Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Viktorija Ķēniņa"'
Autor:
Sabine Kovale, Ruta Terauda, Elina Millere, Gita Taurina, Daiga Murmane, Jekaterina Isakova, Viktorija Kenina, Linda Gailite
Publikováno v:
Case Reports in Neurology, Vol 13, Iss 2, Pp 422-428 (2021)
X-linked Charcot-Marie-Tooth (CMT) disease type I (CMTX1) is the second most frequent type of CMT disease caused by pathogenic variants in the GJB1 gene. We described 2 extended cases (families) with CMTX1 with identified pathogenic variants – p.Va
Externí odkaz:
https://doaj.org/article/30bb1c773fa74c88a1a7c25907d4fa00
Autor:
Elina Millere, Dmitrijs Rots, Ieva Glazere, Gita Taurina, Natalja Kurjane, Viktorija Priedite, Linda Gailite, Kaj Blennow, Henrik Zetterberg, Viktorija Kenina
Publikováno v:
Frontiers in Neurology, Vol 11 (2021)
Background: Spinal and bulbar muscular atrophy (SBMA) or Kennedy disease [OMIM: 313200] is a rare X-linked neuromuscular disease. Patients commonly present with muscle cramps, tremors, leg weakness, dysarthria and dysphagia.Methods: We deeply phenoty
Externí odkaz:
https://doaj.org/article/40caeab967b3455e9f2449ece8f61b48
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:
Kristine Ivanova, Olga Ribakova, Anna Mihailova, Evelina Mozeitovica, Anda Kadisa, Julija Zepa, Viktorija Kenina, Natalja Kurjane, Inita Bulina
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-9 (2024)
Abstract Background Systemic sclerosis (SSc) is considered by many to be one of the most severe autoimmune rheumatic diseases with lower prevalence observed in Northern Europe. No previous studies on the prevalence of SSc in Latvia have been conducte
Externí odkaz:
https://doaj.org/article/c540456a22c240b6a63d34e9e2c33b0e
Autor:
Amol K. Bhandage, Viktorija Kenina, Yu-Fang Huang, Marija Roddate, Gundega Kauke, Arta Grosmane, Violeta Žukova, Niclas Eriksson, Katja Gabrysch, Tanel Punga, Anna Rostedt Punga
Publikováno v:
iScience, Vol 27, Iss 8, Pp 110564- (2024)
Summary: There is an unmet need for objective disease-specific biomarkers in the heterogeneous autoimmune neuromuscular disorder myasthenia gravis (MG). This cross-sectional study identified a signature of 23 inflammatory serum proteins with proximit
Externí odkaz:
https://doaj.org/article/0e664d4197994f5d9651a964aa974e10