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Year Number of Results
2011 1
2019 2
2020 4
2021 3
2022 2
2023 6
2024 0

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17 results

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Page 1
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.
A randomized, double-blind, placebo-controlled phase 2 study to assess safety, tolerability, and efficacy of RT001 in patients with amyotrophic lateral sclerosis.
Weemering DN, Midei M, Milner P, Gopalakrishnan V, Kumar A, Dannenberg AJ, Bunte TM, Foucher J, Ingre C, Ķēniņa V, Rallmann K, van den Berg LH, van Eijk RPA. Weemering DN, et al. Among authors: kenina v. Eur J Neurol. 2023 Dec;30(12):3722-3731. doi: 10.1111/ene.16020. Epub 2023 Aug 21. Eur J Neurol. 2023. PMID: 37550954 Clinical Trial.
The role of HHV-6 and HHV-7 infections in the development of fibromyalgia.
Krumina A, Chapenko S, Kenina V, Mihailova M, Logina I, Rasa S, Gintere S, Viksna L, Svirskis S, Murovska M. Krumina A, et al. Among authors: kenina v. J Neurovirol. 2019 Apr;25(2):194-207. doi: 10.1007/s13365-018-0703-8. Epub 2019 Jan 7. J Neurovirol. 2019. PMID: 30617851 Free PMC article.
Neuroinflammatory Disease as an Isolated Manifestation of Hemophagocytic Lymphohistiocytosis.
Blincoe A, Heeg M, Campbell PK, Hines M, Khojah A, Klein-Gitelman M, Talano JA, Speckmann C, Touzot F, Lankester A, Legger GE, Rivière JG, Garcia-Prat M, Alonso L, Putti MC, Lehmberg K, Maier S, El Chazli Y, Elmaksoud MA, Astigarraga I, Kurjane N, Bulina I, Kenina V, Bryceson Y, Rascon J, Lortie A, Goldstein G, Booth C, Worth A, Wassmer E, Schmitt EG, Warren JT, Bednarski JJ, Ali S, Chiang KY, Krueger J, Henry MM, Holland SM, Marsh RA, Ehl S, Haddad E. Blincoe A, et al. Among authors: kenina v. J Clin Immunol. 2020 Aug;40(6):901-916. doi: 10.1007/s10875-020-00814-6. Epub 2020 Jul 7. J Clin Immunol. 2020. PMID: 32638196
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.
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.
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.
17 results