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Page 1
Navigating the ALS Genetic Labyrinth: The Role of MAPT Haplotypes.
Tourtourikov I, Dabchev K, Todorov T, Angelov T, Chamova T, Tournev I, Kadiyska T, Mitev V, Todorova A. Tourtourikov I, et al. Among authors: chamova t. Genes (Basel). 2023 Oct 30;14(11):2023. doi: 10.3390/genes14112023. Genes (Basel). 2023. PMID: 38002967 Free PMC article.
Phenotypic Variability of LGMD 2C/R5 in a Genetically Homogenous Group of Bulgarian Muslim Roma.
Taneva A, Gresham D, Guergueltcheva V, Chamova T, Bojinova V, Gospodinova M, Katzarova M, Petkov R, Voit T, Aneva L, Asenov O, Georgieva B, Mihaylova V, Bichev S, Todorov T, Todorova A, Kalaydjieva L, Tournev I. Taneva A, et al. Among authors: chamova t. Genes (Basel). 2024 Aug 30;15(9):1144. doi: 10.3390/genes15091144. Genes (Basel). 2024. PMID: 39336735 Free PMC article.
Founder effect of the Glu89Gln TTR mutation in the Bulgarian population.
Kirov A, Sarafov S, Pavlova Z, Todorov T, Chamova T, Gospodinova M, Tournev I, Mitev V, Todorova A. Kirov A, et al. Among authors: chamova t. Amyloid. 2019 Dec;26(4):181-185. doi: 10.1080/13506129.2019.1634539. Epub 2019 Jul 29. Amyloid. 2019. PMID: 31353960
MYH7-related disorders in two Bulgarian families: Novel variants in the same region associated with different clinical manifestation and disease penetrance.
Atemin S, Todorov T, Maver A, Chamova T, Georgieva B, Tincheva S, Pacheva I, Ivanov I, Taneva A, Zlatareva D, Tournev I, Guergueltcheva V, Gospodinova M, Chochkova L, Peterlin B, Mitev V, Todorova A. Atemin S, et al. Among authors: chamova t. Neuromuscul Disord. 2021 Jul;31(7):633-641. doi: 10.1016/j.nmd.2021.04.004. Epub 2021 Apr 26. Neuromuscul Disord. 2021. PMID: 34053846
55 results