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Year Number of Results
2010 1
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Page 1
Efficacy and safety of vutrisiran for patients with hereditary transthyretin-mediated amyloidosis with polyneuropathy: a randomized clinical trial.
Adams D, Tournev IL, Taylor MS, Coelho T, Planté-Bordeneuve V, Berk JL, González-Duarte A, Gillmore JD, Low SC, Sekijima Y, Obici L, Chen C, Badri P, Arum SM, Vest J, Polydefkis M; HELIOS-A Collaborators. Adams D, et al. Amyloid. 2023 Mar;30(1):1-9. doi: 10.1080/13506129.2022.2091985. Epub 2022 Jul 23. Amyloid. 2023. PMID: 35875890 Clinical Trial.
Global uncertainty in the diagnosis of neurological complications of SARS-CoV-2 infection by both neurologists and non-neurologists: An international inter-observer variability study.
Tamborska AA, Wood GK, Westenberg E, Garcia-Azorin D, Webb G, Schiess N, Netravathi M, Baykan B, Dervaj R, Helbok R, Lant S, Özge A, Padovani A, Saylor D, Schmutzhard E, Easton A, Lilleker JB, Jackson T, Beghi E, Ellul MA, Frontera JA, Pollak T, Nicholson TR, Wood N, Thakur KT, Solomon T, Stark RJ, Winkler AS, Michael BD; Global NeuroResearch Coalition. Tamborska AA, et al. J Neurol Sci. 2023 Jun 15;449:120646. doi: 10.1016/j.jns.2023.120646. Epub 2023 Apr 11. J Neurol Sci. 2023. PMID: 37100018 Free PMC article.
Varicella zoster virus infection in neurological patients in Bulgaria.
Shikova E, Kumanova A, Tournev I, Zhelyazkova S, Vassileva E, Ivanov I, Pishmisheva M. Shikova E, et al. Among authors: zhelyazkova s. J Neurovirol. 2021 Apr;27(2):272-278. doi: 10.1007/s13365-021-00952-6. Epub 2021 Mar 4. J Neurovirol. 2021. PMID: 33661458
Case Report: Transthyretin Glu54Leu-a rare mutation with predominant cardiac phenotype.
Gospodinova M, Zhelyazkova S, Chamova T, Asenov O, Pavlova Z, Todorov T, Mikova D, Palashev Y, Gruev I, Kundurdjiev A, Todorova A, Tournev I. Gospodinova M, et al. Among authors: zhelyazkova s. Front Cardiovasc Med. 2023 Oct 31;10:1228410. doi: 10.3389/fcvm.2023.1228410. eCollection 2023. Front Cardiovasc Med. 2023. PMID: 38028480 Free PMC article.
Seven Years of Selective Genetic Screening Program and Follow-Up of Asymptomatic Carriers With Hereditary Transthyretin Amyloidosis in Bulgaria.
Chamova T, Gospodinova M, Asenov O, Todorov T, Pavlova Z, Kirov A, Cherninkova S, Kastreva K, Taneva A, Blagoeva S, Zhelyazkova S, Antimov P, Chobanov K, Todorova A, Tournev I. Chamova T, et al. Among authors: zhelyazkova s. Front Neurol. 2022 Apr 8;13:844595. doi: 10.3389/fneur.2022.844595. eCollection 2022. Front Neurol. 2022. PMID: 35463150 Free PMC article.
Chromosomal microarray analysis of Bulgarian patients with epilepsy and intellectual disability.
Peycheva V, Kamenarova K, Ivanova N, Stamatov D, Avdjieva-Tzavella D, Alexandrova I, Zhelyazkova S, Pacheva I, Dimova P, Ivanov I, Litvinenko I, Bozhinova V, Tournev I, Simeonov E, Mitev V, Jordanova A, Kaneva R. Peycheva V, et al. Among authors: zhelyazkova s. Gene. 2018 Aug 15;667:45-55. doi: 10.1016/j.gene.2018.05.015. Epub 2018 May 9. Gene. 2018. PMID: 29753047
Age and Gender Trends in the Prevalence of Markers for Hepatitis E Virus Exposure in the Heterogeneous Bulgarian Population.
Golkocheva-Markova E, Ismailova C, Kevorkyan A, Raycheva R, Zhelyazkova S, Kotsev S, Pishmisheva M, Rangelova V, Stoyanova A, Yoncheva V, Tenev T, Gladnishka T, Trifonova I, Christova I, Dimitrov R, Bruni R, Ciccaglione AR. Golkocheva-Markova E, et al. Among authors: zhelyazkova s. Life (Basel). 2023 Jun 8;13(6):1345. doi: 10.3390/life13061345. Life (Basel). 2023. PMID: 37374127 Free PMC article.
A novel GEFS+ locus on 12p13.33 in a large Roma family.
Morar B, Zhelyazkova S, Azmanov DN, Radionova M, Angelicheva D, Guergueltcheva V, Kaneva R, Scheffer IE, Tournev I, Kalaydjieva L, Sander JW. Morar B, et al. Among authors: zhelyazkova s. Epilepsy Res. 2011 Nov;97(1-2):198-207. doi: 10.1016/j.eplepsyres.2011.08.009. Epub 2011 Sep 13. Epilepsy Res. 2011. PMID: 21917424
13 results