Projects per year
Personal profile
Education/Academic qualification
3.2 Clinical medicine, Expert, Latvian Council of Science
3 Dec 2020 → 2 Dec 2023
3.2 Clinical medicine, Expert, Latvian Council of Science
21 Sep 2017 → 20 Sep 2020
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Dive into the research topics where Viktorija Ķēniņa is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Network
Recent external collaboration on country/territory level. Dive into details by clicking on the dots or
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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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Discovering biomarkers of disease progression and variability in Charcot-Marie-Tooth neuropathy
Ķēniņa, V., Rots, D. & Gailīte, L.
12/07/21 → 11/07/22
Project: RSU grants
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Predominantly primary antibody deficiencies among adults: solving etiology and causes of clinical variability
Kurjāne, N., Gailīte, L., Rots, D., Kaņepa, A., Lucane, Z., Nartiša, I., Neiburga, K. D., Ozola, L. & Ķēniņa, V.
1/01/21 → 31/12/23
Project: Fundamental and Applied Research Programme
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Discovering biomarkers of disease progression and variability in Charcot-Marie-Tooth neuropathy
Ķēniņa, V., Rots, D., Vilne, B., Gailīte, L. & Isakova, J.
1/09/20 → 31/08/21
Project: RSU grants
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Chronic Inflammatory Demyelinating Polyneuropathy: Characteristics and Epidemiology in Latvia.
Glāzere, I., Roddate, M., Žukova, V., Rots, D., Gailīte, L., Kurjāne, N. & Ķēniņa, V., 2021, p. 164-165. 2 p.Research output: Contribution to conference › Abstract › peer-review
Open Access -
Clinical Phenotyping and Biomarkers in Spinal and Bulbar Muscular Atrophy
Millere, E., Rots, D., Glāzere, I., Tauriņa, G., Kurjāne, N., Priedīte, V., Gailīte, L., Blennov, K., Zetterberg, H. & Ķēniņa, V., 20 Jan 2021, In: Frontiers in Neurology. 11, 8 p., 586610.Research output: Contribution to journal › Article › peer-review
Open AccessFile1 Citation (Scopus) -
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
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Fragile X syndrome and multifocal motor neuropathy coexistance: case report
Millere, E., Mūrmane, D., Daneberga, Z. & Ķēniņa, V., 24 Mar 2021, p. 463.Research output: Contribution to conference › Abstract › peer-review
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GENOTYPE – PHENOTYPE ASSOCIATIONS IN CHARCOT-MARIE-TOOTH DISEASE
Šetlere, S., Millere, E., Kupats, E., Rots, D., Micule, I., Gailīte, L. & Ķēniņa, V., 23 Apr 2021, In: Medicina (Kaunas). 57, Suppl.1, p. 181Research output: Contribution to journal › Meeting Abstract › peer-review
Activities
- 3 Membership of NGOs
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Scientific Panel on Muscle and NMJ disorders of the European Academy of Neurology (External organisation)
Viktorija Ķēniņa (Member)
2018 → …Activity: Membership types › Membership of NGOs
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Scientific Panel on Neuropathies of the European Academy of Neurology (External organisation)
Viktorija Ķēniņa (Member)
2018 → …Activity: Membership types › Membership of NGOs
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Latvian Society of Neuroimmuologists (External organisation)
Viktorija Ķēniņa (Head)
22 Jan 2012 → …Activity: Membership types › Membership of NGOs