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Neuromuscular Disorders : NMD|September 12, 2016
Myotonia congenita type Becker in Bulgaria: First genetically proven cases and mutation screening of two presumable endemic regionsSavina Tincheva, Bilyana Georgieva, Tihomir Todorov, et al.Non-Coding RNA Research|November 30, 2023
miRNAs and related genetic biomarkers according to the WHO glioma classification: From diagnosis to future therapeutic targetsEmiliya Nikolova, Lili Laleva, Milko Milev, et al.Journal of Gastrointestinal and Liver Diseases : JGLD|December 12, 2019
Gastrointestinal Manifestations in Hereditary Transthyretin Amyloidosis associated with Glu89Gln MutationRadislav Nakov, Stayko Sarafov, Ventsislav Nakov, et al.American Journal of Medical Genetics. Part A|March 15, 2019
First case of Roma ethnic origin with Andermann syndrome: A novel frameshift mutation in exon 20 of SLC12A6 geneIliyana Pacheva, Tihomir Todorov, Zeyra Halil, et al.Journal of Cardiovascular Medicine (Hagerstown, Md.)|August 3, 2020
Cardiac involvement, morbidity and mortality in hereditary transthyretin amyloidosis because of p.Glu89Gln mutationMariana Gospodinova, Stayko Sarafov, Teodora Chamova, et al.Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|July 30, 2019
Founder effect of the Glu89Gln TTR mutation in the Bulgarian populationAndrey Kirov, Stayko Sarafov, Zornitza Pavlova, et al.BMJ Case Reports|June 21, 2011
Fragile X mosaic male full mutation/normal allele detected by PCR/MS-MLPATihomir Todorov, Albena Todorova, Andrey Kirov, et al.Epilepsy Research|January 29, 2013
15q13.3 microdeletions in a prospectively recruited cohort of patients with idiopathic generalized epilepsy in BulgariaAndrey Kirov, Petia Dimova, Albena Todorova, et al.Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|June 2, 2021
Characterization of population genetic structure of hereditary transthyretin amyloidosis in BulgariaZornitsa Pavlova, Stayko Sarafov, Tihomir Todorov, et al.Biomedicines|July 27, 2024
CYP21A2 Intron 2 Genetic Variants Might Be Associated with the Clinical Characteristics of Women with PCOSRalitsa Robeva, Silvia Andonova, Tihomir Todorov, et al.Pageof 7