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Page 1
Case Report: Two Families With HPDL Related Neurodegeneration.
Front Genet. 2022 Feb 9;13:780764. doi: 10.3389/fgene.2022.780764. eCollection 2022.
Front Genet. 2022.
PMID: 35222531
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: kidere d.
Neurol Genet. 2022 May 16;8(3):e685. doi: 10.1212/NXG.0000000000000685. eCollection 2022 Jun.
Neurol Genet. 2022.
PMID: 36381256
Free PMC article.
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Impact of the m.13513G>A Variant on the Functions of the OXPHOS System and Cell Retrograde Signaling.
Kidere D, Zayakin P, Livcane D, Makrecka-Kuka M, Stavusis J, Lace B, Lin TK, Liou CW, Inashkina I.
Kidere D, et al.
Curr Issues Mol Biol. 2023 Feb 22;45(3):1794-1809. doi: 10.3390/cimb45030115.
Curr Issues Mol Biol. 2023.
PMID: 36975485
Free PMC article.
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Novel mutations in MYBPC1 are associated with myogenic tremor and mild myopathy.
Stavusis J, Lace B, Schäfer J, Geist J, Inashkina I, Kidere D, Pajusalu S, Wright NT, Saak A, Weinhold M, Haubenberger D, Jackson S, Kontrogianni-Konstantopoulos A, Bönnemann CG.
Stavusis J, et al. Among authors: kidere d.
Ann Neurol. 2019 Jul;86(1):129-142. doi: 10.1002/ana.25494. Epub 2019 May 17.
Ann Neurol. 2019.
PMID: 31025394
Free PMC article.
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Collagen VI-related limb-girdle syndrome caused by frequent mutation in COL6A3 gene with conflicting reports of pathogenicity.
Stavusis J, Micule I, Wright NT, Straub V, Topf A, Panadés-de Oliveira L, Domínguez-González C, Inashkina I, Kidere D, Chrestian N, Lace B.
Stavusis J, et al. Among authors: kidere d.
Neuromuscul Disord. 2020 Jun;30(6):483-491. doi: 10.1016/j.nmd.2020.03.010. Epub 2020 Apr 18.
Neuromuscul Disord. 2020.
PMID: 32448721
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