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Algirdas Utkus

Showing results (51-60 of 102) with videos related to

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Medicina (Kaunas, Lithuania)|August 6, 2021
Aborted Cardiac Arrest in LQT2 Related to Novel <i>KCNH2</i> (<i>hERG</i>) Variant Identified in One Lithuanian FamilyNeringa Bileišienė, Jūratė Barysienė, Violeta Mikštienė, et al.
BMC Endocrine Disorders|April 16, 2021
A novel variant in the PDE4D gene is the cause of Acrodysostosis type 2 in a Lithuanian patient: a case reportGunda Petraitytė, Kamilė Šiaurytė, Violeta Mikštienė, et al.
Nordic Journal of Psychiatry|January 22, 2019
Analysis of Lithuanian CYP2D6 polymorphism and its relevance to psychiatric care of the local populationEdgaras Dlugauskas, Robertas Strumila, Aiste Lengvenyte, et al.
Acta Medica Lituanica|March 31, 2017
Identification of genetic causes of congenital neurodevelopmental disorders using genome wide molecular technologiesEglė Preikšaitienė, Laima Ambrozaitytė, Živilė Maldžienė, et al.
Healthcare (Basel, Switzerland)|December 24, 2021
Effects of Virtual Reality-Based Relaxation Techniques on Psychological, Physiological, and Biochemical Stress IndicatorsEglė Mazgelytė, Virginija Rekienė, Edita Dereškevičiūtė, et al.
Journal of Forensic and Legal Medicine|May 1, 2019
Homicide victims and mechanisms in Lithuania from 2004 to 2016Sigitas Chmieliauskas, Sigitas Laima, Dmitrij Fomin, et al.
Clinical Dysmorphology|October 12, 2014
R368X mutation in MID1 among recurrent mutations in patients with X-linked Opitz G/BBB syndromeEgle Preiksaitiene, Natalija Krasovskaja, Algirdas Utkus, et al.
Acta Medica Lituanica|September 21, 2023
Implementation and Evaluation of Preimplantation Genetic Testing at Vilnius University Hospital Santaros KlinikosEglė Stukaitė-Ruibienė, Živilė Gudlevičienė, Andrė Amšiejienė, et al.
Acta Medica Lituanica|August 16, 2021
Significant Association Between Huntingtin Gene Mutation and Prevalence of Hopelessness, Depression and Anxiety SymptomsAdelė Butėnaitė, Robertas Strumila, Aistė Lengvenytė, et al.
BMC Musculoskeletal Disorders|December 5, 2021
Compound heterozygous c.598_612del and c.1746-20C > G CAPN3 genotype cause autosomal recessive limb-girdle muscular dystrophy-1: a case reportEvelina Siavrienė, Gunda Petraitytė, Birutė Burnytė, et al.
Pageof 11

Showing results (51-60 of 102) with videos related to

Sort By:
Pageof 11
Medicina (Kaunas, Lithuania)|August 6, 2021
Aborted Cardiac Arrest in LQT2 Related to Novel <i>KCNH2</i> (<i>hERG</i>) Variant Identified in One Lithuanian FamilyNeringa Bileišienė, Jūratė Barysienė, Violeta Mikštienė, et al.
BMC Endocrine Disorders|April 16, 2021
A novel variant in the PDE4D gene is the cause of Acrodysostosis type 2 in a Lithuanian patient: a case reportGunda Petraitytė, Kamilė Šiaurytė, Violeta Mikštienė, et al.
Nordic Journal of Psychiatry|January 22, 2019
Analysis of Lithuanian CYP2D6 polymorphism and its relevance to psychiatric care of the local populationEdgaras Dlugauskas, Robertas Strumila, Aiste Lengvenyte, et al.
Acta Medica Lituanica|March 31, 2017
Identification of genetic causes of congenital neurodevelopmental disorders using genome wide molecular technologiesEglė Preikšaitienė, Laima Ambrozaitytė, Živilė Maldžienė, et al.
Healthcare (Basel, Switzerland)|December 24, 2021
Effects of Virtual Reality-Based Relaxation Techniques on Psychological, Physiological, and Biochemical Stress IndicatorsEglė Mazgelytė, Virginija Rekienė, Edita Dereškevičiūtė, et al.
Journal of Forensic and Legal Medicine|May 1, 2019
Homicide victims and mechanisms in Lithuania from 2004 to 2016Sigitas Chmieliauskas, Sigitas Laima, Dmitrij Fomin, et al.
Clinical Dysmorphology|October 12, 2014
R368X mutation in MID1 among recurrent mutations in patients with X-linked Opitz G/BBB syndromeEgle Preiksaitiene, Natalija Krasovskaja, Algirdas Utkus, et al.
Acta Medica Lituanica|September 21, 2023
Implementation and Evaluation of Preimplantation Genetic Testing at Vilnius University Hospital Santaros KlinikosEglė Stukaitė-Ruibienė, Živilė Gudlevičienė, Andrė Amšiejienė, et al.
Acta Medica Lituanica|August 16, 2021
Significant Association Between Huntingtin Gene Mutation and Prevalence of Hopelessness, Depression and Anxiety SymptomsAdelė Butėnaitė, Robertas Strumila, Aistė Lengvenytė, et al.
BMC Musculoskeletal Disorders|December 5, 2021
Compound heterozygous c.598_612del and c.1746-20C > G CAPN3 genotype cause autosomal recessive limb-girdle muscular dystrophy-1: a case reportEvelina Siavrienė, Gunda Petraitytė, Birutė Burnytė, et al.
Pageof 11