Projects per year
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Dive into the research topics where Signe Šetlere is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Projects
- 2 Active
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Discovering biomarkers of disease progression and variability in Charcot-Marie-Tooth neuropathy
Ķēniņa, V., Gailīte, L., Rots, D., Vīksne, K., Šetlere, S., Isakovs, A., Bārdiņa, L. & Glāzere, I.
3/01/22 → 30/12/24
Project: Fundamental and Applied Research Programme
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Support for involving doctoral students in scientific research and studies
Bartuševiča, S., Sīle, L., Lifšics, A., Līcīte, B., Zdanovskis, N., Kiseļova, O., Sokolovska, L., Vinogradova, V. V., Vizgunova-Vikmane, E. E., Miļuna, S., Šneidere, K., Semjonova, G., Kigitoviča, D., Kļaviņa-Makrecka, S., Madelāne, M., Šitovs, A., Kļaviņa, A., Balcere, A., Vanaga, I., Lakiša, S., Grinciuns, M., Mieze, K., Berga-Švītiņa, E., Leidere-Reine, A., Dzudzilo, M., Ozola, M., Avena, L., Brečs, I., Kiščenko, D., Krūmiņa, J., Lucāne, Z., Meidrops, K., Kuļigina, N., Savicka, L., Savickis, V., Šetlere, S., Vargulis, M. & Zariņš, K.
European Social Fund, Latvia State Budget funding
1/04/21 → 30/11/23
Project: EU Structural Funds › ESF
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Alanyl-tRNA synthetase 1 gene variants in hereditary neuropathy genotype and phenotype overview
Setlere, S., Jurcenko, M., Gailite, L., Rots, D. & Kenina, V., 5 Oct 2022, In: Neurology: Genetics. 8, 5, e200019.Research output: Contribution to journal › Article › peer-review
Open AccessFile1 Citation (Scopus)1 Downloads (Pure) -
New-Born Screening for Spinal Muscular Atrophy: Results of a Latvian Pilot Study
Gailite, L., Sterna, O., Konika, M., Isakovs, A., Isakova, J., Micule, I., Setlere, S., Diriks, M. & Auzenbaha, M., Mar 2022, In: International Journal of Neonatal Screening. 8, 1, 15.Research output: Contribution to journal › Article › peer-review
Open AccessFile4 Citations (Scopus)31 Downloads (Pure) -
Overview of Neuromuscular Disorder Molecular Diagnostic Experience for the Population of Latvia
Lace, B., Micule, I., Kenina, V., Setlere, S., Strautmanis, J., Kazaine, I., Taurina, G., Murmane, D., Grinfelde, I., Kornejeva, L., Krumina, Z., Sterna, O., Radovica-Spalvina, I., Vasiljeva, I., Gailite, L., Stavusis, J., Livcane, D., Kidere, D., Malniece, I. & Inashkina, I., 16 Jun 2022, In: Neurology: Genetics. 8, 3, p. 1-8 8 p., e685.Research output: Contribution to journal › Article › peer-review
Open AccessFile1 Citation (Scopus)1 Downloads (Pure) -
Serum Neurofilament Light Chain As Biomarker of Charcot-marie-tooth Disease Type 1x Progression
Grosmane, A., Glazunovs, D., Setlere, S., Gailite, L., Glazere, I., Kalnina, M., Rots, D. & Kenina, V., Jul 2022, In: Journal of the Peripheral Nervous System. 27, S3, p. S181-S181 1 p., 61e.Research output: Contribution to journal › Meeting Abstract › peer-review
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Diagnostic challenges in hereditary peripheral neuropathy in Latvia
Millere, E., Kupats, E., Rots, D., Setlere, S., Mičule, I., Gailīte, L. & Kenina, V., 24 Mar 2021, p. 208.Research output: Contribution to conference › Abstract › peer-review