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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, Kenina V. Rozevska M, et al. Among authors: kenina v. Front Neurol. 2023 Feb 17;14:1084335. doi: 10.3389/fneur.2023.1084335. eCollection 2023. Front Neurol. 2023. PMID: 36873433 Free PMC article.
Sequential targeted exome sequencing of 1001 patients affected by unexplained limb-girdle weakness.
Töpf A, Johnson K, Bates A, Phillips L, Chao KR, England EM, Laricchia KM, Mullen T, Valkanas E, Xu L, Bertoli M, Blain A, Casasús AB, Duff J, Mroczek M, Specht S, Lek M, Ensini M, MacArthur DG; MYO-SEQ consortium; Straub V. Töpf A, et al. Genet Med. 2020 Sep;22(9):1478-1488. doi: 10.1038/s41436-020-0840-3. Epub 2020 Jun 11. Genet Med. 2020. PMID: 32528171 Free PMC article.
Clinical Phenotyping and Biomarkers in Spinal and Bulbar Muscular Atrophy.
Millere E, Rots D, Glazere I, Taurina G, Kurjane N, Priedite V, Gailite L, Blennow K, Zetterberg H, Kenina V. Millere E, et al. Among authors: kenina v. Front Neurol. 2021 Jan 20;11:586610. doi: 10.3389/fneur.2020.586610. eCollection 2020. Front Neurol. 2021. PMID: 33551952 Free PMC article.
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. Lace B, et al. Among authors: kenina v. Neurol Genet. 2022 May 16;8(3):e685. doi: 10.1212/NXG.0000000000000685. eCollection 2022 Jun. Neurol Genet. 2022. PMID: 36381256 Free PMC article.
26 results