Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Elīna Millere"'
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
Autor:
Ance Balode, Margarita Apine, Inese Gobiņa, Anete Kopštāla, Elīna Millere, Aigars Miezītis, Dita Heiberga, Santa Pildava, Elīna Tolmačova
Izdevumā “Intervences plānošana dzīvesveida maiņai” ir apvienoti Interreg Baltijas jūras reģiona programmas projektā BaltCityPrevention izstrādātie materiāli un to praktiskā izmantošanā gūtā pieredze. Projektā kopīgi strādāja
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::12da93b2d300358f8437c8eb5bbed1fa
https://doi.org/10.25143/baltcityprevention-rokasgramata_2020_ipd-804
https://doi.org/10.25143/baltcityprevention-rokasgramata_2020_ipd-804
Publikováno v:
SOCIETY. INTEGRATION. EDUCATION. Proceedings of the International Scientific Conference; Vol 4 (2018): SOCIETY. INTEGRATION. EDUCATION. Proceedings of the International Scientific Conference. May 25th-26th, 2018, Volume IV, SPORTS AND HEALTH, ART AND DESIGN; 154-161
Shift work is prevalent in service industries such as hospitals that provide 24-hour coverage. There is no common accepted definition of shift work, but usually shift work is defined as work hours that are scheduled outside daylight (6 am–6 pm) hou
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