Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Algirdas Utkus

Showing results (91-100 of 102) with videos related to

Pageof 11
Sort By:
Orphanet Journal of Rare Diseases|December 19, 2022
Rare disease education in Europe and beyond: time to actBirute Tumiene, Harm Peters, Bela Melegh, et al.
Frontiers in Pediatrics|November 5, 2021
E-Cigarettes as a Growing Threat for Children and Adolescents: Position Statement From the European Academy of PaediatricsAndrew Bush, Agnieszka Lintowska, Artur Mazur, et al.
Comprehensive Psychoneuroendocrinology|May 13, 2024
Higher levels of plasma Adrenocorticotropic hormone (ACTH) are associated with lower suicidal ideation in depressed patients compared to controls and suicide attempters, independently from depression severityRobertas Strumila, Aiste Lengvenyte, Linas Zdanavicius, et al.
BMC Musculoskeletal Disorders|May 5, 2016
Robust genotyping tool for autosomal recessive type of limb-girdle muscular dystrophiesInna Inashkina, Eriks Jankevics, Janis Stavusis, et al.
BMC Genetics|February 21, 2016
The high frequency of GJB2 gene mutation c.313_326del14 suggests its possible origin in ancestors of Lithuanian populationVioleta Mikstiene, Audrone Jakaitiene, Jekaterina Byckova, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|April 5, 2011
Variation in FGF1, FOXE1, and TIMP2 genes is associated with nonsyndromic cleft lip with or without cleft palateTiit Nikopensius, Inga Kempa, Laima Ambrozaitytė, et al.
Orphanet Journal of Rare Diseases|October 14, 2022
HINT1 neuropathy in Lithuania: clinical, genetic, and functional profilingMatilde Malcorps, Silvia Amor-Barris, Birute Burnyte, et al.
Surgery Today|February 15, 2023
The academic impact and value of an international online surgery lecture seriesDaisuke Hashimoto, Aiste Gulla, Sohei Satoi, et al.
Nutrients|September 23, 2022
Sodium, Potassium and Iodine Intake in an Adult Population of LithuaniaUrte Zakauskiene, Ernesta Macioniene, Lina Zabuliene, et al.
European Journal of Medical Genetics|July 5, 2023
Lack of guidelines and translational knowledge is hindering the implementation of psychiatric genetic counseling and testing within Europe - A multi-professional survey studyKati Koido, Charlotta Ingvoldstad Malmgren, Lejla Pojskic, et al.
Pageof 11

Showing results (91-100 of 102) with videos related to

Sort By:
Pageof 11
Orphanet Journal of Rare Diseases|December 19, 2022
Rare disease education in Europe and beyond: time to actBirute Tumiene, Harm Peters, Bela Melegh, et al.
Frontiers in Pediatrics|November 5, 2021
E-Cigarettes as a Growing Threat for Children and Adolescents: Position Statement From the European Academy of PaediatricsAndrew Bush, Agnieszka Lintowska, Artur Mazur, et al.
Comprehensive Psychoneuroendocrinology|May 13, 2024
Higher levels of plasma Adrenocorticotropic hormone (ACTH) are associated with lower suicidal ideation in depressed patients compared to controls and suicide attempters, independently from depression severityRobertas Strumila, Aiste Lengvenyte, Linas Zdanavicius, et al.
BMC Musculoskeletal Disorders|May 5, 2016
Robust genotyping tool for autosomal recessive type of limb-girdle muscular dystrophiesInna Inashkina, Eriks Jankevics, Janis Stavusis, et al.
BMC Genetics|February 21, 2016
The high frequency of GJB2 gene mutation c.313_326del14 suggests its possible origin in ancestors of Lithuanian populationVioleta Mikstiene, Audrone Jakaitiene, Jekaterina Byckova, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|April 5, 2011
Variation in FGF1, FOXE1, and TIMP2 genes is associated with nonsyndromic cleft lip with or without cleft palateTiit Nikopensius, Inga Kempa, Laima Ambrozaitytė, et al.
Orphanet Journal of Rare Diseases|October 14, 2022
HINT1 neuropathy in Lithuania: clinical, genetic, and functional profilingMatilde Malcorps, Silvia Amor-Barris, Birute Burnyte, et al.
Surgery Today|February 15, 2023
The academic impact and value of an international online surgery lecture seriesDaisuke Hashimoto, Aiste Gulla, Sohei Satoi, et al.
Nutrients|September 23, 2022
Sodium, Potassium and Iodine Intake in an Adult Population of LithuaniaUrte Zakauskiene, Ernesta Macioniene, Lina Zabuliene, et al.
European Journal of Medical Genetics|July 5, 2023
Lack of guidelines and translational knowledge is hindering the implementation of psychiatric genetic counseling and testing within Europe - A multi-professional survey studyKati Koido, Charlotta Ingvoldstad Malmgren, Lejla Pojskic, et al.
Pageof 11