Projects per year
Personal profile
Expertise related to UN Sustainable Development Goals
In 2015, UN member states agreed to 17 global Sustainable Development Goals (SDGs) to end poverty, protect the planet and ensure prosperity for all. This person’s work contributes towards the following SDG(s):
External positions
Clinical Geneticist, Children's Clinical University Hospital
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Collaborations and top research areas from the last five years
Projects
- 1 Finished
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The exploration of genetic factors underlying malformations of cortical development in patients with surgically treated refractory epilepsy
Mičule, I. (Project leader) & Lāce, B. (Supervisor)
1/10/20 → 30/09/24
Project: PhD projects
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Clinical and genetic characterization of Netherton syndrome due to SPINK5 founder variant in Latvian population
Nartisa, I. (Corresponding Author), Kirsteina, R., Neiburga, K. D., Zigure, S., Ozola, L., Grantina, I., Micule, I., Murmane, D., Slisere, B., Gailite, L., Vilne, B., Rots, D., Taurina, G. & Kurjane, N., 1 Apr 2023, In: Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology. 34, 4, e13937.Research output: Contribution to journal › Article › peer-review
Open AccessFile41 Downloads (Pure) -
DYSMORPHIC FEATURES IN A PATIENT WITH GLYCOGEN STORAGE DISEASE TYPE 4: A RARE PHENOTYPIC VARIATION
Rozevska, M., Zariņa, A. & Mičule, I., 2023, p. 60-60. 1 p.Research output: Contribution to conference › Poster › peer-review
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Exploring the role of the SHH gene in development: A case report of two children with Variant of Uncertain Significance
Rozevska, M., Lāce, B., Mičule, I., Grīnfelde, I., Mūrmane, D., Locmele, D., Masinska, M., Piruška, I., Skrabule, L. & Tauriņa, G., 2023, p. 230 - 230. 1 p.Research output: Contribution to conference › Poster › peer-review
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HINT1 NEUROPATHY IN LATVIA: CLINICAL, GENETIC, AND FUNCTIONAL PROFILING
Rozevska, M., Rots, D., Gailīte, L., Linde, R., Mironovs, S., Timčenko, M., Ļiņovs, V., Locmele, D., Mičule, I., Lace, B. & Ķēniņa, V., 2023, In: Medicina (Kaunas). 59, Suppl.2, p. 262 -262 1 p.Research output: Contribution to journal › Meeting Abstract › peer-review
Open Access -
The most common European HINT1 neuropathy variant phenotype and its case studies
Rozevska, M., Rots, D., Gailite, L., Linde, R., Mironovs, S., Timcenko, M., Linovs, V., Locmele, D., Micule, I., Lace, B. (Corresponding Author) & Kenina, V., 2023, In: Frontiers in Neurology. 14, p. 1084335 1084335.Research output: Contribution to journal › Article › peer-review
Open AccessFile1 Citation (Scopus)18 Downloads (Pure)
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HINT1 Neuropathy in Latvia: Clinical, Genetic, and Functional Profiling
Rozevska, M. (Speaker), Rots, D. (Co-author), Gailīte, L. (Co-author), Linde, R. (Co-author), Mironovs, S. (Co-author), Timčenko, M. (Co-author), Ļiņovs, V. (Co-author), Locmele, D. (Co-author), Mičule, I. (Co-author), Lāce, B. (Co-author) & Ķēniņa, V. (Co-author)
29 Mar 2023Activity: Talk or presentation types › Poster presentation
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Diagnostic challenges in patients with suspicions for primary immunodeficiencies in Latvia
Kurjāne, N. (Speaker), Murmane, D. (Speaker), Mičule, I. (Co-author), Kreile, M. (Co-author), Grīnfelde, I. (Co-author), Nartiša, I. (Co-author), Rots, D. (Co-author), Gailīte, L. (Co-author) & Taurina, G. (Co-author)
23 Apr 2021 → 24 Apr 2021Activity: Talk or presentation types › Oral presentation
Press/Media
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Children's Clinical University Hospital Researchers Reveal New Findings on Neuropathy (The most common European HINT1 neuropathy variant phenotype and its case studies)
Rots, D., Mičule, I. & Gailīte, L.
2/03/23
1 item of Media coverage
Press/Media