Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Viktorija Ķēniņa"'
Autor:
Kristīne Ivanova, Maksims Zolovs, Kaj Blennow, Henrik Zetterberg, Nataļja Kurjāne, Viktorija Ķēniņa
Publikováno v:
Frontiers in Medicine, Vol 11 (2024)
IntroductionSystemic sclerosis (SSc) is a rare autoimmune disease with multiple organ involvement; however, the contribution of the nervous system (NS) remains relatively understudied. There are no specific data on the role of the autoimmune response
Externí odkaz:
https://doaj.org/article/4e1eb746b21a4b3a98ffe5da0dd1535d
Autor:
Arta Grosmane, Ieva Roze, Marija Roddate, Gundega Ķauķe, Violeta Žukova, Ieva Glāzere, Maksims Zolovs, Viktorija Ķēniņa
Publikováno v:
Frontiers in Neurology, Vol 15 (2024)
IntroductionOur aim was to translate, adapt and validate the Myasthenia Gravis Activities of Daily Living scale into the Latvian language and to evaluate this instrument (MG-ADL-L) in terms of construct validity and reliability.MethodsWe enrolled pat
Externí odkaz:
https://doaj.org/article/c66271902711439d99530a86b885733a
Publikováno v:
Medicina, Vol 59, Iss 5, p 935 (2023)
Background and Objectives: Parkinson’s disease (PD) is a chronic, progressive illness with a profound impact on health-related quality of life, and it is crucial to know what factors influence the quality of life throughout the course of the diseas
Externí odkaz:
https://doaj.org/article/c595e75d406e433a94ab00aed23efb6f
Autor:
Kristīne Ivanova, Daniils Žukovs, Evelīna Možeitoviča, Dmitrijs Rots, Nataļja Kurjāne, Viktorija Ķēniņa
Publikováno v:
Neurologia i Neurochirurgia Polska. 57:206-211
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::15f6f7e6782861a43f996b856bdc04cd
https://doi.org/10.5603/pjnns.a2023.0018
https://doi.org/10.5603/pjnns.a2023.0018
Autor:
Vladimirs Krutovs, Gundega Ķauķe, Marija Roddate, Maksims Timčenko, Evija Miglāne, Viktorija Ķēniņa
Publikováno v:
International Journal of Scientific Reports. 9:157-160
Myasthenia gravis is an autoimmune disease that causes weakness in the skeletal muscles. It is considered to be a relatively rare disease. Most commonly the first symptoms are associated with ocular muscle weakness resulting in ptosis and/or diplopia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c19d1f0f5b3c634b57aa5b14459598ae
https://doi.org/10.18203/issn.2454-2156.intjscirep20231012
https://doi.org/10.18203/issn.2454-2156.intjscirep20231012
Publikováno v:
Proceedings of the Latvian Academy of Sciences. Section B. Natural, Exact, and Applied Sciences.. 76:232-238
Inherited peripheral neuropathies (IPN) are a clinically and genetically heterogeneous group of disorders. The most common IPN is Charcot-Marie-Tooth (CMT) disease. Here we describe IPN clinical variability and diagnostic characteristics in the Latvi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::892929aaaff69fc33fad9c3bbdbf85fc
https://doi.org/10.2478/prolas-2022-0035
https://doi.org/10.2478/prolas-2022-0035
Autor:
Dace Ziemele, Marija Litviņenko, Viktorija Ķēniņa, Mārīte Karlovska, Guntis Karelis, Lana Vainšteine
Publikováno v:
Journal of Pharmacy and Pharmacology. 6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4715e9e7dae643aabb239f7b42a7f864
https://doi.org/10.17265/2328-2150/2018.02.002
https://doi.org/10.17265/2328-2150/2018.02.002
Autor:
Viktorija Ķēniņa, Guntis Karelis, Lana Vainšteine, Natalja Zlobina, Andrejs Kostiks, Angelika Krūmiņa
Publikováno v:
Proceedings of the Latvian Academy of Sciences. Section B, Natural Sciences, Vol 69, Iss 5, Pp 269-273 (2015)
Terapeitiska plazmas apmaiņa (TPA) tiek lietota noteiktu neiroloģisku saslimšanu gadījumos ar mērķi no organisma izvadīt imūnglobulīnus un citas imunoloģiski aktīvas substances. Pētījumā tika ietverti un izvērtēti pacienti, kas ārst
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::427d8b02eed89ec7cbde3a6afdbb1518
https://doi.org/10.1515/prolas-2015-0041
https://doi.org/10.1515/prolas-2015-0041
Publikováno v:
Proceedings of the Latvian Academy of Sciences. Section B, Natural Sciences, Vol 69, Iss 5, Pp 223-227 (2015)
Visbiežāk atrastās autoantivielas asociācijā ar perifērām neiropātijām ir pret gangliozīdiem GM1, GQ1b, asialo-GM1, GM2, GD1a un GD1b. Atzīta diagnostiska vērtība ir divām no tām - anti-GM1 un anti-GQ1b. Tika veikts retrospektīvs pēt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e3282ee46d9091eebb0974664b5776a
https://doaj.org/article/b289a2b9fc214a0c82318ffd3581a7e8
https://doaj.org/article/b289a2b9fc214a0c82318ffd3581a7e8
Autor:
Inese Kamša, Viktorija Ķēniņa, Maruta S. Naudiņa, Anete Zieda, Lelde Pelčere, Kristīne Rāviņa, Nataļja Kurjāne
Publikováno v:
Proceedings of the Latvian Academy of Sciences. Section B, Natural Sciences, Vol 69, Iss 5, Pp 210-214 (2015)
Myasthenia gravis (MG) ir autoimūna saslimšana, ko raksturo muskuļu vājums un pastiprināta nogurdināmība auto-antivielu izraisītu neiromuskulārās pārvades traucējumu dēļ. Šo auto-antivielu produkcijā ir iesaistīts aizkrūts dziedzeri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::337b8f93ebbf9e0d186c25e4b2490087
https://doaj.org/article/7b7bf2c2b436420f9cc2f78543317208
https://doaj.org/article/7b7bf2c2b436420f9cc2f78543317208