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Issue DateTitleAuthor(s)
5-Oct-2022Alanyl-tRNA synthetase 1 gene variants in hereditary neuropathy genotype and phenotype overviewSetlere, Signe; Jurcenko, Marija; Gailite, Linda; Rots, Dmitrijs; Kenina, Viktorija; Department of Doctoral Studies; Scientific Laboratory of Molecular Genetics; Department of Biology and Microbiology
2023The most common European HINT1 neuropathy variant phenotype and its case studiesRozevska, Marija; Rots, Dmitrijs; Gailite, Linda; Linde, Ronalds; Mironovs, Stanislavs; Timcenko, Maksims; Linovs, Viktors; Locmele, Dzintra; Micule, Ieva; Lace, Baiba; Kenina, Viktorija; Scientific Laboratory of Molecular Genetics
23-Jun-2021GJB1 Gene Analysis in Two Extended Families with X-Linked Charcot-Marie-Tooth DiseaseKovale, Sabine; Terauda, Ruta; Millere, Elina; Taurina, Gita; Murmane, Daiga; Isakova, Jekaterina; Kenina, Viktorija; Gailite, Linda; Scientific Laboratory of Molecular Genetics
16-Jun-2022Overview of Neuromuscular Disorder Molecular Diagnostic Experience for the Population of LatviaLace, Baiba; Micule, Ieva; Kenina, Viktorija; Setlere, Signe; Strautmanis, Jurgis; Kazaine, Inese; Taurina, Gita; Murmane, Daiga; Grinfelde, Ieva; Kornejeva, Liene; Krumina, Zita; Sterna, Olga; Radovica-Spalvina, Ilze; Vasiljeva, Inta; Gailite, Linda; Stavusis, Janis; Livcane, Diana; Kidere, Dita; Malniece, Ieva; Inashkina, Inna; Rīga Stradiņš University; Scientific Laboratory of Molecular Genetics
2020Clinical and neurophysiological spectrum of polyneuropathies in childrenMillere, Elīna; Gribuste, Laura; Kazaine, Inese; Strautmanis, Jurgis; Gailite, Linda; Kenina, Viktorija; Rīga Stradiņš University

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