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Algirdas Utkus

Showing results (11-20 of 102) with videos related to

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Acta Dermatovenerologica Croatica : ADC|September 3, 2020
A Familial 4q12 Deletion Involving KIT Gene Causes PiebaldismJustas Arasimavičius, Evelina Dilytė, Algirdas Utkus, et al.
Genes|August 26, 2023
Implementing Core Genes and an Omnigenic Model for Behaviour Traits Prediction in GenomicsTautvydas Rancelis, Ingrida Domarkiene, Laima Ambrozaityte, et al.
Health Economics Review|January 24, 2026
Cost analysis of financial, productivity, and informal care burdens in families raising children with congenital anomaliesEvelina Marija Vaitėnienė, Audronė Jakaitienė, Liubovė Murauskienė, et al.
Genes|June 2, 2021
Variants in the Myostatin Gene and Physical Performance Phenotype of Elite AthletesValentina Ginevičienė, Audronė Jakaitienė, Erinija Pranckevičienė, et al.
Endokrynologia Polska|May 10, 2021
Dysregulation of microRNAs as the risk factor of lymph node metastasis in papillary thyroid carcinoma: systematic reviewRomena Laukiene, Valentinas Jakubkevicius, Laima Ambrozaityte, et al.
Neurology. Genetics|April 14, 2023
Cerebellar Ataxia and Peripheral Neuropathy in a Family With <i>PNPLA8</i>-Associated DiseaseBirute Burnyte, Ramune Vilimiene, Kristina Grigalioniene, et al.
Medicina (Kaunas, Lithuania)|December 6, 2007
[Fabry's disease: a clinical case and literature review]Rasa Dobrovolskiene, Algirdas Utkus, Birute Tumiene, et al.
Prilozi (Makedonska Akademija Na Naukite I Umetnostite. Oddelenie Za Medicinski Nauki)|May 7, 2014
Introducing standards of the best medical practice for patients with inherited alpha-1-antitrypsin deficiency in Central Eastern EuropeArũnas Valiulis, Algirdas Utkus, Rimantas Stukas, et al.
Journal of Clinical Medicine|April 27, 2024
Neuropsychiatric Aspects of Sotos Syndrome: Explorative Review Building Multidisciplinary Bridges in Clinical PracticeSigita Lesinskiene, Reda Montvilaite, Kamile Pociute, et al.
International Journal of Ophthalmology|November 20, 2018
X-linked juvenile retinoschisis: phenotypic and genetic characterizationRasa Strupaitė, Laima Ambrozaitytė, Loreta Cimbalistienė, et al.
Pageof 11

Showing results (11-20 of 102) with videos related to

Sort By:
Pageof 11
Acta Dermatovenerologica Croatica : ADC|September 3, 2020
A Familial 4q12 Deletion Involving KIT Gene Causes PiebaldismJustas Arasimavičius, Evelina Dilytė, Algirdas Utkus, et al.
Genes|August 26, 2023
Implementing Core Genes and an Omnigenic Model for Behaviour Traits Prediction in GenomicsTautvydas Rancelis, Ingrida Domarkiene, Laima Ambrozaityte, et al.
Health Economics Review|January 24, 2026
Cost analysis of financial, productivity, and informal care burdens in families raising children with congenital anomaliesEvelina Marija Vaitėnienė, Audronė Jakaitienė, Liubovė Murauskienė, et al.
Genes|June 2, 2021
Variants in the Myostatin Gene and Physical Performance Phenotype of Elite AthletesValentina Ginevičienė, Audronė Jakaitienė, Erinija Pranckevičienė, et al.
Endokrynologia Polska|May 10, 2021
Dysregulation of microRNAs as the risk factor of lymph node metastasis in papillary thyroid carcinoma: systematic reviewRomena Laukiene, Valentinas Jakubkevicius, Laima Ambrozaityte, et al.
Neurology. Genetics|April 14, 2023
Cerebellar Ataxia and Peripheral Neuropathy in a Family With <i>PNPLA8</i>-Associated DiseaseBirute Burnyte, Ramune Vilimiene, Kristina Grigalioniene, et al.
Medicina (Kaunas, Lithuania)|December 6, 2007
[Fabry's disease: a clinical case and literature review]Rasa Dobrovolskiene, Algirdas Utkus, Birute Tumiene, et al.
Prilozi (Makedonska Akademija Na Naukite I Umetnostite. Oddelenie Za Medicinski Nauki)|May 7, 2014
Introducing standards of the best medical practice for patients with inherited alpha-1-antitrypsin deficiency in Central Eastern EuropeArũnas Valiulis, Algirdas Utkus, Rimantas Stukas, et al.
Journal of Clinical Medicine|April 27, 2024
Neuropsychiatric Aspects of Sotos Syndrome: Explorative Review Building Multidisciplinary Bridges in Clinical PracticeSigita Lesinskiene, Reda Montvilaite, Kamile Pociute, et al.
International Journal of Ophthalmology|November 20, 2018
X-linked juvenile retinoschisis: phenotypic and genetic characterizationRasa Strupaitė, Laima Ambrozaitytė, Loreta Cimbalistienė, et al.
Pageof 11