Dietary habits of pregnant women in Bulgaria

por Chamova, R, Panteleeva, M
Publicado 2022

Clinical and genetic diversity of SMN1-negative proximal spinal muscular atrophies

por Peeters, Kristien, Chamova, Teodora, Jordanova, Albena
Publicado 2014

Prevalence and Manifestations of Doctor-Diagnosed Allergies in Bulgarian Families with Atopy

por Pancheva, R, Chamova, R, Toneva, A, Marinova, M
Publicado 2023

Axonal neuropathy with neuromyotonia: there is a HINT

por Peeters, Kristien, Chamova, Teodora, Tournev, Ivailo, Jordanova, Albena
Publicado 2017

Cognitive Impairment and Brain Imaging Characteristics of Patients with Congenital Cataracts, Facial Dysmorphism, Neuropathy Syndrome

por Chamova, Teodora, Zlatareva, Dora, Raycheva, Margarita, Bichev, Stoyan, Kalaydjieva, Luba, Tournev, Ivailo
Publicado 2015

Screening for hereditary transthyretin amyloidosis in Bulgaria

por Nakov, Radislav, Nakov, Ventsislav, Gospodinova, Mariana, Todorov, Tihomir, Todorova, Albena, Chamova, Teodora, Tournev, Ivailo
Publicado 2021

Link between COVID-19 Vaccination Attitudes and Support for Mandatory Childhood Vaccinations

por Chamova, R, Pancheva, R, Rohova, M, Ivanova, E, Hadjieva, S, Mikhailov, N, Kolarova, M, Radeva, N, Paunov, T
Publicado 2023

Description of the first two cases of Pompe disease in Bulgaria

por Tournev, I, Chamova, T, Sinigerska, I, Guergueltcheva, V, Gospodinova, M, Ganova, P, Stoilov, R, Todorova, A, Todorov, T
Publicado 2013

Cardiac involvement and clinical follow up of patients with hereditary transthyretin related amyloidosis associated with Glu89Gln mutation

por Gospodinova, Mariana, Sarafov, Stayko, Guergueltcheva, Velina, Kirov, Andrey, Chamova, Teodora, Todorova, Albena, Tournev, Ivailo, Denchev, Stefan
Publicado 2015

Cardiomyopathy and peripheral polyneuropathy severity in patients with Glu89Gln mutation at the time of diagnosis

por Gospodinova, Mariana, Sarafov, Stayko, Guergueltcheva, Velina, Kirov, Andrey, Chamova, Teodora, Todorova, Albena, Tournev, Ivailo, Denchev, Stefan
Publicado 2015

Association Between Loss of Dp140 and Cognitive Impairment in Duchenne and Becker Dystrophies

por Chamova, T, Guergueltcheva, V, Raycheva, M, Todorov, T, Genova, J, Bichev, S, Bojinova, V, Mitev, V, Tournev, I, Todorova, A
Publicado 201

Epidemiology of Familial Amyloid Polyneuropathy in Bulgaria

por Sarafov, Stayko, Gospodinova, Mariana, Velina, Velina Guergueltcheva, Kirov, Andrei, Teodora, Chamova, Todorov, Tihomir, Todorova, Alebena, Tournev, Ivailo
Publicado 2015

Peripheral myelin protein 2 – a novel cluster of mutations causing Charcot-Marie-Tooth neuropathy

por Palaima, Paulius, Chamova, Teodora, Jander, Sebastian, Mitev, Vanyo, Van Broeckhoven, Christine, Tournev, Ivailo, Peeters, Kristien, Jordanova, Albena
Publicado 2019

Fear of infection or fear of protection – driving factors of COVID-19 vaccine uptake in Bulgaria: Stanislava Hadzhieva

por Rohova, M, Pancheva, R, Mihaylov, NL, Radeva, N, Ivanova, E, Chamova, R, Paunov, Ts, Kolarova, M, Hadzhieva, S
Publicado 2022

Attitudes towards mandatory vaccinations during the COVID-19 pandemic in Bulgaria: Stanislava Hadzhieva

por Hadzhieva, S, Chamova, R, Ivanova, E, Radeva, N, Rohova, M, Mihaylov, NL, Paunov, Ts, Kolarova, M, Pancheva, R
Publicado 2022

Navigating the ALS Genetic Labyrinth: The Role of MAPT Haplotypes

por Tourtourikov, Ivan, Dabchev, Kristiyan, Todorov, Tihomir, Angelov, Teodor, Chamova, Teodora, Tournev, Ivailo, Kadiyska, Tanya, Mitev, Vanyo, Todorova, Albena
Publicado 2023

Novel variant c.92T > G (p.Val31Gly) in the PFN1 gene (ALS18) responsible for a specific phenotype in a large Bulgarian amyotrophic lateral sclerosis pedigree

por Angelov, Teodor, Chamova, Teodora, Atemin, Slavena, Todorov, Tihomir, Ormandzhiev, Slavko, Tourtourikov, Ivan, Todorova, Albena, Devos, David, Tournev, Ivailo
Publicado 2023

Case Report: Transthyretin Glu54Leu—a rare mutation with predominant cardiac phenotype

por Gospodinova, Mariana, Zhelyazkova, Sashka, Chamova, Teodora, Asenov, Ognyan, Pavlova, Zornitsa, Todorov, Tihomir, Mikova, Dilyana, Palashev, Yordan, Gruev, Ivan, Kundurdjiev, Atanas, Todorova, Albena, Tournev, Ivailo
Publicado 2023

Challenges of diagnostic exome sequencing in an inbred founder population

por Azmanov, Dimitar N, Chamova, Teodora, Tankard, Rick, Gelev, Vladimir, Bynevelt, Michael, Florez, Laura, Tzoneva, Dochka, Zlatareva, Dora, Guergueltcheva, Velina, Bahlo, Melanie, Tournev, Ivailo, Kalaydjieva, Luba
Publicado 2013

Seven Years of Selective Genetic Screening Program and Follow-Up of Asymptomatic Carriers With Hereditary Transthyretin Amyloidosis in Bulgaria

por Chamova, Teodora, Gospodinova, Mariana, Asenov, Ognian, Todorov, Tihomir, Pavlova, Zornitsa, Kirov, Andrey, Cherninkova, Sylvia, Kastreva, Kristina, Taneva, Ani, Blagoeva, Stanislava, Zhelyazkova, Sashka, Antimov, Plamen, Chobanov, Kaloian, Todorova, Albena, Tournev, Ivailo
Publicado 2022