gabriele; Mataityte-Dirziene, Jurga; Stumbrys, Daumantas; Utkus, Algirdas; Lesinskas, Eugenijus
Journal:
International journal of pediatric otorhinolaryngology
Issue:
Volume 134(2020:Jul.)
Page Start:
Record Type:
Journal Article
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3. The high frequency of GJB2 gene mutation c.313_326del14 suggests its possible origin in ancestors of Lithuanian population. Issue 1 (December 2016)

Authors:
Mikstiene, Violeta; Jakaitiene, Audrone; Byckova, Jekaterina; Gradauskiene, Egle; Preiksaitiene, Egle; Burnyte, Birute; Tumiene, Birute; Matuleviciene, Ausra; Ambrozaityte, Laima; Uktveryte, Ingrida; Domarkiene, Ingrida; Rancelis, Tautvydas; Cimbalistiene, Loreta; Lesinskas, Eugenijus; Kucinskas,...
Journal:
BMC genetics
Issue:
Volume 17:Issue 1(2016)
Page Start:
1
Record Type:
Journal Article
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4. Thiamine responsive megaloblastic anemia syndrome: A novel homozygous SLC19A2 gene mutation identified. (23rd February 2015)

Authors:
Mikstiene, Violeta; Songailiene, Jurgita; Byckova, Jekaterina; Rutkauskiene, Giedre; Jasinskiene, Edita; Verkauskiene, Rasa; Lesinskas, Eugenijus; Utkus, Algirdas
Journal:
American journal of medical genetics
Issue:
Volume 167:Number 7(2015:Jul.)
Page Start:
1605
Record Type:
Journal Article
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